Faculty Profiles - HASHIMOTO Masato

写真a

HASHIMOTO Masato

Name of department

Faculty of Systems Engineering, Chemistry

Job title

Professor

Mail Address

Homepage

External link

Education

1986

-

1991

The University of Tokyo Graduate School of Science Department of Chemistry, MSc and PhD
1982

-

1986

The University of Tokyo Faculty of Science 化学

Degree

Doctor of Science 1991
Master of Science 1988

Academic & Professional Experience

2020.04

-

Now

Wakayama University 評議員
2015.04

-

2018.03

和歌山大学システム工学部副学部長
2010.10

-

Now

Wakayama University システム工学部 Professor
1997.04

-

2010.09

Wakayama University, Associate professor システム工学部助教授(准教授)
1994.05

-

1997.03

Umeå University, Sweden, Posdoc researcher
1991.04

-

1994.04

The University of Tokyo, Research associate 工学部合成化学科助手

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Association Memberships

近畿工業化学会
ドイツ化学会
日本結晶学会
日本化学会
王立化学会(イギリス)
触媒学会
アメリカ化学会
IUPAC

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Research Areas

Nanotechnology/Materials / Inorganic and coordination chemistry / 無機合成化学、無機構造化学、無機溶液化学、ポリオキソメタレート、ペルオキソメタレート

Classes (including Experimental Classes, Seminars, Graduation Thesis Guidance, Graduation Research, and Topical Research)

2023 Introductory Seminar in Systems Engineering Specialized Subjects
2023 Scientific and Technical English B Specialized Subjects
2023 Graduation Research Specialized Subjects
2023 Experiments in Applied Chemistry Specialized Subjects
2023 Advanced Lectures in Chemistry Specialized Subjects
2023 Experiments in Chemistry Ⅲ Specialized Subjects
2023 Inorganic Chemistry Ⅱ Specialized Subjects
2023 Experiments in Chemistry IV Specialized Subjects
2023 Structural Chemistry Specialized Subjects
2023 Inorganic Chemistry Ⅰ Specialized Subjects
2022 Inorganic Chemistry Ⅱ Specialized Subjects
2022 Inorganic Chemistry Ⅰ Specialized Subjects
2022 Graduation Research Specialized Subjects
2022 Graduation Research Specialized Subjects
2022 Experiments in Material Science andChemistry C Specialized Subjects
2022 Seminar in Material Science and Chemistry ⅡA Specialized Subjects
2022 Seminar in Material Science and Chemistry ⅠA Specialized Subjects
2022 Structural Chemistry Specialized Subjects
2022 Scientific and Technical English B Specialized Subjects
2022 Advanced Lectures in Chemistry Specialized Subjects
2022 Experiments in Chemistry IV Specialized Subjects
2022 Experiments in Chemistry Ⅲ Specialized Subjects
2022 Experiments in Applied Chemistry Specialized Subjects
2021 Graduation Research Specialized Subjects
2021 Structural Chemistry Specialized Subjects
2021 Experiments in Chemistry Ⅲ Specialized Subjects
2021 Advanced Lectures in Chemistry Specialized Subjects
2021 Experiments in Applied Chemistry Specialized Subjects
2021 Inorganic Chemistry Ⅰ Specialized Subjects
2021 Inorganic Chemistry Ⅱ Specialized Subjects
2021 Graduation Research Specialized Subjects
2021 Graduation Research Specialized Subjects
2021 Scientific and Technical English B Specialized Subjects
2021 Experiments in Chemistry IV Specialized Subjects
2021 Introductory Seminar in Systems Engineering Specialized Subjects
2021 Experiments in Material Science andChemistry C Specialized Subjects
2021 Seminar in Material Science and Chemistry ⅡA Specialized Subjects
2021 Seminar in Material Science and Chemistry ⅠA Specialized Subjects
2020 Graduation Research Specialized Subjects
2020 Graduation Research Specialized Subjects
2020 Experiments in Chemistry IV Specialized Subjects
2020 Experiments in Chemistry Ⅲ Specialized Subjects
2020 Scientific and Technical English B Specialized Subjects
2020 Experiments in Applied Chemistry Specialized Subjects
2020 Advanced Lectures in Chemistry Specialized Subjects
2020 Structural Chemistry Specialized Subjects
2020 Seminar in Material Science and Chemistry ⅡA Specialized Subjects
2020 Seminar in Material Science and Chemistry ⅠA Specialized Subjects
2020 Experiments in Material Science andChemistry C Specialized Subjects
2020 Inorganic Chemistry Ⅱ Specialized Subjects
2020 Inorganic Chemistry Ⅰ Specialized Subjects
2019 Graduation Research Specialized Subjects
2019 Experiments in Chemistry Ⅲ Specialized Subjects
2019 Scientific and Technical English B Specialized Subjects
2019 Experiments in Material Science and Chemistry Specialized Subjects
2019 Experiments in Applied Chemistry Specialized Subjects
2019 Advanced Lectures in Chemistry Specialized Subjects
2019 Structural Chemistry Specialized Subjects
2019 Introduction to Majors 2 Specialized Subjects
2019 Introduction to Majors 2 Specialized Subjects
2019 Seminar in Material Science and Chemistry ⅡA Specialized Subjects
2019 Seminar in Material Science and Chemistry ⅠA Specialized Subjects
2019 Experiments in Material Science andChemistry C Specialized Subjects
2019 Inorganic Chemistry Ⅱ Specialized Subjects
2019 Inorganic Chemistry Ⅰ Specialized Subjects
2019 Experiments in Material Science andChemistry B Specialized Subjects
2018 Structural Chemistry Specialized Subjects
2018 Exercises in Majors A Specialized Subjects
2018 Introduction to Majors 2 Specialized Subjects
2018 Introduction to Majors 1 Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Exercises in Majors C Specialized Subjects
2018 Exercises in Majors B Specialized Subjects
2018 Introduction to Majors 2 Specialized Subjects
2018 Introduction to Majors 1 Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Scientific and Technical English B Specialized Subjects
2018 Experiments in Material Science and Chemistry Specialized Subjects
2018 Experiments in Applied Chemistry Specialized Subjects
2018 Advanced Lectures in Chemistry Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Introductory Seminar in Systems Engineering Specialized Subjects
2018 Seminar in Material Science and Chemistry ⅡA Specialized Subjects
2018 Seminar in Material Science and Chemistry ⅠA Specialized Subjects
2018 Special Lecture Ⅱ for Nano-science Specialized Subjects
2018 Special Lecture Ⅰ for Nano-science Specialized Subjects
2018 Experiments in Material Science andChemistry C Specialized Subjects
2018 Inorganic Chemistry Ⅱ Specialized Subjects
2018 Inorganic Chemistry Ⅰ Specialized Subjects
2017 Exercises in Majors C Specialized Subjects
2017 Exercises in Majors B Specialized Subjects
2017 Exercises in Majors A Specialized Subjects
2017 Experiments in Material Science and Chemistry Specialized Subjects
2017 Structural Chemistry Specialized Subjects
2017 Introduction to Majors 2 Specialized Subjects
2017 Introduction to Majors 2 Specialized Subjects
2017 Introduction to Majors 1 Specialized Subjects
2017 Introduction to Majors 1 Specialized Subjects
2017 Introductory Seminar in Systems Engineering Specialized Subjects
2017 Seminar in Material Science and Chemistry ⅡA Specialized Subjects
2017 Seminar in Material Science and Chemistry ⅠA Specialized Subjects
2017 Special Lecture Ⅱ for Nano-science Specialized Subjects
2017 Special Lecture Ⅰ for Nano-science Specialized Subjects
2017 Experiments in Material Science andChemistry C Specialized Subjects
2017 Inorganic Chemistry Ⅱ Specialized Subjects
2017 Inorganic Chemistry Ⅰ Specialized Subjects
2017 Experiments in Material Science andChemistry B Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Seminar in Material Science and Chemistry ⅡA Specialized Subjects
2016 Seminar in Material Science and Chemistry ⅠA Specialized Subjects
2016 Experiments in Material Science andChemistry C Specialized Subjects
2016 Experiments in Material Science andChemistry B Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Experiments in Material Science andChemistry A Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Introductory Seminar in Systems Engineering Specialized Subjects
2016 Structural Chemistry Specialized Subjects
2016 Exercises in Majors C Specialized Subjects
2016 Exercises in Majors B Specialized Subjects
2016 Exercises in Majors A Specialized Subjects
2016 Introduction to Majors 2 Specialized Subjects
2016 Introduction to Majors 2 Specialized Subjects
2016 Introduction to Majors 1 Specialized Subjects
2016 Introduction to Majors 1 Specialized Subjects
2016 Special Lecture Ⅱ for Nano-science Specialized Subjects
2016 Special Lecture Ⅰ for Nano-science Specialized Subjects
2016 Inorganic Chemistry Ⅰ Specialized Subjects
2015 Inorganic Chemistry A Specialized Subjects
2015 Experiments in Material Science andChemistry C Specialized Subjects
2015 Experiments in Material Science andChemistry A Specialized Subjects
2015 Seminar in Material Science and Chemistry ⅠA Specialized Subjects
2015 Introduction to Majors 2 Specialized Subjects
2015 Introduction to Majors 2 Specialized Subjects
2015 Introduction to Majors 1 Specialized Subjects
2015 Introduction to Majors 1 Specialized Subjects
2015 Special Lecture Ⅱ for Nano-science Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Introductory Seminar in Systems Engineering Specialized Subjects
2015 Inorganic Chemistry B Specialized Subjects
2015 Experiments in Material Science andChemistry B Specialized Subjects
2015 Seminar in Material Science and Chemistry ⅡA Specialized Subjects
2015 Advanced Material Science andChemistry Ⅱ Specialized Subjects
2015 Exercises in Majors C Specialized Subjects
2015 Exercises in Majors B Specialized Subjects
2015 Exercises in Majors A Specialized Subjects
2015 Special Lecture Ⅰ for Nano-science Specialized Subjects
2014 Seminar in Material Science and Chemistry ⅡA Specialized Subjects
2014 Seminar in Material Science and Chemistry ⅠA Specialized Subjects
2014 Inorganic Chemistry B Specialized Subjects
2014 Inorganic Chemistry A Specialized Subjects
2014 Advanced Material Science andChemistry Ⅱ Specialized Subjects
2014 Advanced Material Science andChemistry Ⅰ Specialized Subjects
2014 Special Lecture Ⅱ for Nano-science Specialized Subjects
2014 Special Lecture Ⅰ for Nano-science Specialized Subjects
2014 Experiments in Material Science andChemistry C Specialized Subjects
2014 Introduction to Material Science andChemistry Specialized Subjects
2014 Experiments in Material Science andChemistry B Specialized Subjects
2014 Experiments in Material Science andChemistry A Specialized Subjects
2014 Introductory Seminar Liberal Arts and Sciences Subjects
2013 Graduation Research Specialized Subjects
2013 Graduation Research Specialized Subjects
2013 Seminar in Material Science and Chemistry ⅡA Specialized Subjects
2013 Seminar in Material Science and Chemistry ⅠA Specialized Subjects
2013 Inorganic Chemistry B Specialized Subjects
2013 Inorganic Chemistry A Specialized Subjects
2013 Advanced Material Science andChemistry Ⅱ Specialized Subjects
2013 Advanced Material Science andChemistry Ⅰ Specialized Subjects
2013 Special Lecture Ⅱ for Nano-science Specialized Subjects
2013 Special Lecture Ⅰ for Nano-science Specialized Subjects
2013 Experiments in Material Science andChemistry C Specialized Subjects
2013 Introduction to Material Science andChemistry Specialized Subjects
2013 Experiments in Material Science andChemistry B Specialized Subjects
2013 Experiments in Material Science andChemistry A Specialized Subjects
2013 Chemistry in Environments Liberal Arts and Sciences Subjects
2013 Introductory Seminar Liberal Arts and Sciences Subjects
2012 Graduation Research Specialized Subjects
2012 Inorganic Chemistry A Specialized Subjects
2012 Introduction to Material Science andChemistry Specialized Subjects
2012 Experiments in Material Science andChemistry C Specialized Subjects
2012 Experiments in Material Science andChemistry A Specialized Subjects
2012 Advanced Material Science andChemistry Ⅰ Specialized Subjects
2012 Chemistry in Environments Liberal Arts and Sciences Subjects
2012 Introductory Seminar Liberal Arts and Sciences Subjects
2012 Special Lecture Ⅱ for Nano-science Specialized Subjects
2012 Inorganic Chemistry B Specialized Subjects
2012 Experiments in Material Science andChemistry B Specialized Subjects
2012 Advanced Material Science andChemistry Ⅱ Specialized Subjects
2012 Special Lecture Ⅰ for Nano-science Specialized Subjects
2011 Experiments in Material Science andChemistry C Specialized Subjects
2011 Experiments in Material Science andChemistry B Specialized Subjects
2011 Experiments in Material Science andChemistry A Specialized Subjects
2011 Advanced Material Science andChemistry Ⅱ Specialized Subjects
2011 Advanced Material Science andChemistry Ⅰ Specialized Subjects
2011 Special Lecture Ⅱ for Nano-science Specialized Subjects
2011 Special Lecture Ⅰ for Nano-science Specialized Subjects
2011 Inorganic Chemistry B Specialized Subjects
2011 Inorganic Chemistry A Specialized Subjects
2011 Chemistry in Environments Liberal Arts and Sciences Subjects
2010 Graduation Research Specialized Subjects
2010 Chemistry in Environments Specialized Subjects
2010 Practices in Chemistry Specialized Subjects
2010 Inorganic Chemistry A Specialized Subjects
2010 Inorganic Chemistry B Specialized Subjects
2010 NA Specialized Subjects
2010 NA Specialized Subjects
2010 NA Specialized Subjects
2010 NA Specialized Subjects
2010 NA Specialized Subjects
2010 NA Specialized Subjects
2010 NA Specialized Subjects
2009 NA Specialized Subjects
2009 NA Specialized Subjects
2009 NA Specialized Subjects
2009 NA Specialized Subjects
2009 NA Specialized Subjects
2009 NA Specialized Subjects
2009 NA Specialized Subjects
2009 NA Specialized Subjects
2009 NA Specialized Subjects
2009 NA Specialized Subjects
2009 Graduation Research Specialized Subjects
2009 Chemistry in Environments Liberal Arts and Sciences Subjects
2008 NA Specialized Subjects
2008 NA Specialized Subjects
2008 NA Specialized Subjects
2008 NA Specialized Subjects
2008 NA Specialized Subjects
2008 NA Specialized Subjects
2008 NA Specialized Subjects
2008 NA Specialized Subjects
2008 NA Specialized Subjects
2008 NA Specialized Subjects
2008 Introduction to Material Science andChemistry Specialized Subjects
2008 Graduation Research Specialized Subjects
2008 Chemistry in Environments Liberal Arts and Sciences Subjects
2007 NA Specialized Subjects
2007 NA Specialized Subjects
2007 NA Specialized Subjects
2007 NA Specialized Subjects
2007 NA Specialized Subjects
2007 NA Specialized Subjects
2007 NA Specialized Subjects
2007 NA Specialized Subjects
2007 NA Specialized Subjects
2007 NA Specialized Subjects
2007 Graduation Research Specialized Subjects
2007 Chemistry in Environments Liberal Arts and Sciences Subjects

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Classes

2023 Systems Engineering SeminarⅠA Master's Course
2023 Systems Engineering SeminarⅠB Master's Course
2023 Systems Engineering SeminarⅡA Master's Course
2023 Systems Engineering SeminarⅡB Master's Course
2023 Chemistry of Inorganic Reactions Master's Course
2023 Systems Engineering Project SeminarⅠA Master's Course
2023 Systems Engineering Project SeminarⅠB Master's Course
2023 Systems Engineering Project SeminarⅡA Master's Course
2023 Systems Engineering Project SeminarⅡB Master's Course
2023 Systems Engineering Advanced Seminar Ⅰ Doctoral Course
2023 Systems Engineering Advanced Seminar Ⅰ Doctoral Course
2023 Systems Engineering Advanced Seminar Ⅱ Doctoral Course
2023 Systems Engineering Advanced Seminar Ⅱ Doctoral Course
2023 Systems Engineering Advanced Research Doctoral Course
2023 Systems Engineering Advanced Research Doctoral Course
2023 Systems Engineering Global Seminar Ⅰ Doctoral Course
2023 Systems Engineering Global Seminar Ⅰ Doctoral Course
2023 Systems Engineering Global Seminar Ⅱ Doctoral Course
2023 Systems Engineering Global Seminar Ⅱ Doctoral Course
2022 Systems Engineering Global Seminar Ⅱ Doctoral Course
2022 Systems Engineering Global Seminar Ⅰ Doctoral Course
2022 Systems Engineering Advanced Research Doctoral Course
2022 Systems Engineering Advanced Seminar Ⅱ Doctoral Course
2022 Systems Engineering Advanced Seminar Ⅰ Doctoral Course
2022 Systems Engineering Project SeminarⅡB Master's Course
2022 Systems Engineering Project SeminarⅡA Master's Course
2022 Systems Engineering Project SeminarⅠB Master's Course
2022 Systems Engineering Project SeminarⅠA Master's Course
2022 Chemistry of Inorganic Reactions Master's Course
2022 Systems Engineering SeminarⅡB Master's Course
2022 Systems Engineering SeminarⅡA Master's Course
2022 Systems Engineering SeminarⅠB Master's Course
2022 Systems Engineering SeminarⅠA Master's Course
2021 Systems Engineering Global Seminar Ⅱ Doctoral Course
2021 Systems Engineering Global Seminar Ⅰ Doctoral Course
2021 Systems Engineering Advanced Research Doctoral Course
2021 Systems Engineering Advanced Seminar Ⅱ Doctoral Course
2021 Systems Engineering Advanced Seminar Ⅰ Doctoral Course
2021 Systems Engineering Project SeminarⅡB Master's Course
2021 Systems Engineering Project SeminarⅡA Master's Course
2021 Systems Engineering Project SeminarⅠB Master's Course
2021 Systems Engineering Project SeminarⅠA Master's Course
2021 Chemistry of Inorganic Reactions Master's Course
2021 Systems Engineering SeminarⅡB Master's Course
2021 Systems Engineering SeminarⅡA Master's Course
2021 Systems Engineering SeminarⅠB Master's Course
2021 Systems Engineering SeminarⅠA Master's Course
2020 Systems Engineering Global Seminar Ⅱ Doctoral Course
2020 Systems Engineering Global Seminar Ⅰ Doctoral Course
2020 Systems Engineering Advanced Research Doctoral Course
2020 Systems Engineering Advanced Seminar Ⅱ Doctoral Course
2020 Systems Engineering Advanced Seminar Ⅰ Doctoral Course
2020 Systems Engineering Project SeminarⅡB Master's Course
2020 Systems Engineering Project SeminarⅡA Master's Course
2020 Systems Engineering Project SeminarⅠB Master's Course
2020 Systems Engineering Project SeminarⅠA Master's Course
2020 Chemistry of Inorganic Reactions Master's Course
2020 Systems Engineering SeminarⅡB Master's Course
2020 Systems Engineering SeminarⅡA Master's Course
2020 Systems Engineering SeminarⅠB Master's Course
2020 Systems Engineering SeminarⅠA Master's Course
2019 Chemistry of Inorganic Reactions Master's Course
2019 Systems Engineering Advanced Seminar Ⅱ Doctoral Course
2019 Systems Engineering Advanced Seminar Ⅱ Doctoral Course
2019 Systems Engineering Advanced Seminar Ⅰ Doctoral Course
2019 Systems Engineering Advanced Seminar Ⅰ Doctoral Course
2019 Systems Engineering Advanced Research Doctoral Course
2019 Systems Engineering Advanced Research Doctoral Course
2019 Systems Engineering SeminarⅡB Master's Course
2019 Systems Engineering SeminarⅡA Master's Course
2019 Systems Engineering SeminarⅠB Master's Course
2019 Systems Engineering SeminarⅠA Master's Course
2019 Systems Engineering Project SeminarⅡB Master's Course
2019 Systems Engineering Project SeminarⅠB Master's Course
2019 Systems Engineering Project SeminarⅠA Master's Course
2018 Systems Engineering Advanced Research Doctoral Course
2018 Systems Engineering Advanced Research Doctoral Course
2018 Systems Engineering Advanced Seminar Ⅰ Doctoral Course
2018 Systems Engineering Advanced Seminar Ⅰ Doctoral Course
2018 Systems Engineering Project SeminarⅡB Master's Course
2018 Systems Engineering Project SeminarⅡA Master's Course
2018 Systems Engineering Project SeminarⅠB Master's Course
2018 Systems Engineering Project SeminarⅠA Master's Course
2018 Systems Engineering SeminarⅡB Master's Course
2018 Systems Engineering SeminarⅡA Master's Course
2018 Systems Engineering SeminarⅠB Master's Course
2018 Systems Engineering SeminarⅠA Master's Course
2018 Chemistry of Inorganic Reactions Master's Course
2017 Systems Engineering Advanced Research Doctoral Course
2017 Systems Engineering Advanced Research Doctoral Course
2017 Systems Engineering Advanced Seminar Ⅰ Doctoral Course
2017 Systems Engineering Project SeminarⅡB Master's Course
2017 Systems Engineering Project SeminarⅡA Master's Course
2017 Systems Engineering Project SeminarⅠB Master's Course
2017 Systems Engineering Project SeminarⅠA Master's Course
2017 Chemistry of Inorganic Reactions Master's Course
2017 Systems Engineering SeminarⅡB Master's Course
2017 Systems Engineering SeminarⅡA Master's Course
2017 Systems Engineering SeminarⅠB Master's Course
2017 Systems Engineering SeminarⅠA Master's Course
2016 Systems Engineering Global Seminar Ⅱ Doctoral Course
2016 Systems Engineering Global Seminar Ⅱ Doctoral Course
2016 Systems Engineering Advanced Research Doctoral Course
2016 Systems Engineering Advanced Research Doctoral Course
2016 Systems Engineering Advanced Research Doctoral Course
2016 Systems Engineering Advanced Research Doctoral Course
2016 Systems Engineering Advanced Seminar Ⅱ Doctoral Course
2016 Systems Engineering Advanced Seminar Ⅱ Doctoral Course
2016 Systems Engineering Project SeminarⅡB Master's Course
2016 Systems Engineering Project SeminarⅡA Master's Course
2016 Systems Engineering Project SeminarⅠB Master's Course
2016 Systems Engineering Project SeminarⅠA Master's Course
2016 Systems Engineering SeminarⅡB Master's Course
2016 Systems Engineering SeminarⅡA Master's Course
2016 Systems Engineering SeminarⅠB Master's Course
2016 Systems Engineering SeminarⅠA Master's Course
2016 Chemistry of Inorganic Reactions Master's Course
2015 Systems Engineering Advanced Seminar Ⅱ
2015 Systems Engineering Advanced Seminar Ⅰ
2015 Systems Engineering Advanced Research
2015 Systems Engineering SeminarⅡA
2015 Systems Engineering SeminarⅠA
2015 Systems Engineering Project SeminarⅡA
2015 Systems Engineering Project SeminarⅠA
2015 Systems Engineering Global Seminar Ⅰ
2015 Chemistry of Inorganic Reactions
2015 Systems Engineering Advanced Seminar Ⅱ
2015 Systems Engineering Advanced Seminar Ⅰ
2015 Systems Engineering Advanced Research
2015 Systems Engineering SeminarⅡB
2015 Systems Engineering SeminarⅠB
2015 Systems Engineering Project SeminarⅡB
2015 Systems Engineering Project SeminarⅠB
2015 Systems Engineering Global Seminar Ⅰ
2014 Systems Engineering Global Seminar Ⅱ
2014 Systems Engineering Global Seminar Ⅱ
2014 Systems Engineering Advanced Research
2014 Systems Engineering Advanced Research
2014 Systems Engineering Advanced Seminar Ⅱ
2014 Systems Engineering Advanced Seminar Ⅱ
2014 Systems Engineering Advanced Seminar Ⅰ
2014 Systems Engineering Advanced Seminar Ⅰ
2014 Systems Engineering Project SeminarⅡB
2014 Systems Engineering Project SeminarⅡA
2014 Systems Engineering Project SeminarⅠB
2014 Systems Engineering Project SeminarⅠA
2014 Solid State Chemistry
2014 Systems Engineering SeminarⅡB
2014 Systems Engineering SeminarⅡA
2014 Systems Engineering SeminarⅠB
2014 Systems Engineering SeminarⅠA
2013 Systems Engineering Advanced Research
2013 Systems Engineering Advanced Research
2013 Systems Engineering Advanced Seminar Ⅱ
2013 Systems Engineering Advanced Seminar Ⅱ
2013 Systems Engineering Advanced Seminar Ⅰ
2013 Systems Engineering Advanced Seminar Ⅰ
2013 Systems Engineering Project SeminarⅡB
2013 Systems Engineering Project SeminarⅡA
2013 Systems Engineering Project SeminarⅠB
2013 Systems Engineering Project SeminarⅠA
2013 Solid State Chemistry
2013 Systems Engineering SeminarⅡB
2013 Systems Engineering SeminarⅡA
2013 Systems Engineering SeminarⅠB
2013 Systems Engineering SeminarⅠA
2012 Systems Engineering Advanced Seminar Ⅱ
2012 Systems Engineering Advanced Seminar Ⅰ
2012 Systems Engineering Advanced Research
2012 Systems Engineering SeminarⅡA
2012 Systems Engineering SeminarⅠA
2012 Systems Engineering Project SeminarⅡA
2012 Systems Engineering Project SeminarⅠA
2012 Solid State Chemistry
2012 Systems Engineering Advanced Seminar Ⅱ
2012 Systems Engineering Advanced Seminar Ⅰ
2012 Systems Engineering Advanced Research
2012 Systems Engineering SeminarⅡB
2012 Systems Engineering SeminarⅠB
2012 Systems Engineering Project SeminarⅡB
2012 Systems Engineering Project SeminarⅠB
2011 Systems Engineering Project SeminarⅡB
2011 Systems Engineering Project SeminarⅡA
2011 Systems Engineering Project SeminarⅠB
2011 Systems Engineering Project SeminarⅠA
2011 Systems Engineering Advanced Research
2011 Systems Engineering Advanced Research
2011 NA
2011 NA
2011 Systems Engineering Advanced Seminar Ⅱ
2011 Systems Engineering Advanced Seminar Ⅱ
2011 Systems Engineering Advanced Seminar Ⅰ
2011 Systems Engineering Advanced Seminar Ⅰ
2011 Solid State Chemistry
2010 Solid State Chemistry Master's Course
2010 NA Master's Course
2010 NA Master's Course
2010 NA Master's Course
2010 NA Master's Course
2009 Reactions of Coordination Compounds Master's Course
2009 NA Master's Course
2009 NA Master's Course
2009 NA Master's Course
2009 NA Master's Course
2008 Reactions of Coordination Compounds Master's Course
2008 NA Master's Course
2008 NA Master's Course
2008 NA Master's Course
2008 NA Master's Course
2007 Reactions of Coordination Compounds Master's Course
2007 NA Master's Course
2007 NA Master's Course
2007 NA Master's Course
2007 NA Master's Course

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Research Interests

synthetic inorganic chemistry
polyoxometalate
peroxometalate
structural inorganic chemistry

Published Papers

Control over the preference for binding sites of polyoxometalates to silver ethynide clusters by surface charge modification

Sho Tamari, Kosuke Ono, Masato Hashimoto, Tomoji Ozeki

DALTON TRANSACTIONS ( ROYAL SOC CHEMISTRY ) 44 ( 44 ) 19056 - 19058 2015 [Refereed]

　View Summary

A polyoxometalate-silver ethynide composite cluster, [Ag-42(CO3)-{ C = CC(CH3)(3)}(27)(alpha-A-SiW9Nb3O40)(2)](-) (1), demonstrates that we can select the binding site of a polyoxometalate to the silver alkynide cluster by tuning the surface charge of the precursor polyoxometalate. Multidimensional and multinuclear NMR spectra revealed that 1 maintains its precise atomic connectivity in the solution.

DOI
Synthesis, structure and spectroscopic analyses of aquachloridooxidodiperoxidomolybdate(VI)

Masa-aki Saito, Masato Hashimoto

DALTON TRANSACTIONS ( ROYAL SOC CHEMISTRY ) 43 ( 2 ) 402 - 405 2014 [Refereed]

　View Summary

A novel aquachloridooxidodiperoxidomolybdate(VI), [MoClO(O-2)(2)(OH2)](-), was crystallised as tetraethylammonium and triethylmethylammonium salts from strongly acidic aqueous solutions, and was structurally analysed by single crystal X-ray diffraction and NMR spectroscopy. The aqueous behaviour of the present anion observed by O-17 NMR agrees with that reported in a previous speciation study.

DOI
Calcium and strontium salts of (glycinato-κ2 N,O)oxidobis(peroxido-κ2O,O′)vanadate(V) tetrahydrate

Takeshi Higuchi, Ayana Uchida, Masato Hashimoto

Acta Crystallographica Section C: Crystal Structure Communications 69 ( 12 ) 1494 - 1497 2013.12 [Refereed]

　View Summary

The title salts calcium (glycinato-κ2 N,O) oxidobis(peroxido-κ2 O,O′)vanadate(V) tetrahydrate, Ca[VO(O2)2(NH2CH2COO)] ·4H2O, and strontium (glycinato-κ2 N,O)oxidobis(peroxido-κ2 O,O′)vanadate(V) tetrahydrate, Sr[VO(O2)2(NH2CH2COO)] ·4H2O, crystallized at pH ca 7.4 with similar lattice parameters. The glycinate anion acts as a bidentate N,O-chelating ligand, and the V atom has a pentagonal bipyramidal geometry, with two η2- peroxo groups and the glycinate N atom in the equatorial plane, and one terminal oxo and a glycinate O atom at the axial positions. The H atoms of three of the four water molecules in the strontium salt exhibited disorder over three positions for each molecule. © 2013 International Union of Crystallography.

DOI
Dipotassium Diaquadiphosphatooctaperoxotetramolybdate, [K-2(P2O7){MoO(O-2)(2)}(2){MoO(O-2)(2)(OH2)}(2)](2-) - a One-Dimensional Double Chain Array of Polyanions Linked by Potassium Cations

Koji Aoki, Keisuke Iwata, Takahiro Iwata, Masato Hashimoto

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY ( WILEY-V C H VERLAG GMBH ) ( 10-11 ) 1808 - 1814 2013.04 [Refereed]

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A dipotassium diaquadiphosphatooctaperoxotetramolybdate, [K2(P2O7){MoO(O2)2}2{MoO(O2)2(OH2)}2]2, was crystallised as a tetramethylammonium salt and its structure was determined by single-crystal X-ray diffraction. The diaquadiphosphatooctaperoxotetramolybdate moiety (POPMo4) consists of four molybdenum decahedra and one 4-diphosphate group. All Mo atoms bear two peroxo groups at their equatorial positions. Two of the four Mo atoms are also coordinated by a water molecule. The four molybdenum decahedra are separated and linked by the diphosphate group. The POPMo4 moieties are linked by potassium atoms to form an infinite anionic 1D double chain. The chains are connected by hydrogen bonds to water of crystallisation molecules to form a 2D network. POPMo4 or its precursor gives a 31P NMR signal at = 7.3 ppm in the reaction solution and is stable at low pH and a high Mo/diphosphate molar ratio.

DOI
Potassium, rubidium and ammonium salts of -(formato-2O:O)--oxido-bis[oxidobis(peroxido-2O,O)molybdate(VI)]

Masaki Takehara, Masato Hashimoto

ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS ( WILEY-BLACKWELL ) 69 37 - + 2013.01 [Refereed]

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The unit-cell parameters of the three title salts, namely, tripotassium, K3[Mo2(CHO2)O3(O2)4], trirubidium, Rb3[Mo2(CHO2)O3(O2)4], and triammonium -(formato-2O:O)--oxido-bis[oxidobis(peroxido-2O,O)molybdate(VI)], (NH4)3[Mo2(CHO2)O3(O2)4], which were all crystallized at pH 3, are quite similar, but the potassium and rubidium salt structures are noncentrosymmetric, whereas that of the ammonium salt is centrosymmetric. Formate acts as an O:O-bridging ligand in the complex anion and is bound to a -oxido-bis(oxidodiperoxidomolybdate) unit.

DOI
Bis(trimethylphenylammonium) μ-oxalato-bis[oxidodiperoxidomolybdate(VI)]

Ayaka Oba, Masato Hashimoto

Acta Crystallographica Section E: Structure Reports Online 68 ( 12 ) m1467 2012.12 [Refereed]

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A trimethylphenylammonium salt of a dinuclear μ-oxalate complex of diperoxidomonomolybdate units, (C9H14N)2[Mo2(C2O4)(O2)4O2], was obtained from an acidic aqueous solution
the dianion is located about a centre of inversion. Each Mo atom bears two peroxide groups together with one O atom from the oxalate group in its equatorial positions and one terminal O atom as well as another O atom from the oxalate in axial positions. The oxalate group acts as a tetradentate bridging ligand and bridges between the diperoxidomolybdate units.

DOI
Role of p(Z)-pi(Ar/Nap) conjugation in structures of 1-(arylchalcogena)-naphthalenes for Z = Te versus Se, S and O: experimental and theoretical investigations

Takahito Nakai, Mitsuhiro Nishino, Satoko Hayashi, Masato Hashimoto, Waro Nakanishi

DALTON TRANSACTIONS ( ROYAL SOC CHEMISTRY ) 41 ( 25 ) 7485 - 7497 2012 [Refereed]

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Magnitudes of the p(Z)-pi(Ar/Nap) conjugation were evaluated for 1-(arylchalcogena)naphthalenes (1-(ArZ)Nap, 1-(p-YC(6)H(4)Z)C10H7; 1 (Z = Te), 2 (Se), 3 (S) and 4 (O)). Structures of 1 were determined by X-ray analysis for Y = NMe2 (b), OMe (c) and CN (i). For 1b and 1c that have electron donating Y, the Z-C-Ar bond is located on the naphthyl plane with Z-C-Nap being perpendicular to the aryl plane, which we define as (B: pd). On the other hand, the structure of 1i with electron donating Y is (A: pl), of which Z-C-Ar is placed almost perpendicular to the naphthyl plane with Z-C-Nap being located on the aryl plane. Each structure of 1a (Y = H), 1b, 1c, 1d (Me), 1e (F), 1f (Cl), 1g (Br), 1h (COOEt), 1i and 1j (NO2) was determined by NMR in chloroform-d. Structures of 1 in the solutions are (B: pd) for b, c and e that have electron donating Y, (A: pl) for f-j with electron accepting Y, and in equilibrium between (B: pd) and (A: pl) for a and d of which Yare rather neutral. The results for 2-4 are very similar to those of 1 in solutions. Quantum chemical calculations were performed on 1-4 with Yof a, b' (NH2), d, f and j. Magnitudes of the p(Z)-pi(Ar/Nap) conjugation were well-evaluated by NBO (natural bond orbital) analysis. The values were 12.6 and 13.0 kcal mol(-1) for the typical forms of (A: pl) and (B: pd) of 1a, respectively, resulting in a much smaller energy difference between the two (0.4 kcal mol(-1)), which should correspond to the observed result. It is well-demonstrated that the p(Te)-p(Ar/Nap) conjugation operates effectively in 1, although the magnitudes increase in the order of Z = Te < Se < S < O. Thermal effect of the Gibbs free energies is shown to play an important role in the energy profiles of 1a-4a.

DOI
A P-31-NMR study of the H+-MoO42--(HP)O-3(2-)-HPO42--(C6H5P)O-3(2-)-(CH3P)O-3(2-) system at low Mo-tot/P-tot ratio - Formation of mixed-hetero X2M5-type polyanions

Masato Hashimoto, Ingegaerd Andersson, Lage Pettersson

DALTON TRANSACTIONS ( ROYAL SOC CHEMISTRY ) ( 17 ) 3321 - 3327 2009 [Refereed]

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Formation of X2M5-type heteropolyanions in the aqueous mixed-hetero H+-MoO42--(HP)O-3(2-)-HPO42--(C6H5P)O-3(2-)- (C6H3P)O-3(2-) system has been studied by P-31-NMR at [Mo](tot)/[P-all](tot) = 1.5 at 298(1) K in 0.600 M Na(Cl) ionic medium. The -log[H+] range 1.4-6.2 has been covered. The pK(a) values of methylphosphonate were determined from P-31-NMR chemical shift data in the range of 0 < -log[H+] < 13.2 as H(CH3P)O-3(-) 7.30 and H-2(CH3P)O-3 2.05. All four-component H+-MoO42--P1-P2 subsystems (P1 and P2 are two of the four phosphorus-containing components), except H+-MoO(4)2(-)-(HP)O-3(2-)-HPO42-, which has been studied previously, were examined instead of the full six-component system in order to simplify the evaluation of the NMR spectra. The concentrations were adjusted to [Mo](tot) = 60 mM and [P1](tot) = [P2](tot) = 20 mM in the measurements. All conceivable P2M5 and (P1)(P2)M5 heteropolyanions were identified. The following novel X2M5-type polyanions were found and their formation constants are given in logarithmic values with 36 in parentheses: (CH3P)(2)Mo5O214- 69.68(7), (HP)(C6HSP)Mo5O214- 67.09(4), (C6H5P)PMo5O225- 63.23(5), H(C6H5P)PMo5O224- 68.11(4), (HP)(CH3P)Mo5O214-- 67.85(4), (CH3P)PMo5O225- 64.14(7), H(CH3P)Mo5O224- 68.89(4) and (C6H5P)(CH3P)Mo5O214- 69.18(4). The equilibrium conditions are illustrated in distribution diagrams. Phosphite proved to bind more weakly in X2M5-type polyoxometallates than phosphate or phosphonates, which are almost equally favoured in complexation.

DOI
Preparation and Characterization of an alpha-Wells-Dawson-Type [V2Mo18O62](6-) Complex

Sadayuki Himeno, Keishi Kawasaki, Masato Hashimoto

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN ( CHEMICAL SOC JAPAN ) 81 ( 11 ) 1465 - 1471 2008.11 [Refereed]

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An orange-yellow vanadomolybdate complex was prepared by heating a 100 mM Mo-VI-20 mM V-V-0.45 M HCl-20% (v/v) CH3CN system at 70 degrees C for 24 h, being isolated as the tetrapropylammonium (Pr4N+) salt. The Pr4N+ salt crystallized in the orthorhombic space group P2(1)2(1)2; the lattice constants were a = 18.417(4), b = 20.869(5), c = 15.280(3) angstrom, V = 5873(2) angstrom(3), and Z = 2. The crystallographic study revealed that the structure consists of The alpha-Wells-Dawson-type [V2Mo18O62](6-) anion, in which vanadates serve as the central tetrahedra. alpha-[V2Mo18O62](6-) complex underwent a two-step one-electron reduction in CH3CN, and the presence of acid caused the one-electron waves to be converted into three two-electron waves. The formation conditions were elucidated by V-51 NMR measurements.

DOI
An equilibrium analysis of the aqueous H+-MoO42--(HP)O-3(2-)-H+MoO42--(HP)O-3(2-)-(HPO)(4)(2-) and systems

Masato Hashimoto, Ingegaerd Andersson, Lage Pettersson

DALTON TRANSACTIONS ( ROYAL SOC CHEMISTRY ) ( 1 ) 124 - 132 2007.01 [Refereed]

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The speciation in the phosphitomolybdate system, H+-MoO42--(HP)O-3(2-), has been determined from combined potentiometric and P-31 NMR measurements in 0.600 M Na(Cl) medium at 298(1) K. Potentiometric titration data were collected in the ranges 2.5 < -log[H+] < 6.2, 40.0 <= [Mo](tot) <= 240.0 mM, 10.0 <= [P](tot) <= 40.0 mM and l <= [Mo](tot)/[P](tot) <= 10. P-31 NMR data were collected in the same ranges with the exception that -log[H+] was decreased to 0.8. The pK(a) values of phosphite were determined by means of potentiometric (1.5 < -log[H+] < 8.6) and P-31 NMR chemical shift data (0.0 < -log[H+] < 12.0). The following log beta (3 sigma) values were deduced: H(HP)O-3(-), 6.09(2); H-2(HP)O-3, 7.23(4) (pK(a) = 1. 14). In the phosphitomolybdate system, the following complexes were found along with their formation constants ((HP) denotes phosphite): Mo-5(HP)(2)(4-), 65.31(4); Mo-6(HP)(2)(5-), 71.94(5); Mo-5(HP)(4-), 51.25(8); Mo-5(HP)(3-), 54.9(3); Mo-6(HP)(2-), 68.99(9); Mo-7(Hp)(5-), 71.25(3); Mo-7(HP)(4-), 74.2(2). Because hydrolysis and oxidation of phosphite to phosphate were observed by NMR, with a mixed-hetero species of low [Mo](tot)/[P](tot) ratio being detected, the four-component H+-MoO42-(HP)-O-3(2-)-HPO42- system was also studied in the same way over the range 0.8 < -log[H+] < 6.2 and [Mo](tot)/[P](tot) fixed at 1.5. The following mixed heteropolyanion species have been found (P denotes the phosphate group): Mo-5(HP)P5-, 62.27(6); Mo-5(HP)P4-, 66.76(4). The equilibrium speciation in the two systems are illustrated by distribution diagrams. In addition, the aqueous structures are proposed for all the species formed in the systems.

DOI
Preparation, structure, and characterization of a novel diphosphoheptadecatungstate complex, [(P2O7)W17O51](4-)

S Himeno, T Katsuta, M Takamoto, M Hashimoto

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN ( CHEMICAL SOC JAPAN ) 79 ( 1 ) 100 - 105 2006.01 [Refereed]

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A novel diphosphoheptadecatungstate complex, [(P2O7)W17O51](4-) was prepared from a 200 mM (M = mol dm(-3)) W(VI)-10 mM P2O74--0.6 M HCl-40% (v/v) CH3CN system, and characterized by IR, UV-vis, P-31 NMR, and W-183 NMR spectroscopy, and voltammetry. Single-crystal X-ray analysis was made on [(C2H5)(4)N](4)[(P2O7)W17O51]center dot CH3CN, which crystallized in the monoclinic space group P2(1)/n, with cell parameters a = 16.1877(8), b = 22.103(1), c = 21670(1) angstrom, beta = 90.847(1)degrees, V = 8110.3(7) angstrom(3), and Z = 4. The anion consists of a PW8O31 fragment derived from a beta-Keggin-type [PW12O40](3-) structure, and two PW8O31 units are linked by five oxygen atoms and a WO5 square pyramid. The [(P2O7)W17O51](4-) anion exhibited a four-step reversible one-electron redox wave in CH3CN, and a three-step two-electron redox wave resulted in the presence of acid. This is the first example of an electrochemically-active diphosphotungstate complex.

DOI
First transition metal complex of 1,8-bis(dimethylamino)naphthalene (proton sponge)

T Yamasaki, N Ozaki, Y Saika, K Ohta, K Goboh, F Nakamura, M Hashimoto, S Okeya

CHEMISTRY LETTERS ( CHEMICAL SOC JAPAN ) 33 ( 7 ) 928 - 929 2004.07 [Refereed]

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First transition metal complexes of 1,8-bis(dimethyl-amino)naphthalene (proton sponge), N,N'-chelated Pd(II) complexes, were prepared and the strong coordination ability of the proton sponge was demonstrated. The high transition energy for the coordination could be lowered by the existence of the intermediate charge-transfer complex which was isolated.

DOI
Preparation and characterization of an alpha-Keggin-type [SW12O40](2)-complex

S Himeno, M Takamoto, M Hoshiba, A Higuchi, M Hashimoto

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN ( CHEMICAL SOC JAPAN ) 77 ( 3 ) 519 - 524 2004.03 [Refereed]

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A divanadium-substituted derivative of 12-tungstosulfate(VI), [S(V2W10)O-40](4-) was prepared as the tetrabutylammonium (n-Bu4N+) salt by heating a 50 nM (M = mol dm(-3)) W(VI)-20 mM V(V)-0.5 M H2SO4-50% (v/v) CH3CN system at 70 degreesC for 24 h. The [S(V2W10)O-40](4-) anion Was transformed spontaneously into a monovanadium-substituted derivative, [S(VW11)O-40](3-) in a 70% (v/v) CH3CN-1.0 M HCl system at 70 degreesC. Oil the other hand, [SW12O40](2-) was precipitated as the n-Bu4N+ salt upon heating a 95% (v/v) CH3CN-0.5 M HCl system containing [S(V2W10)O-40](4-). The single-crystal X-ray structural analysis revealed that the structure consisted of an alpha-Keggin-type [SW12O40](2-) anion. The [SW12O40](2-) anion was characterized by IR and UV-vis spectroscopy, and voltammetry.

DOI
Synthesis and Crystal Structure of Cs2(CN3H6)3[(C2H5)2NH2][W7O22(O2)2].3H2O

Hiroyuki Suzuki, Masato Hashimoto, Seichi Okeya

Eur. J. Inorg. Chem. 2632 - 2634 2004 [Refereed]
Synthesis and structural characterization of [HxCp*TiMo5O18]((3-x)-) (x=0, 1, 2); new insights into protonation patterns in polyoxometalates

H Akashi, J Chen, H Hasegawa, M Hashimoto, T Hashimoto, T Sakuraba, A Yagasaki

POLYHEDRON ( PERGAMON-ELSEVIER SCIENCE LTD ) 22 ( 20 ) 2847 - 2854 2003.09 [Refereed]

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Reaction Of [(n-C4H9)(4)N](2)[Mo2O7], Cp*TiCl3, and [(n-C4H9)(4)N]OH in CH3CN yields [(n-C4H9)(4)N](3)[Cp*TiMo5O18].CH3CN [a = 12.863(4) Angstrom b = 26.608(6) Angstrom, c = 24.534(4) Angstrom, beta = 103.88(2)degrees, Z = 4, space group P2(1)/c (no. 14)]. Similar reaction without [(n-C4H9)(4)N]OH yields monoprotonated complex [(n-C4H9)(4)N](2)[HCp*TiMo5O18], where, according to a single-crystal X-ray diffraction study [a = 19.9550(4) Angstrom, b = 25.5420(8) Angstrom, c = 11.8820(3) Angstrom, beta = 100.31(2)degrees, Z = 4, space group P2(1)/n (no. 14)], the anion is protonated at one of OMo2 doubly-bridging oxygens. Reaction of [(n-C4H9)(4)N](2)[HCp*TiMo5O18] with CCl3COOH in CHCl3 followed by crystallization from CH3CN/Et2O yields diprotonated [(n-C4H9)(4)N][H2Cp*TiMO5O18].1/4(C2H5)(2)O, which, according to a single-crystal X-ray diffraction study [a = 12.319(2) Angstrom, b = 16.105(3) Angstrom, c = 12.001(2) Angstrom, alpha = 110. 74(1)degrees, beta = 100.31(2)degrees, gamma = 82.777(5) Z = 2, space group P (1) over bar (no. 2)], contains hydrogen-bonded dimers of [H,,Cp*TiMo5O19](-) ions. The [Cp*TiMo5O18](3-) is basic enough to form stable organometallic adducts like [(eta-C8H12)Ir(Cp*TiMo5O18)](2-) and [(eta-C8H14)Rh(Cp*TiMo5O18)](2-). (C) 2003 Elsevier Ltd. All rights reserved.

DOI
O-17 NMR study of aqueous peroxoisopolymolybdate equilibria at lower peroxide/Mo ratios

L Pettersson, Andersson, I, F Taube, Toth, I, M Hashimoto, OW Howarth

DALTON TRANSACTIONS ( ROYAL SOC CHEMISTRY ) ( 1 ) 146 - 152 2003 [Refereed]

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Aqueous peroxomolybdates have been studied using O-17 NMR together with equilibrium measurements and calculations, over a wide range of conditions. Ten peroxo species are identified, mostly in more than one state of protonation. Some are already known in the solid state, or from equilibrium analysis, but structural information is also obtained for MoO3 (HO2)(-) and the new or previously tentative species Mo2O5 (O-2)(2)(2-), HpMo7O23 (O-2)(2)(p-6) and HpMo7O23 (O-2)(p-6) (p = 0-2). Sites of protonation are identified, as are O-17 resonances from both bidentate and monodentate peroxide. Several oxygen exchange processes are also seen, including a probable dimer-tetramer exchange.

DOI
A breathing ionic crystal displaying selective binding of small alcohols and nitriles: K-3[Cr3O(OOCH)(6)(H2O)(3)][alpha-SiW12O40]center dot 16H(2)O

S Uchida, M Hashimoto, N Mizuno

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION ( WILEY-V C H VERLAG GMBH ) 41 ( 15 ) 2814 - + 2002 [Refereed]
[Ni(H2O6)]2[Na(H2O)3]2 V10O28・4H2O

Tomoyuki Higami, Masato Hashimoto, Seichi Okeya

Acta Crystallogr. Sect. C C58 i144 - i146 2002 [Refereed]
Characterisation of aqueous peroxomolybdate catalysts applicable to pulp bleaching

F Taube, M Hashimoto, Andersson, I, L Pettersson

JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS ( ROYAL SOC CHEMISTRY ) ( 6 ) 1002 - 1008 2002 [Refereed]

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The equilibrium speciation in the system p H++ q MoO42-+ rH(2)O(2) + sSO(4)(2-) reversible arrow(H+)(p) (MoO42-)(q) (H2O2)(r) (SO42-)s in 0.300 M Na-2 (SO4) medium at 25 degreesC has been determined from potentiometric titration data in the ranges 2.0 less than or equal topH less than or equal to5.5, 5.00 less than or equal to[Mo](tot)/mM less than or equal to80.00, 0 less than or equal to[H2O2](tot)/mM less than or equal to245 and 273.07 less than or equal to[SO42-](tot)/mM less than or equal to320.20. Species with the following compositions were found: MoX- (1,1,1,0), MoX (2,1,1,0), MoX2- (1,1,2,0), MoX2 (2,1,2,0), MoX2S2- (2,1,2,1), Mo2X42- (2,2,4,0), Mo7X6- (8,7,1,0), Mo7X5- (9,7,1,0), Mo7X4- (10,7,1,0) and Mo7X3- (11,7,1,0). The numbers in parentheses refer to the values of p, q, r and s in the formula above. The numbers and charges of molybdenum (Mo), peroxide (X) and sulfate (S) in each species are given in the abbreviated formula MoqXrSs(2q + 2s - p)-. The following formation constants with 3sigma were obtained; logbeta(1,1,1,0) = 8.53 +/- 0.03, log beta(2,1,1,0) = 11.22 +/- 0.04 (pK(a) = 2.69), log beta(1,1,2,0) = 11.61 +/- 0.03, log beta(2,1,2,0) = 13.77 (+/- 0.06) (pK(a) = 2.16), log beta(2,1,2,1) = 14.50 +/- 0.06, log beta(2,2,4,0) = 23.77 +/- 0.11, log beta(8,7,1,0) = 56.71 +/- 0.11, log beta(9,7,1,0) = 62.00 +/- 0.05 (pK(a) = 5.29), log beta(10,7,1,0) = 65.74 +/- 0.06 (pK(a) = 3.74), log beta(11,7,1,0) = 68.23 +/- 0.08 (pK(a) = 2.49). Most complexes have been verified by Mo-95 NMR, O-17 NMR, and the novel MoX2S2- complex also by FTIR spectroscopy.

DOI
Origin of microporosity of ammonium dodecatungstophosphate unveiled by single crystal structure analysis

T Ito, M Hashimoto, S Uchida, N Mizuno

CHEMISTRY LETTERS ( CHEMICAL SOC JAPAN ) ( 12 ) 1272 - 1273 2001.12 [Refereed]

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The single crystals of ammonium dodecatungstophosphate were successfully synthesized and the structure was analyzed. The intrinsic crystal structure (cubic, Pn (3) over barm) had no cavity. It follows that the microporosity observed for the powdery sample originated from narrow spaces surrounded by the fine nanocrystallites.
Synthesis, structure, and characterization of an alpha-Dawson-type [S2W18O62](4-) complex

S Himeno, H Tatewaki, M Hashimoto

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN ( CHEMICAL SOC JAPAN ) 74 ( 9 ) 1623 - 1628 2001.09 [Refereed]

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A yellow sulfatotungstate complex was formed by heating a 50 mM W(Vl)-2 M H2SO4-40% (v/v) CH3CN system at 70 degreesC for 14 days, being isolated as the tetrapropylammonium (n-Pr4N+) salt. An X-ray structural analysis (orthorhombic, Pca2(1) (No. 29) a = 27.181(1), b = 14.1428(6), c = 27.7292(9) Angstrom, and Z = 4) revealed that the structure consists of an alpha -Dawson-type [S2W18O62](4-) anion. The alpha-[S2W18O62](4-) complex underwent a four-step reversible one-electron reduction in CH3CN, and the presence of acid caused the one-electron waves to be converted into three two-electron waves. The formation conditions were elucidated by a combined Raman and voltammetric study.

DOI
A P-31-NMR study of peroxo species formed during oxidation of cyclohexene with hydrogen peroxide in tri-n-butylphosphate catalyzed by heteropolyacids

M Hashimoto, K Itoh, KY Lee, M Misono

TOPICS IN CATALYSIS ( KLUWER ACADEMIC/PLENUM PUBL ) 15 ( 2-4 ) 265 - 271 2001 [Refereed]

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In the oxidation of cyclohexene with H2O2 in monophasic tri-n-butylphosphate (TBP) solution catalyzed by Keggin-type 12-heteropolyacids, i.e., H3PMo12-xWxO40 (x = 0-12), several peroxo species were observed by P-31-NMR spectroscopy in lower field than the original heteropolyacids. Their composition varied regularly with that of the starting catalyst. The P-containing peroxo species formed was deduced as [PM4O8(O-2)(8)](3-) (M = Mo, W). The peroxo species formed more easily with a decrease in the W content, x of H3PMo12-xWxO40. It was further indicated from the reactivity with cyclohexene and the comparison with catalytic performance that W-rich peroxo species were catalytically more active than Mo-rich peroxo species for the oxidation of cyclohexene in this reaction system.
Facile formation and dissociation behaviour of C-C bond resulted from the nucleophilic attack of carbanions on a carbonyl carbon in [Pt(hfac)(2)]

S Okeya, M Hashimoto, F Nakamura, Y Kusuyama, M Kobayashi, R Arakawa

CHEMISTRY LETTERS ( CHEMICAL SOC JAPAN ) ( 10 ) 1130 - 1131 2000.10 [Refereed]

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[Pt(hfac)(2)] (hfac: hexafluoroacetylacetonate) reacts with MeNH2 in CH2Cl2/MeOH to give an -NHMe adduct complex on one of the carbonyl carbons, (MeNH3) [Pt(hfac)(hfac-NHMe)] 1 which is a tetrahedral intermediate of a Schiff base complex, [Pt(CF3COCHC(NMe)CF3)(2)] 2. Complex 1 activates H2O, MeOH, MeNO2 or acetone in solution to form the corresponding conjugate base adducts. The C-C bond in -CH2NO2 adduct 6, easily cleaves and generates nitromethane in solution.
Reactivity of organometallic molybdate toward lanthanide cations. Synthesis and structure of polynuclear lanthanide-molybdate complexes

M Hashimoto, M Takata, A Yagasaki

INORGANIC CHEMISTRY ( AMER CHEMICAL SOC ) 39 ( 16 ) 3712 - + 2000.08 [Refereed]

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Novel polynuclear rare earth compounds [La-3(OH2)(7)-(Cp*MoO3)(2)(NO3)(7)] and [La-3(OH2)(5)(THF)(Cp*MoO3)(2)-(NO3)(6)](2)(NO3)(2) were synthesized by reacting [(n-C4H9)(4)N][CP*MoO3] With La(NO3)(3). 6H(2)O in THF. X-ray crystal structural analyses revealed that both these compounds are composed of a La3Mo2O6 unit in which the metal atoms arrange themselves into a trigonal bipyramid. The Ce analogues were also obtained.
[GRAPHICS]

DOI
[NH4]3[VO2(SO4)2(OH2)2].1.5H2O

Masato Hashimoto, Michiru Kubata, Atsushi Yagasaki

Acta Crystallogr., Sect. C C56 1411 - 1412 2000 [Refereed]
Multicomponent polyanions. 52. Crystal structure of hexacaesium monohydrogen decamolybdo(VI)divanado(IV)phosphate(7-) dihydrate

M Hashimoto, A Selling, M Hakansson, L Pettersson

ACTA CHEMICA SCANDINAVICA ( MUNKSGAARD INT PUBL LTD ) 53 ( 5 ) 305 - 313 1999.05 [Refereed]

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The structure of the title compound, (Cs6HPMo10V2O40)-V-VI-O-IV. 2H(2)O has been determined by a single-crystal X-ray diffraction method. The compound crystallises in two different space groups. Crystal A: monoclinic P2(1), a = 10.988(3), b = 10.615(3), c = 17.472(2) Angstrom, beta = 91.55(1)degrees, V = 2037(7) Angstrom(3) and Z = 2. Crystal B: monoclinic, Pn, a = 10.982(2), b = 10.614(3), c = 17.487(3) Angstrom, beta = 91.64(1)degrees, V = 2037(7) Angstrom(3) and Z = 2. The R-values based on F were 0.0487 for A and 0.0485 for B for 4491 (A) and 4464 (B) reflections with F-o > 4.0 sigma (F-o) and 353 parameters, and S = 1.048 (A) and 1.026 (B). The polyanion has a so-called alpha-Keggin structure in each crystal. The two vanadium atoms are delocalised in the 12 addenda atom positions in the anion.
Formation and conversion of molybdophosphate and -arsenate complexes in aqueous solution

S Himeno, M Hashimoto, T Ueda

INORGANICA CHIMICA ACTA ( ELSEVIER SCIENCE SA ) 284 ( 2 ) 237 - 245 1999.01 [Refereed]

　View Summary

The difference between the formation and conversion processes of molybdophosphate and -arsenate complexes was elucidated in a 100 mM Mo(VI)-0.5 M HCl system as a function of the P(V) or As(V) concentration. In the Mo(VI)-P(V) system, the Keggin-type [PMo12O40](3-) complex was stable only at P(V) concentrations <7 mM; further addition of P(V) caused the [PMo12O40](3-) complex to decompose mainly into the A-[PMo9O34H6](3-) complex at an ambient temperature. The latter was subsequently converted into the Dawson-type [P2Mo18O62](6-) complex at an elevated temperature; the Dawson complex was kinetically stable even in the presence of excess of P(V). At As(V) concentrations <10 mM, in contrast, the corresponding Mo(VI)-As(V) system did not produce the Keggin-type [AsMo12O40](3-) complex but the previously unknown complex (tentatively formulated as [AsMo10O37H5](4-)) at an ambient temperature; with further addition of As(V), the [AsMo10O37H5](4-) complex was transformed directly into the [As2Mo6O26H2](4-) complex. The Dawson-type [As2Mo18O62](6-) complex, which was formed upon heating the system at 80 degrees C for 5 h, also underwent subsequent transformation into the [As2Mo6O26H2](4-) complex at As(V) concentrations >20 mM. (C) 1999 Elsevier Science S.A. All rights reserved.
Multicomponent polyanions. 53. Structure of tetrakis(trimethylammonium) tetra-mu-oxo-bis(triaquahexadecaoxo(trioxophenylphosphato)hexamolybdate) dihydrate, [NH(CH3)(3)](4)[{(C6H5P)Mo6O21(H2O)(3)}(2)].2H(2)O

DG Lyxell, D Bostrom, M Hashimoto, L Pettersson

ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE ( MUNKSGAARD INT PUBL LTD ) 54 424 - 430 1998.08 [Refereed]

　View Summary

The title compound crystallized in the monoclinic space group P2(1)/n (No. 14) [a = 11.211 (5), b = 12.862 (3), c = 23.05 (1) Angstrom, beta = 94.37 (3)degrees, V = 3314 (2) Angstrom(3), Z = 2]. The polyanion can be regarded as a dimer of a phenylphosphonatohexamolybdate, (C6H5P)Mo6O23(H2O)(3), Linked by four O atoms. In this monomeric unit the six molybdenum octahedra are grouped into two parts consisting of four and two edge-sharing octahedra, respectively. These two parts are connected by two corner-sharing O atoms to form a bent Mo-6 ring. The phenylphosphonate group coordinates to the Mo-6 ring from the narrow side as a tripodal Ligand. The {(C6H5P)Mo6O21 (H2O)(3)}(2) units form layers parallel to (001) and the structure is stabilized by hydrogen bonds between water and neighboring anions. The monomeric unit has been shown to be a key structure in the process of deducing the aqueous solution structures of the (C6H5P)Mo-6(2-) and (C6H5P)Mo-7(4-) species found in a previous equilibrium study of the H+-MoO42-(C6H5P)O-3(2-) system.
Voltammetric determination of vanadium(V) and vanadium(IV) through the formation of a 12-molybdovanadate(V) complex

S Himeno, K Kusuyama, M Hashimoto, N Ishio

ANALYTICAL SCIENCES ( JAPAN SOC ANALYTICAL CHEM ) 14 ( 4 ) 681 - 685 1998.08 [Refereed]

　View Summary

A simple voltammetric method has been developed for the determination of V(V) and V(IV). When a mixture of V(V) and V(IV) is added last of all to a 50 mM Mo(VI)-0.3 M HCl-70%(v/v) CH3CN system, only V(V) reacts with Mo(VI) to form a 12-molybdovanadate(V) complex which undergoes a two-step reduction at the glassy carbon (GC) electrode; the reduction current is directly proportional to the V(V) concentration in the mixture. On the other hand, when HCl is added last after heating the Mo(VI)-CH3CN system containing a mixture of V(V) and V(IV) at 60 degrees C for 10 min, V(IV) is completely oxidized to V(V), and the total concentration of vanadium is determined. The V(IV) concentration is determined by subtracting the V(V) concentration before oxidation from the total concentration of vanadium. Interferences from foreign ions are also discussed.
Syntheses, structures and solution dynamics of anionic 5-coordinate Pt(II) complexes with halide

S Okeya, M Hashimoto, T Matsuo, K Yamanaka, T Sumino, H Hashimoto, N Kanehisa, Y Kai

CHEMISTRY LETTERS ( CHEMICAL SOC JAPAN ) ( 6 ) 541 - 542 1998.06 [Refereed]

　View Summary

Five-coordinate anionic complexes, [Pt(hfac)(2)X](-) (X = Cl, Pr, I), were prepared by reaction of [Pt(hfac)(2)] and [PPh4]X in CH2Cl2. A distorted square pyramidal structure was revealed by the X-ray analysis. The variable-temperature H-1 and F-19 NMR spectra of these complexes were explained by two independent dynamic motions in solution, which were considered good models for the ligand exchange and cis-trans isomerization reactions.
Multicomponent polyanions. 54. Crystal structure of tetracaesium monohydrogen phosphato(phosphito)pentamolybdate dihydrate, Cs-4[H(HP)PMo5O22]center dot 2H(2)O

DG Lyxell, D Bostrom, M Hashimoto, L Pettersson

ACTA CHEMICA SCANDINAVICA ( MUNKSGAARD INT PUBL LTD ) 52 ( 4 ) 425 - 430 1998.04 [Refereed]

　View Summary

The crystal structure of tetracaesium monohydrogen phosphato (phosphito)pentamolybdate dihydrate was determined by single-crystal X-ray diffraction. The compound crystallises in the triclinic space group P (1) over bar, a=10.284(2), b= 10.791(2) and c=13.047(3) Angstrom, alpha=109.34(2), beta=99.92(2) and gamma=102.85(2)degrees, V=1283.4(5) Angstrom(3) and Z=2. The final R-values are R=0.066, wR=0.039 and S=1.3667. The H(HP)PMo5O224- anion has common features with the Strandberg X2M5-type heteropolyanion. The five MoO6 octahedra form a five-membered ring by one corner-sharing and four edge-sharing connections, and the tripodal phosphate and phosphite ligands protrude from each side of this ring in opposite directions. This is the first example of the structure of the heteropolyoxometalate having both P-III and P-V as heteroatoms.
均一沈殿法による12-タングストリン酸アンモニウム酸性塩触媒の調製とその構造

犬丸啓, 中島仁, 橋本正人, 御園生誠

日本化学会誌 390 - 397 1998 [Refereed]
Heteropoly compounds .30. Alkane oxidation with mixed addenda heteropoly catalysts containing Ru(III) and Rh(III)

Y Matsumoto, M Asami, M Hashimoto, M Misono

JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL ( ELSEVIER SCIENCE BV ) 114 ( 1-3 ) 161 - 168 1996.12 [Refereed]

　View Summary

Oxidation of alkanes, mainly of cyclohexane, with t-butyl hydroperoxide (TBHP) catalyzed by alkylammonium salts of mixed addenda heteropoly compounds having Keggin-type polyanions were studied in benzene solutions, with regard to the relative catalytic activity, reaction orders and the stability of catalysts. Tetra-n-hexylammonium salts of SiRu(H2O)W11O395- and SiRh(H2O)W11O395- showed higher catalytic activities than the corresponding Fe- and Go-substituted catalysts for the selective oxidation of cyclohexane to cyclohexanol and cyclohexanone. Although the Ru catalyst was possibly a mixture, it consisted mainly of SiRu(H2O)W11O395- and gave reproducible catalytic performance for repeated preparations. The initial rates were approximately proportional to the concentrations of cyclohexane, TBHP and the catalyst. Although the rate decreased with the consumption of TBHP, the initial rate was resumed by the addition of TBHP, indicating the absence of the deterioration of catalytic activity. Similarly alcohols and ketones were selectively formed from n-decane and ethylbenzene.

DOI
Multicomponent polyanions .48. The crystal structure of trihydrogen dodecamolybdophosphate-benzene(1/3)

DG Lyxell, D Bostrom, M Hashimoto, L Pettersson

ACTA CHEMICA SCANDINAVICA ( MUNKSGAARD INT PUBL LTD ) 50 ( 11 ) 985 - 990 1996.11 [Refereed]

　View Summary

A novel organic solvated heteropoly compound, H3Mo12PO40. 3(C6H6), crystallised in the monoclinic form, P2(1)/n (No. 14), with a = 12.189(2), b = 13.981(2), c = 12.978(1) Angstrom and beta = 98.59(1)degrees. The refinement of 340 parameters with 3705 reflections [I > 3.0 sigma(I)] gave a final R-value of 0.061 (R(w) = 0.067). The polyanion, having a so-called alpha-Keggin structure, is disordered around an inversion centre. One of three benzene molecules is sandwiched between polyanions, and the other two are accommodated in a cavity surrounded by polyanions. The links between polyanions and benzene rings are mainly due to hydrogen bonds. The phosphate and benzene in the compound were formed by hydrolysis of phenylphosphonate. (C) Acta Chemica Scandinavica 1996.
Preparation and structure of tetramethylammonium hydrogen triperoxotrimolybdodisulfate trihydrate, [N(CH3)4]3[H(SO4) 2-(MoO2(O2))3]·3H 2O

Masato Hashimoto, Hikaru Ichida, Yukiyoshi Sasaki

Journal of Coordination Chemistry ( Taylor and Francis Ltd. ) 37 ( 1-4 ) 349 - 359 1996 [Refereed]

　View Summary

A novel peroxopolyoxomolybdate compound, [N(CH3)4]3 [H(SO4)2 (MoO2(O2))3]·3H2O, has been obtained from a strongly acidic aqueous solution of a molybdate-sulfate system as the monoclinic crystal of P21/n, a = 13.497(3), b = 15.231 (4), c = 32.603(2) Å, β= 103.113(9)°, and V = 6577(2) Å3. The final R-value was 0.0986 for 395 parameters using 7162 reflections. Each of the two crystallographically independent polyanions contains three molybdenum atoms with five O2-, one O2 2-, and two sulfate groups, one of which is a tripod ligand apical to the molybdenum plane, and the other is a bipod ligand equatorial to the Mo plane. © 1996 OPA (Overseas Publishers Association) Amsterdam B.V. Published in The Netherlands under license by Gordon and Breach Science Publishers SA.

DOI
SYNTHESIS AND CHARACTERIZATION OF A BIDENTATE CHELATING DIISONITRILE LIGAND WITH 2 THIOETHEREAL SULFURS IN A BRIDGING GROUP AND ITS COPPER(I), RHODIUM(I) AND PALLADIUM(II) COMPLEXES

K SAKATA, K MATSUMOTO, M HASHIMOTO

INORGANICA CHIMICA ACTA ( ELSEVIER SCIENCE SA LAUSANNE ) 227 ( 1 ) 113 - 118 1994.12 [Refereed]

　View Summary

The diisonitrile ligand (L) has been synthesized in five reaction steps from t-butylbenzene with an overall yield of 7.3%. The reaction of palladium(II) chloride with L leads to the palladium(II) complex, PdLCl(2), whereas the rhodium(I) complexes, RhL(2)Cl and RhL(2)BF(4), and the copper(I) complex, CuL(2)BF(4), are prepared by ligand exchange reactions. These complexes were investigated by means of mass, infrared, nuclear magnetic resonance (NMR) and electronic spectra, as well as molar conductances. Judging from the molar conductances of the RhL(2)Cl, RhL(2)BF(4), and CuL(2)BF(4), complexes, tetrafluoroborate and chloride anions are ionized in acetonitrile. This is also supported by mass spectral data. The strong band at 2100 cm(-1) is assigned to the N drop C stretching mode. This band shifts to higher frequency upon metal coordination because of the inductive effect produced by the positive charge of the metal ions. This shift increases with increasing charge on the complex. The methy]ene proton signals of the benzy] group and the bridging group in the ligand are shifted slightly downfield on formation of the complexes. Since the magnitude of the shift is approximately proportional to the oxidation number in the metal complexes, the oxidation number could be distinguished by proton NMR studies of the methy]ene groups. These results indicate that the N drop C group in the ligand serves as a sigma-donor and the thioethereal sulfur in the bridging group is not coordinated to the metal atoms. It is surprising that L does not coordinate through the sulfur atoms rather than the isonitriles, because the S-coordinated form would have a stable five-membered-ring structure and the isonitrile coordination gives a fifteen-membered-ring structure.
CD(2,2'-BIPYRIDINE-N,N')NI(CN)4, A HIGHLY BENT CLOSE 2-DIMENSIONAL NETWORK OF [CD-((NC)NI1/4)4]N

M HASHIMOTO, T IWAMOTO

ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS ( MUNKSGAARD INT PUBL LTD ) 50 496 - 498 1994.04 [Refereed]

　View Summary

The crystal structure of poly[(2,2'-bipyridine-N,N')cadmium(II) tetra-mu-cyanonickelate(II)], [Cd(CoH8N2)][Ni(CN)4], has been determined. The tetracyanonickelate(II) ion, Ni(CN)42-, bridges four Cd+ ions to form an infinite two-dimensional folded network stacking along the b axis. The 2,2'-bipyridine ligands chelate to the Cd atoms alternately above and below the folded network. The distortion about the octahedrally coordinated Cd atom is so large, as a result of the unusual coordination behaviour of the Ni(CN)4 in the network formation, that one of the Cd-N-C angles is markedly bent [143.1 (3)-degrees].
ACID STRENGTH OF HETEROPOLYACIDS AND ITS CORRELATION WITH CATALYTIC ACTIVITY

T OKUHARA, CW HU, M HASHIMOTO, M MISONO

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN ( CHEMICAL SOC JAPAN ) 67 ( 4 ) 1186 - 1188 1994.04 [Refereed]

　View Summary

UV spectrophotometry of a Hammett indicator revealed that the acid strength of the Keggin-type heteropolyacids having W as addenda atoms increased as the valency of the central atom increased (Co < B < Si, Ge < P). The catalytic activity for the decomposition of isobutyl propionate in a homogeneous system was correlated well with the acid strength.
[(C5H5N)2H]3[PW12O40]

M HASHIMOTO, M MISONO

ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS ( MUNKSGAARD INT PUBL LTD ) 50 231 - 233 1994.02 [Refereed]

　View Summary

The crystal structure of tris(dipyridinium) dodecatung-stophosphate has been determined. The [PW12O40]3- heteropolyanion, having T(d) symmetry, is disordered by the 3 symmetry. The pyridine molecules are paired around H+ forming (C5H5N)-H+-(NC5H5) cations with their molecular planes almost parallel to the ab plane of the crystal.

DOI
SELECTIVE OXIDATION OF CYCLOPENTENE AND CYCLOHEXENE BY HYDROGEN-PEROXIDE CATALYZED BY HETEROPOLYACIDS

KY LEE, K ITOH, M HASHIMOTO, N MIZUNO, M MISONO

NEW DEVELOPMENTS IN SELECTIVE OXIDATION II ( ELSEVIER SCIENCE PUBL B V ) 82 583 - 591 1994 [Refereed]

　View Summary

Oxidation of cycloolefins by hydrogen peroxide catalyzed by various Keggin-type heteropolyacids, H3PMo12-xWxO40, x=0-12, were studied in homogeneous tri-n-butyl phosphate solution, placing stress on the effects of the constituent elements of heteropoly anion. Remarkable synergistic effect of mixed addenda atoms, Mo and W, was observed and high yields of dialdehyde were obtained. A reaction scheme was proposed based on the time course and stoichiometry of reaction, and the reactivity of products.
CRYSTAL-STRUCTURE OF TETRACAESIUMDIHYDROGENDECAVANADATE TRIHYDRATE, CS4H2V10O28-CENTER-DOT-3H2O - A LAYERED CRYSTAL-STRUCTURE OF DECAVANADATE

M HASHIMOTO, M MISONO, M HIBINO, J OI, T KUDO

POLYHEDRON ( PERGAMON-ELSEVIER SCIENCE LTD ) 12 ( 22 ) 2745 - 2747 1993.11 [Refereed]

　View Summary

The title compound Cs4H2V10O28.3H2O was obtained from a polyvanadate system containing H2O2. No peroxo group or hydrogen peroxide molecule was found in the structure. The polyanions are ordered parallel to the bc-plane forming a layered structure. The water molecules and the caesium ions make a hydrogen bonding network with decavanadate ions and each other to support the whole crystal structure.
CATALYSIS BY HETEROPOLY COMPOUNDS .22. REACTIONS OF ESTERS AND ESTERIFICATION CATALYZED BY HETEROPOLYACIDS IN A HOMOGENEOUS LIQUID-PHASE EFFECTS OF THE CENTRAL ATOM OF HETEROPOLYANIONS HAVING TUNGSTEN AS THE ADDENDA ATOM

CW HU, M HASHIMOTO, T OKUHARA, M MISONO

JOURNAL OF CATALYSIS ( ACADEMIC PRESS INC JNL-COMP SUBSCRIPTIONS ) 143 ( 2 ) 437 - 448 1993.10 [Refereed]
Second Harmonic Generation in Inorganic-Organic Complexes. 1. Control of Bulk Dipolar Alignment of p-Nitroaniline Crystal upon Complexing with Hydrobromic Acid

Takeshi Gotoh, Noritaka Mizuno, Masakazu Iwamoto, Satoshi Hashimoto, Masahiro Kawasaki, Masato Hashimoto, Makoto Misono

Chemistry of Materials 4 ( 3 ) 502 - 504 1992.02 [Refereed]

DOI
THE TWISTED SKELETON OF 1,9-DIAMINONONANE IN CATENA-[CATENA-MU-(1,9-DIAMINONONANE)CADMIUM(II) TETRA-MU-CYANONICKELATE(II)]-O-XYLENE(2/1)A

M HASHIMOTO, T KITAZAWA, T HASEGAWA, T IWAMOTO

JOURNAL OF INCLUSION PHENOMENA AND MOLECULAR RECOGNITION IN CHEMISTRY ( KLUWER ACADEMIC PUBL ) 11 ( 2 ) 153 - 158 1991.09 [Refereed]

　View Summary

The Hofmann-danon-type o-xylene clathrate Cd[NH2(CH2)9NH2]Ni(CN)4.0.5(CH3)2C6H4, crystallizes in the triclinic space group P1BAR with a = 15.118(3), b = 14.048(4), c = 7.325(1) angstrom, alpha = 91.50(2), beta = 131.66(3), and gamma = 107.50(2)-degrees, V = 1051(1) angstrom 3 and Z = 2. The structure, refined to R = 0.047 using 2851 reflections, reveals a three-dimensional host framework built of the layers of a two-dimensional catena-[cadmium tetra-mu-cyanonickelate(II)] network and of the ambidentate 1,9-diaminononane (danon) bridging the Cd atoms in adjacent networks. The guest o-xylene molecule is accommodated in the cavity formed in the interlayer space similar to that in the Hofmann-daotn-type. The skeleton of the danon in the Cd-NC9N-Cd linkage takes a (gauche)2(trans)8 conformation twisted at the (gauche)2 part in contrast with the all-trans conformation of 1,8-diaminooctane in the Hofmann-daotn-type clathrate. The twisted (gauche)2 part of the danon skeleton occupies the interlayer space to such an extent that void space available for the guest o-xylene molecule decreases to half that in the Hofmann-daotn-type clathrate Cd[NH2(CH2)8NH2]Ni(CN)4.G.

DOI
Preparation and X-ray crystal structure of [N(CH3)4]4[{H(SO4)W3O7(O2)2}2O]

Masato Hashimoto, Toschitake Iwamoto, Hikaru Ichida, Yukiyoshi Sasaki

Polyhedron 10 ( 6 ) 649 - 651 1991 [Refereed]

　View Summary

The title peroxotungstosulphate as the first example of a polytungstosulphate has been prepared and its structure determined. The salt crystallizes under the conditions: [WO42-] = 0.3-1.0 mol dm-3, [WO42-]/[SO42-] = 1-1/4, [WO42-]/[H2O2] = 1/2-1/4 and pH &lt
1. The SO42- tetrahedron shares its three vertices with two WO5(O2)2 decahedra and one WO6 octahedron to form a diperoxotritungstosulphate moiety
the polyanion is made of the two moieties bridged with three gm-oxo groups. © 1991.

DOI
CRYSTAL-STRUCTURES OF (18-CROWN-6)-(2-HYDROXYETHYLAMMONIUM) TETRACYANONICKELATE(II) AND 10-AMINODECYLAMMONIUM TETRACYANONICKELTATE(II)

M HASHIMOTO, T IWAMOTO

JOURNAL OF COORDINATION CHEMISTRY ( GORDON BREACH SCI PUBL LTD ) 23 ( 1-4 ) 269 - 276 1991 [Refereed]
CATENA-MU-(1,9-DIAMINONONANE)CADMIUM(II) ARRAY IN THE CRYSTAL-STRUCTURE OF CATENA-[BIS-CATENA-MU-(1,9-DIAMINONONANE)CADMIUM(II) CIS-DI-MU-CYANO-DICYANONICKELATE(II)]-(2,4-XYLIDINE) (1/2) DIFFERENT FROM THAT IN THE 2,3-ISOMER ANALOG

M HASHIMOTO, T IWAMOTO

CHEMISTRY LETTERS ( CHEMICAL SOC JAPAN ) ( 9 ) 1531 - 1534 1990.09 [Refereed]

DOI
NOVEL 3-DIMENSIONAL METAL-COMPLEX HOST STRUCTURES OF CATENA-[PROPYLENEDIAMINECADMIUM(II) TETRA-MU-CYANONICKELATE(II)] AND CATENA-[PROPYLENEDIAMINECADMIUM(II) TETRA-MU-CYANOCADMATE(II)]

KM PARK, M HASHIMOTO, T KITAZAWA, T IWAMOTO

CHEMISTRY LETTERS ( CHEMICAL SOC JAPAN ) ( 9 ) 1701 - 1704 1990.09 [Refereed]
IR, RAMAN AND C-13 NMR-SPECTRA OF PEROXOTUNGSTOOXALATE

M HASHIMOTO, T IWAMOTO, H ICHIDA, Y SASAKI, T KUDO

INORGANICA CHIMICA ACTA ( ELSEVIER SCIENCE SA LAUSANNE ) 166 ( 1 ) 17 - 20 1989.12 [Refereed]

DOI
CRYSTAL-STRUCTURE OF CATENA-[CATENA-BIS-MU-(1,9-DIAMINONONANE)CADMIUM CIS-DI-MU-CYANO-DICYANONICKELATE(II)]-(2,3-XYLIDINE)(1/2)

M HASHIMOTO, T HASEGAWA, H ICHIDA, T IWAMOTO

CHEMISTRY LETTERS ( CHEMICAL SOC JAPAN ) ( 8 ) 1387 - 1390 1989.08 [Refereed]
OXALATO COMPLEXES DIRECTLY FORMED BY THE REACTION OF INTERSTITIAL CARBIDES WITH HYDROGEN-PEROXIDE

T KUDO, Y SASAKI, M HASHIMOTO, K MATSUMOTO

INORGANICA CHIMICA ACTA ( ELSEVIER SCIENCE SA LAUSANNE ) 145 ( 2 ) 205 - 209 1988.05 [Refereed]

DOI
FORMATION OF PEROXO OXALATO COMPLEX OF TUNGSTEN(VI) DIRECTLY FROM TUNGSTEN CARBIDE AND HYDROGEN-PEROXIDE - A NEW PATH TO THE TOTAL SYNTHESIS OF THE ORGANIC-COMPOUND

T KUDO, Y SASAKI, M HASHIMOTO, H ICHIDA, K MATSUMOTO

INORGANICA CHIMICA ACTA ( ELSEVIER SCIENCE SA LAUSANNE ) 133 ( 2 ) 201 - 203 1987.10 [Refereed]
CRYSTAL-STRUCTURE OF TETRABUTYLAMMONIUM MU-OXALATOBIS(OXODIPEROXOTUNGSTATE) (2-), [(N-C4H9)4N]2[WO(O2)2(C2O4)WO(O2)2]

M HASHIMOTO, T OZEKI, H ICHIDA, Y SASAKI, K MATSUMOTO, T KUDO

CHEMISTRY LETTERS ( CHEMICAL SOC JAPAN ) ( 9 ) 1873 - 1876 1987 [Refereed]

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Misc

INOR 711-Characterization and 31P NMR study of [X2{PW3O9.5(O2)3(OH)0.5(OH2)}4]8-(X=K+, Rb+, NH4+)

Shinya Kitaura, Kiyotaka Kihara, Masato Hashimoto, Seichi Okeya

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY ( AMER CHEMICAL SOC ) 234 2007.08
INOR 906-Speciation study of phosphorus-containing Strandberg type heteropolymolybdate anions

Masato Hashimoto, Ingegaerd Andersson, Lage Pettersson

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY ( AMER CHEMICAL SOC ) 234 2007.08
INOR 693-Novel peroxodiphosphatomolybdate -structural and 31P NMR study-

Koji Aoki, Keisuke Iwata, Masato Hashimoto, Seichi Okeya

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY ( AMER CHEMICAL SOC ) 234 2007.08
INOR 704-31P NMR study of peroxophosphatotunstates in aqueous/acetonitrile mixed media

Yusuke Hamamatsu, Shinya Kitaura, Kiyotaka Kihara, Takahiro Terada, Masato Hashimoto, Seichi Okeya

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY ( AMER CHEMICAL SOC ) 234 2007.08
INOR 696-Characterization and 31P NMR study of [PMo10O35(O2)]7-with various counter cations

Keisuke Iwata, Koji Yamanaka, Koji Aoki, Masato Hashimoto, Seichi Okeya

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY ( AMER CHEMICAL SOC ) 234 2007.08
Future Opportunities in Organic Synthesis by Heteropoly Acid Catalysts

MISONO M.

Shokubai ( 触媒学会 ) 34 ( 3 ) p152 - 158 1992.04

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Works

環境調和型選択酸化触媒のナノ構造制御

2003

Conference Activities & Talks

三リン酸を含むペルオキソポリオキソタングステートの合成

中村悠人, 橋本正人

錯体化学会第73回討論会 2023.09.22
2種のペルオキソヘキサタングステートの合成法の最適化

池端祐人, 橋本正人

錯体化学会第73回討論会 2023.09.22
Pをヘテロ原子とする環状ペルオキソタングステートの結晶の質の改善とキャラクタリゼーション

大西正剛, 橋本正人

錯体化学会第73回討論会 2023.09.22
二リン酸をヘテロ原子団とする希土類含有ペルオキソポリオキソモリブデートの合成と構造解析

藏富勇人, 橋本正人

錯体化学会第73回討論会 2023.09.22
Synthesis of W11 peroxopolytungstate containing diphosphates and rare earth elements and its porous crystal structure

Yuu Yamazaki, Masato Hashimoto

錯体化学会第73回討論会 2023.09.21
有機配位子により架橋されたRE2W4型希土類含有ペルオキソタングステート誘導体の合成と構造

安上昂輝, 佐々木祐二, 橋本正人

錯体化学会第73回討論会 2023.09.21
環状三リン酸をヘテロ原子団とするペルオキソモリブデートの合成と錯形成時の溶液内での挙動

水野雄樹, 橋本正人

錯体化学会第73回討論会 2023.09.21
二リン酸と希土類によって集積化した W25 核ペルオキソポリタングステートの合成と構造

山崎優, 橋本正人

第39回希土類討論会 2023.05.31
二リン酸をヘテロ原子団とするペルオキソタングステートの合成と構造および溶液内挙動の追跡

植田悠斗, 橋本正人

錯体化学会第72回討論会 2022.09.27
カルボキレートを配位させたぺルオキソポリオキソタングステートの合成と構造解析

奥田裕一, 橋本正人

錯体化学会第72回討論会 2022.09.27
希土類イオンと二リン酸によって構造が支持されたW11核ペルオキソヘテロポリタングステートの合成と構造

山﨑優, 橋本正人

錯体化学会第72回討論会 2022.09.27
ギ酸基で架橋された無限鎖型希土類含有ペルオキソタングステートの合成と構造

安上昂輝, 橋本正人

錯体化学会第72回討論会 2022.09.27
八核ペルオキソジフォスファトモリブデートの合成方法の最適化と錯形成反応

藏富勇人, 橋本正人

錯体化学会第72回討論会 2022.09.26
トリメタリン酸をヘテロ原子団とするペルオキソモリブデートの反応溶液内での錯形成挙動

水野雄樹, 橋本正人

錯体化学会第72回討論会 2022.09.26
RE2W4型希⼟類含有ペルオキソタングステート誘導体の合成と構造

安上昂輝, 橋本正人

錯体化学会第71回討論会 2021.09.16
SiおよびTeをヘテロ原⼦とするペルオキソモリブデートの合成

古川裕太, 橋本正人

錯体化学会第71回討論会 2021.09.16
⼆リン酸をヘテロ原⼦団とした、希⼟類含有環状ペルオキソポリタングステートの合成と結晶構造

山﨑優, 橋本正人

錯体化学会第71回討論会 2021.09.16
新規ぺルオキソ・オキソ⼆重架橋ぺルオキソメタレートダイマーの合成・構造解析および溶液内挙動の追跡

奥田裕一, 橋本正人

錯体化学会第71回討論会 2021.09.16
⼆リン酸をヘテロ原⼦団とする⼆核ペルオキソタングステートの合成と構造および溶液内挙動の追跡

植田悠斗, 橋本正人

錯体化学会第71回討論会 2021.09.16
Ishii-Venturello型ペルオキソヘテロタングステートの合成検討と触媒反応過程の追跡

平谷直也, 橋本正人

錯体化学会第71回討論会 2021.09.16
プロピオン酸基を配位子としたペルオキソタングステートの合成と構造解析

奥田裕一, 橋本正人

錯体化学会第70回討論会 2020.09.30
ペルオキソジホスファトタングステートの合成と溶液内挙動の追跡

植田悠斗, 橋本正人

錯体化学会第70回討論会 2020.09.29
硫酸基を配位子として含むペルオキソモリブデートの合成と構造

古川裕太, 橋本正人

錯体化学会第70回討論会 2020.09.29
希土類(III)イオンを含むペルオキソイソモリブデートの合成、構造解析と発光特性およびタングステン類似体との比較

大川裕太, 橋本正人

錯体化学会第70回討論会 2020.09.29
31P, 51V NMRを用いた高濃度多リン酸ペルオキソバナデート系の錯形成挙動の調査と形成錯体の単離

櫃本雄一朗, 橋本正人

錯体化学会第70回討論会 2020.09.29
2種類のサンドイッチ型ペルオキソホスファトタングステートの合成と錯体形成の相互関係

祝田佑介, 橋本正人

錯体化学会第70回討論会 2020.09.29
希土類元素を含み、二リン酸をヘテロ原子団とするペルオキソヘテロポリタングステートの合成

山﨑優, 橋本正人

錯体化学会第70回討論会 2020.09.29
触媒反応過程の追跡を目的としたIshii-Venturello型ペルオキソヘテロタングステートの合成検討と溶液内挙動

平谷直也, 橋本正人

錯体化学会第70回討論会 2020.09.29
二リン酸をヘテロ原子団とするペルオキソモリブデートの合成と溶液内挙動の追跡

浅野翔, 橋本正人

錯体化学会第70回討論会 2020.09.29
硫酸を配位子として含むペルオキソモリブデートの新規合成法と構造

古川裕太, 橋本正人

第69回錯体化学討論会 2019.09.23
希土類元素を含むペルオキソイソタングステートの合成と構造、及び89Y, 183W NMR

山本雄介, 橋本正人

第69回錯体化学討論会 2019.09.23
未帰属シグナルを持つ多リン酸ペルオキソバナデート系の31P, 51V NMRを用いた溶液内挙動の調査

櫃本雄一朗, 橋本正人

第69回錯体化学討論会 2019.09.23
サンドイッチ型ペルオキソホスファトタングステートの合成と31P NMRによる溶液内挙動の追跡

祝田佑介, 橋本正人

第69回錯体化学討論会 2019.09.23
希土類イオンを組み込んだペルオキソイソモリブデートの発行特性および類似構造を持つタングステートとの比較

大川裕太, 橋本正人

第69回錯体化学討論会 2019.09.23
二リン酸をヘテロ原子団とするペルオキソモリブデートの合成と溶液内挙動の追跡

浅野翔, 橋本正人

第69回錯体化学討論会 2019.09.23
Triphosphatotriperoxodivanadate that survives in wide acidic conditions

Nagito Hirano, Masato Hashimoto

11th International Vanadium Symposium 2018.11.07
Ishii-Venturello type peroxovanadates with oligophosphates

Yuichiro Hitsumoto, Masato Hashimoto

11th International Vanadium Symposium 2018.11.06
ペルオキソジホスファトタングステートの合成と溶液内挙動の追跡

貴志智弥, 橋本正人

第68回錯体化学討論会 2018.07.29
直鎖多リン酸をヘテロ原子団とするペルオキソモリブデート

浅野翔, 橋本正人

第68回錯体化学討論会 2018.07.29
イリジウムを組み込んだペルオキソホスファト/イソモリブデートの合成と31P NMRによる溶液内挙動の追跡

山下達也, 橋本正人

第68回錯体化学討論会 2018.07.29
サンドイッチ型および環状ペルオキソヘテロタングステートの合成と構造

祝田佑介, 橋本正人

第68回錯体化学討論会 2018.07.29
環状・鎖状多リン酸とトリペルオキソジバナデートとの錯形成および形成錯体の単離・構造決定

平野凪斗, 橋本正人

第68回錯体化学討論会 2018.07.28
多リン酸を含むペルオキソバナデートの合成と構造およびアニオン形成反応

櫃本雄一朗, 橋本正人

第68回錯体化学討論会 2018.07.28
希土類(III)イオンを組み込んだペルオキソイソポリタングステートの合成と構造および89Y, 183W NMR

山本雄介, 橋本正人

第68回錯体化学討論会 2018.07.28
希土類元素を組み込んだペルオキソホスホタングステートの合成と構造決定

田中智史, 橋本正人

第68回錯体化学討論会 2018.07.28
希土類イオンを組み込んだペルオキソイソモリブデートの合成と構造

大川裕太, 橋本正人

第68回錯体化学討論会 2018.07.28
イリジウムとリンを組み込んだペルオキソタングステートの合成と31P NMRによる溶液内挙動の追跡

山下達也, 橋本正人

第67回錯体化学討論会 2017.09.16
多リン酸を含むペルオキソバナデート

平野凪斗, 橋本正人

第67回錯体化学討論会 2017.09.16
希土類元素(III)を組み込んだペルオキソイソポリタングステートの合成と構造および溶液内挙動の追跡

山本雄介, 橋本正人

第67回錯体化学討論会 2017.09.16
二リン酸をヘテロ原子団とするペルオキソタングステート

貴志智弥, 橋本正人

第67回錯体化学討論会 2017.09.16
希土類元素を組み込んだぺるオキソホスホタングステートの合成と構造解析

田中智史, 橋本正人

第67回錯体化学討論会 2017.09.16
W3ユニット[W3O14-x(O2)x]を含むペルオキソタングステートの形成と構造

小山直哉, 橋本正人

第67回錯体化学討論会 2017.09.16
Peroxovanadates and oligophosphates

Shunsuke Sorihashi, Nagito Hirano, Masato Hashimoto

10th International Vanadium Symposium 2016.11.07
希土類(III)イオンを含む捻じれ型ペルオキソイソタングステートの合成と構造

北村智哉, 橋本正人

第66回錯体化学討論会 2016.09.11
Pt(IV)含有ペルオキソヘテロポリタングステートの合成、構造および31P, 195Pt NMRによる溶液内挙動の検討

朝日聖晶, 橋本正人

第66回錯体化学討論会 2016.09.11
'W3ユニット'[W3O14-x(O2)x]をビルディングユニットとするペルオキソタングステートの形成と構造

小山直哉, 橋本正人

第66回錯体化学討論会 2016.09.11
直鎖多リン酸を含むペルオキソバナデートの合成と構造

反橋俊介, 橋本正人

第66回錯体化学討論会 2016.09.11
直鎖三リン酸―ペルオキソモリブデート系における錯形成反応の31P NMRによる追跡と形成錯体のキャラクタリゼーション

尾山諒輔, 橋本正人

第66回錯体化学討論会 2016.09.11
イリジウムを組み込んだペルオキソホスファトタングステートの合成と31P NMRによる溶液内挙動の追跡

山下達也, 橋本正人

第66回錯体化学討論会 2016.09.11
水溶液中における環状リン酸を含むペルオキソバナデート系の溶液内挙動

平野凪斗, 橋本正人

第66回錯体化学討論会 2016.09.10
希土類元素を組み込んだペルオキソイソ/ヘテロバナデートの合成

福井孝則, 橋本正人

第66回錯体化学討論会 2016.09.10
直鎖状リン酸をヘテロ原子団とするペルオキソタングステートの合成および31P NMRによる溶液内反応の検討

貴志智弥, 橋本正人

第66回錯体化学討論会 2016.09.10
二リン酸を含むペルオキソヘテロバナデートの合成と構造

反橋俊介, 橋本正人

第65回錯体化学討論会 2015.09.22
希土類元素を組み込んだペルオキソバナデートの合成

福井孝則, 橋本正人

第65回錯体化学討論会 2015.09.22
直鎖三リン酸をヘテロ原子団とするペルオキソモリブデートの合成と31P NMRによる溶液内挙動の追跡

尾山諒輔, 橋本正人

第65回錯体化学討論会 2015.09.22
水溶液系におけるリン酸により架橋されたペルオキソタングステート二量体の合成および31P NMRによる形成反応の検討

吉田祐基, 橋本正人

第65回錯体化学討論会 2015.09.21
Pt(IV)を組み込んだペルオキソヘテロポリタングステートの合成とNMRによる溶液内挙動の追跡

朝日聖晶, 橋本正人

第65回錯体化学討論会 2015.09.21
Pt(IV)を含むペルオキソタングステートの合成と形成反応の追跡

岩田貴大, 橋本正人

第65回錯体化学討論会 2015.09.21
Triphosphatoperoxotungstates - 31P NMR and Structural Study

Yusuke Kunigita, Masato Hashimoto

40th International Conference on Coordination Chemistry 2012.09.12
Structure and Anion Formation of Novel Diphosphatodecaperoxopentatungstate

Yusuke Kunigita, Masato Hashimoto

40th International Conference on Coordination Chemistry 2012.09.11
An Overview on Peroxopolyoxometallate

Masato Hashimoto [Invited]

GDCh-Wissenschaftsforum Chemie 2011 2011.09.07
Novel Diphosphatoperoxohexamolybdate

Kenji Konishi, Yusuke Kunigita, Masato Hashimoto

GDCh-Wissenschaftsforum Chemie 2011 2011.09.05
Triphosphatoperoxotungstates -31P NMR and Structural Study-

Yusuke Kunigita, Masato Hashimoto

GDCh-Wissenschaftsforum Chemie 2011 2011.09.05
Polymeric Peroxometalates

Masato Hashimoto [Invited]

PACIFICHEM2010 2010.12.19
Novel Peroxohexatungstate

Akitsugu Shiga, Masato Hashimoto

PACIFICHEM2010 2010.12.18
Novel Octaperoxophosphatotetratungstate

Shin-ya Kitaura, Katsutoshi Kato, Masato Hashimoto

PACIFICHEM2010 2010.12.18
Diphosphato complexes of vanadates and peroxovanadates

Masato Hashimoto

7th International Vanadium Symposium 2010.10.07
Novel peroxodiphosphatotungstates

Yuto Hirata, Masayuki Hanano, Kiyotaka Kihara, Masato Hashimoto

International Polyoxometalate Symposium 2009.07.30
A brief introduction of peroxoheteropolytungstates at low peroxide/W ratio

Masato Hashimoto [Invited]

International Polyoxometalate Symposium 2009.07.30
Simple peroxovanadate-amino acid complexes

Masato Hashimoto, Takeshi Higuchi, Seichi Okeya [Invited]

6th International Vanadium Symposium 2008.07.17
Synthesis and characterisation of novel [VO(O2)2L] (L=ligand) type complexes

Takeshi Higuchi, Masato Hashimoto, Seichi Okeya

6th International Vanadium Symposium 2008.07.17
Speciation study of phosphorus-containing Strandberg type heteromolybdate anions

Masato Hashimoto, Ingegärd Andersson, Lage Petterson [Invited]

234th The American Chemical Society National Meeing 2007.08.23
Characterization and 31P NMR study of [X2{PW3O9.5(O2)3(OH)0.5(OH2)}4]8- (X=K+, Rb+, NH4+)

Shin-ya Kitaura, Kiyotaka Kihara, Masato Hashimoto, Seichi Okeya

234th The American Chemical Society National Meeing 2007.08.21
Novel peroxodiphosphatomolybdate -structural and 31P NMR study-

Koji Aoki, Keisuke Iwata, Masato Hashimoto, Seichi Okeya

234th The American Chemical Society National Meeing 2007.08.21
31P NMR study of peroxophosphotungstates in aqueous/acetonitrile mixed media

Yusuke Hamamatsu, Takahiro Terada, Shin-ya Kitaura, Kiyotaka Kihara, Masato Hashimoto, Seichi Okeya

234th The American Chemical Society National Meeing 2007.08.21
Characterization and 31P NMR study of [PMo10O35(O2)]7-

Keisuke Iwata, Koji Yamanaka, Masato Hashimoto, Seichi Okeya

234th The American Chemical Society National Meeing 2007.08.21
Syntheses, structures and NMR studies of novel peroxopolytungstates coordinated by organic ligands

PACIFICHEM2005 2005.12.19
Peroxopolyoxometalates as assemblies of building units

Masato Hashimoto

PACIFICHEM2005 2005.12.19
Keggin- and Dawson-type tungstosulfuric acids applicable as super strong acid catalysts

Masayuki Hanano, Hiroki Ozaki, Masato Hashimoto, Seichi Okeya

PACIFICHEM2005 2005.12.18
Formation, Synthesis and Structure of Peroxoheteropolytungstates obtained from Aqueous-Organic Mixed Media

Yusuke Hamamatsu, Masato Hashimoto, Seichi Okeya

11th Asian Chemical Congress 2005.08.25
Recent Progress on Peroxopolyoxometallates

Masato Hashimoto [Invited]

28th International Conference on Solution Chemistry 2002.07.23
Structure of [PMo10O35(O2)]7-. A Novel Capped Lacunary Keggin Type Heteropolyanion

Koji Yamanaka, Masato Hashimoto, Seichi Okeya

35th International Conference on Coordination Chemistry 2002.07.23
The synthesis and structure of a novel peroxoisopolytungstate [W7O22(O2)2]6-

Hiroyuki Suzuki, Masato Hashimoto, Seichi Okeya

9th Nordic Symposium on Coordination Chemistry 2002.06.15
Structures of novel peroxoisopolymolybdates formed in aqueous-organic medium

Takashi Tanaka, Masato Hashimoto, Seichi Okeya

9th Nordic Symposium on Coordination Chemistry 2002.06.15
Perspective Aspects on Peroxopolyoxometallates

Masato Hashimoto [Invited]

9th Nordic Symposium on Coordination Chemistry 2002.06.15
The structures of novel 3D [V10O28]6- transition metal complexes

Tomoyuki Higami, Masato Hashimoto, Seichi Okeya

3rd International Symposium on Vanadium Chemistry and Biochemistry 2001.11.28
Peroxomolybdates -Preparation and Structure-

Tomohiro Minami, Masato Hashimoto, Seichi Okeya

PACIFICHEM2000 2000.12.17

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Research Exchange

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KAKENHI

ペルオキソへテロポリタングステートの構造制御-溶媒と陽イオンが担う役割とは?-

2007.04

-

2011.03

Grant-in-Aid for Scientific Research(C) Principal investigator
ビルディングブロックの集積によるイオン性金属過酸化物ポリマーの分子構築

2003.04

-

2006.03

Grant-in-Aid for Exploratory Research Principal investigator
平面四角形型錯体の反応モデルとしての五配位錯体

1999.04

-

2002.03

Grant-in-Aid for Scientific Research(C) Co-investigator

Joint or Subcontracted Research with foundation, company, etc.

ナフタレン誘導体の試験研究

2024.06

-

2024.07

Contracted research Principal investigator

Instructor for open lecture, peer review for academic journal, media appearances, etc.

非常勤講師

2015.04

-

2015.09

広島大学大学院工学研究院

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非常勤講師等

非常勤講師,任期:2015/04/08～2015/09/30
論文審査

2013.04

-

Now

Inorganic Chemistry Communications, Journal of Molecular Catalysisなど　( Elsevier)

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学術雑誌等の編集委員・査読・審査員等

論文審査,任期:継続中
南紀熊野サテライト講義

2010.04

和歌山大学

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公開講座・講演会の企画・講師等

南紀熊野サテライト講義「みんなの科学入門」を行なった。(7コマ分),日付:2010.11～2010.12

Committee member history in academic associations, government agencies, municipalities, etc.

公益社団法人日本化学会　オリンピック小委員会委員

2023.03.01

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2024.02.28

日本化学会

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化学オリンピック

代表生徒の選抜及び教育訓練
公益社団法人日本化学会　オリンピック小委員会委員

2022.03.01

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化学オリンピック

代表生徒の選抜及び教育訓練
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2021.03.01

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化学オリンピック

代表生徒の選抜及び教育訓練
学協会、政府、自治体等の公的委員

2020.03

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2021.03

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2020.02

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2021.02

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学協会、政府、自治体等の公的委員

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2019.11

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2020.10

公益社団法人日本化学会近畿支部　2020年度公益社団法人日本化学会

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（近畿支部選出）2020年度代議員,任期:2019年11月～2020年10月
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2019.10

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2020.09

日本化学会

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代議員,任期:1年
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2019.03

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2020.02

公益財団法人日本化学会グランプリ小委員会

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国や地方自治体、他大学・研究機関等での委員

委員,任期:2019年3月～2020年2月
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2019.02

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2020.02

日本化学会

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学協会、政府、自治体等の公的委員

化学グランプリ・オリンピック委員会化学オリンピック小委員会,任期:1年
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2018.02

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2019.02

日本化学会

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化学グランプリ・オリンピック委員会化学オリンピック小委員会,任期:1年
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2017.04

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2018.02

平成29年教育・普及部門の委員会

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国や地方自治体、他大学・研究機関等での委員

委員,任期:2017年～2018年２月
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2017.03

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2018.02

平成29年教育・普及部門の委員会

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国や地方自治体、他大学・研究機関等での委員

委員,任期:2017年3月-2018年2月
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2017.02

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2018.02

日本化学会

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学協会、政府、自治体等の公的委員

化学グランプリ・オリンピック委員会化学オリンピック小委員会,任期:1年
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2016.03

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2017.02

オリンピック小委員会

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国や地方自治体、他大学・研究機関等での委員

委員,任期:2016年3月-2017年2月
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2016.02

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2017.02

日本化学会

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化学グランプリ・オリンピック委員会化学オリンピック小委員会,任期:1年
委員長

2015.02

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2016.02

日本化学会

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化学グランプリ・オリンピック委員会化学オリンピック小委員会,任期:1年
理事

2014.06

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2015.06

一般社団法人和歌山県発明協会

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国や地方自治体、他大学・研究機関等での委員

理事,任期:2014/06/03～2015/06/03
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2014.06

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2015.03

和歌山県起業家支援施設等入居審査委員会

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2014.06

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2015.03

公益財団法人わかやま産業振興財団わかやま中小企業元気ファンド事業審査委員会

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国や地方自治体、他大学・研究機関等での委員

委員,任期:2014/06/04～2015/03/31
評議員

2014.05

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2015.03

公益財団法人わかやま産業振興財団

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国や地方自治体、他大学・研究機関等での委員

評議員,任期:2014/05/08～2015/03/31
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2014.03

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2015.02

公益社団法人日本化学会　化学グランプリ・オリンピック委員会　オリンピック小委員会

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国や地方自治体、他大学・研究機関等での委員

国や地方自治体、他大学・研究機関等での委員,任期:2014/03/01～2017/02/28
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2014.02

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2016.02

教育・普及部門の委員会

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国や地方自治体、他大学・研究機関等での委員

委員,任期:2015/02/26～2016/02/28
講師

2013.04

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2014.03

鳥取県

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科学を創造する人材育成事業
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2013.03

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2015.02

オリンピック小委員会

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国や地方自治体、他大学・研究機関等での委員

委員,任期:2014/03/01～2015/02/28
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2012.03

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2015.02

日本化学会

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学協会、政府、自治体等の公的委員

化学グランプリ・オリンピック委員会化学オリンピック小委員会
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2009.10

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2010.03

第7回バナジウム国際会議国内組織委員会

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学会開催のための準備等,任期:2009.10～2010.3
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2009.04

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2010.02

日本化学会

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学協会、政府、自治体等の公的委員

学協会、政府、自治体等の公的委員,任期:2009.4～2010.2
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2007.07

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2007.08

和歌山県

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国や地方自治体、他大学・研究機関等での委員

戦略的研究開発プラン外部審査員 ,任期:2007.7～2007.8
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2007.04

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2010.03

化学系研究設備有効活用ネットワーク協議会

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共同利用機器の選定、活動方針の決定、予算決算の承認、など,任期:2007.4～2010.3

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