Development of Group4 Transition Metal Polyhydride Complexes for Dinitrogen Activation
Project/Area Number |
24750063
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Inorganic chemistry
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Research Institution | Institute of Physical and Chemical Research |
Principal Investigator |
SHIMA Takanori 独立行政法人理化学研究所, 侯有機金属化学研究室, 専任研究員 (60391976)
|
Project Period (FY) |
2012-04-01 – 2014-03-31
|
Project Status |
Completed (Fiscal Year 2013)
|
Budget Amount *help |
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2013: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Fiscal Year 2012: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
|
Keywords | 窒素活性化 / ヒドリド錯体 / 多金属錯体 / チタン / チタンヒドリド錯体 / 水素化 / アンモニア / ジルコニウム / ハフニウム / ポリヒドリド錯体 |
Research Abstract |
We successfully created a novel multi-metallic titanium polyhydride compound that can cleave the dinitrogen bond and form nitrogen-hydrogen bond at ambient temperature and pressure without additional reducing agents or proton sources. The titanium polyhydride compound can generate sufficient electrons to break nitrogen triple bonds by elimination of H2, which is a source of two electrons for each H2 unit lost, and act as a hydrogen source for ammonia precursors. Furthermore, the metal centers might enhance N2 activation through cooperative effects seen in biological nitrogen fixation and the Haber-Bosch process. This is unprecedented to observe N2 activation, bond cleavage and N-H bond formation steps in one reaction. This result offers hope in the search for mild dinitrogen reduction catalysts.
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Report
(3 results)
Research Products
(29 results)