期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 136, 期 27, 页码 9719-9731出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja5044243
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资金
- Funding Program for Next Generation World-Leading Researchers [GR025]
- Japan Society for the Promotion of Science (JSPS) [26288044, 26620075, 26105708, 22245028, 24109014]
- Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT)
- MEXT Project of Integrated Research on Chemical Synthesis
- MEXT Project of Elements Strategy Initiative to Form Core Research Center
- JSPS
- Grants-in-Aid for Scientific Research [26288044, 13J08163, 24109014, 26620075, 26888008, 26105708] Funding Source: KAKEN
A series of dinitrogen-bridged dimolybdenum-dinitrogen complexes bearing 4-substituted PNP-pincer ligands are synthesized by the reduction of the corresponding molybdenum trichloride complexes under 1 atm of molecular dinitrogen. In accordance with a theoretical study, the catalytic activity is enhanced by the introduction of an electron-donating group to the pyridine ring of PNP-pincer ligand, and the complex bearing 4-methoxy-substituted PNP-pincer ligands is found to work as the most effective catalyst, where 52 equiv of ammonia are produced based on the catalyst (26 equiv of ammonia based on each molybdenum atom of the catalyst), together with molecular dihydrogen as a side-product. Time profiles for the catalytic reactions indicate that the rates of the formation of ammonia and molecular dihydrogen depend on the nature of the substituent on the PNP-pincer ligand of the complexes. The formation of ammonia and molecular dihydrogen is complementary in the reaction system.
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