期刊
INORGANIC CHEMISTRY FRONTIERS
卷 7, 期 9, 页码 1845-1850出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9qi01431d
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资金
- National Research Foundation of Korea - Korean government (MIST) [NRF-2018R1A5A1025208]
A diphosphinoamido cobalt scaffold was employed for studying catalytic CO2 hydrogenation. Particularly, the dissociative ligand loss of a cobalt catalyst induced by a formate product has been investigated. A structurally rigidified ligand leads to the reduction of the basicity of an amido moiety of a cobalt complex, thus revealing higher catalyst performance relative to the original ligand. With a robust N-Co moiety, the hydrolytic stability of the catalyst toward an accumulated conjugate acid [DBUH][OCHO] has been dramatically improved.
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