Affiliation:
1. Engineering Research Center of Advanced Rare Earth Materials (Ministry of Education), Center of Basic Molecular Science (CBMS) Department of Chemistry Tsinghua University Beijing 100084 China
2. Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 P. R. China
Abstract
AbstractThe reactivity of metal‐hydride complexes can be harnessed by the modification of ancillary ligands. With the aim of improving the hydride‐donor ability of the key Mn−H intermediate and reducing steric hindrance, we herein report the rational design of a versatile and efficient NHC‐based NNC‐pincer Mn catalyst for hydrogenation reactions. This newly developed catalyst exhibited higher activity than the corresponding NNP‐pincer Mn catalyst owing to its reduced steric hindrance and enhanced Mn−H σ‐bonding orbital energy level through a π‐antibonding interaction. Using this highly active NNC‐pincer Mn catalyst, a rich array of polar unsaturated compounds (>80 examples) including esters, N‐heteroarenes, amides, carbonates, and urea derivatives, were successfully hydrogenated under relatively mild conditions. This work represents a rare example of a general phosphine‐free Mn‐catalyzed hydrogenation system.
Funder
National Natural Science Foundation of China
Cited by
1 articles.
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