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CH2 Linkage Effects on the Reactivity of Bis(aminophosphine)-Ruthenium Complexes for Selective Hydrogenation of Esters into Alcohols.


ABSTRACT: A novel ruthenium complex binding to two subtly different aminophosphine ligands, (o-PPh2C6H4CH2NH2)(o-PPh2C6H4NH2)RuCl2, was successfully isolated. This bis(aminophosphine)-ruthenium complex shows efficient activity in both dimethyl oxalate (DMO) and methyl benzoate (MB) hydrogenation. On the contrast, similar complexes (o-PPh2C6H4NH2)2RuCl2 and (o-PPh2C6H4CH2NH2)2RuCl2, can only effectively catalyze the hydrogenation of DMO and MB, respectively. Our experimental studies in combination of theoretical calculations reveal that the remarkable substrate selectivity in the hydrogenation of esters arises from the nonbonding interactions operated by the CH2 linkage of the ligand.

SUBMITTER: Fang X 

PROVIDER: S-EPMC5479805 | biostudies-other | 2017 Jun

REPOSITORIES: biostudies-other

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CH<sub>2</sub> Linkage Effects on the Reactivity of Bis(aminophosphine)-Ruthenium Complexes for Selective Hydrogenation of Esters into Alcohols.

Fang Xiaolong X   Sun Mingjun M   Zheng Jianwei J   Li Bin B   Ye Linmin L   Wang Xiaoping X   Cao Zexing Z   Zhu Hongping H   Yuan Youzhu Y  

Scientific reports 20170621 1


A novel ruthenium complex binding to two subtly different aminophosphine ligands, (o-PPh<sub>2</sub>C<sub>6</sub>H<sub>4</sub>CH<sub>2</sub>NH<sub>2</sub>)(o-PPh<sub>2</sub>C<sub>6</sub>H<sub>4</sub>NH<sub>2</sub>)RuCl<sub>2</sub>, was successfully isolated. This bis(aminophosphine)-ruthenium complex shows efficient activity in both dimethyl oxalate (DMO) and methyl benzoate (MB) hydrogenation. On the contrast, similar complexes (o-PPh<sub>2</sub>C<sub>6</sub>H<sub>4</sub>NH<sub>2</sub>)<sub>2</  ...[more]

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