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...

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Autores principales: Xiaolong Fang, Mingjun Sun, Jianwei Zheng, Bin Li, Linmin Ye, Xiaoping Wang, Zexing Cao, Hongping Zhu, Youzhu Yuan
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Publicado: Nature Portfolio 2017
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spelling oai:doaj.org-article:eb96cef5dc944821b337e7fb530eba842021-12-02T15:05:47ZCH2 Linkage Effects on the Reactivity of Bis(aminophosphine)–Ruthenium Complexes for Selective Hydrogenation of Esters into Alcohols10.1038/s41598-017-04362-92045-2322https://doaj.org/article/eb96cef5dc944821b337e7fb530eba842017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-04362-9https://doaj.org/toc/2045-2322Abstract 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.Xiaolong FangMingjun SunJianwei ZhengBin LiLinmin YeXiaoping WangZexing CaoHongping ZhuYouzhu YuanNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Xiaolong Fang
Mingjun Sun
Jianwei Zheng
Bin Li
Linmin Ye
Xiaoping Wang
Zexing Cao
Hongping Zhu
Youzhu Yuan
CH2 Linkage Effects on the Reactivity of Bis(aminophosphine)–Ruthenium Complexes for Selective Hydrogenation of Esters into Alcohols
description 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.
format article
author Xiaolong Fang
Mingjun Sun
Jianwei Zheng
Bin Li
Linmin Ye
Xiaoping Wang
Zexing Cao
Hongping Zhu
Youzhu Yuan
author_facet Xiaolong Fang
Mingjun Sun
Jianwei Zheng
Bin Li
Linmin Ye
Xiaoping Wang
Zexing Cao
Hongping Zhu
Youzhu Yuan
author_sort Xiaolong Fang
title CH2 Linkage Effects on the Reactivity of Bis(aminophosphine)–Ruthenium Complexes for Selective Hydrogenation of Esters into Alcohols
title_short CH2 Linkage Effects on the Reactivity of Bis(aminophosphine)–Ruthenium Complexes for Selective Hydrogenation of Esters into Alcohols
title_full CH2 Linkage Effects on the Reactivity of Bis(aminophosphine)–Ruthenium Complexes for Selective Hydrogenation of Esters into Alcohols
title_fullStr CH2 Linkage Effects on the Reactivity of Bis(aminophosphine)–Ruthenium Complexes for Selective Hydrogenation of Esters into Alcohols
title_full_unstemmed CH2 Linkage Effects on the Reactivity of Bis(aminophosphine)–Ruthenium Complexes for Selective Hydrogenation of Esters into Alcohols
title_sort ch2 linkage effects on the reactivity of bis(aminophosphine)–ruthenium complexes for selective hydrogenation of esters into alcohols
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/eb96cef5dc944821b337e7fb530eba84
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