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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2017
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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) |
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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 |
work_keys_str_mv |
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1718388742199181312 |