A substrate-dependent mechanism for the reactions of a hydrido(hydrosilylene)ruthenium complex with carbonyl compounds: insights from quantum chemical calculations
Author:
Affiliation:
1. Department of Applied Chemistry
2. Zhejiang Gongshang University
3. Hangzhou 310018
4. People's Republic of China
5. Department of Chemistry
6. Zhejiang University
7. Hangzhou 310027
Abstract
The reactivity difference between ketones and aldehydes towards the ruthenium silylene hydride complex is dependent on the substituents of the carbonyl substrates.
Funder
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2017/NJ/C6NJ02361D
Reference40 articles.
1. Redistribution of Methyl Groups between Silicon Centers in Bis(silyl)tungsten Complexes: Silyl Silylene Complex Intermediates as the Source of Interligand Reactivity
2. Activation of the Si-Si Bond by Transition Metal Complexes
3. Stoichiometric and Catalytic Behavior of Cationic Silyl and Silylene Complexes
4. Reactivity of silylene complexes
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1. Ruthenium and Osmium Complexes Containing NHC and π-Acid Ligands;Comprehensive Organometallic Chemistry IV;2022
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