Cp* non-innocence and the implications of (η4-Cp*H)Rh intermediates in the hydrogenation of CO2, NAD+, amino-borane, and the Cp* framework – a computational study
Author:
Affiliation:
1. Coordination Chemistry and Catalysis Unit, Okinawa Institute of Science and Technology, 1919-1 Tancha, Onna-son, Okinawa, 904-0495, Japan
Abstract
Publisher
Royal Society of Chemistry (RSC)
Subject
Inorganic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/DT/D2DT03611H
Reference61 articles.
1. Pentamethylcyclopentadienylrhodium and -iridium halides. I. Synthesis and properties
2. J.Okuda and T.Eberle , in Metallocenes , Wiley-VCH Verlag GmbH , Weinheim, Germany , 2008 , pp. 415–453
3. Base-Free Iridium-Catalyzed Hydrogenation of Esters and Lactones
4. Hydrogenation of Carboxylic Acids Catalyzed by Half-Sandwich Complexes of Iridium and Rhodium
5. Ambient-pressure hydrogenation of ketones and aldehydes by a metal-ligand bifunctional catalyst [Cp*Ir(2,2′-bpyO)(H2O)] without using base
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1. Assessment of the applicability of DFT methods to [Cp*Rh]‐catalyzed hydrogen evolution processes;Journal of Computational Chemistry;2024-07-25
2. Protonolysis of BH4– Leads to Intermediacy of BH3-σ(H2) That Evolves H2 and Furnishes Borane as the Key Reducing Agent;Organometallics;2023-10-31
3. Computational Insights into the Influence of Ligands on Hydrogen Generation with [Cp*Rh] Hydrides;The Journal of Physical Chemistry A;2023-07-12
4. Cyclopentadienyl ring activation in organometallic chemistry and catalysis;Nature Reviews Chemistry;2023-05-31
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