A mechanistic exploration of the Wilkinson hydrogenation catalyst. Part 1: Model templates
Author:
Abstract
Geoffrey Wilkinson first reported his famous work on the hydrogenation catalyst that now bears his name in 1965[1] and I met him at Imperial College around 1969 and again when I returned there in 1977.
Publisher
Front Matter
Link
https://api.rogue-scholar.org/posts/10.59350/66mt7-bk491.pdf
Reference7 articles.
1. Hydride intermediates in homogeneous hydrogenation reactions of olefins and acetylenes using rhodium catalysts,1965
2. Two-dimensional δ/J-resolved31P n.m.r. spectroscopy of [bis(diphenylphosphino)methane](trimethylphosphine)chlororhodium(I),1982
3. Trimethyl and diethylphenylphosphine complexes of rhenium(I, III, IV, V) and their reactions. X-ray crystal structures of a bis(η5-cyclopentadienyl)-ethane-bridged dirhenium(I) complex obtained from phenylacetylene, tetrakis-(diethylphenylphosphine) (dinitrogen) hydridorhenium (I), tetrakis(trimethyl-phosphine) (η2-dimethylphosphinomethyl) rhenium(I) and tetrakis(trimethylphosphine) (iodo)methyl rhenium(III) iodide-tetramethylphosphonium iodide,1982
4. Bis(diphenylphosphino)methane trimethylphosphine alkyl and η5-cyclopentadienyl compounds of rhodium(I); 31P{1H} two dimensional δ/J resolved and Overhauser effect nuclear magnetic resonance spectroscopy,1982
5. Harnessing FAIR data: A suggested useful persistent identifier (PID) for quantum chemical calculations.,2018
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