Kinetic and Computational Analysis of CO Substitution in a Dinuclear Osmium Carbonyl Complex: Intersection between Dissociative and Dissociative-Interchange Mechanisms
Author:
Affiliation:
1. Department of Chemistry, Texas A&M University, College Station, Texas 77843, United States
2. Department of Chemistry & Biochemistry, Abilene Christian University, Abilene, Texas 79699, United States
Funder
Welch Foundation
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.1c02797
Reference28 articles.
1. Sawhorse-type diruthenium tetracarbonyl complexes
2. Dinuclear ruthenium complexes as active catalyst precursors for the low pressure hydroformylation of alkenes into aldehydes
3. Alkene isomerization by non-hydridic phosphine substituted ruthenium carbonyl carboxylates
4. Ruthenium complexes with 1,1′-biisoquinoline as ligand. Synthesis and hydrogenation activity
5. On the behaviour of Ru(I) and Ru(II) carbonyl acetates in the presence of H2 and/or acetic acid and their role in the catalytic hydrogenation of acetic acid
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1. Theoretical Investigation of Linear Relationships between the Dihedral Torsion Angles and Diosmium Bond Distances in Diosmium Sawhorse Complexes;Inorganic Chemistry;2024-01-18
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