Comparative Analysis of the Donor Properties of Isomeric Pyrrolyl Phosphine Ligands
Author:
Affiliation:
1. Department of Chemistry, University of Richmond, Richmond, Virginia 23173, United States
2. Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, United States
Funder
Division of Chemistry
University of Richmond
American Chemical Society Petroleum Research Fund
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.3c00467
Reference57 articles.
1. N-Pyrrolyl Phosphines: An Unexploited Class of Phosphine Ligands with Exceptional .pi.-Acceptor Character
2. Synthesis of Pyrrolyl-, Indolyl-, and Carbazolylphosphanes and Their Catalytic Application as Ligands in the Hydroformylation of 2-Pentene
3. N-Pyrrolylphosphines as ligands for highly regioselective rhodium-catalyzed 1-butene hydroformylation: effect of water on the reaction selectivity
4. Chelating N-pyrrolylphosphino-N′-arylaldimine ligands: synthesis, ligand behaviour and applications in catalysis
5. Disentangling Ligand Effects on Metathesis Catalyst Activity: Experimental and Computational Studies of Ruthenium–Aminophosphine Complexes
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1. Effects of Substituted Triarylphosphine Ligands on Electron Transfer in [(p-Cymene)Ru] Complexes;Organometallics;2024-08-17
2. N^N^C-Cyclometalated rhodium(iii) complexes with isomeric pyrimidine-based ligands: unveiling the impact of isomerism on structural motifs, luminescence and cytotoxicity;Dalton Transactions;2024
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