Competing Thermal and Photochemical Ligand Substitution Reactions of the Dimetallacycle (CO)4Mo(μ-PMD)2Mo(CO)4 (PMD = Pentamethylenediazirine). Mechanistic Information from Entering Nucleophile and Pressure Dependences
Author:
Affiliation:
1. Institute for Inorganic Chemistry, University of Erlangen-Nürnberg, Egerlandstrasse 1, 91058 Erlangen, Germany
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om961047p
Reference54 articles.
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4. "Mixed" Complexes of Group VIb Metal Carbonyls
5. Kinetic studies of phosphite ligand substitution in o-phenanthroline complexes of Group VIb metal carbonyls
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1. Organometallic Chemistry of Polypyridine Ligands I;Advances in Heterocyclic Chemistry Volume 93;2007
2. The interpretation and mechanistic significance of activation volumes for organometallic reactions;Advances in Physical Organic Chemistry;2006
3. Systematic Tuning of the Photosubstitution Mechanism of M(CO)4(1,10-phenanthroline) by Variation of the Metal, Entering Nucleophile, Excitation Wavelength, and Pressure;Inorganic Chemistry;1998-02-07
4. Chapter 28. Mechanisms of reactions in solution;Annual Reports Section "A" (Inorganic Chemistry);1998
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