Dinuclear (d3−d3) Diolate Complexes of Molybdenum and Tungsten. 3.1 Bridging and Chelating Isomers of M2(NMe2)2(O∼∼CHMe∼∼O)2, Where O∼∼CHMe∼∼O Is the Dianion of 2,2‘-Ethylidenebis(4,6-di-tert-butylphenol). Kinetic versus Thermodynamic Considerations
Author:
Affiliation:
1. Department of Chemistry and Molecular Structure Center, Indiana University, Bloomington, Indiana 47405
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ic9708430
Reference14 articles.
1. Dinuclear (d3−d3) Diolate Complexes of Molybdenum and Tungsten. 2.1 Derivatives of 2,2‘-Methylenebis(6-tert-butyl-4-methylphenoxide). Direct Observation of the Conversion of Bridged to Chelate Isomers (M = Mo) and Reversible Carbon−Hydrogen Bond Oxidative Addition (M = W)
2. Kinetics and Mechanism of Reactions of Transition Metal Complexes
3. The coordination chemistry of dinuclear molybdenum(III) and tungsten(III): d3-d3 dimers
4. Unbridged and bridged isomers of W2(PCy2)2(NMe2)4: preparations, characterizations, and comments on thermodynamic and activation parameters for the closing of phosphido bridges in d3-d3 dinuclear compounds
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