Effect of Pressure on the Reversible Binding of Acetonitrile to the “Co(I)−CO2” Adduct To Form Cobalt(III) Carboxylate
Author:
Affiliation:
1. Chemistry Department, Brookhaven National Laboratory, Upton, New York 11973-5000, and Institute for Inorganic Chemistry, University of ErlangenNürnberg, Egerlandstrasse 1, 91058 Erlangen, Germany
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ic971044k
Reference37 articles.
1. For example: (a)Catalytic Activation of Carbon Dioxide; Ayers, W. M., Ed.; ACS Symposium Series 363; American Chemical Society: Washington, DC, 1988. (b) Behr, A.Carbon Dioxide Activation by MetalComplexes; VCH: Weinheim, 1988. (c)Electrochemical and ElectrocatalyticReactions of Carbon Dioxide; Sullivan; B. P., Ed.; Elsevier: Amsterdam, 1993. (d)Proceedings of the Fourth International Symposium on Chemical Fixationof Carbon Dioxide, Kyoto, Japan, Sept. 7−11, 1997; Inui, T., et al., Eds.; Elsevier: Amsterdam, 1998.
2. Electrocatalytic reduction of carbon dioxide by using macrocycles of nickel and cobalt
3. Homogeneous catalysis of the photoreduction of water by visible light. Mediation by a tris(2,2'-bipyridine)ruthenium(II)-cobalt(II) macrocycle system
4. A study of the mechanism for the electrocatalysis of carbon dioxide reduction by nickel and cobalt square planar complexes in solution
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