Tin-Capped Trinuclear Nickel Clusters: Redox Isomerism between μ3-Stannyl and μ3-Stannylene Clusters of the Class [Ni3(dppm)3(μ3-I)(μ3-SnClx)]n+ (x = 2, n = 1; x = 3, n = 0)
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California at San Diego, 9500 Gilman Drive, La Jolla, California 92093-0358, and Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-1393
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ic020108a
Reference12 articles.
1. Infrared spectroelectrochemical and electrochemical kinetics studies of the reaction of nickel cluster radicals [Ni3(μ2-dppm)3(μ3-L) (μ3I)]•(L = CNR, R = CH3, i-C3H7, C6H11, CH2C6H5, t-C4H9, 2,6-Me2C6H3; L = CO) with carbon dioxide
2. Carbon dioxide chemistry of the trinuclear complex [Ni3(.mu.3-CNMe)(.mu.3-I)(dppm)3][PF6]. Electrocatalytic reduction of carbon dioxide
3. Synthesis and characterization of .mu.2-.eta.2- and .mu.2-.eta.3-CO2 complexes of iron and rhenium
4. Sodium [NN′-ethylenebis(salicylideneiminato)cobaltate(I)], a reversible carbon dioxide carrier
5. Carbon dioxide activation by cobalt macrocycles: evidence of hydrogen bonding between bound CO2 and the macrocycle in solution
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