Ring opening versus phenyl–phosphorus bond cleavage in incorporating a phosphole into triosmium clusters
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/1991/DT/DT9910003381
Reference16 articles.
1. Oxidative addition of phenylphosphole: X-ray crystal structures of two ring-opened products [Os3(μ3-PhPC4H4)(CO)x] where x = 8 or 9
2. Carbon–hydrogen cleavage versus ring opening in the oxidative addition reactions of furan, thiophene, selenophene and tellurophene with [Os3(CO)10(MeCN)2]
3. Crystal structures of the clusters [Os3H2(XCH:CHC:C)(CO)9] where X = NMe or S containing triply bridging ligands derived from n-methylpyrrole and thiophene
4. Triosmium clusters formed by oxidative addition and decarbonylation of 2-formylpyrrole: crystal structures of three triosmium clusters containing aromatic or nonaromatic heterocyclic ligands derived from pyrrole
5. Triosmium Clusters
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3. Fluxional behaviour of phosphole and phosphine ligands on triosmium clusters;Journal of Organometallic Chemistry;2015-12
4. Synthesis and characterization of trinuclear osmium clusters containing diallylphosphines as hemilabile ligands: Experimental and theoretical studies of their reactivity with nucleophilic molecules;Journal of Organometallic Chemistry;2014-12
5. Reactivity of triosmium clusters with 3,4-dimethyl-1-phenylphosphole and cyanoethyldi-tert-butylphosphine ligands: X-ray crystal structures of [Os3(CO)9(μ-OH)(μ-H)(η1-PhPC4H2Me2)] and [Os3(CO)11(η1- t Bu2PC2H4CN)];Transition Metal Chemistry;2013-12-29
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