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Journal ArticleDOI

Reaction de metathese des olefines induite photochimiquement en presence d'un complexe de metal de transition : VI. Existence probable d'un metallodichlorocarbene primaire

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TLDR
In this paper, a mechanism for the formation of these compounds is outlined, and the mechanism for their formation is described in terms of the insertion of metalladichlorocarbene moieties into the carbon double bond.
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This article is published in Journal of Organometallic Chemistry.The article was published on 1980-02-19. It has received 35 citations till now. The article focuses on the topics: Enol & Double bond.

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Photocatalyse appliquee a la metathese dans le cas du systeme W(CO)6/CCl4/hv. Proprietes des precurseurs et role du solvant

TL;DR: In this paper, the authors investigate the role of catalyseurs actifs in the phase d'irradiation of W(CO) 6 in the reaction of metathese des olefines.
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A novel heterobimetallic W–Ge compound. X-ray crystal structure of [W(μ-Cl)(GeCl3)(CO)3(η4-C7H8)]

TL;DR: In this paper, a new heterobimetallic complex [W(μ-Cl)(GeCl3)(CO)3(η4-C7H8)] (1) has been prepared by photochemical reaction of W(CO)6 with bicyclo[2.2]hepta-2,5-diene (NBD) and GeCl4.
Journal ArticleDOI

Photochemical reactions of Group 6 metal carbonyls catalytic transformation of alkenes and alkynes

TL;DR: In this paper, the most interesting approaches in each of three photocatalytic reactions: polymerization of alkynes, isomerization of alkenes, and metathesis of ynes are summarized.
Journal ArticleDOI

M(CO)6–RCln–hν catalysts (M = W, Mo; RCln= PhCCl3, Ph2CCl2): new catalyst systems for the metathesis polymerization of substituted acetylenes and cycloalkenes

TL;DR: The M(CO)6-RCln-hν system as discussed by the authors was proposed to provide high molecular weight polymers in good yields, where RCln are sufficient in catalytic amounts unlike CCl4.
Journal ArticleDOI

Oxidative substitution reaction of the osmochrome Os(OEP)[P(OMe)3]2 in chlorinated solvents

TL;DR: Steady state photolysis of octaethylporphine in chlorinated solvents at 365 and 405 nm and at 22 °C results in the formation of an osmium(IV) porphyrin identified as Os(OEP)Cl2.
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