Issue 13, 2004

Reactivity of an anionic Pd(ii) metallacycle with CH2X2 (X = Cl, Br, I): formal insertion of methylene into a Pd–Caryl bond

Abstract

Whereas the reaction of the anionic palladium metallacycle [K{P[upper bond 1 start]d(CH2CMe2-o-C[upper bond 1 end]6H4)(κ2-Tp)}] with CH2Cl2 leads to the isolation of the stable Pd(IV) chloromethyl complex [P[upper bond 1 start]d(CH2CMe2-o-C[upper bond 1 end]6H4)(κ3-Tp)(CH2Cl)], the analogous reactions with CH2Br2 and CH2I2 give rise to the six membered metallacycles [P[upper bond 1 start]d(CH2CMe2-o-C6H4(C[upper bond 1 end]H2))(κ3-Tp)X] (X = Br or I), as a result of the formal insertion of CH2 into the Pd–Caryl bond.

Graphical abstract: Reactivity of an anionic Pd(ii) metallacycle with CH2X2 (X = Cl, Br, I): formal insertion of methylene into a Pd–Caryl bond

Supplementary files

Article information

Article type
Communication
Submitted
04 Mar 2004
Accepted
19 Apr 2004
First published
24 May 2004

Chem. Commun., 2004, 1490-1491

Reactivity of an anionic Pd(II) metallacycle with CH2X2 (X = Cl, Br, I): formal insertion of methylene into a Pd–Caryl bond

J. Cámpora, P. Palma, D. del Río, J. A. López and P. Valerga, Chem. Commun., 2004, 1490 DOI: 10.1039/B403411B

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