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Unprecedented 1,3-migration of the arylligand in metallacyclic aryl α-naphthyl Pt(iv) difluorides to produce β-arylnaphthyl Pt(ii) complexes†
Ina S. Dubinsky-Davidchik,Israel Goldberg,Arkadi Vigalok,Andrei N. Vedernikov
Chemical Communications Pub Date : 03/08/2013 00:00:00 , DOI:10.1039/C3CC41079J
Abstract

Electrophilic fluorination of aryl α-naphthyl Pt(II) complexes leads to an unprecedented 1,3-migration of the aryl ligand to the β-position of the naphthyl group. The reaction proceeds via the initial oxidative addition of two fluoro ligands to the Pt center followed by C(sp2)–C(sp2) coupling and aryl migration.

Graphical abstract: Unprecedented 1,3-migration of the aryl ligand in metallacyclic aryl α-naphthyl Pt(iv) difluorides to produce β-arylnaphthyl Pt(ii) complexes
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