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Binucleating behaviour of a proximally-diphosphinated calix[4]arene†
Mouhamad Awada,Catherine Jeunesse,Dominique Matt,Loic Toupet,Richard Welter
Dalton Transactions Pub Date : 08/30/2011 00:00:00 , DOI:10.1039/C1DT10375J
Abstract

The long diphosphine 5,11-diphenylphosphanyl-25,26-dipropyloxy-27,28-bis(2-propenyloxy) calix[4]arene (cone) (5), in which the two phosphorus atoms are separated by a semi-rigid linking unit, was prepared in four steps starting from calix[4]arene. Reaction of 5 with AuCl(SEt2) or [RuCl2(p-cymene)]2 led to calixarenes bearing two metallated pendant arms, [5·(AuCl)2] and [5·{RuCl2(p-cymene)}2], respectively. In the presence of AgBF4 or [Ni(C5H5)(1,5-cyclooctadiene)]BF4, diphosphine 5 displayed a marked tendency to form oligomeric material, but under high dilution conditions dimeric species were obtained selectively. The inability of 5 to form chelate complexes was further illustrated by its reaction with [PdCl2(1,5-cyclooctadiene)2], which led quantitatively to a rare complex in which a diphosphine spans across the dinuclear [PdCl(μ-Cl)2PdCl] unit.

Graphical abstract: Binucleating behaviour of a proximally-diphosphinated calix[4]arene
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