Dinuclear Cu(I) complexes prepared from 2-diphenylphosphino-6-methylpyridine

Abstract

A series of reactions have been performed by mixing 2-diphenylphosphino-6-methyl-pyridine (dpPyMe) and [Cu(CH3CN)4]BF4 in different molar ratios. Starting from equimolar quantities of dpPyMe and Cu+, a dinuclear Cu(I) complex with two P,N binucleating bridging ligands has been obtained. This compound is stable in the solid state, however ligand exchange reactions leading to a mixture of species have been evidenced in solution. By increasing the amount of dpPyMe, the reaction of dpPyMe and [Cu(CH3CN)4]BF4 afforded the dinuclear Cu(I) complex [Cu2(?-dpPyMe)3(CH3CN)](BF4)2 in which the three bridging dpPyMe ligands are in a head-to-head arrangement. This compound is remarkably stable in solution. It has been also shown that the axial CH3CN ligand of [Cu2(?-dpPyMe)3(CH3CN)](BF4)2 can be suitably exchanged with other nitrile ligands [benzonitrile, 4-(dimethylamino)-benzonitrile, 4-nitrobenzonitrile and bromoacetonitrile] but also with triphenylphosphine oxide. The electrochemical and photophysical properties of the resulting complexes have been systematically investigated. The [Cu2(?-dpPyMe)3(L)](BF4)2 derivatives are weak emitters in solution but remarkable emission quantum yields (6 to 46%) have been found in rigid matrices at room temperature. One complex was utilized as active material for preliminary tests in LEC devices.


Autore Pugliese

Tutti gli autori

  • Cid J.J.; Mohanraj J.; Mohankumar M.; Holler M.; Monti F.; Accorsi G.; Karmazin-Brelot L.; Nierengarten I.; Malicka J.M.; Cocchi M.; Delavaux-Nicot B.; Armaroli N.; Nierengarten J.F.

Titolo volume/Rivista

Polyhedron


Anno di pubblicazione

2014

ISSN

0277-5387

ISBN

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Numero di citazioni Wos

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Settori ERC

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Codici ASJC

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