Luminescent Three- and Four-Coordinate Dinuclear Copper(I) Complexes Triply Bridged by Bis(diphenylphosphino)methane and Functionalized 3-(2′-Pyridyl)-1,2,4-triazole Ligands

Abstract

A new series of bimetallic Cu(I) complexes 1 – 5 triply bridged by a monoanionic or charge-neutral functionalized 3-(2′-pyridyl)-1,2,4-triazole in a μ–η 1 (N),η 2 (N,N) tridentate binding mode and two bis(diphenylphosphino)methane (dppm) ligands have been synthesized. Complexes 1 – 5 are singly or doubly charged dinuclear Cu(I) species with an eight-membered Cu 2 C 2 P 4 ring of {Cu(μ-dppm) 2 Cu} unit, in which 3 and 4 adopt the boat–boat conformation, while 1, 2, and 5 display the chair–boat form. In these dimeric copper(I) complex cations, one of the two Cu(I) ions is four-coordinated, in a highly distorted N 2 P 2 tetrahedral environment and the other is three-coordinated, in a distorted NP 2 trigonal planar arrangement. All these Cu(I) complexes exhibit a comparatively weak low-energy absorption in CH 2 Cl 2 solution, ascribed to the charge-transfer transitions with appreciable 1 MLCT contribution, as suggested by time-dependent density functional theory (TDDFT) analyses. Complexes 1 – 5 display good emission properties in both solution and solid states at ambient temperature, which are well-modulated via structural modification of 3-(2′-pyridyl)-1,2,4-triazole, including the alteration of the substituent type (−CF 3, −H, −CH 3, and −C(CH 3 ) 3 ) and position ( ortho -, meta -, and para -position). Furthermore, the variation of the substituent (−CF 3 and −C(CH 3 ) 3 ) on the 5-site of the 1,2,4-triazolyl ring markedly influences the proton activity of the 1,2,4-triazolyl-NH, thus leading to the formation of both singly and doubly charged bimetallic Cu(I) species regulated by the NH ↔ N – conversion, resulting from NH deprotonation of the 1,2,4-triazolyl ring.