Accessing bimetallic complexes through a variable bridging ligand strategy

Dalton Trans. 2024 Nov 26. doi: 10.1039/d4dt02903h. Online ahead of print.

Abstract

In this contribution we are introducing a Variable Bridging Ligand (VBL) strategy for the preparation of heterometallic complexes. One synthetic challenge associated with other methods described in the existing literature stems from the fact that if there is a need to change the donor groups on a metalloligand, both the initial ligand and the resulting metalloligand must be synthesized all over again. To circumvent this problem, we reasoned that if a metal complex would have one labile ligand that can be easily replaced by various bridging polytopic species, several metalloligands can thus be generated starting from the same starting material. Experimentally, we describe here the synthesis and characterization of a new ligand, bis(pyrazol-1-yl)-N-(quinolin-8-yl)acetamide, HLQ2Pz (Pz = pyrazolyl ring) and its reactions with copper(II) centers. In a first step, pro-metalloligand preparation was investigated using Cu(II) primary metallic centers and the HLQ2Pz main ligand to produce (LQ2Pz)Cu(OAc)·H2O, (LQ2Pz)Cu(BF4), and (LQ2Pz)Cu(ClO4)·MeCN complexes. Using (LQ2Pz)Cu(ClO4)·MeCN as a pro-metalloligand, two metalloligands (LQ2Pz)Cu[O2CCH(pz)2] and (LQ2Pz)Cu[O2CCH(CH2pz)2] were prepared. Employing the latter metalloligand, two mixed valence CuII/CuI complexes, {(LQ2Pz)CuII[O2CCH(CH2pz)2CuI(PPh3)2]}NO3 and {(LQ2Pz)CuII[O2CCH(CH2pz)2]}2CuI(PF6) were synthesized. These compounds were characterized by NMR, UV-Vis, and IR spectroscopy, and in solid state by single crystal X-ray diffraction.