Synthesis, structural characterization and luminescent properties of a series of Cu(i) complexes based on polyphosphine ligands

摘要

A series of Cu(i) complexes with a [Cu(NN)(PP)]~+ moiety, [Cu(phen)(pba)](BF_4) (1a), [Cu_2(phen)_2(pbaa)] (BF_4)_2 (2a), [Cu_2(phen)_2(pnaa)] (BF_4)_2 (3a), [Cu_2(phen)_2(pbbaa)] (BF_4)_2 (4a), [Cu(dmp)(pba)](BF_4) (1b), [Cu _2(dmp)_2(pbaa)](BF_4)_2 (2b), [Cu _2(dmp)_2(pnaa)](BF_4)_2 (3b) and [Cu_2(dmp)_2(pbbaa)](BF_4)_2 (4b) (phen = 1,10-phenanthroline, dmp = 2,9-dimethyl-1,10-phenanthroline, pba = N,N-bis((diphenylphosphino)methyl)benzenamine, pbaa = N,N,N′,N′- tetrakis((diphenylphosphino)methyl)benzene-1,4-diamine, pnaa = N,N,N′,N′-tetrakis((diphenylphosphino)methyl)naphthalene-1, 5-diamine and pbbaa = N,N,N′,N′-tetrakis((diphenylphosphino)methyl) biphenyl-4,4′-diamine), were rationally designed and synthesized. These complexes were characterized by ~1H and ~(31)P NMR, electrospray mass spectrometry, elemental analysis and X-ray crystal structure analysis. Introduction of different central arene spacers (phenyl, naphthyl, biphenyl) into ligands, resulting in the size variation of these complexes, aims to tune the photophysical properties of the complexes. Each Cu(i) ion in these complexes adopts a distorted tetrahedral geometry constructed by the chelating diimine and phosphine groups. Intermolecular C-H?π and/or π?π interactions are involved in the solid states. The dmp-containing complex exhibits better emission relative to the corresponding phen complex due to the steric encumbrance of bulky alkyl groups. Furthermore, for complexes with identical diimine but different phosphine ligands, the tendency of increased emission lifetime as well as blue-shifted emission in the solid state follows with the decrease in size of complexes. Intermolecular C-H?π interactions have an influence on the final solid state photophysical properties through vibrationally relaxed non-radiative energy transfer in the excited state. Smaller-sized complexes show better photophysical properties due to less vibrationally relaxed behavior related to flexible C-H?π bonds. Nevertheless, the tendency for increased quantum yield and emission lifetime, as well as blue-shifted emission in dilute solution goes with the increase in size of complexes. The central arene ring (phenyl, naphthyl or biphenyl) has an influence on the final photophysical properties. The larger the π-conjugated extension of central arene ring is, the better the photophysical properties of complex are. The rigid and large-sized complex 3b, with a high quantum yield and long lifetime, is the best luminophore among these complexes.