Heteroleptic [Cu(BIPHEP)(N^N)][PF] complexes (BIPHEP = 1,1'-biphenyl-2,2'-diylbis(diphenylphosphane)), in which N^N is 2,2'-bipyridine (bpy), 6-methyl-2,2'-bipyridine (6-Mebpy), 6-ethyl-2,2'-bipyridine (6-Etbpy), or 5,5'-dimethyl-2,2'-bipyridine (5,5'-Mebpy), have been synthesized and characterized using multinuclear NMR spectroscopies and electrospray ionization mass spectrometry. The single crystal structures of [Cu(BIPHEP)(bpy)][PF]∙CHCl, [Cu(BIPHEP)(5,5'-Mebpy)][PF]∙CHCl, [Cu(BIPHEP)(6-Mebpy)][PF]∙EtO∙0.5HO and [Cu(BIPHEP)(6-Etbpy)][PF] confirm distorted tetrahedral {Cu(P^P)(N^N)} coordination environments. Each compound shows a quasi-reversible Cu/Cu process. In deaerated solution, the compounds are weak emitters. Powdered samples are yellow emitters ( in the range 558-583 nm) and [Cu(BIPHEP)(5,5'-Mebpy)][PF] exhibits the highest photoluminescence quantum yield (PLQY = 14%). On cooling to 77 K (frozen 2-methyloxolane), the emission maxima are red-shifted and the excited state lifetimes increase from < 8 μs, to values of up to 53 μs, consistent with the compounds with N^N = 6-Mebpy, 6-Etbpy and 5,5'-Mebpy exhibiting thermally activated delayed fluorescence (TADF).
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864541 | PMC |
http://dx.doi.org/10.3390/molecules24213934 | DOI Listing |
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