A new phosphorescent iridium metal with cyclometalated and dimethyl carboxylate bipyridine ligands complex 1 was synthesized and characterized. The ester functional were designed and connected as amine recognition group. The UVVis absorption and luminescence properties of complex 1 were investigated with amine. The result show that complex 1 exhibited high selectivity and efficient signaling behavior n-butylamine in acid catalyst.
Organic light emitting diodes (OLEDs), charged iridium(III) complexes, spiro ligand Abstract. We report the synthesis, characterization and photophysical properties of a cationic cyclometalated Ir(III) complexes of general formula [Ir(ppy)2(spbpy)]+Cl, [Ir(diFppy)2(spbpy)]+Cland [Ir(thiopy)2(spbpy)]+Clwhere ppy, spbpy, diFppy and thiopy are 2-phenylpyridine, 4,5-diaza-9,9′-spirobifluorene, 2-(2′,4′-difluorophenyl)-pyridine and 2-(thiophen-2′-yl)-pyridine, respectively. The complexes exhibit strong absorption bands in the UV region in solution spectra, due to spin-allowed ligand-centred (LC) and weaker absorption bands at longer wavelengths from metal-to-ligand charge transfer (MLCT). The photoluminescence spectra of all the complexes were characterised by a combination of 3MLCT and3π→π*states. The emission color of a cationic cyclometalated Ir(III) complexes in solution have successfully tuned from green to orange (501-582 nm).
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