期刊
INORGANICA CHIMICA ACTA
卷 550, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2023.121446
关键词
Platinum(II) complexes; Dipyridylbenzene; Phosphorescence; Thiolate
Substituting the chloride ligand of the cyclometalated complexes [Pt(5-R-dpyb)Cl] (R = methyl, 2-thienyl; dpyb = 1,3-di(2-pyridyl)benzene) with 1-phenyl-1H-tetrazole-5-thiolate leads to the thiolato complexes [Pt(5-R-dpyb)(1-phenyl-1H-tetrazole-5-thiolate)], which have been fully characterized. The photophysical properties of these complexes were determined in degassed dichloromethane solution at room temperature. It was found that the emission color can be controlled by the substituents on the benzene ring, with the introduction of a donor group such as 2-thienyl resulting in a significant red-shift.
Substitution of the chlorido ligand of the cyclometalated complexes [Pt(5-R-dpyb)Cl] (R = methyl, 2-thienyl; dpyb = 1,3-di(2-pyridyl)benzene) by 1-phenyl-1H-tetrazole-5-thiolate leads to the related thiolato complexes [Pt(5-R-dpyb)(1-phenyl-1H-tetrazole-5-thiolate)], which have been fully characterised. Their photophysical properties were determined in degassed dichloromethane solution at room temperature. It turned out that the color of the phosphorescence can be tuned by the nature of the substituents on the benzene ring, with the introduction of a donor group such as 2-thienyl allowing a large red-shift of the emission. Substitution of the chloride ligand with 1-phenyl-1H-tetrazole-5-thiolate has a negligible effect on the emission maxima and life-times, since both parameters remain in a narrow range which is very close to the original value. However, the use of this thiolate as ancillary ligand can lead to very high quantum yields, approaching unity.
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