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Synthesis, Characterization and Photophysical Properties of Thiophene-containing Chloro Re(I) Complex

机译:含噻吩的氯Re(i)复合物的合成,表征和光物理性质

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Two tricarbonyl rhenium complexes with the formula of [Re(CO)_3(L)Cl], where L=1,10-phenanthroline (Phen-Re) and 2-(3-thienyl)-imidazo[4,5-f]-1,10-phenanthroline (TIPh-Re), were successfully synthesized and characterized by ~1H NMR and UV-Vis with the aim to analyze the effect of the thiophene(TI) moiety on the photophysical properties of TIPh-Re. It was found that the introduction of an π-electron density moiety into diimine ligands leads to a dramatic red shift of the absorption of the corresponding Re(I) complex. At the same time, the results verify that the triplet metal-to-ligand charge-transfer dπ(Re)→π~*(N-N) emission (3MLCT) of Phen-Re and TIPh-Re centered at ca. 566 nm and ca.569 nm, respectively.
机译:两种三羰基铼配合物,其中[Re(CO)_3(L)Cl]的式,其中L = 1,10-菲林(Phen-Re)和2-(3-噻吩基)-imidazo [4,5-F] -1,10-菲咯啉(Tiph-Re)被成功地合成并表征〜1H NMR和UV-Vis,目的是分析噻吩(Ti)部分对Tiph-Re的光学性质的影响。发现将π-电子密度部分引入二嘧啶配体,导致相应的RE(I)复合物的吸收的剧烈红移。同时,结果验证了三元金属 - 配体电荷 - 转移dπ(Re)→π〜*(n-n)发射(3mlct)的Phen-Re和Tiph-Re以CA为中心。分别为566纳米和约569纳米。

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