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发蓝光的双核 N-杂环二碳烯金(I)配合物,具有近乎单位的量子产率。

Blue-emitting dinuclear N-heterocyclic dicarbene gold(I) complex featuring a nearly unit quantum yield.

机构信息

Dipartimento di Scienze Chimiche, Università di Padova, via Marzolo 1, 35131 Padova, Italy.

出版信息

Inorg Chem. 2012 Feb 6;51(3):1778-84. doi: 10.1021/ic2020786. Epub 2012 Jan 23.

Abstract

Dinuclear N-heterocyclic dicarbene gold(I) complexes of general formula Au(2)(RIm-Y-ImR)(2)(2) (R = Me, Cy; Y = (CH(2))(1-4), o-xylylene, m-xylylene) have been synthesized and screened for their luminescence properties. All the complexes are weakly emissive in solution whereas in the solid state some of them show significant luminescence intensities. In particular, crystals or powders of the complex with R = Me, Y = (CH(2))(3) exhibit an intense blue emission (λ(max) = 450 nm) with a high quantum yield (Φ(em) = 0.96). The X-ray crystal structure of this complex is characterized by a rather short intramolecular Au···Au distance (3.272 Ǻ). Time dependent density functional theory (TDDFT) calculations have been used to calculate the UV/vis properties of the ground state as well as of the first excited state of the complex, the latter featuring a significantly shorter Au···Au distance.

摘要

具有通式Au(2)(RIm-Y-ImR)(2)(2)(R = Me,Cy;Y = (CH(2))(1-4),邻-二甲苯,间-二甲苯)的双核 N-杂环二碳烯金(I)配合物已被合成并对其发光性能进行了筛选。所有配合物在溶液中均具有弱发光性,而在固态中,其中一些则显示出显著的发光强度。特别是具有 R = Me,Y = (CH(2))(3)的配合物的晶体或粉末显示出强蓝色发射(λ(max) = 450nm),量子产率高(Φ(em) = 0.96)。该配合物的 X 射线晶体结构的特点是分子内 Au···Au 距离相当短(3.272 Ǻ)。时变密度泛函理论(TDDFT)计算已用于计算配合物基态和第一激发态的 UV/vis 性质,后者具有明显较短的 Au···Au 距离。

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