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A new 3D copper(I) iodide hybrid, [Cu4I4(TMEDA)2]n(1, TMEDA = N,N,N',N'-tetramethylethylenediamine), has been solvothermally synthesized and characterized by singlecrystal X-ray diffraction, IR spectroscopy, elemental analysis, powder X-ray diffractions and thermogravimetric analysis. Compound 1 crystallizes in tetragonal space group P42/n with a = b = 11.5663(7) A, c = 9.2456(11) A, V = 1236.87(18) A3, Z = 8, C3H8 CuIN, Mr = 248.54, Dc = 3.507 g/cm3, F(000) = 920, μ(MoKα) = 8.388 mm–1, the final R = 0.0244 and wR = 0.0573 for 1118 observed reflections(I 2σ(I)). The hybrid framework is built up from cubane-like Cu4I4 cluster and flexible acyclic aliphatic diamine TMEDA, which can be simplified into a twofold interpenetrating dia network. The solid state luminescence spectrum displays a strong yellow emission band at room temperature(Aex = 340 nm, Aem = 530 nm). Results reveal that steric effect of N-substituted methyl groups in TMEDA have obvious influence on the structure and photoluminescent property of compound 1. 相似文献
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Ultrafast proton transfer dynamics of 2-(2'-hydroxyphenyl)benzoxazole dye in different solvents 下载免费PDF全文
The excited-state intramolecular proton transfer of 2-(2-hydroxyphenyl)benzoxazole dye in different solvents is investigated using ultrafast femtosecond transient absorption spectroscopy combined with quantum chemical calculations.Conformational conversion from the syn-enol configuration to the keto configuration is proposed as the mechanism of excited-state intramolecular proton transfer.The duration of excited-state intramolecular proton transfer is measured to range from 50 fs to 200 fs in different solvents.This time is strongly dependent on the calculated energy gap between the N-S;and T-S;structures in the S;state.Along the proton transfer reaction coordinate,the vibrational relaxation process on the S;state potential surface is observed.The duration of the vibrational relaxation process is determined to be from8.7 ps to 35 ps dependent on the excess vibrational energy. 相似文献
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