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Intermolecular hydrogen bond and twisted intramolecular charge transfer in excited state of fast violet B (FVB) in methanol solution

机译:固溶紫B(FVB)在甲醇溶液中处于激发态的分子间氢键和扭曲的分子内电荷转移

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摘要

The excited state hydrogen bonding dynamics and corresponding photophysical processes of fast violet B(FVB) in hydrogen-donating methanol (MeOH) solution are investigated by using time-dependent density functional theory (TDDFT) method. In the FVB molecule, there are -C=O, -N-H groups which could act as hydrogen acceptor and donor. It is demonstrated that both the intramolecular hydrogen bond O...H-N in FVB and intermolecular hydrogen bond C=O...H-O between FVB and MeOH are formed in the ground state S_0 and strengthened in the excited state S_1. The absorption spectra are obviously red shifted for the hydrogen-bonded complex in comparison with FVB monomer in the low energy range. The theoretical investigation demonstrates that the twisted intramolecular charge transfer takes place in the excited states for both isolated FVB and hydrogen-bonded complex, and the dominant twisting is along N2-C3 bond. The potential energy curve is investigated to understand the photophysics process of FVB and hydrogen-bonded complex.
机译:利用时变密度泛函理论(TDDFT)研究了快紫色B(FVB)在供氢甲醇(MeOH)溶液中的激发态氢键动力学及相应的光物理过程。在FVB分子中,有-C = O,-N-H基团可以充当氢受体和供体。结果表明,FVB中的分子内氢键O ... H-N和FVB与MeOH之间的分子间氢键C = O ... H-O均在基态S_0处形成并在激发态S_1处增强。在低能量范围内,与FVB单体相比,氢键配合物的吸收光谱明显红移。理论研究表明,对于分离的FVB和氢键复合物,分子内电荷的扭曲都发生在激发态,并且主要的扭曲是沿着N2-C3键。研究势能曲线以了解FVB和氢键配合物的光物理过程。

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