Casado Juan, Ortiz Rocío Ponce, Ruiz Delgado Mari C, Azumi Reiko, Oakley Richard T, Hernandez Víctor, López Navarrete Juan T
Departamento de Química Física, Facultad de Ciencias, Universidad de Malaga, 29071 Malaga, Spain.
J Phys Chem B. 2005 May 26;109(20):10115-25. doi: 10.1021/jp0446175.
In this article, we investigate a series of alpha,omega-dicyano end-capped oligothiophenes NC(C(4)H(2)S)(n)()CN ranging in length from the dimer to the hexamer (n = 2-6), in the neutral state as pure solids, by means of Fourier transform IR and Fourier transform Raman (FT-Raman) spectroscopies. The cyclic voltammetry analysis of the compounds in dichloromethane reveals that most of them show two oxidation and two reduction waves (i.e., a dual or amphoteric electrochemical behavior), associated with the injection of either positive or negative charges into the pi-conjugated system. The doped species are characterized by in situ vis-near-IR and FT-Raman spectrochemistries. Density functional theory calculations have been also performed, at the B3LYP/6-31G level, to assess information about the molecular geometries and vibrational features of the neutral and doped species and about the topologies of the molecular orbitals involved in the main electronic transitions that appear for the neutral forms in the visible spectral region and for the doped species in the near-IR region.
在本文中,我们通过傅里叶变换红外光谱和傅里叶变换拉曼光谱(FT - 拉曼光谱),对一系列α,ω - 二氰基封端的寡聚噻吩NC(C₄H₂S)ₙCN(长度从二聚体到六聚体,n = 2 - 6)在中性状态下作为纯固体进行了研究。对这些化合物在二氯甲烷中的循环伏安分析表明,它们中的大多数显示出两个氧化波和两个还原波(即双重或两性电化学行为),这与向π共轭体系中注入正电荷或负电荷有关。通过原位可见 - 近红外光谱和FT - 拉曼光谱对掺杂物种进行了表征。还在B3LYP/6 - 31G水平上进行了密度泛函理论计算,以评估有关中性和掺杂物种的分子几何结构、振动特征以及参与中性形式在可见光谱区域和掺杂物种在近红外区域出现的主要电子跃迁的分子轨道拓扑结构的信息。