Delgado Ledesma Salvador, Ponce Ortiz Rocío, Ruiz Delgado Mari Carmen, Vida Yolanda, Pérez-Inestrosa E, Casado Juan, Hernández Víctor, Kim Oh-Kil, Lehn Jean-Marie, López Navarrete Juan T
Departamento de Química Física, Facultad de Ciencias, Universidad de Málaga, 29071 Málaga, Spain.
Chemistry. 2004 Aug 6;10(15):3805-16. doi: 10.1002/chem.200305752.
A series of nonlinear optical (NLO) donor-acceptor (D-A) chromophores containing a fused terthiophene, namely dithienothiophene (DTT), as the electron relay, the same donor group, and acceptors of various strengths, has been investigated by means of infrared and Raman spectroscopies, both in the solid state as well as in a variety of solvents, to evaluate the effectiveness of the intramolecular charge transfer from the electron-donor to the electron-acceptor end groups. The Raman spectral profiles of these NLO-phores measured from their dilute solutions have been found to be rather similar to those of the corresponding solids, and thus their intramolecular charge transfer (ICT) shows very little dependence on the solvent polarity. The experimental results obtained for the DTT-containing NLO-phore with a 4-(N,N-dibutylamino)styryl end group as the donor and a 2,2-dicyanoethen-1-yl end group as the acceptor differ from those previously obtained for two parent "push-pull" chromophores with the same D-A pair but built-up around either a bis(3,4-ethylenedioxythienyl) (BEDOT) or a bithienyl (BT) electron relay. Vibrational spectroscopy shows that DTT is significantly more efficient as an electron relay than BT (which has the same number of conjugated C=C bonds) or BEDOT (which can be viewed as a rigidified version of BT on account of noncovalent intramolecular interactions between heteroatoms of adjacent rings). Density functional theory (DFT) calculations have also been performed on these NLO-phores to assign their main electronic and vibrational features and to obtain information about their structures. An additional merit of these molecular materials was revealed by the infrared spectra of the DTT-based NLO-phores recorded at different temperatures. Thus, spectra recorded between -170 and 150 degrees C did not show any substantial change, indicating that the materials have a high thermal stability, which is of significance for their use as active components in optoelectronic devices.
通过红外光谱和拉曼光谱,研究了一系列含有稠合三联噻吩(即二噻吩并噻吩,DTT)作为电子中继体、相同供体基团以及不同强度受体的非线性光学(NLO)供体-受体(D-A)发色团,这些研究是在固态以及多种溶剂中进行的,目的是评估从电子供体端基到电子受体端基的分子内电荷转移的有效性。从这些NLO发色团的稀溶液中测得的拉曼光谱轮廓与相应固体的光谱轮廓相当相似,因此它们的分子内电荷转移(ICT)对溶剂极性的依赖性很小。以4-(N,N-二丁基氨基)苯乙烯基端基作为供体、2,2-二氰基乙烯-1-基端基作为受体的含DTT的NLO发色团所获得的实验结果,与之前针对两个具有相同D-A对但围绕双(3,4-亚乙基二氧噻吩基)(BEDOT)或联噻吩(BT)电子中继体构建的母体 “推-拉” 发色团所获得的结果不同。振动光谱表明,作为电子中继体,DTT比BT(具有相同数量的共轭C = C键)或BEDOT(由于相邻环的杂原子之间的非共价分子内相互作用,可视为BT的刚性化形式)效率显著更高。还对这些NLO发色团进行了密度泛函理论(DFT)计算,以确定它们的主要电子和振动特征,并获取有关其结构的信息。基于DTT的NLO发色团在不同温度下记录的红外光谱揭示了这些分子材料的另一个优点。因此,在-170至150摄氏度之间记录的光谱没有显示出任何实质性变化,表明这些材料具有高热稳定性,这对于它们作为光电器件中的活性成分的应用具有重要意义。