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Suppression of chromophore coupling in thin films by chemical substitution of a perylene tetracarboxylic acid diimide

机译:通过chemical四羧酸二酰亚胺的化学取代来抑制薄膜中的发色团偶联

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摘要

Thin films (1-100 nm) of 1,6,7, 12-tetrachloro-N,N'-dimethyl perylene tetracarboxylic acid diimide(Cl_4MePTCDI) were prepared on glass and quartz substrates bydrop coating from solution and by physical vapor depositionunder variation of substrate temperature and deposition rate.Optical absorption spectra were measured in situ in dependenceon average film thickness during film growth under variation ofdeposition rate and substrate temperature and following filmpreparation ex situ in dependence on sample temperature. Theresults are compared to those obtained earlier (J. Phys. Chem., B1999, 103, 3078) at thin films of unsubstituted N, N'-dimethylperylene tetracarboxylic acid diimide (MePTCDI). In contrast tounsubstituted MePTCDI no significant chromophore couplingcould be detected in films of Cl_4MePTCDI. A relative highoptical emission signal for thin films of Cl4MePTCDI withcharacteristics quite similar to the solution spectrum clearlyconfirmed this interpretation. A twisted structure of the moleculeas indicated earlier (J. Phys. Chem., 1992, 96, 7988) is discussedas the basis of changes in the solid state structure relative tounsubstituted MePTCDI which has a planar aromatic system andgrows in crystalline films.
机译:在玻璃和石英衬底上通过溶液滴涂和改变温度下的物理气相沉积制备1,6,7,12-四氯-N,N'-二甲基ylene四羧酸二酰亚胺(Cl_4MePTCDI)的薄膜(1-100 nm)。在沉积速率和基底温度变化的情况下,根据薄膜生长过程中的平均薄膜厚度,在原位测量光学吸收光谱,并根据样品温度进行非原位制膜。将结果与早先在未取代的N,N′-二甲基per四羧酸二酰亚胺(MePTCDI)的薄膜上获得的结果(J.Phys.Chem。,B1999,103,3078)进行比较。与未取代的MePTCDI相反,在Cl_4MePTCDI膜中未检测到显着的生色团偶联。具有与溶液光谱非常相似的特性的Cl4MePTCDI薄膜的相对高光发射信号清楚地证实了这种解释。讨论了如前所述(J.Phys.Chem。,1992,96,7988)的分子的扭曲结构,作为相对于具有平面芳族体系并且在结晶膜中生长的未取代的MePTCDI相对于固态结构变化的基础。

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