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Infrared Absorption Spectroscopic Studies of ¥á,¥?-Diphenylpolyenyl Anions with Odd Numbered Polyene Molecules

机译:¥á,¥?-二苯基多烯基阴离子与奇数多烯分子的红外吸收光谱研究

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Infrared absorption spectra of メ,-diphenylpolyenyl anions Ph(CH)nPh- (DPn-, n=7, 9, and 13) in the tetrahydrofuran-d6 solutions was measured in the range of 1700 and 1200 cm-1 . The infrared spectra obtained from anions (DPn) showed considerable difference from their neutral species (DPn); their intensities were enhanced at least two orders of magnitude stronger than their neutral species. The in-plane CH bending modes at 1464 and 1375 cm-1 are correspondingly strengthened with the chain length increased, but the C=C stretching at 1541 cm-1 is weakened and frequencies are not changed. We provide an IR evidence for the first time that the bond order or bond alternations of the anions (soliton) are different from those of radical anions (polaron) as well as neutral species.
机译:メ,-二苯基多烯基阴离子Ph(CH) n Ph -(DP n -,在四氢呋喃-d 6 溶液中测得的n = 7、9和13)的范围为1700和1200 cm -1 。从阴离子(DP n )获得的红外光谱与中性物质(DP n )存在很大差异;它们的强度比中性物种至少增强了两个数量级。随着链长的增加,在1464和1375 cm -1 处的面内CH弯曲模式相应增强,但在1541 cm -1 处的C = C拉伸减弱并且频率不变。我们首次提供IR证据,表明阴离子(孤子)的键序或键交替与自由基阴离子(极化子)以及中性离子的键序或键交替不同。

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