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首页> 外文期刊>Inorganic Chemistry Communications >Optical properties of bis-(2,4,6-trimethylpyridine)iodine(I) cation: absorption and emission
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Optical properties of bis-(2,4,6-trimethylpyridine)iodine(I) cation: absorption and emission

机译:双-(2,4,6-三甲基吡啶)碘(I)阳离子的光学性质:吸收和发射

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摘要

With regard to its electronic structure, the cation Icolla_2~+ (coll = collidine or 2,4,6-trimethylpyridine) is viewed as a coordination compound of iodine(I) with a p~4 electron configuration. The lowest-energy excited state of Icoll_2~+ is suggested to be a pipi~* collidine intraligand (IL) triplet which appears in absorption (lambda_max = 332 nm, epsilon = max = 405 nm, phi = 0.001, tau approx 90 ns). Owing to the heavy-atom effect of iodine this phosphorescence occurs at r.t. The longest-wavelength pp absorption is apparently obscured by the intense spin-allowed IL band at lambda_max = 268 nm.
机译:就其电子结构而言,阳离子Icolla_2〜+(coll =可力丁或2,4,6-三甲基吡啶)被视为具有p〜4电子构型的碘(I)的配位化合物。 Icoll_2〜+的最低能量激发态被认为是pipi〜*可力丁内配体(IL)三重态,出现在吸收中(lambda_max = 332 nm,epsilon = max = 405 nm,phi = 0.001,tau约90 ns) 。由于碘的重原子效应,该磷光发生在室温下。在lambda_max = 268 nm处,强烈的自旋允许IL带明显掩盖了最长波长的pp吸收。

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