首页> 外文期刊>Journal of Solution Chemistry >Spectroscopic Study of Charge-Transfer Complexation of Iodine with DB18C6 in Chloroform, Dichloromethane and Their 1:1 Mixture
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Spectroscopic Study of Charge-Transfer Complexation of Iodine with DB18C6 in Chloroform, Dichloromethane and Their 1:1 Mixture

机译:碘与DB18C6在氯仿,二氯甲烷及其1:1混合物中的电荷转移配合物的光谱研究

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摘要

The charge-transfer complexes of dibenzo-18-crown-6(DB18C6) (L) with iodine, as a typical sigma-acceptor, were studied spectrophotometrically in chloroform, dichloromethane and their 1:1 (v/v) mixture at 25.0 +/- A 0.1 A degrees C. Spectral data, formation constants and the effect of the solvent have been determined. Spectral characteristics and formation constants are discussed in the terms of donor molecular structure and solvent polarity. The stoichiometry of the complexes was established to be 1:1. The formation constants (K (CT)) of the complexes were determined. The complexes were isolated and characterized by FTIR and H-1-NMR spectroscopy. The observed time dependence of the charge-transfer band and subsequent formation of in solution were related to the slow transformation of the initial 1:1 L:I-2 outer complex to an inner electron donor-acceptor complex, followed by fast reaction of the inner complex with iodine to form a triiodide ion. The pseudo-first-order rate constants for the transformation process were evaluated in different solvent systems.
机译:在25.0 +的氯仿,二氯甲烷及其1:1(v / v)混合物中用分光光度法研究了二苯并18冠6(DB18C6)(L)与碘的电荷转移络合物(作为典型的σ受体)。 /-0.1 A摄氏度。已经确定了光谱数据,形成常数和溶剂的作用。根据供体分子结构和溶剂极性讨论了光谱特征和形成常数。络合物的化学计量确定为1:1。确定复合物的形成常数(K(CT))。分离复合物并通过FTIR和H-1-NMR光谱表征。观察到的电荷转移带的时间依赖性以及随后在溶液中的形成与最初的1:1 L:I-2外复合物向内电子给体-受体复合物的缓慢转化,随后的快速反应有关。与碘形成内部络合物,形成三碘离子。在不同的溶剂体系中评估了转化过程的拟一级反应速率常数。

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