Hasani Masoumeh, Akbari Sakineh
Department of Chemistry, College of Science, Bu-Ali Sina University, Hamadan, Iran.
Spectrochim Acta A Mol Biomol Spectrosc. 2007 Nov;68(3):409-13. doi: 10.1016/j.saa.2006.12.003. Epub 2006 Dec 8.
The formation of charge transfer complex between 4'-aminobenzo-15-crown-5 (AB15C5) and iodine is investigated spectrophotometrically in chloroform, dichloromethane (DCM) and 1,2-dichloroethane (DCE) solutions at 25 degrees C. The continuous variation method clearly revealed the formation of 1:1 charge transfer complex in solution. The observed time dependence of the charge transfer band and subsequent formation of I 3- in solution were related to the slow transformation of the initially formed 1:1 AB15C5.I2 outer complex to an inner electron donor-acceptor (EDA) 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 from the absorbance-time data and found to vary in the order of 1,2-DCE>DCM>CHCl3. The values of the formation constant, KDA, for each complex are evaluated from Benesi-Hilebrand equation. Stability of the resulting complex in three solvents was also found to vary in the order of 1,2-DCE>DCM>CHCl3.
在25℃下,采用分光光度法研究了4'-氨基苯并-15-冠-5(AB15C5)与碘在氯仿、二氯甲烷(DCM)和1,2-二氯乙烷(DCE)溶液中电荷转移络合物的形成。连续变化法清楚地表明溶液中形成了1:1的电荷转移络合物。观察到的电荷转移带的时间依赖性以及溶液中随后I₃⁻的形成与最初形成的1:1 AB15C5·I₂外层络合物缓慢转化为内层电子供体-受体(EDA)络合物有关,随后内层络合物与碘快速反应形成三碘离子。从吸光度-时间数据评估了转化过程的伪一级速率常数,发现其变化顺序为1,2-DCE>DCM>CHCl₃。根据贝内西-希勒布兰德方程评估了每种络合物的形成常数KDA。还发现所得络合物在三种溶剂中的稳定性变化顺序为1,2-DCE>DCM>CHCl₃。