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某些偶氮磺酰基喹啉配体和铀酰配合物的 D.C.电导率和传导机制。

D.C. electrical conductivity and conduction mechanism of some azo sulfonyl quinoline ligands and uranyl complexes.

机构信息

Department of Physics, Faculty of Science at Demiatta, Mansoura University (Damietta branch), Egypt.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2011 Dec;83(1):61-6. doi: 10.1016/j.saa.2011.07.042. Epub 2011 Aug 10.

Abstract

Supramolecular coordination of dioxouranium(VI) heterochelates 5-sulphono-7-(4'-X phenylazo)-8-hydroxyquinoline HL(n) (n=1, X=CH(3); n=2, X=H; n=3, X=Cl; n=4, X=NO(2)) have been prepared and characterized with various physico-chemical techniques. The infrared spectral studies showed a monobasic bidentate behavior with the oxygen and azonitrogen donor system. The temperature dependence of the D.C. electrical conductivity of HL(n) ligands and their uranyl complexes has been studied in the temperature range 305-415 K. The thermal activation energies E(a) for HL(n) compounds were found to be in the range 0.44-0.9 eV depending on the nature of the substituent X. The complexation process decreased E(a) values to the range 0.043-045 eV. The electrical conduction mechanism has been investigated for all samples under investigation. It was found to obey the variable range hopping mechanism (VRH).

摘要

二氧铀(VI)杂环配合物 5-磺基-7-(4'-X 苯基偶氮)-8-羟基喹啉 HL(n)(n=1,X=CH(3);n=2,X=H;n=3,X=Cl;n=4,X=NO(2))的超分子配位已被制备并通过各种物理化学技术进行了表征。红外光谱研究表明,该配合物具有单核双齿配位行为,配位原子为氧和偶氮氮。HL(n)配体及其铀酰配合物的直流电导率随温度在 305-415 K 范围内进行了研究。HL(n)化合物的热激活能 E(a)值范围为 0.44-0.9 eV,取决于取代基 X 的性质。配合过程将 E(a)值降低到 0.043-045 eV 范围内。对所有研究样品的电传导机制进行了研究。发现其符合变程跳跃机制(VRH)。

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