首页> 外文期刊>Journal of the Chinese Chemical Society >Electrode Kinetics and Complex Formation of [Zn-Antibiotics-Cephalothin] System vis a vis Kinetics of Electrode Reactions
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Electrode Kinetics and Complex Formation of [Zn-Antibiotics-Cephalothin] System vis a vis Kinetics of Electrode Reactions

机译:电极反应动力学中的[Zn-抗生素-头孢菌素]体系的电极动力学和复合物形成

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Charge transfer reactions between a dropping mercury electrode and a [Mn-antibiotics-cephalothin] system were studied at pH = 7.30 ± 0.01, μ = 1.0 M NaClO_4 at 298 K. The antibiotics were doxycycline, chlortetracycline, oxytetracycline, tetracycline, minocycline, amoxicillin and chloramphenicol used as primary ligands and cephalothin as secondary ligand formed 1:1:1, 1:1:2 and 1:2:1 complexes with Zn~2. Electrode kinetics was discussed on the basis of kinetic parameters viz. transfer coefficient (α), degree of irreversibility (λ), diffusion coefficient (D) and rate constant (k). The values of a varied from 0.40 to 0.57 (0.50) confirm that 'transition state' behaves between reactant and product response to applied potential and it lies always between d.m.e. and solution interface. A small variation in potential affects the rate and rate constant greatly.
机译:在298 K的pH = 7.30±0.01,μ= 1.0 M NaClO_4的条件下,研究了滴汞电极与[Mn-抗生素-头孢菌素]系统之间的电荷转移反应。抗生素为强力霉素,金霉素,土霉素,四环素,米诺环素,阿莫西林氯霉素为主要配体,头孢噻吩为次要配体与Zn〜2形成1:1:1、1:1:2和1:2:1的配合物。在动力学参数的基础上讨论了电极动力学。传递系数(α),不可逆度(λ),扩散系数(D)和速率常数(k)。从0.40到0.57(0.50)的变化值证实,反应物和产物对施加电势的反应之间的``过渡态''表现为始终处于d.m.e.和解决方案界面。电位的微小变化会极大地影响速率和速率常数。

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