Electrochemistry and Catalytic Properties for Dioxygen Reduction Using Ferrocene-Substituted Cobalt Porphyrins

详细信息    查看全文

• 作者：Bin Sun ; Zhongping Ou ; Deying Meng ; Yuanyuan Fang ; Yang Song ; Weihua Zhu ; Pavlo V. Solntsev ; Victor N. Nemykin ; Karl M. Kadish
• 刊名：Inorganic Chemistry
• 出版年：2014
• 出版时间：August 18, 2014
• 年：2014
• 卷：53
• 期：16
• 页码：8600-8609
• 全文大小：530K
• ISSN：1520-510X

文摘

Cobalt porphyrins having 0鈥? meso-substituted ferrocenyl groups were synthesized and examined as to their electrochemical properties in N,N鈥?dimethylformamide (DMF) containing 0.1 M tetra-n-butylammonium perchlorate as a supporting electrolyte. The examined compounds are represented as (Fc)_n(CH₃Ph)_4鈥?i>nPorCo, where Por is a dianion of the substituted porphyrin, Fc and CH₃Ph represent ferrocenyl and/or p-CH₃C₆H₄ groups linked at the four meso-positions of the macrocycle, and n varies from 0 to 4. Each porphyrin undergoes two reversible one-electron reductions and two to six one-electron oxidations in DMF, with the exact number depending upon the number of Fc groups on the compound. The first electron addition is metal-centered to generate a Co(I) porphyrin. The second is porphyrin ring-centered and leads to formation of a Co(I) 蟺-anion radical. The first oxidation of each Co(II) porphyrin is metal-centered to generate a Co(III) derivative under the given solution conditions. Each ferrocenyl substituent can also be oxidized by one electron, and this occurs at more positive potentials. Each compound was investigated as a catalyst for the electoreduction of dioxygen when adsorbed on a graphite electrode in 1.0 M HClO₄. The number of electrons transferred (n) during the catalytic reduction was 2.0 for the three ferrocenyl substituted compounds, consistent with only H₂O₂ being produced as a product of the reaction. Most monomeric cobalt porphyrins exhibit n values between 2.6 and 3.1 under the same solution conditions, giving a mixture of H₂O and H₂O₂ as a reduction product, although some monomeric porphyrins can give an n value of 4.0. Our results in the current study indicate that appending ferrocene groups directly to the meso positions of a porphyrin macrocycle will increase the selectivity of the oxygen reduction, resulting in formation of only H₂O₂ as a reaction product. This selectivity of the electrocatalytic oxygen reduction reaction is explained on the basis of steric hindrance by the ferrocene substituents which prevent dimerization.