Speciation of a water-soluble chromium porphyrin by spectral and electrochemical methods

被引:4
作者
Cheng, CF
Hung, CL
Su, YO [1 ]
Cheng, SH
机构
[1] Natl Taiwan Univ, Dept Chem, Taipei 106, Taiwan
[2] Natl Chi Nan Univ, Dept Appl Chem, Nantou Hsien 545, Taiwan
关键词
chromium porphyrin; speciation; electrocatalysis; oxidation; spectroelectrochemistry;
D O I
10.1016/j.jelechem.2003.11.023
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A water-soluble chromium porphyrin, [Cr(111)TF(4)TMAP](5+) (chromium(III) meso-tetrakis(2,3,5,6-tetrafluoro-N,N,N-trimethyl-4-anilinium)yl) porphyrin) was synthesized and the spectral and electrochemical properties were examined. In aqueous solution, [Cr(111)TF(4)TMAp](5+) exhibits two pK(a)s at 7.04 and 10.07. The cyclic voltammogram showed that a reversible reduction wave appeared at -0.84 V in pH 5.0 buffer solution, which is assigned as the Cr-III/II redox couple. The oxidation formal potentials were obtained by spectroelectrochemistry. With suitable control of the oxidation potentials and solution conditions, the high valent oxo-Cr-1V and oxo-Cr-v porphyrins were obtained. The ligand trans to the oxygen atom is either H2O or OH-, depending on the pH of the solution. In this paper, oxo-(CrTF)-T-v (4)TMAP is thus the first reported water-soluble Cr-v porphyrin that can be generated electrochemically and chemically. Electrogenerated oxo-Cr-v porphyrin species catalyzed the oxidation of cyclopent-2-ene-1-acetic acid to cyclopent-2-ene-4-one-1-acetic acid in the presence of dioxygen and returned to oxo-Cr-1v porphyrin, which is not reactive toward the substrate. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 175
页数:7
相关论文
共 31 条
[1]  
[Anonymous], 2000, PORPHYRIN HDB
[2]   New manganese β-polynitroporphyrins as particularly efficient catalysts for biomimetic hydroxylation of aromatic compounds with H2O2 [J].
Bartoli, JF ;
Mouries-Mansuy, V ;
Le Barch-Ozette, K ;
Palacio, M ;
Battioni, P ;
Mansuy, D .
CHEMICAL COMMUNICATIONS, 2000, (10) :827-828
[3]   Axial ligand effects on the redox reactions of manganese porphyrins [J].
Chang, CH ;
Cheng, SH ;
Su, YO .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 1999, 46 (02) :221-227
[4]   Electrocatalytic oxidation of styrene by a high valent ruthenium porphyrin cation radical [J].
Chen, CY ;
Cheng, SH ;
Su, YO .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2000, 487 (01) :51-56
[5]  
COTTON FA, 1998, ADV INORG CHEM, P1455
[6]   ELECTROCHEMICAL STUDIES OF OXO(MESO-TETRAPHENYLPORPHINATO)CHROMIUM(IV) - DIRECT EVIDENCE FOR EPOXIDATION OF OLEFINS BY AN ELECTROCHEMICALLY GENERATED FORMAL CHROMIUM(V) STATE [J].
CREAGER, SE ;
MURRAY, RW .
INORGANIC CHEMISTRY, 1985, 24 (23) :3824-3828
[7]   MODEL AND ENZYMATIC STUDIES WITH CYTOCHROME-P-450 [J].
DOLPHIN, D ;
JAMES, BR ;
LEUNG, T .
INORGANICA CHIMICA ACTA-BIOINORGANIC CHEMISTRY, 1983, 79 (1-6) :25-27
[8]   IS A LINEAR RELATIONSHIP BETWEEN THE FREE-ENERGIES OF ACTIVATION AND ONE-ELECTRON OXIDATION POTENTIAL EVIDENCE FOR ONE-ELECTRON TRANSFER BEING RATE DETERMINING - INTERMEDIATES IN THE EPOXIDATION OF ALKENES BY CYTOCHROME-P-450 MODELS .4. EPOXIDATION OF A SERIES OF ALKENES BY OXO(MESO-TETRAKIS(2,6-DIBROMOPHENYL)PORPHINATO)-CHROMIUM(V)N [J].
GARRISON, JM ;
OSTOVIC, D ;
BRUICE, TC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (13) :4960-4966
[9]   EPOXIDATION OF ALKENES BY OXO(5,10,15,20-TETRAKIS(2,6-DIMETHYL-3-SULFONATOPHENYL)PORPHINATO)CHROMIUM(V) IN AQUEOUS-SOLUTION [J].
GARRISON, JM ;
LEE, RW ;
BRUICE, TC .
INORGANIC CHEMISTRY, 1990, 29 (10) :2019-2021
[10]   HYDROXYLATION BY CYTOCHROME-P-450 AND METALLOPORPHYRIN MODELS - EVIDENCE FOR ALLYLIC REARRANGEMENT [J].
GROVES, JT ;
SUBRAMANIAN, DV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (07) :2177-2181