Role of proton-coupled electron transfer in O-O bond activation

被引:357
作者
Rosenthal, Joel [1 ]
Nocera, Daniel G. [1 ]
机构
[1] MIT, Dept Chem 6335, Inst Technol, Cambridge, MA 02139 USA
关键词
D O I
10.1021/ar7000638
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The selective reduction of oxygen to water requires four electrons and four protons. The design of catalysts that promote oxygen reduction therefore requires the management of both electron and proton inventories. Pacman and Hangman porphyrins provide a cleft for oxygen binding, a redox shuttle for oxygen reduction, and functionality for tuning the acidbase properties of bound oxygen and its intermediates. With proper control of the proton-coupled electron transfer events, O-O bond breaking of oxygen, and more generally oxygenated substrates, may be achieved with high efficiencies. The rule set developed for oxygen reduction may be applied to a variety of other small molecule activation reactions of consequence to energy conversion.
引用
收藏
页码:543 / 553
页数:11
相关论文
共 63 条
[1]   Factors governing oxygen reduction in solid oxide fuel cell cathodes [J].
Adler, SB .
CHEMICAL REVIEWS, 2004, 104 (10) :4791-4843
[2]  
[Anonymous], 1985, STANDARD POTENTIALS
[3]   Modeling cytochrome oxidase:: A quantum chemical study of the O-O bond cleavage mechanism [J].
Blomberg, MRA ;
Siegbahn, PEM ;
Babcock, GT ;
Wikström, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (51) :12848-12858
[4]   Functional analogues of the dioxygen reduction site in cytochrome oxidase:: Mechanistic aspects and possible effects of CuB [J].
Boulatov, R ;
Collman, JP ;
Shiryaeva, IM ;
Sunderland, CJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (40) :11923-11935
[5]   Controlled uncoupling and recoupling of proton pumping in cytochrome c oxidase [J].
Brändén, G ;
Pawate, AS ;
Gennis, RB ;
Brzezinski, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (02) :317-322
[6]   Proton-coupled O-O activation on a redox platform bearing a hydrogen-bonding scaffold [J].
Chang, CJ ;
Chng, LL ;
Nocera, DG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (07) :1866-1876
[7]   Electrocatalytic four-electron reduction of oxygen to water by a highly flexible cofacial cobalt bisporphyrin [J].
Chang, CJ ;
Deng, YQ ;
Shi, CN ;
Chang, CK ;
Anson, FC ;
Nocera, DG .
CHEMICAL COMMUNICATIONS, 2000, (15) :1355-1356
[8]   The Pacman effect: A supramolecular strategy for controlling the excited-state dynamics of pillared cofacial bisporphyrins [J].
Chang, CJ ;
Loh, ZH ;
Deng, YQ ;
Nocera, DG .
INORGANIC CHEMISTRY, 2003, 42 (25) :8262-8269
[9]   Xanthene-bridged cofacial bisporphyrins [J].
Chang, CJ ;
Deng, YQ ;
Heyduk, AF ;
Chang, CK ;
Nocera, DG .
INORGANIC CHEMISTRY, 2000, 39 (05) :959-966
[10]   Structural, spectroscopic, and reactivity comparison of xanthene- and dibenzofuran-bridged cofacial bisporphyrins [J].
Chang, CJ ;
Baker, EA ;
Pistorio, BJ ;
Deng, YQ ;
Loh, ZH ;
Miller, SE ;
Carpenter, SD ;
Nocera, DG .
INORGANIC CHEMISTRY, 2002, 41 (12) :3102-3109