Thermodynamics and kinetics of proton-coupled electron transfer: stepwise vs. concerted pathways

被引:182
作者
Mayer, JM [1 ]
Rhile, IJ [1 ]
机构
[1] Univ Washington, Dept Chem, Seattle, WA 98195 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2004年 / 1655卷 / 1-3期
关键词
proton-coupled electron transfer; hydrogen atom transfer; electron transfer; proton transfer; Marcus theory; iron;
D O I
10.1016/j.bbabio.2003.07.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Reactions that involve transfer of an electron and a proton can proceed by stepwise pathways involving initial electron transfer (ET) or initial proton transfer (PT), or by a concerted pathway without an intermediate. The concerted mechanism is termed proton-coupled electron transfer (PCET). Understanding such reactions requires knowledge of the thermodynamics of the possible ET, PT, and PCET steps. Many reactions have a large thermochemical bias favoring the PCET pathway. This bias is often sufficient to rule out stepwise mechanisms. The DeltaGdegrees for ET, PT or PCET has a strong influence on the rate of that step. Using the terminology of Marcus theory, PT and PCET reactions at C-H bonds have higher intrinsic barriers than such reactions at O-H or N-H bonds. The intrinsic barriers to ET and PCET are often similar when there is a small intrinsic barrier to PT. Reactions with a thermochemical bias toward PCET and with similar intrinsic barriers for all the pathways are most likely to occur by concerted PCET. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:51 / 58
页数:8
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