Driving Force Dependence of Rates for Nonadiabatic Proton and Proton-Coupled Electron Transfer: Conditions for Inverted Region Behavior

被引:33
作者
Edwards, Sarah J. [1 ]
Soudackov, Alexander V. [1 ]
Hammes-Schiffer, Sharon [1 ]
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
基金
美国国家科学基金会;
关键词
RADICAL-ION PAIR; POLAR ENVIRONMENT;
D O I
10.1021/jp907808t
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The driving force dependence of the rate constants for nonadiabatic electron transfer (ET), proton transfer (PT), and proton-coupled electron transfer (PCET) reactions is examined. Inverted region behavior, where the rate constant decreases as the reaction becomes more exoergic (i.e., as Delta G(0) becomes more negative), has been observed experimentally for ET and FIT. This behavior was predicted theoretically for ET but is not well understood for PT and PCET. The objective of this Letter is to predict the experimental conditions that Could lead to observation of inverted region behavior for PT and PCET. The driving force dependence of the rate constant is qualitatively different for PT and PCET than for ET because of the high proton vibrational frequency and substantial shift between the reactant and product proton vibrational wave functions. As a result, inverted region behavior is predicted to be experimentally inaccessible for PT and PCET if only the driving force is varied. This behavior may be observed for PT over a limited range of rates and driving forces if the solvent reorganization energy is low enough to cause observable oscillations. Moreover, this behavior may be observed for PT or PCET if the proton donor-acceptor distance increases as Delta G(0) becomes more negative. Thus, a plausible explanation for experimentally observed inverted region behavior for PT or PCET is that varying the driving force also impacts other properties of the system, such as the proton donor-acceptor distance.
引用
收藏
页码:14545 / 14548
页数:4
相关论文
共 21 条
[1]   Evidence for inverted region behavior in proton transfer to carbanions [J].
Andrieux, CP ;
Gamby, J ;
Hapiot, P ;
Savéant, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (33) :10119-10124
[2]   DYNAMIC THEORY OF PROTON TUNNELING TRANSFER RATES IN SOLUTION - GENERAL FORMULATION [J].
BORGIS, D ;
HYNES, JT .
CHEMICAL PHYSICS, 1993, 170 (03) :315-346
[3]   INTRAMOLECULAR LONG-DISTANCE ELECTRON-TRANSFER IN ORGANIC-MOLECULES [J].
CLOSS, GL ;
MILLER, JR .
SCIENCE, 1988, 240 (4851) :440-447
[4]   Proton-coupled electron transfer [J].
Cukier, RI ;
Nocera, DG .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1998, 49 :337-369
[5]   Analysis of Kinetic Isotope Effects for Proton-Coupled Electron Transfer Reactions [J].
Edwards, Sarah J. ;
Soudackov, Alexander V. ;
Hammes-Schiffer, Sharon .
JOURNAL OF PHYSICAL CHEMISTRY A, 2009, 113 (10) :2117-2126
[6]   Concerted electron and proton transfer: Transition from nonadiabatic to adiabatic proton tunneling [J].
Georgievskii, Y ;
Stuchebrukhov, AA .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (23) :10438-10450
[7]   Predicting Hydrogen-Bond Strengths from Acid-Base Molecular Properties. The pKa Slide Rule: Toward the Solution of a Long-Lasting Problem [J].
Gilli, Paola ;
Pretto, Loretta ;
Bertolasi, Valerio ;
Gilli, Gastone .
ACCOUNTS OF CHEMICAL RESEARCH, 2009, 42 (01) :33-44
[8]   Proton-Coupled Electron Transfer in Solution, Proteins, and Electrochemistry [J].
Hammes-Schiffer, Sharon ;
Soudackov, Alexander V. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (45) :14108-14123
[9]   Proton-coupled electron transfer [J].
Huynh, My Hang V. ;
Meyer, Thomas J. .
CHEMICAL REVIEWS, 2007, 107 (11) :5004-5064
[10]   Kinetic isotope effects for nonadiabatic proton transfer reactions in a polar environment. 1. Interpretation of tunneling kinetic isotopic effects [J].
Kiefer, PM ;
Hynes, JT .
JOURNAL OF PHYSICAL CHEMISTRY A, 2004, 108 (52) :11793-11808