Role of entropy in increased rates of intramolecular reactions

被引:16
作者
Armstrong, AA [1 ]
Amzel, LM [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biophys & Biophys Chem, Baltimore, MD 21205 USA
关键词
D O I
10.1021/ja0344359
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The rates of intramolecular condensation of a series of monoesters of dicarboxylic acids have been shown to be highly dependent on the nature of the intervening groups. To understand the origin of this effect, we estimated DeltaS(NAC,S), the entropy difference between the ensemble of accessible ground state conformers and a single ground state conformer having transition-state-like geometry. DeltaS(NAC,S) differs from the activation entropy for the reaction by DeltaS(TS,NAC), the difference in vibrational entropy between the selected ground state conformer and the transition state. The estimated values of DeltaS(NAC,S) correlate well (R-2 = 0.96 and 0.73 using dielectric constant values of 80 and 1, respectively) with experimentally determined reaction rate constants. Normal-mode analysis performed on minimized ground state conformations of each molecule suggests that the change in vibrational entropy makes only a small contribution to the total activation entropy. These results indicate that the conformational entropy difference between the transition and the ground states contributes significantly to the free energy of activation.
引用
收藏
页码:14596 / 14602
页数:7
相关论文
共 18 条
[1]  
AKHAOV YY, 1981, DIELECTRIC PROPERTIE
[2]   CHARMM - A PROGRAM FOR MACROMOLECULAR ENERGY, MINIMIZATION, AND DYNAMICS CALCULATIONS [J].
BROOKS, BR ;
BRUCCOLERI, RE ;
OLAFSON, BD ;
STATES, DJ ;
SWAMINATHAN, S ;
KARPLUS, M .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 1983, 4 (02) :187-217
[3]   GEM EFFECT .4. ACTIVATION PARAMETERS ACCOMPANYING INCREASED STERIC REQUIREMENTS OF 3,5' SUBSTITUENTS IN SOLVOLYSIS OF MONO-P-BROMOPHENYL GLUTARATES [J].
BRUICE, TC ;
BRADBURY, WC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (14) :3808-&
[5]   CONCEPT OF ORBITAL STEERING IN CATALYTIC REACTIONS [J].
BRUICE, TC ;
BROWN, A ;
HARRIS, DO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1971, 68 (03) :658-&
[6]   Ground state and transition state contributions to the rates of intramolecular and enzymatic reactions [J].
Bruice, TC ;
Lightstone, FC .
ACCOUNTS OF CHEMICAL RESEARCH, 1999, 32 (02) :127-136
[7]   SIDE-CHAIN ENTROPY OPPOSES ALPHA-HELIX FORMATION BUT RATIONALIZES EXPERIMENTALLY DETERMINED HELIX-FORMING PROPENSITIES [J].
CREAMER, TP ;
ROSE, GD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) :5937-5941
[8]  
D'Aquino JA, 2000, PROTEINS, P93
[9]  
Jencks W. P., 1969, CATALYSIS CHEM ENZYM
[10]  
KARPLUS M, 1981, MACROMOLECULES, V14, P325, DOI 10.1021/ma50003a019