Indices for predicting the quality of leaving groups

被引:127
作者
Ayers, PW [1 ]
Anderson, JSM [1 ]
Rodriguez, JI [1 ]
Jawed, Z [1 ]
机构
[1] McMaster Univ, Dept Chem, Hamilton, ON L8S 4M1, Canada
关键词
D O I
10.1039/b500996k
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 inherent quality of leaving groups in chemical reactions is related to their ionization potential and electron affinity using a quadratic model for the dependence of the energy on the number of electrons. A good leaving group for nucleophilic substitution/elimination reactions is one where the difference in energy between the system with the "optimum'' number of electrons and the anion is small. Similarly, a good leaving group for electrophilic substitution/elimination reactions is one where the difference in energy between the system with the optimum number of electrons and the cation is small. This insight allows us to define indices for the quality of leaving groups in nucleophilic and electrophilic reactivity, which we term the nucleofugality and the electrofugality, respectively. These indices are useful not only for predicting the quality of leaving groups in organic reactions, but also for explaining the stability of carbocations, carbanions, and trends in pK(a).
引用
收藏
页码:1918 / 1925
页数:8
相关论文
共 34 条
[1]   Perturbative perspectives on the chemical reaction prediction problem [J].
Ayers, PW ;
Anderson, JSM ;
Bartolotti, LJ .
INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2005, 101 (05) :520-534
[2]   Variational principles for describing chemical reactions. Reactivity indices based on the external potential [J].
Ayers, PW ;
Parr, RG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (09) :2007-2017
[3]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[4]  
Carey F. A., 1984, Advanced Organic Chemistry Part A Structure and Mechanism
[5]   Reactivity dynamics in atom-field interactions: A quantum fluid density functional study [J].
Chattaraj, PK ;
Maiti, B .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (01) :169-183
[6]  
*CRC, 1990, CRC HDB CHEM PHYS
[7]   Electron affinities of the first- and second-row atoms:: Benchmark ab initio- and density-functional calculations [J].
de Oliveira, G ;
Martin, JML ;
de Proft, F ;
Geerlings, P .
PHYSICAL REVIEW A, 1999, 60 (02) :1034-1045
[8]   Correlating acidities, electron affinities, and bond dissociation energies. Measure one, get all three! [J].
Fattahi, A ;
Kass, SR .
JOURNAL OF ORGANIC CHEMISTRY, 2004, 69 (26) :9176-9183
[9]  
Frisch M.J., 1998, GAUSSIAN 98
[10]   Solvent assistance in the solvolysis of secondary substrates. I. The 2-adamantyl system, a standard for limiting solvolysis in a secondary substrate [J].
Fry, JL ;
Lancelot, CJ ;
Lam, LKM ;
Harris, JM ;
Bingham, RC ;
Raber, DJ ;
Hall, RE ;
Schleyer, PV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1970, 92 (08) :2538-2540