Conceptual density-functional theory for general chemical reactions, including those that are neither charge- nor frontier-orbital-controlled. 1. Theory and derivation of a general-purpose reactivity indicator

被引:129
作者
Anderson, James S. M.
Melin, Junia
Ayers, Paul W.
机构
[1] McMaster Univ, Dept Chem, Hamilton, ON L8S 4M1, Canada
[2] Kansas State Univ, Dept Chem, Manhattan, KS 66506 USA
关键词
D O I
10.1021/ct600164j
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
A new general-purpose reactivity indicator is derived. Unlike existing indicators, this indicator can describe the reactivity of molecules that lie between the electrostatic (or charge) control and electron-transfer (or frontier-orbital) control paradigms. Depending on the parameters in the indicator, it describes electrostatic control (where the electrostatic potential is the appropriate indicator), electron-transfer control (where the Fukui function's potential is the appropriate indicator), and intermediate cases (where linear combinations of the electrostatic potential and the Fukui function's potential are appropriate indicators). Our analysis gives some insight into the origins of the local hard/soft-acid/base principle. The "minimum Fukui function" rule for hard reagents also emerges naturally from our analysis: if (1) a reaction is strongly electrostatically controlled and (2) there are two sites that are equally favorable from an electrostatic standpoint, then the most reactive of the electrostatically equivalent sites is the site with the smallest Fukui function. An analogous electrostatic potential rule for soft reagents is also introduced: if (1) a reaction is strongly electron-transfer-controlled and (2) there are two sites where the Fukui function's potential are equivalent, then the most reactive of the Fukui-equivalent sites will be the one with greatest electrostatic potential (for electrophilic attack on a nucleophile) or smallest electrostatic potential (for nucleophilic attack on an electrophile).
引用
收藏
页码:358 / 374
页数:17
相关论文
共 69 条
[1]  
Albright T.A., 1985, ORBITAL INTERACTIONS
[2]   Conceptual density-functional theory for general chemical reactions, including those that are neither charge- nor frontier-orbital-controlled. 2. Application to molecules where frontier molecular orbital theory fails [J].
Anderson, James S. M. ;
Melin, Junia ;
Ayers, Paul W. .
JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2007, 3 (02) :375-389
[3]   The physical basis of the hard/soft acid/base principle [J].
Ayers, Paul W. .
FARADAY DISCUSSIONS, 2007, 135 :161-190
[4]   Elucidating the hard/soft acid/base principle: A perspective based on half-reactions [J].
Ayers, Paul W. ;
Parr, Robert G. ;
Pearson, Ralph G. .
JOURNAL OF CHEMICAL PHYSICS, 2006, 124 (19)
[5]   Can one oxidize an atom by reducing the molecule that contains it? [J].
Ayers, Paul W. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2006, 8 (29) :3387-3390
[6]   Atoms in molecules, an axiomatic approach. I. Maximum transferability [J].
Ayers, PW .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (24) :10886-10898
[7]   Indices for predicting the quality of leaving groups [J].
Ayers, PW ;
Anderson, JSM ;
Rodriguez, JI ;
Jawed, Z .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2005, 7 (09) :1918-1925
[8]   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
[9]   An elementary derivation of the hard/soft-acid/base principle [J].
Ayers, PW .
JOURNAL OF CHEMICAL PHYSICS, 2005, 122 (14)
[10]   Perspective on "Density functional approach to the frontier-electron theory of chemical reactivity" - Parr RG, Yang W (1984) J Am Chem Soc 106: 4049-4050 [J].
Ayers, PW ;
Levy, M .
THEORETICAL CHEMISTRY ACCOUNTS, 2000, 103 (3-4) :353-360