Energy decomposition analysis

被引:714
作者
von Hopffgarten, Moritz [1 ]
Frenking, Gernot [1 ]
机构
[1] Univ Marburg, Fachbereich Chem, D-3550 Marburg, Germany
关键词
METAL-LIGAND BOND; C-CL BONDS; DENSITY-FUNCTIONAL THEORY; QUANTUM CONTRIBUTIONS; PARTITIONING ANALYSIS; ACTIVATION STRAIN; OXIDATIVE ADDITION; CHEMICAL-BOND; BINUCLEAR COMPLEXES; TRANSITION-METALS;
D O I
10.1002/wcms.71
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The energy decomposition analysis (EDA) is a powerful method for a quantitative interpretation of chemical bonds in terms of three major expressions. The instantaneous interaction energy ?Eint between two fragments A and B in a molecule AB is partitioned in three terms, namely, (1) the quasiclassical electrostatic interaction ?Eelstat between the fragments, (2) the repulsive exchange (Pauli) interaction ?EPauli between electrons of the two fragments having the same spin, and (3) the orbital (covalent) interaction ?Eorb, which comes from the orbital relaxation and the orbital mixing between the fragments. The latter term can be decomposed into contributions of orbitals with different symmetry, which makes it possible to distinguish between s, p, and d bonding. After a short introduction into the theoretical background of the EDA, we present illustrative examples of main group and transition metal chemistry. The results show that the EDA terms can be interpreted in a chemically meaningful way, thus providing a bridge between quantum chemical calculations and heuristic bonding models of traditional chemistry. (c) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:43 / 62
页数:20
相关论文
共 104 条
[1]  
[Anonymous], 2005, CHEM REV, V105
[2]  
[Anonymous], 2001, Chem. Rev, V101
[3]  
[Anonymous], ANGEW CHEM
[4]  
Bader R. F. W., 1994, ATOMS MOL QUANTUM TH
[5]   Nucleophilicity and leaving-group ability in frontside and backside SN2 reactions [J].
Bento, A. Patricia ;
Bickelhaupt, F. Matthias .
JOURNAL OF ORGANIC CHEMISTRY, 2008, 73 (18) :7290-7299
[6]   Why is BCl3 a stronger Lewis acid with respect to strong bases than BF3? [J].
Bessac, F ;
Frenking, G .
INORGANIC CHEMISTRY, 2003, 42 (24) :7990-7994
[7]   OXIDATIVE INSERTION AS FRONTSIDE S(N)2 SUBSTITUTION - A THEORETICAL-STUDY OF THE MODEL REACTION SYSTEM PD+CH3CL [J].
BICKELHAUPT, FM ;
ZIEGLER, T ;
SCHLEYER, PV .
ORGANOMETALLICS, 1995, 14 (05) :2288-2296
[8]   THEORETICAL INVESTIGATION ON BASE-INDUCED 1,2-ELIMINATIONS IN THE MODEL SYSTEM F-+CH3CH2F - THE ROLE OF THE BASE AS A CATALYST [J].
BICKELHAUPT, FM ;
BAERENDS, EJ ;
NIBBERING, NMM ;
ZIEGLER, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (20) :9160-9173
[9]  
Bickelhaupt FM, 1999, J COMPUT CHEM, V20, P114, DOI 10.1002/(SICI)1096-987X(19990115)20:1<114::AID-JCC12>3.0.CO
[10]  
2-L