The nature of bonding in pericyclic and pseudopericyclic transition states: Thermal chelotropic decarbonylations

被引:41
作者
Chamorro, E [1 ]
机构
[1] Univ Andres Bello, Fac Ecol & Recursos Nat, Dept Ciencias Quim, Santiago, Chile
关键词
D O I
10.1063/1.1566740
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 electron localization function (ELF), a local measure of the Pauli repulsion, is shown like a useful descriptor of bonding at pericyclic and pseudopericyclic transition states. The main differences between these two relevant topologies have been investigated in detail through the examination of well-characterized typical allowed-symmetry thermal decarbonylations. It is shown that results based on the electron fluctuation between the ELF basin populations at the reaction center, provides a consistent description of bonding which complements the traditional Woodward-Hoffmann symmetry-orbital based analysis. (C) 2003 American Institute of Physics.
引用
收藏
页码:8687 / 8698
页数:12
相关论文
共 50 条
[1]   On the mechanism of conversion of N-acyl-4-acyloxy-β-lactams into 2-substituted 1,3-oxazin-6-ones.: Can a low-barrier transition state be antiaromatic? [J].
Alajarín, M ;
Sánchez-Andrada, P ;
Cossío, FP ;
Arrieta, A ;
Lecea, B .
JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (25) :8470-8477
[2]   Conversion of N-acyl-4-acyloxy-β-lactams into 1,3-oxazin-6-ones:: Two consecutive pseudopericyclic processes [J].
Alajarín, M ;
Vidal, A ;
Sánchez-Andrada, P ;
Tovar, F ;
Ochoa, G .
ORGANIC LETTERS, 2000, 2 (07) :965-968
[3]  
Bader F.W., 1994, Atoms in molecules: a quantum theory
[4]  
BADER RFW, 1976, LOCALIZATION DELOCAL, V1
[5]   A SIMPLE MEASURE OF ELECTRON LOCALIZATION IN ATOMIC AND MOLECULAR-SYSTEMS [J].
BECKE, AD ;
EDGECOMBE, KE .
JOURNAL OF CHEMICAL PHYSICS, 1990, 92 (09) :5397-5403
[6]   Comparison of lithium and hydrogen bonds in (X•••Li•••X)- and (X•••H•••X)- (X=F, Cl and Br) complexes:: Topological analysis of electron localization function [J].
Berski, S ;
Latajka, Z .
INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2002, 90 (03) :1108-1120
[7]   Electrocyclic ring openings of 2-furylcarbene and related carbenes: A comparison between pseudopericyclic and coarctate reactions [J].
Birney, DM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (44) :10917-10925
[8]   Pericyclic and pseudopericyclic thermal cheletropic decarbonylations: When can a pericyclic reaction have a planar, pseudopericyclic transition state? [J].
Birney, DM ;
Ham, S ;
Unruh, GR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (19) :4509-4517
[9]  
Birney DM, 1999, ANGEW CHEM INT EDIT, V38, P189, DOI 10.1002/(SICI)1521-3773(19990115)38:1/2<189::AID-ANIE189>3.0.CO
[10]  
2-V