Deeper Insight into the Diels-Alder Reaction through the Activation Strain Model

被引:52
作者
Fernandez, Israel [1 ]
Bickelhaupt, F. Matthias [2 ,3 ,4 ]
机构
[1] Univ Complutense Madrid, Dept Quim Organ 1, Ciudad Univ, E-28040 Madrid, Spain
[2] Vrije Univ Amsterdam, Dept Theoret Chem, De Boelelaan 1083, NL-1081 HV Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, ACMM, De Boelelaan 1083, NL-1081 HV Amsterdam, Netherlands
[4] Radboud Univ Nijmegen, Inst Mol & Mat, Heyendaalseweg 135, NL-6525 AJ Nijmegen, Netherlands
关键词
activation strain model; chemical reactivity; cycloaddition; Diels-Alder; energy decomposition analysis; selectivity; POLYCYCLIC AROMATIC-HYDROCARBONS; SECONDARY ORBITAL INTERACTIONS; WALLED CARBON NANOTUBES; HYPERCONJUGATIVE AROMATICITY; ADDITION-REACTIONS; STERIC COURSE; CYCLOADDITIONS; DISTORTION/INTERACTION; 1,3-DIPOLAR; DIENES;
D O I
10.1002/asia.201601203
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this Focus Review, we present the application of the so-called Activation Strain Model of chemical reactivity to the Diels-Alder cycloaddition reaction. To this end, representative recent examples have been selected to illustrate the power of this new computational approach to gain a deeper quantitative understanding of this fundamental process in chemistry. We cover a wide range of issues, such as, the "endo-rule", reactivity trends emerging from systematic variation in the reactants' strain, and cycloaddition reactions involving relevant species in material science, that is, fullerenes, polycyclic aromatic hydrocarbons and nanotubes.
引用
收藏
页码:3297 / 3304
页数:8
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