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Calculated stabilities and structures for carbocations and singlet carbenes bearing electron‐withdrawing groups
Author(s) -
Gronert Scott,
Keeffe James R.
Publication year - 2013
Publication title -
journal of physical organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.325
H-Index - 66
eISSN - 1099-1395
pISSN - 0894-3230
DOI - 10.1002/poc.3167
Subject(s) - carbocation , chemistry , polarizability , main group element , computational chemistry , singlet state , isodesmic reaction , enthalpy , trifluoromethyl , cyclobutadiene , stereochemistry , molecule , crystallography , chemical physics , density functional theory , photochemistry , alkyl , atomic physics , organic chemistry , thermodynamics , physics , excited state , transition metal , catalysis
Carbocations and carbenes, as electron‐deficient species, require electron donation from the remainder of the molecule to the carbon center by whatever means available. Classical interactions include resonance, polar and polarizability effects, but neighboring group participation of several sorts can also serve as stabilizing factors. Simple carbocations with directly attached electron‐withdrawing groups (EWGs), that is, EWG–CH 2 + ions, comprise one group by which these interactions may be probed. This article provides computational evidence at the MP2/6‐311 + G** level for variable but significant stabilizing interactions between the carbocation center and common EWGs, many via bridging (partial or symmetrical), neighboring group participation, homoconjugation or π interactions. Bridging from atoms possessing nonbonding electron pairs is a common motif. Removal of bridging by application of geometric constraints nullifies bridging stabilization, but does not eliminate the possibility of other stabilizing interactions, for example polar, polarizability and π donation from the EWG. The potential for π donation from strong EWGs has not been widely appreciated in the past. A carbocation stabilization enthalpy, CSE+, is defined as the enthalpy of the isodesmic reaction CH 3 + + R–H → CH 4 + R + . Comparisons are made with singlet carbenes bearing EWGs for which many structural features are similar. Copyright © 2013 John Wiley & Sons, Ltd.