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Natural bond orbital (NBO) analysis of the angular group induced bond alternation (AGIBA) substituent effect
The geometries, natural charges, and resonance structures of 11 monosubstituted benzene derivatives were analyzed at the B3LYP/6‐311++G(d,p) and HF/6‐311++G(d, p) levels of theory. The following angular substituents were chosen: OCH3, CH2CH3, OH, SH, NHCH3, NHNH2, NO, CHCH2, NCH2, NNH, and CHO....
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Published in: | Journal of physical organic chemistry 2010-06, Vol.23 (6), p.551-556 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The geometries, natural charges, and resonance structures of 11 monosubstituted benzene derivatives were analyzed at the B3LYP/6‐311++G(d,p) and HF/6‐311++G(d, p) levels of theory. The following angular substituents were chosen: OCH3, CH2CH3, OH, SH, NHCH3, NHNH2, NO, CHCH2, NCH2, NNH, and CHO. The analysis of resonance structures was performed by using two different methodologies: harmonic oscillator stabilization energies (HOSE) and natural resonance theory (NRT). Also, the natural bond orbital (NBO) donor–acceptor stabilization energies for different resonance structures were calculated. We found that for all the substituents, the purely geometric resonance stabilization parameter (HOSE) is linearly correlated with quantum chemically derived resonance structure weight (NRT) of a given structure. Also, the calculations provide qualitative support for the earlier assumption of a through space angular group induced bond alternation (AGIBA) effect. Copyright © 2010 John Wiley & Sons, Ltd.
The angular group induced bond alternation (AGIBA) substituent effect was analyzed within the natural resonance theory (NRT). Good correlation between quantum‐mechanical NRT resonance structure weights and empirical harmonic oscillator stabilization energy (HOSE) model were found. |
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ISSN: | 0894-3230 1099-1395 |
DOI: | 10.1002/poc.1647 |