Literature DB >> 17143865

Rehybridization as a general mechanism for maximizing chemical and supramolecular bonding and a driving force for chemical reactions.

Igor V Alabugin1, Mariappan Manoharan.   

Abstract

Dynamic variations in hybridization patterns (rehybridization) were analyzed at B3LYP/6-31G** and MP2/6-31+G* levels. Computations clearly illustrate the generality of rehybridization in a variety of chemical phenomena, which involve structural reorganization in hydrogen-bonded complexes, nonhyperconjugative stereoelectronic effects in saturated heterocycles, Mills-Nixon effect, and contrasting substituent effects in cycloaromatization reactions. Copyright (c) 2006 Wiley Periodicals, Inc.

Entities:  

Year:  2007        PMID: 17143865     DOI: 10.1002/jcc.20524

Source DB:  PubMed          Journal:  J Comput Chem        ISSN: 0192-8651            Impact factor:   3.376


  3 in total

1.  Non-covalent interactions - QTAIM and NBO analysis.

Authors:  Sławomir J Grabowski
Journal:  J Mol Model       Date:  2012-07-08       Impact factor: 1.810

2.  Fine-tuning alkyne cycloadditions: Insights into photochemistry responsible for the double-strand DNA cleavage via structural perturbations in diaryl alkyne conjugates.

Authors:  Wang-Yong Yang; Samantha A Marrone; Nalisha Minors; Diego A R Zorio; Igor V Alabugin
Journal:  Beilstein J Org Chem       Date:  2011-06-16       Impact factor: 2.883

3.  Bioorthogonal Hydroamination of Push-Pull-Activated Linear Alkynes.

Authors:  Dahye Kang; Sheldon T Cheung; Justin Kim
Journal:  Angew Chem Int Ed Engl       Date:  2021-06-24       Impact factor: 16.823

  3 in total

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