Literature DB >> 17979314

Radical hydrogen bonding: origin of stability of radical-molecule complexes.

Heriberto Hernández-Soto1, Frank Weinhold, Joseph S Francisco.   

Abstract

Natural bond orbital analysis is used to investigate the nature of hydrogen bonding in a series of binary open-shell complexes involving hydroperoxy radical HO(2)...X and analogous closed-shell H(2)O(2)...X complexes (where X = H(2)O, H(2)O(2), HONO, HONO(2), CH(3)OH, HCOOH, CH(3)COOH, and H(2)SO(4)) in order to elucidate and identify the electronic factors responsible for the strength of radical hydrogen bonds. Results from this study suggest that the radical species strongly alters the strength of the characteristic n --> sigma(*) donor-acceptor interaction in the hydrogen bonding. This interaction is found to contribute to the unusually strong binding in radical-molecule complexes. These findings have important new ramifications for our fundamental understanding of radical hydrogen bonds.

Entities:  

Year:  2007        PMID: 17979314     DOI: 10.1063/1.2784558

Source DB:  PubMed          Journal:  J Chem Phys        ISSN: 0021-9606            Impact factor:   3.488


  3 in total

1.  Spectroscopic identification and stability of the intermediate in the OH + HONO2 reaction.

Authors:  Bridget A O'Donnell; Eunice X J Li; Marsha I Lester; Joseph S Francisco
Journal:  Proc Natl Acad Sci U S A       Date:  2008-08-04       Impact factor: 11.205

2.  Hydrogen bonded and stacked geometries of the temozolomide dimer.

Authors:  Okuma Emile Kasende; Jules Tshishimbi Muya; Vincent de Paul N Nziko; Steve Scheiner
Journal:  J Mol Model       Date:  2016-03-14       Impact factor: 1.810

3.  Enantioselective Hydroamination of Alkenes with Sulfonamides Enabled by Proton-Coupled Electron Transfer.

Authors:  Casey B Roos; Joachim Demaerel; David E Graff; Robert R Knowles
Journal:  J Am Chem Soc       Date:  2020-03-20       Impact factor: 15.419

  3 in total

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