Literature DB >> 14624556

Radical reactions of didehydroarenes with a 1,4-relationship.

F Sedinam Amegayibor1, John J Nash, Hilkka I Kenttämaa.   

Abstract

A gas-phase study of the radical reactivities of didehydroarenes with a 1,4-relationship reveals that electronic effects (due to singlet-triplet state splittings) can be offset by polar effects.

Entities:  

Year:  2003        PMID： 14624556     DOI： 10.1021/ja0360079

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN： 0002-7863            Impact factor:   15.419


  3 in total

1.  Reactivity of aromatic sigma, sigma-biradicals toward riboses.

Authors:  Anthony Adeuya; Linan Yang; F Sedinam Amegayibor; John J Nash; Hilkka I Kenttämaa
Journal:  J Am Soc Mass Spectrom       Date:  2006-08-28       Impact factor: 3.109

2.  Substituent Effects on the Reactivity of the 2,4,6-Tridehydropyridinium Cation, an Aromatic σ,σ,σ-Triradical.

Authors:  Jinshan Gao; Bartłomiej J Jankiewicz; Huaming Sheng; Lindsey Kirkpatrick; Xin Ma; John J Nash; Hilkka I Kenttämaa
Journal:  European J Org Chem       Date:  2018-11-15

3.  Generation and characterization of a distonic biradical anion formed from an enediynone prodrug in the gas phase.

Authors:  Linan Yang; Tefsit Bekele; Mark A Lipton; Hilkka I Kenttämaa
Journal:  J Am Soc Mass Spectrom       Date:  2013-03-20       Impact factor: 3.109
  3 in total

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