Literature DB >> 24248898

The thiomethyl anion: Formation, reactivity, and thermodynamic properties.

S R Kass1, H Guo, G D Dahlke.   

Abstract

The thiomethyl anion (1) has been generated by fluorodesilylation of trimethylsilylmethanethiol in a variable-temperature flowing afterglow device. The proton affinity (1649 ± 12 kJ mol(-1)) and electron affinity (0.67 ± .13 eV) were determined and compared to a previously reported molecular orbital calculation. Isomerization via a 1,2-proton shift does not take place between -40° and 100°C despite a 156 kJ mol(-1) driving force. Ion-molecule reactions of 1 were examined with a number of reagents including N20, O2, CS2, COS, and CO2, Hydride ion transfer was observed in every case, along with other products, and thermodynamic information has been derived.

Entities:  

Year:  1990        PMID: 24248898     DOI: 10.1016/1044-0305(90)85016-F

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  3 in total

1.  The acidity of uracil and uracil analogs in the gas phase: four surprisingly acidic sites and biological implications.

Authors:  Mary Ann Kurinovich; Jeehiun K Lee
Journal:  J Am Soc Mass Spectrom       Date:  2002-08       Impact factor: 3.109

2.  Reactions of strong bases with vinyl fluoride formation and characterization of 1-fluorovinyl anion and the fluoride-acetylene hydrogen-bonded complex.

Authors:  J J Rabasco; S R Kass
Journal:  J Am Soc Mass Spectrom       Date:  1992-02       Impact factor: 3.109

3.  Effects of Environmental and Electric Perturbations on the pKa of Thioredoxin Cysteine 35: A Computational Study.

Authors:  Valeria D'Annibale; Donatella Fracassi; Paolo Marracino; Guglielmo D'Inzeo; Marco D'Abramo
Journal:  Molecules       Date:  2022-09-30       Impact factor: 4.927

  3 in total

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