Experimental and theoretical evidence of decrease of both the enthalpy difference and the isomerization barrier of some thioester compounds when the molecular ion is formed-Reference-Cited by-同舟云学术

Experimental and theoretical evidence of decrease of both the enthalpy difference and the isomerization barrier of some thioester compounds when the molecular ion is formed

Published:1994-01 Issue:1-2 Volume:317 Page:165-169
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Védova C.O.Della,Furlong J.J.P.,Mack H.-G.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference30 articles.

1. Towards the absolute determination of the conformation in thioester compounds through the first pre-resonance Raman study in X-NSO molecules. Preparation and properties of S(N-sulphinylimine) chlorocarbonylsulphane, ClC(O)SNSO: IR, pre-resonant Raman, 13C NMR, mass and UV spectroscopic and conformational study

2. Conformational properties and gas-phase structure of (fluorocarbonyl)sulfenyl chloride, FC(O)SCl; electron diffraction, vibrational analysis, and ab initio calculations

3. Preparation and properties of fluorocarbonylsulphenyl bromide, FC(O) SBr

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3. Ionic Fragmentation on ClC(O)SCl. Evidence of a Highly Charged Molecular Ion and Confirmation of Unusual Dissociation Mechanisms for Halocarbonylsulfenyl Chlorides;The Journal of Physical Chemistry A;2004-12-23

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