Geometrical structures, energies and vibrational frequencies of phenylthiyl, p -aminophenylthiyl and their disulfides by using quantum chemical calculations-Reference-Cited by-同舟云学术

Geometrical structures, energies and vibrational frequencies of phenylthiyl, p -aminophenylthiyl and their disulfides by using quantum chemical calculations

Published:2000-10 Issue:1-3 Volume:531 Page:51-64
ISSN:0166-1280
Container-title:Journal of Molecular Structure: THEOCHEM
language:en
Short-container-title:Journal of Molecular Structure: THEOCHEM

Author:

Kamisuki T,Hirose C

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference38 articles.

1. Flash photolysis of aromatic sulfur molecules

2. Spectral shifts of the p-aminophenylthyl radical absorption and emission in solution

3. Evaluation of addition rates of thiyl radicals to vinyl monomers by flash photolysis. 4. Solvent effects on rates of free-radical reactions. Addition of the p-aminobenzenethiyl radical to styrene

4. The extinction coefficient for the p-aminophenylthiyl radical as determined by reaction with galvinoxyl

5. Estimation of extinction coefficient and radiative lifetime of a free radical, p-aminophenylthiyl

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Oxidative Addition of S−S Bonds to Dimethylplatinum(II) Complexes: Evidence for a Binuclear Mechanism;Organometallics;2008-10-30

2. Theoretical Investigation of Molecular Properties of the First Excited State of the Thiophenoxyl Radical;The Journal of Physical Chemistry A;2008-10-24

3. Electronic properties of para-substituted thiophenols and disulfides from 13C NMR spectroscopy and ab initio calculations: relations to the Hammett parameters and atomic chargesElectronic supplementary information (ESI) available: all characterization data are tabulated in Table S1. A figure showing the dependence of the natural charge of the C1 atom of the disulfides on the 13C NMR chemical shift is also provided. See http://www.rsc.org/suppdata/nj/b3/b300048f/;New Journal of Chemistry;2003