E Z Stereoisomerization in Methylene bis-Dithiocarbamate and N,N,S Trimethyldithiocarbamate
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Authors
Pharr, Caroline
Thorburn, John
Advisor
Ron Wilde
Jon Salzsieder
Debra Bernardi
Jon Salzsieder
Debra Bernardi
Editor
Date of Issue
2003-04-01
Subject Keywords
trimethyldithiocarbamate, methylene bis-dithiocarbamate, selective inversion recovery
Publisher
Citation
Series/Report No.
item.page.identifier
Title
E Z Stereoisomerization in Methylene bis-Dithiocarbamate and N,N,S Trimethyldithiocarbamate
Other Titles
Type
thesis
Description
Abstract
Rates of rotation about the carbon-nitrogen partial double bond in N,N,Strimethyldithiocarbamate (1) and methylene bis-dithiocarbamate (2) were measured by the dynamic NMR technique known as selective inversion recovery. Free energies of activation (AG*) for the rotational barrier about the carbon-nitrogen partial double bond in compounds 1 and 2 were determined in a variety of solvents. Compound 1 was found to have a lower rotational barrier than compound 2. As solvent polarity increased, an increase in rotational barrier was observed. Contrary to expectations, hydroxylic solvents lowered the rotational barrier for compounds 1 and 2 based on their increased solvent polarity and hydrogen bonding capabilities. These results have implications for determining switching rates in dithiocarbamate chiroptical switches.
Sponsors
Degree Awarded
Bachelor's
Semester
Spring
Department
Chemistry & Physics