Award Date
12-1-2014
Degree Type
Thesis
Degree Name
Master of Science (MS)
Department
Chemistry and Biochemistry
First Committee Member
Kenneth Czerwinski
Second Committee Member
Frederic Poineau
Third Committee Member
Paul Forster
Fourth Committee Member
David Hatchett
Fifth Committee Member
Thomas Hartmann
Number of Pages
60
Abstract
The reaction of bidentate aniline oligomers with pentavalent technetium has been investigated previously through the reaction of (n-Bu4N)TcOCl4 with o-phenylenediamine (PDA). The initial studies found that PDA reacted in a 1 to 2 molar ratio with pentavalent technetium in in ethanol. This study was expanded by the examination of a second aniline derivatives, 2-aminophenol (AMP)) and two thiobenzene derivatives (2-mercaptophenol (MP) and thiosalicylic acid (TSA)) to evaluate the kinetic formation of these complexes with pentavalent technetium. The pentavalent technetium complexes all showed reactivity with technetium having a coordination numbers of 5 with all ligands reacting in a 1 to 2 metal to ligand ratio, which was confirmed by the use of electrospray ionization mass spectrometry (ESI- MS). Kinetic measurements were performed by UV-visible spectroscopy in a 24 hours period. Separate spectra were also obtained of the metal ligand complex at varying ratios of metal to ligand concentration to determine extinction coefficients for each metal-ligand complex based on Beer-Lambert's equation. While most of the reactions took about 24 hours to reach completion, the complex of TcO(TSA)2- has the fastest formation rate while the TcO(PDA)2- had that fastest reaction rate for the analine derivatives
Keywords
Aniline; Derivatives; Pentavalent; Speciation; Oligomers; Phenylenediamines; Technetium; Thiobenzene
Disciplines
Chemistry | Polymer Chemistry
File Format
Degree Grantor
University of Nevada, Las Vegas
Language
English
Repository Citation
Childs, Kyle E., "Speciation of Pentavalent Technetium Complexes with Aniline and Thiobenzene Derivatives" (2014). UNLV Theses, Dissertations, Professional Papers, and Capstones. 2250.
http://dx.doi.org/10.34917/7048172
Rights
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