Ams, Mark R.
(2007)
Intramolecularly Sensitized Precipitons.
Doctoral Dissertation, University of Pittsburgh.
(Unpublished)
Abstract
This dissertation describes the first intramolecularly activated precipitons. The isomerization process is induced by intramolecular triplet energy transfer from a covalently attached sensitizer. The intramolecular sensitization leads to a more rapid isomerization than can be achieved by intermolecular sensitization at accessible concentrations. Two different types of intramolecularly sensitized precipitons were investigated. The first precipiton receives intramolecular sensitization from a covalently attached metal complex (Ru(bpy)3Cl2). It was used in a model study for the sequestration of metal contaminants. The second precipiton receives intramolecular sensitization from a covalently attached organic compound (benzil). The preparation, photophysical properties, and photoisomerization kinetics of these precipitons, as well as the precipitation event, are discussed.
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Details
Item Type: |
University of Pittsburgh ETD
|
Status: |
Unpublished |
Creators/Authors: |
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ETD Committee: |
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Date: |
15 June 2007 |
Date Type: |
Completion |
Defense Date: |
26 March 2007 |
Approval Date: |
15 June 2007 |
Submission Date: |
10 April 2007 |
Access Restriction: |
No restriction; Release the ETD for access worldwide immediately. |
Institution: |
University of Pittsburgh |
Schools and Programs: |
Dietrich School of Arts and Sciences > Chemistry |
Degree: |
PhD - Doctor of Philosophy |
Thesis Type: |
Doctoral Dissertation |
Refereed: |
Yes |
Uncontrolled Keywords: |
benzil; cis; isomerization; separation; stilbene; trans; precipiton; ruthenium |
Other ID: |
http://etd.library.pitt.edu/ETD/available/etd-04102007-154650/, etd-04102007-154650 |
Date Deposited: |
10 Nov 2011 19:35 |
Last Modified: |
15 Nov 2016 13:39 |
URI: |
http://d-scholarship.pitt.edu/id/eprint/6956 |
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