eprintid: 8904
rev_number: 4
userid: 6
dir: disk0/00/00/89/04
datestamp: 2011-11-10 19:57:17
lastmod: 2016-11-15 13:48:14
status_changed: 2011-11-10 19:57:17
type: thesis_degree
metadata_visibility: show
contact_email: vaslo77@gmail.com
item_issues_count: 0
eprint_status: archive
creators_name: Vaslowski, Gregory
creators_email: vaslo77@gmail.com
title: Studies on the Alternatives to Stilbene Based Precipitons and Further Applications and Designs of Precipitons.
ispublished: unpub
divisions: sch_as_chemistry
full_text_status: public
keywords: azo; azobenzene; chemical separations; fluorous; green; organic chemistry; recyclable; scavengers; sythesis; thioureas
abstract: Precipitons, solubility-based phase tags, can be used in similar fashion to other solution based phase tags without many of the disadvantages. Structures based on azobenzene have been studied as alternatives to stilbene-based precipitons. The double bond between nitrogens in azobenzene can be interconverted between cis and trans by UV irradiation, unlike stilbene which only isomerizes in the cis to trans direction. The analogous nature of azobenzene to stilbene was the basis for the creation and study of possible recyclable alternatives to the studied stilbene orignal. Stilbene-based precipiton reagent tags have also been studied. Previous studies show the effectiveness of precipitons as a substrate tag. To show the precipiton's effectiveness as a reagent scavenger, several carbodiimide-based tags have been synthesized and tested as reagent scavengers. Finally, various sulfoxides tagged with a stilbene-based precipiton have been synthesized in order to demonstrate isolation of small molecules by sublimation from solids. Proof of principle is demonstrated by isomerizing precipiton tagged sulfoxides which are subsequently heated in oil and release several small allyl protected products. These products are isolated and characterized by common methods.
date: 2007-09-19
date_type: completed
institution: University of Pittsburgh
refereed: TRUE
etdcommittee_type: committee_chair
etdcommittee_type: committee_member
etdcommittee_type: committee_member
etdcommittee_name: Wilcox, Craig S
etdcommittee_name: Grabowski, Joseph J
etdcommittee_name: Nelson, Scott G
etdcommittee_email: daylite@pitt.edu
etdcommittee_email: joeg@pitt.edu
etdcommittee_email: sgnelson@pitt.edu
etdcommittee_id: DAYLITE
etdcommittee_id: JOEG
etdcommittee_id: SGNELSON
etd_defense_date: 2007-08-03
etd_approval_date: 2007-09-19
etd_submission_date: 2007-08-05
etd_access_restriction: immediate
etd_patent_pending: FALSE
assigned_doi: doi:10.5195/pitt.etd.2011.8904
thesis_type: thesis
degree: MS
committee: Craig S. Wilcox (daylite@pitt.edu) - Committee Chair
committee: Joseph J. Grabowski (joeg@pitt.edu) - Committee Member
committee: Scott G. Nelson (sgnelson@pitt.edu) - Committee Member
etdurn: etd-08052007-190054
other_id: http://etd.library.pitt.edu/ETD/available/etd-08052007-190054/
other_id: etd-08052007-190054
citation:   Vaslowski, Gregory  (2007) Studies on the Alternatives to Stilbene Based Precipitons and Further Applications and Designs of Precipitons.  Master's Thesis, University of Pittsburgh.    (Unpublished)  
document_url: http://d-scholarship-dev.library.pitt.edu/8904/1/GregoryVaslowski-8-10-2007-MSThesis.pdf