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HERO ID
6622889
Reference Type
Journal Article
Title
Anionic synthesis and detection of fluorescence-labeled polymers with a terminal anhydride group
Author(s)
Moon, B; Hoye, TR; Macosko, CW; ,
Year
2000
Is Peer Reviewed?
Yes
Journal
Journal of Polymer Science. Part A, Polymer Chemistry
ISSN:
0887-624X
EISSN:
1099-0518
Publisher
JOHN WILEY & SONS INC
Location
NEW YORK
Volume
38
Issue
12
Page Numbers
2177-2185
Language
English
DOI
10.1002/(SICI)1099-0518(20000615)38:12<2177::AID-POLA60>3.0.CO;2-5
Web of Science Id
WOS:000087239700006
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033726231&doi=10.1002%2f%28SICI%291099-0518%2820000615%2938%3a12%3c2177%3a%3aAID-POLA60%3e3.0.CO%3b2-5&partnerID=40&md5=83ccb5bfa5bd2537ab3453abf565996e
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Abstract
To monitor polymer-polymer coupling reactions between two different monofunctional polymers in dilute polymer blends, fluorescence-labeled anhydride-functional polystyrene (PS) and poly(methyl methacrylate) (PMMA) were prepared by conventional anionic polymerization. Sequential trapping of lithiopolystyrene by 1-(2-anthryl)-1-phenylethylene (APE) and then di-t-butyl maleate (4) provided, after pyrolysis, anhydride-functional fluorescent PS. Fluorescent PMMA anhydride (8) was synthesized with sec-butyllithium/APE as an initiator for the anionic polymerization of methyl methacrylate, trapping by 4, and pyrolysis. These polymers could be reacted with amine-functional polymers by melt blending, and the reaction progress could be monitored by gel permeation chromatography coupled with fluorescence detection. This technique not only allows monitoring of the coupling reaction with high sensitivity (ca. 100 times more sensitive than refractive index detection) but also permits selective detection because unlabeled polymers are invisible to fluorescence detection. This highly sensitive and selective detection methodology was also used to monitor the coupling reaction of 8 with PS-NH2 at a thin-film interface, which was otherwise difficult to detect by conventional methods. (C) 2000 John Wiley & Sons, Inc.
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