Chemical modification of polysulfone: anionic synthesis of dipyridyl functionalized polysulfone

Citation
Gj. Summers et al., Chemical modification of polysulfone: anionic synthesis of dipyridyl functionalized polysulfone, POLYMER, 42(2), 2001, pp. 397-402
Citations number
20
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
POLYMER
ISSN journal
00323861 → ACNP
Volume
42
Issue
2
Year of publication
2001
Pages
397 - 402
Database
ISI
SICI code
0032-3861(200101)42:2<397:CMOPAS>2.0.ZU;2-L
Abstract
A new method for the synthesis of dipyridyl functionalized polysulfone is d escribed. The functionalization process involves the formation of lithiated polysulfone from polysulfone (1) and subsequent reaction with 2,2'-vinylid enedipyridine (2) in tetrahydrofuran at -78 degrees C under argon atmospher e. The dipyridyl functionalized polysulfone (3) was evaluated for the chela tion of trace heavy metal ions such as copper and nickel in aqueous medium. The dipyridyl functionalized polysulfone shows better complexing affinity for nickel ions at specific concentrations of test solutions. Quaternizatio n reactions of dipyridyl functionalized polysulfone with dimethyl sulfate i n the presence of perchloric acid quantitatively affords the corresponding polymeric pyridinium perchlorate derivative (4). (C) 2000 Elsevier Science Ltd. All rights reserved.