A versatile synthetic path to thiol containing polysiloxanes
Author(s) -
Perju Elena,
Dünki Simon J.,
Opris Dorina M.
Publication year - 2016
Publication title -
journal of polymer science part a: polymer chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.768
H-Index - 152
eISSN - 1099-0518
pISSN - 0887-624X
DOI - 10.1002/pola.28179
Subject(s) - thiol , thioester , surface modification , polymer chemistry , chemistry , polymer , elastomer , organic chemistry , enzyme
A synthetic strategy to polydimethylsiloxanes and polymethylsiloxanes containing thiol functions as end‐ or side‐groups, respectively, is presented. Such polymers are important starting materials for elastomeric networks and postpolymerization modifications. The synthesis starts either with vinyl end‐functionalized polydimethylsiloxanes or with polymethylvinylsiloxanes. The vinyl groups are reacted either with thioacetic acid or with a thioacetic acid/butanethiol mixture via a UV‐initiated thiol‐ene reaction to form the respective thioester quantitatively within few minutes. The thioesters are subsequently deprotected to the respective thiols by reduction with LiAlH 4 . The resulting thiol containing polysiloxanes can be used for the formation of networks or another functionalization. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54 , 2940–2948
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