TY - JOUR
T1 - Preparation of linear and hyperbranched fluorinated poly(aryl ether-thioether) through para-fluoro-thiol click reaction
AU - Baysak, Elif
AU - Tunca, Umit
AU - Hizal, Gurkan
AU - Durmaz, Hakan
N1 - Publisher Copyright:
© 2018 Wiley Periodicals, Inc.
PY - 2018/8/15
Y1 - 2018/8/15
N2 - The para-fluoro-thiol “click” reaction (PFTCR) was utilized to prepare linear and hyperbranched fluorinated poly (aryl ether-thioether). For this purpose, 1,2-bis(perfluorophenoxy)ethane was prepared and reacted with 1,6-hexandithiol and trimethylolpropane tris(3-mercaptopropionate), respectively. While hyperbranched polymers were prepared using 0.5 M concentrations of starting materials at room temperature, the linear polymer syntheses were performed at different reaction temperatures and concentrations. The resulting polymers were mainly characterized by NMR measurements and a very distinct fluorine signals regarding meta- and ortho- positions in the 19F NMR were found for both polymer topologies. In addition to NMR analyses, both linear and hyperbranched polymers were further characterized by using Fourier transform infrared spectroscopy (FT-IR), gel permeation chromatography (GPC), and differential scanning calorimetry (DSC).
AB - The para-fluoro-thiol “click” reaction (PFTCR) was utilized to prepare linear and hyperbranched fluorinated poly (aryl ether-thioether). For this purpose, 1,2-bis(perfluorophenoxy)ethane was prepared and reacted with 1,6-hexandithiol and trimethylolpropane tris(3-mercaptopropionate), respectively. While hyperbranched polymers were prepared using 0.5 M concentrations of starting materials at room temperature, the linear polymer syntheses were performed at different reaction temperatures and concentrations. The resulting polymers were mainly characterized by NMR measurements and a very distinct fluorine signals regarding meta- and ortho- positions in the 19F NMR were found for both polymer topologies. In addition to NMR analyses, both linear and hyperbranched polymers were further characterized by using Fourier transform infrared spectroscopy (FT-IR), gel permeation chromatography (GPC), and differential scanning calorimetry (DSC).
KW - fluorinated poly(aryl ether-thioether)
KW - hyperbranched polymers
KW - linear polymers
KW - para-fluoro-thiol “click” reaction
UR - http://www.scopus.com/inward/record.url?scp=85052068769&partnerID=8YFLogxK
U2 - 10.1002/pola.29068
DO - 10.1002/pola.29068
M3 - Article
AN - SCOPUS:85052068769
SN - 0887-624X
VL - 56
SP - 1853
EP - 1859
JO - Journal of Polymer Science, Part A: Polymer Chemistry
JF - Journal of Polymer Science, Part A: Polymer Chemistry
IS - 16
ER -