4.7 Article

Thiol-functionalized branched and linear poly(ε-caprolactone): Direct synthesis, characterization and application in stabilizing silver nanoparticles

Journal

POLYMER
Volume 80, Issue -, Pages 88-94

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.polymer.2015.10.053

Keywords

Rare earth phenolates; Chemoselectivity; Thiol functionalized poly(epsilon-caprolactone); Ring-opening polymerization; Silver nanoparticle

Funding

  1. National Natural Science Foundation of China [21504039]
  2. National High Technology Research and Development Program of China [2014AA021201]
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions

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Yttrium trisphenolates was developed as highly chemoselective catalyst toward thiol, primary and secondary hydroxyl. By utilizing yttrium trisphenolates, well-defined thiol-functionalized branched and linear poly(epsilon-caprolactone) were directly synthesized via ring-opening polymerization of epsilon-caprolactone in the presence of unprotected 3-mercaptopropane-1, 2-diol and 2-mercapto-1-ethanol as initiator respectively. The expected structures were characterized by H-1 NMR, MALDI TOF MS and SEC. High thiol fidelities (>70%) and yields (>90%) of products were obtained with controlled molecular weights. The resultant thiol-functionalized poly(epsilon-caprolactone) were used to stabilize silver nanoparticles through two-phase method. The red shift of the UVevis absorption band of linear poly(epsilon-caprolactone) protected nanoparticles was observed comparing with the branched counterpart. Both two kinds of nanoparticles were well-dispersed with diameters around 2-3 nm according to TEM. (C) 2015 Elsevier Ltd. All rights reserved.

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