Evaluation of different catalyst systems for bulk polymerization through “click” chemistry

“Click” chemistry is a frequently used technique in polymer chemistry for coupling polymer end groups to construct novel copolymer architectures and as a step-growth polymerization technique. In this study, the bulk polymerization of a diyne and a bisazide were achieved through the copper-catalyzed...

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Published inPolymer (Guilford) Vol. 52; no. 20; pp. 4435 - 4441
Main Authors Sheng, Xia, Rock, Darman M., Mauldin, Timothy C., Kessler, Michael R.
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 12.09.2011
Elsevier
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Summary:“Click” chemistry is a frequently used technique in polymer chemistry for coupling polymer end groups to construct novel copolymer architectures and as a step-growth polymerization technique. In this study, the bulk polymerization of a diyne and a bisazide were achieved through the copper-catalyzed alkyne-azide 1,3-cycloaddition (CuAAC) with different catalysts, including the homogeneous catalyst Cu(PPh3)3Br and a heterogeneous Cu/C catalyst. The effects of different catalyst systems on the kinetics of the “click” polymerization were evaluated by differential scanning calorimetry (DSC) and oscillatory rheology. Additionally, the thermomechanical properties of resulting polymers were evaluated by temperature-ramp oscillatory rheology and thermal stabilities by thermogravimetry. [Display omitted]
Bibliography:http://dx.doi.org/10.1016/j.polymer.2011.07.018
ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0032-3861
1873-2291
DOI:10.1016/j.polymer.2011.07.018