Stereospecific radical polymerization of N -tert -butoxycarbonylacrylamide in the presence of fluorinated alcohols
Author:
Publisher
Wiley
Subject
Materials Chemistry,Organic Chemistry,Polymers and Plastics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pola.24373/fullpdf
Reference23 articles.
1. Stereospecific Living Radical Polymerization: Dual Control of Chain Length and Tacticity for Precision Polymer Synthesis
2. Hydrogen-bond-assisted stereocontrol in the radical polymerization ofN-isopropylacrylamide with primary alkyl phosphate: The effect of the chain length of the straight ester group
3. Direct synthesis of syndiotactic-rich poly(N-isopropylacrylamide) via radical polymerization of hydrogen-bond-complexed monomer
4. Dual roles of alkyl alcohols as syndiotactic-specificity inducers and accelerators in the radical polymerization ofN-isopropylacrylamide and some properties of syndiotactic poly(N-isopropylacrylamide)
5. Remarkable effect of hydrogen-bonding interaction on stereospecificity in the radical polymerization of N-vinylacetamide
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1. Dual role for alkali metal cations in enhancing the low-temperature radical polymerization of N,N-dimethylacrylamide;Polymer Chemistry;2015
2. Syndiotactic- and heterotactic-specific radical polymerizations of N-n-propyl-α-fluoroacrylamide and phase-transition behaviors of aqueous solutions of poly(N-n-propyl-α-fluoroacrylamide);Journal of Polymer Science Part A: Polymer Chemistry;2012-03-23
3. Syndiotactic-specific radical polymerization ofN-isopropylacrylamide in toluene at low temperatures in the presence of silyl alcohols;Polymer International;2012-02-06
4. Control of stereospecificity in the radical polymerization of N ‐methyl‐ N ‐(2‐pyridyl)acrylamide by conformational switching of the monomer with protonation;Journal of Polymer Science Part A: Polymer Chemistry;2011-07-22
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