Synthesis of novel trithiocarbonate and allyl sulfide containing monomers
文献信息
Christopher R. Fenoli
In this study, we present a mild, efficient, and high yield synthesis of a variety of trithiocarbonates and allyl sulphide-containing AFT (addition–fragmentation termination) monomers containing terminal (meth)acrylate functional groups. The trithiocarbonate moiety core was synthesized with reaction yields often above 95%. Synthesis of monomers with allyl sulphide cores gave yields ranging from 48–92%. These monomers, designated as CRAFT (Controllable Reversible Addition Chain Transfer) monomers, offer the ability to control the mechanical and polymerization properties of the resulting thiol-Michael and chain-growth polymer networks in a previously unattainable manner. The triothiocarbonates reached 70–81% acrylate conversion in 10–200 s of light exposure while the allyl sulphide monomers reached 74–85% conversion in 10–50 s.
期刊推荐

New Journal of Chemistry

Russian Journal of Bioorganic Chemistry

Chemical Communications

Journal of Natural Medicines

Crystallography Reports

Russian Journal of Organic Chemistry

Acta Materialia

Current Opinion in Colloid & Interface Science

Russian Chemical Bulletin

Chemistry Education Research and Practice
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Polymer Chemistry

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![[(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-Diacetyloxy-15-[(2R,3S)-3-benzamido-3-phenyl-2-(2,2,2-trichloroethoxycarbonyloxy)propanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate structure [(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-Diacetyloxy-15-[(2R,3S)-3-benzamido-3-phenyl-2-(2,2,2-trichloroethoxycarbonyloxy)propanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate structure](https://cnstatic.chemtradehub.com/structs/100/100431-55-8-7104.webp)


