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Novel Unsaturated Sucrose Ethers and Their Application as Monomers

Novel unsaturated ethers were synthesised in good yields starting from sucrose, using a two-step mild and efficient procedure based on the Gassman method, which consists in forming a vinyl group by the elimination of ethanol from mixed acetals with trimethylsilyl trifluoromethanesulfonate in the pre...

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Detalles Bibliográficos
Autores principales: Crucho, Carina C., Petrova, Krasimira T., Pinto, Rui C., Barros, Maria T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245388/
https://www.ncbi.nlm.nih.gov/pubmed/18463572
http://dx.doi.org/10.3390/molecules13040762
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author Crucho, Carina C.
Petrova, Krasimira T.
Pinto, Rui C.
Barros, Maria T.
author_facet Crucho, Carina C.
Petrova, Krasimira T.
Pinto, Rui C.
Barros, Maria T.
author_sort Crucho, Carina C.
collection PubMed
description Novel unsaturated ethers were synthesised in good yields starting from sucrose, using a two-step mild and efficient procedure based on the Gassman method, which consists in forming a vinyl group by the elimination of ethanol from mixed acetals with trimethylsilyl trifluoromethanesulfonate in the presence of alkyl amines. Mixed acetals are readily obtained from the corresponding alcohols and ethyl vinyl ether, using an acidic catalyst. Conventional etherification involving a primary halide was also examined. The monomers thus obtained were successfully polymerised by a free radical mechanism, yielding unbranched linear and soluble polymers with pending sucrose moieties, and some of their physical properties were determined.
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spelling pubmed-62453882018-11-26 Novel Unsaturated Sucrose Ethers and Their Application as Monomers Crucho, Carina C. Petrova, Krasimira T. Pinto, Rui C. Barros, Maria T. Molecules Communication Novel unsaturated ethers were synthesised in good yields starting from sucrose, using a two-step mild and efficient procedure based on the Gassman method, which consists in forming a vinyl group by the elimination of ethanol from mixed acetals with trimethylsilyl trifluoromethanesulfonate in the presence of alkyl amines. Mixed acetals are readily obtained from the corresponding alcohols and ethyl vinyl ether, using an acidic catalyst. Conventional etherification involving a primary halide was also examined. The monomers thus obtained were successfully polymerised by a free radical mechanism, yielding unbranched linear and soluble polymers with pending sucrose moieties, and some of their physical properties were determined. MDPI 2008-03-28 /pmc/articles/PMC6245388/ /pubmed/18463572 http://dx.doi.org/10.3390/molecules13040762 Text en © 2008 by MDPI (http://www.mdpi.org). Reproduction is permitted for noncommercial purposes.
spellingShingle Communication
Crucho, Carina C.
Petrova, Krasimira T.
Pinto, Rui C.
Barros, Maria T.
Novel Unsaturated Sucrose Ethers and Their Application as Monomers
title Novel Unsaturated Sucrose Ethers and Their Application as Monomers
title_full Novel Unsaturated Sucrose Ethers and Their Application as Monomers
title_fullStr Novel Unsaturated Sucrose Ethers and Their Application as Monomers
title_full_unstemmed Novel Unsaturated Sucrose Ethers and Their Application as Monomers
title_short Novel Unsaturated Sucrose Ethers and Their Application as Monomers
title_sort novel unsaturated sucrose ethers and their application as monomers
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245388/
https://www.ncbi.nlm.nih.gov/pubmed/18463572
http://dx.doi.org/10.3390/molecules13040762
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