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Synthesis and Characterization of Organotin Containing Copolymers: Reactivity Ratio Studies
Organotin monomers containing dibutyltin groups – dibutyltin citraconate (DBTC) as a new monomer and dibutyltin maleate (DBTM) – were synthesized. Free radical copolymerizations of the organotin monomers with styrene (ST) and butyl acrylate (BA) were performed. The overall conversion was kept low (≤...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257311/ https://www.ncbi.nlm.nih.gov/pubmed/20336013 http://dx.doi.org/10.3390/molecules15031784 |
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author | Al-Deyab, Salem S. Al-Hazmi, Ali Mohsen El-Newehy, Mohamed H. |
author_facet | Al-Deyab, Salem S. Al-Hazmi, Ali Mohsen El-Newehy, Mohamed H. |
author_sort | Al-Deyab, Salem S. |
collection | PubMed |
description | Organotin monomers containing dibutyltin groups – dibutyltin citraconate (DBTC) as a new monomer and dibutyltin maleate (DBTM) – were synthesized. Free radical copolymerizations of the organotin monomers with styrene (ST) and butyl acrylate (BA) were performed. The overall conversion was kept low (≤15% wt/wt) for all studied samples and the copolymers composition was determined from tin analysis using the Gillman and Rosenberg method. The reactivity ratios were calculated from the copolymer composition using the Fineman-Ross (FR) method. The synthesized monomers were characterized by elemental analysis, (1)H-, (13)C-NMR and FTIR spectroscopy. |
format | Online Article Text |
id | pubmed-6257311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-62573112018-12-04 Synthesis and Characterization of Organotin Containing Copolymers: Reactivity Ratio Studies Al-Deyab, Salem S. Al-Hazmi, Ali Mohsen El-Newehy, Mohamed H. Molecules Article Organotin monomers containing dibutyltin groups – dibutyltin citraconate (DBTC) as a new monomer and dibutyltin maleate (DBTM) – were synthesized. Free radical copolymerizations of the organotin monomers with styrene (ST) and butyl acrylate (BA) were performed. The overall conversion was kept low (≤15% wt/wt) for all studied samples and the copolymers composition was determined from tin analysis using the Gillman and Rosenberg method. The reactivity ratios were calculated from the copolymer composition using the Fineman-Ross (FR) method. The synthesized monomers were characterized by elemental analysis, (1)H-, (13)C-NMR and FTIR spectroscopy. Molecular Diversity Preservation International 2010-03-12 /pmc/articles/PMC6257311/ /pubmed/20336013 http://dx.doi.org/10.3390/molecules15031784 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license ( (http://creativecommons.org/licenses/by/3.0/) http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Al-Deyab, Salem S. Al-Hazmi, Ali Mohsen El-Newehy, Mohamed H. Synthesis and Characterization of Organotin Containing Copolymers: Reactivity Ratio Studies |
title | Synthesis and Characterization of Organotin Containing Copolymers: Reactivity Ratio Studies |
title_full | Synthesis and Characterization of Organotin Containing Copolymers: Reactivity Ratio Studies |
title_fullStr | Synthesis and Characterization of Organotin Containing Copolymers: Reactivity Ratio Studies |
title_full_unstemmed | Synthesis and Characterization of Organotin Containing Copolymers: Reactivity Ratio Studies |
title_short | Synthesis and Characterization of Organotin Containing Copolymers: Reactivity Ratio Studies |
title_sort | synthesis and characterization of organotin containing copolymers: reactivity ratio studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257311/ https://www.ncbi.nlm.nih.gov/pubmed/20336013 http://dx.doi.org/10.3390/molecules15031784 |
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