Reactivity Ratios for Organotin Copolymer Systems

Di(tri-n-butyltin) itaconate (DTBTI) and monoethyl tributyltin fumarate (METBTF) were synthesized as organotin monomers. The organotin monomers were copolymerized with styrene (ST) and methyl methacrylate (MMA) via a free radical polymerization technique. The overall conversion was kept low (°15% wt...

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Autores principales: El-Newehy, Mohamed H., Al-Deyab, Salem S., Al-Hazmi, Ali Mohsen Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2010
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257256/
https://www.ncbi.nlm.nih.gov/pubmed/20428076
http://dx.doi.org/10.3390/molecules15042749
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author El-Newehy, Mohamed H.
Al-Deyab, Salem S.
Al-Hazmi, Ali Mohsen Ali
author_facet El-Newehy, Mohamed H.
Al-Deyab, Salem S.
Al-Hazmi, Ali Mohsen Ali
author_sort El-Newehy, Mohamed H.
collection PubMed
description Di(tri-n-butyltin) itaconate (DTBTI) and monoethyl tributyltin fumarate (METBTF) were synthesized as organotin monomers. The organotin monomers were copolymerized with styrene (ST) and methyl methacrylate (MMA) via a free radical polymerization technique. The overall conversion was kept low (°15% wt/wt) for all studied samples and the copolymer composition was determined from tin analysis. The synthesized monomers and copolymers were characterized by elemental analysis, (1)H- and (13)C-NMR, and FTIR spectroscopy.
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spelling pubmed-62572562018-11-30 Reactivity Ratios for Organotin Copolymer Systems El-Newehy, Mohamed H. Al-Deyab, Salem S. Al-Hazmi, Ali Mohsen Ali Molecules Article Di(tri-n-butyltin) itaconate (DTBTI) and monoethyl tributyltin fumarate (METBTF) were synthesized as organotin monomers. The organotin monomers were copolymerized with styrene (ST) and methyl methacrylate (MMA) via a free radical polymerization technique. The overall conversion was kept low (°15% wt/wt) for all studied samples and the copolymer composition was determined from tin analysis. The synthesized monomers and copolymers were characterized by elemental analysis, (1)H- and (13)C-NMR, and FTIR spectroscopy. Molecular Diversity Preservation International 2010-04-15 /pmc/articles/PMC6257256/ /pubmed/20428076 http://dx.doi.org/10.3390/molecules15042749 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ 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/).
spellingShingle Article
El-Newehy, Mohamed H.
Al-Deyab, Salem S.
Al-Hazmi, Ali Mohsen Ali
Reactivity Ratios for Organotin Copolymer Systems
title Reactivity Ratios for Organotin Copolymer Systems
title_full Reactivity Ratios for Organotin Copolymer Systems
title_fullStr Reactivity Ratios for Organotin Copolymer Systems
title_full_unstemmed Reactivity Ratios for Organotin Copolymer Systems
title_short Reactivity Ratios for Organotin Copolymer Systems
title_sort reactivity ratios for organotin copolymer systems
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257256/
https://www.ncbi.nlm.nih.gov/pubmed/20428076
http://dx.doi.org/10.3390/molecules15042749
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