Preparation of single-site tin(IV) compounds and their use in the polymerization of ε-caprolactone

Butyltin(IV) carboxylate compounds were obtained by reactions of butyltrichlorotin(IV) with potassium pivalate, perfluoroheptanoate, methacrylate, 2,6-pyridinedicarboxylate, and phthalate. The synthesized complexes were fully characterized by nuclear magnetic resonance (1H-, 13C-NMR), Fourier transf...

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Main Authors: Begum Canan Yildiz, Asgar Kayan
Format: Article
Language:English
Published: Taylor & Francis Group 2017-01-01
Series:Designed Monomers and Polymers
Subjects:
NMR
Online Access:http://dx.doi.org/10.1080/15685551.2016.1231032
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spelling doaj-19b7be5e1a044833baf4ee2ca1425ff32020-11-25T01:17:52ZengTaylor & Francis GroupDesigned Monomers and Polymers1568-55512017-01-01201899610.1080/15685551.2016.12310321231032Preparation of single-site tin(IV) compounds and their use in the polymerization of ε-caprolactoneBegum Canan Yildiz0Asgar Kayan1Kocaeli UniversityKocaeli UniversityButyltin(IV) carboxylate compounds were obtained by reactions of butyltrichlorotin(IV) with potassium pivalate, perfluoroheptanoate, methacrylate, 2,6-pyridinedicarboxylate, and phthalate. The synthesized complexes were fully characterized by nuclear magnetic resonance (1H-, 13C-NMR), Fourier transform infrared (FTIR), mass spectroscopies (MS) and elemental analysis. These tin complexes were used as catalysts for the ring opening polymerization of ε-caplolactone and the conversion of monomers to polymers was completed in just 1 h. The structures of polymers were characterized by a combination of spectroscopic techniques (NMR, FTIR, MS), differential scanning calorimeter (DSC) and gel permeation chromatography. In this study, the ε-caplolactone polymers with different average molecular weights between 5000 and 40,000 Da having a regular structure were obtained.http://dx.doi.org/10.1080/15685551.2016.1231032Single-site tin catalystcarboxylatesε-caplolactonering-openingNMR
collection DOAJ
language English
format Article
sources DOAJ
author Begum Canan Yildiz
Asgar Kayan
spellingShingle Begum Canan Yildiz
Asgar Kayan
Preparation of single-site tin(IV) compounds and their use in the polymerization of ε-caprolactone
Designed Monomers and Polymers
Single-site tin catalyst
carboxylates
ε-caplolactone
ring-opening
NMR
author_facet Begum Canan Yildiz
Asgar Kayan
author_sort Begum Canan Yildiz
title Preparation of single-site tin(IV) compounds and their use in the polymerization of ε-caprolactone
title_short Preparation of single-site tin(IV) compounds and their use in the polymerization of ε-caprolactone
title_full Preparation of single-site tin(IV) compounds and their use in the polymerization of ε-caprolactone
title_fullStr Preparation of single-site tin(IV) compounds and their use in the polymerization of ε-caprolactone
title_full_unstemmed Preparation of single-site tin(IV) compounds and their use in the polymerization of ε-caprolactone
title_sort preparation of single-site tin(iv) compounds and their use in the polymerization of ε-caprolactone
publisher Taylor & Francis Group
series Designed Monomers and Polymers
issn 1568-5551
publishDate 2017-01-01
description Butyltin(IV) carboxylate compounds were obtained by reactions of butyltrichlorotin(IV) with potassium pivalate, perfluoroheptanoate, methacrylate, 2,6-pyridinedicarboxylate, and phthalate. The synthesized complexes were fully characterized by nuclear magnetic resonance (1H-, 13C-NMR), Fourier transform infrared (FTIR), mass spectroscopies (MS) and elemental analysis. These tin complexes were used as catalysts for the ring opening polymerization of ε-caplolactone and the conversion of monomers to polymers was completed in just 1 h. The structures of polymers were characterized by a combination of spectroscopic techniques (NMR, FTIR, MS), differential scanning calorimeter (DSC) and gel permeation chromatography. In this study, the ε-caplolactone polymers with different average molecular weights between 5000 and 40,000 Da having a regular structure were obtained.
topic Single-site tin catalyst
carboxylates
ε-caplolactone
ring-opening
NMR
url http://dx.doi.org/10.1080/15685551.2016.1231032
work_keys_str_mv AT begumcananyildiz preparationofsinglesitetinivcompoundsandtheiruseinthepolymerizationofecaprolactone
AT asgarkayan preparationofsinglesitetinivcompoundsandtheiruseinthepolymerizationofecaprolactone
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