Polyorthocarbonates

Abstract Hitherto unreported aromatic polyorthocarbonates have been synthesized by the reaction of dichlorodiphenoxymethane and various aromatic dihydroxy compounds. magnified image The polymers possess the structure of a methanetetra‐ol ether (carbonic acid orthoester) in the main chain. The direct...

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Published in:Journal of Polymer Science Part A-1: Polymer Chemistry
Main Author: Takekoshi, Tohru
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 1972
Subjects:
Online Access:http://dx.doi.org/10.1002/pol.1972.170101207
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fpol.1972.170101207
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spelling crwiley:10.1002/pol.1972.170101207 2024-06-02T08:05:11+00:00 Polyorthocarbonates Takekoshi, Tohru 1972 http://dx.doi.org/10.1002/pol.1972.170101207 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fpol.1972.170101207 https://onlinelibrary.wiley.com/doi/pdf/10.1002/pol.1972.170101207 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Journal of Polymer Science Part A-1: Polymer Chemistry volume 10, issue 12, page 3509-3518 ISSN 0449-296X 1542-9350 journal-article 1972 crwiley https://doi.org/10.1002/pol.1972.170101207 2024-05-03T11:10:10Z Abstract Hitherto unreported aromatic polyorthocarbonates have been synthesized by the reaction of dichlorodiphenoxymethane and various aromatic dihydroxy compounds. magnified image The polymers possess the structure of a methanetetra‐ol ether (carbonic acid orthoester) in the main chain. The direct structural evidence was obtained by 13 C NMR. High molecular weight, linear polyorthocarbonates were derived from sterically unhindered bisphenols. The polymers were noncrystalline, and clear, flexible films were obtained by casting from solution. Aromatic polyorthocarbonates decomposed above 360°C under nitrogen. The polymers were extremely stable under basic conditions but were unstable in strongly acidic media, particularly at elevated temperatures. Article in Journal/Newspaper Carbonic acid Wiley Online Library Journal of Polymer Science Part A-1: Polymer Chemistry 10 12 3509 3518
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract Hitherto unreported aromatic polyorthocarbonates have been synthesized by the reaction of dichlorodiphenoxymethane and various aromatic dihydroxy compounds. magnified image The polymers possess the structure of a methanetetra‐ol ether (carbonic acid orthoester) in the main chain. The direct structural evidence was obtained by 13 C NMR. High molecular weight, linear polyorthocarbonates were derived from sterically unhindered bisphenols. The polymers were noncrystalline, and clear, flexible films were obtained by casting from solution. Aromatic polyorthocarbonates decomposed above 360°C under nitrogen. The polymers were extremely stable under basic conditions but were unstable in strongly acidic media, particularly at elevated temperatures.
format Article in Journal/Newspaper
author Takekoshi, Tohru
spellingShingle Takekoshi, Tohru
Polyorthocarbonates
author_facet Takekoshi, Tohru
author_sort Takekoshi, Tohru
title Polyorthocarbonates
title_short Polyorthocarbonates
title_full Polyorthocarbonates
title_fullStr Polyorthocarbonates
title_full_unstemmed Polyorthocarbonates
title_sort polyorthocarbonates
publisher Wiley
publishDate 1972
url http://dx.doi.org/10.1002/pol.1972.170101207
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fpol.1972.170101207
https://onlinelibrary.wiley.com/doi/pdf/10.1002/pol.1972.170101207
genre Carbonic acid
genre_facet Carbonic acid
op_source Journal of Polymer Science Part A-1: Polymer Chemistry
volume 10, issue 12, page 3509-3518
ISSN 0449-296X 1542-9350
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1002/pol.1972.170101207
container_title Journal of Polymer Science Part A-1: Polymer Chemistry
container_volume 10
container_issue 12
container_start_page 3509
op_container_end_page 3518
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