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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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 |
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Wiley Online Library |
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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 |
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10 |
container_issue |
12 |
container_start_page |
3509 |
op_container_end_page |
3518 |
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1800749954807889920 |