Polymers of carbonic acid, 8. Linear polybiurets
Abstract Linear polybiurets can be synthesized by polycondensation of chloroformyl isocyanate and N , N ′‐bis(trimethylsilyl)‐α,ω‐diaminoalkanes or silylated aromatic diamines. The polybiurets were characterized by elemental analyses, inherent viscosity measurements, IR spectroscopy, 1 H, 13 C, 15 N...
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crwiley:10.1002/macp.1992.021931012 2024-06-02T08:05:11+00:00 Polymers of carbonic acid, 8. Linear polybiurets Kricheldorf, Hans R. Meier‐Haack, Jochen 1992 http://dx.doi.org/10.1002/macp.1992.021931012 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmacp.1992.021931012 https://onlinelibrary.wiley.com/doi/pdf/10.1002/macp.1992.021931012 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Die Makromolekulare Chemie volume 193, issue 10, page 2631-2645 ISSN 0025-116X 0025-116X journal-article 1992 crwiley https://doi.org/10.1002/macp.1992.021931012 2024-05-03T11:35:07Z Abstract Linear polybiurets can be synthesized by polycondensation of chloroformyl isocyanate and N , N ′‐bis(trimethylsilyl)‐α,ω‐diaminoalkanes or silylated aromatic diamines. The polybiurets were characterized by elemental analyses, inherent viscosity measurements, IR spectroscopy, 1 H, 13 C, 15 N NMR spectroscopy in solution, differential scanning calorimetry (DSC) measurements, wide‐angle X‐ray scattering (WAXS) and thermogravimetric analyses. All polybiurets are semicrystalline materials with a low rate of crystallization and unexpectedly low melting points. 13 C and 15 N NMR cross‐polarization/magic angle spinning (CP/MAS) spectra of the solid polybiurets indicate different conformations for the amorphous and crystalline phase. All polybiurets gradually decompose upon heating above 200°C. Synthetic methods and properties of linear biurets were also checked by synthesis and characterization of N , N ′‐dioctylbiuret. Article in Journal/Newspaper Carbonic acid Wiley Online Library Die Makromolekulare Chemie 193 10 2631 2645 |
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English |
description |
Abstract Linear polybiurets can be synthesized by polycondensation of chloroformyl isocyanate and N , N ′‐bis(trimethylsilyl)‐α,ω‐diaminoalkanes or silylated aromatic diamines. The polybiurets were characterized by elemental analyses, inherent viscosity measurements, IR spectroscopy, 1 H, 13 C, 15 N NMR spectroscopy in solution, differential scanning calorimetry (DSC) measurements, wide‐angle X‐ray scattering (WAXS) and thermogravimetric analyses. All polybiurets are semicrystalline materials with a low rate of crystallization and unexpectedly low melting points. 13 C and 15 N NMR cross‐polarization/magic angle spinning (CP/MAS) spectra of the solid polybiurets indicate different conformations for the amorphous and crystalline phase. All polybiurets gradually decompose upon heating above 200°C. Synthetic methods and properties of linear biurets were also checked by synthesis and characterization of N , N ′‐dioctylbiuret. |
format |
Article in Journal/Newspaper |
author |
Kricheldorf, Hans R. Meier‐Haack, Jochen |
spellingShingle |
Kricheldorf, Hans R. Meier‐Haack, Jochen Polymers of carbonic acid, 8. Linear polybiurets |
author_facet |
Kricheldorf, Hans R. Meier‐Haack, Jochen |
author_sort |
Kricheldorf, Hans R. |
title |
Polymers of carbonic acid, 8. Linear polybiurets |
title_short |
Polymers of carbonic acid, 8. Linear polybiurets |
title_full |
Polymers of carbonic acid, 8. Linear polybiurets |
title_fullStr |
Polymers of carbonic acid, 8. Linear polybiurets |
title_full_unstemmed |
Polymers of carbonic acid, 8. Linear polybiurets |
title_sort |
polymers of carbonic acid, 8. linear polybiurets |
publisher |
Wiley |
publishDate |
1992 |
url |
http://dx.doi.org/10.1002/macp.1992.021931012 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmacp.1992.021931012 https://onlinelibrary.wiley.com/doi/pdf/10.1002/macp.1992.021931012 |
genre |
Carbonic acid |
genre_facet |
Carbonic acid |
op_source |
Die Makromolekulare Chemie volume 193, issue 10, page 2631-2645 ISSN 0025-116X 0025-116X |
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http://onlinelibrary.wiley.com/termsAndConditions#vor |
op_doi |
https://doi.org/10.1002/macp.1992.021931012 |
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Die Makromolekulare Chemie |
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193 |
container_issue |
10 |
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2631 |
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2645 |
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1800749970191548416 |