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Ionic Porous Organic Polymers Based on Functionalized Tetraarylborates

Lithium tetrakis(4-boronatoaryl)borates were subjected to polycondensation reactions with selected polyhydroxyl monomers such as 2,3,6,7,10,11-hexahydroxytriphenylene (HHTP) and 2,3,6,7-tetrahydroxy-9,10-dimethylanthracene (THDMA). Obtained boronate-type ionic porous polymers TAB1–4 were characteriz...

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Autores principales: Tomaszewski, Patryk, Wiszniewski, Marcin, Gontarczyk, Krzysztof, Wieciński, Piotr, Durka, Krzysztof, Luliński, Sergiusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6630441/
https://www.ncbi.nlm.nih.gov/pubmed/31234284
http://dx.doi.org/10.3390/polym11061070
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author Tomaszewski, Patryk
Wiszniewski, Marcin
Gontarczyk, Krzysztof
Wieciński, Piotr
Durka, Krzysztof
Luliński, Sergiusz
author_facet Tomaszewski, Patryk
Wiszniewski, Marcin
Gontarczyk, Krzysztof
Wieciński, Piotr
Durka, Krzysztof
Luliński, Sergiusz
author_sort Tomaszewski, Patryk
collection PubMed
description Lithium tetrakis(4-boronatoaryl)borates were subjected to polycondensation reactions with selected polyhydroxyl monomers such as 2,3,6,7,10,11-hexahydroxytriphenylene (HHTP) and 2,3,6,7-tetrahydroxy-9,10-dimethylanthracene (THDMA). Obtained boronate-type ionic porous polymers TAB1–4 were characterized by PXRD, (6)Li and (11)B magic-angle spinning nuclear magnetic resonance (MAS NMR), FT-IR, SEM, and TGA. They exhibit relatively good sorption of H(2) (up to 75 cm(3)/g STP), whereas N(2) uptake at 77 K for lower pressure range is relatively poor (up to 50 cm(3)/g STP below P/P(0) = 0.8). In addition, the effect of elongation of aryl arms in the tetraarylborate core on the materials’ properties was studied. Thus, it was found that replacement of the 4-boronatophenyl with 4-boronatobiphenylyl group has a negative impact on the sorption characteristics.
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spelling pubmed-66304412019-08-19 Ionic Porous Organic Polymers Based on Functionalized Tetraarylborates Tomaszewski, Patryk Wiszniewski, Marcin Gontarczyk, Krzysztof Wieciński, Piotr Durka, Krzysztof Luliński, Sergiusz Polymers (Basel) Article Lithium tetrakis(4-boronatoaryl)borates were subjected to polycondensation reactions with selected polyhydroxyl monomers such as 2,3,6,7,10,11-hexahydroxytriphenylene (HHTP) and 2,3,6,7-tetrahydroxy-9,10-dimethylanthracene (THDMA). Obtained boronate-type ionic porous polymers TAB1–4 were characterized by PXRD, (6)Li and (11)B magic-angle spinning nuclear magnetic resonance (MAS NMR), FT-IR, SEM, and TGA. They exhibit relatively good sorption of H(2) (up to 75 cm(3)/g STP), whereas N(2) uptake at 77 K for lower pressure range is relatively poor (up to 50 cm(3)/g STP below P/P(0) = 0.8). In addition, the effect of elongation of aryl arms in the tetraarylborate core on the materials’ properties was studied. Thus, it was found that replacement of the 4-boronatophenyl with 4-boronatobiphenylyl group has a negative impact on the sorption characteristics. MDPI 2019-06-21 /pmc/articles/PMC6630441/ /pubmed/31234284 http://dx.doi.org/10.3390/polym11061070 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tomaszewski, Patryk
Wiszniewski, Marcin
Gontarczyk, Krzysztof
Wieciński, Piotr
Durka, Krzysztof
Luliński, Sergiusz
Ionic Porous Organic Polymers Based on Functionalized Tetraarylborates
title Ionic Porous Organic Polymers Based on Functionalized Tetraarylborates
title_full Ionic Porous Organic Polymers Based on Functionalized Tetraarylborates
title_fullStr Ionic Porous Organic Polymers Based on Functionalized Tetraarylborates
title_full_unstemmed Ionic Porous Organic Polymers Based on Functionalized Tetraarylborates
title_short Ionic Porous Organic Polymers Based on Functionalized Tetraarylborates
title_sort ionic porous organic polymers based on functionalized tetraarylborates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6630441/
https://www.ncbi.nlm.nih.gov/pubmed/31234284
http://dx.doi.org/10.3390/polym11061070
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