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Locating the Reaction Site of 1,2,3,4-Butanetetracarboxylic Acid Carboxyl and Cellulose Hydroxyl in the Esterification Cross-Linking
[Image: see text] The modification of cellulose with polycarboxylic acid is an important technology to functionalize the substrate. 1,2,3,4-Butanetetracarboxylic acid (BTCA) can significantly improve the anti-wrinkle performance of treated cotton fabrics by cross-linking with cellulose. However, the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552472/ https://www.ncbi.nlm.nih.gov/pubmed/34723036 http://dx.doi.org/10.1021/acsomega.1c04718 |
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author | Ji, Bolin Wang, Xiaowen Gong, Shoujia Zhong, Weibing Xie, Ruyi |
author_facet | Ji, Bolin Wang, Xiaowen Gong, Shoujia Zhong, Weibing Xie, Ruyi |
author_sort | Ji, Bolin |
collection | PubMed |
description | [Image: see text] The modification of cellulose with polycarboxylic acid is an important technology to functionalize the substrate. 1,2,3,4-Butanetetracarboxylic acid (BTCA) can significantly improve the anti-wrinkle performance of treated cotton fabrics by cross-linking with cellulose. However, the reaction site of BTCA carboxyl and the cellulose hydroxyl has not yet been clarified, which hinders the in-depth understanding about the reaction mechanism and the development of new cross-linking reagents. This study combines Fourier transform infrared and two-dimensional correlation spectroscopy to try to make it clear. Results confirmed that BTCA anhydride is an active intermediate (corresponding to the generally accepted theory) to esterify with cellulose hydroxyl, especially the O(6)–H(6) and O(2)–H(2). Cellobiose was taken as a model of cellulose to react with BTCA at variable temperatures, proving the above conclusion. In addition, the C14- or C11-containing carboxyl of BTCA showed a higher reactivity. Based on calculating reaction kinetics and thermodynamics with Gaussian 09W software, the most likely reaction route between BTCA and cellulose was as follows: BTCA → BTCA C5C14 anhydride → C14O15 ester → C14O15 ester C31C34 anhydride → C14O15C33O ester. |
format | Online Article Text |
id | pubmed-8552472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85524722021-10-29 Locating the Reaction Site of 1,2,3,4-Butanetetracarboxylic Acid Carboxyl and Cellulose Hydroxyl in the Esterification Cross-Linking Ji, Bolin Wang, Xiaowen Gong, Shoujia Zhong, Weibing Xie, Ruyi ACS Omega [Image: see text] The modification of cellulose with polycarboxylic acid is an important technology to functionalize the substrate. 1,2,3,4-Butanetetracarboxylic acid (BTCA) can significantly improve the anti-wrinkle performance of treated cotton fabrics by cross-linking with cellulose. However, the reaction site of BTCA carboxyl and the cellulose hydroxyl has not yet been clarified, which hinders the in-depth understanding about the reaction mechanism and the development of new cross-linking reagents. This study combines Fourier transform infrared and two-dimensional correlation spectroscopy to try to make it clear. Results confirmed that BTCA anhydride is an active intermediate (corresponding to the generally accepted theory) to esterify with cellulose hydroxyl, especially the O(6)–H(6) and O(2)–H(2). Cellobiose was taken as a model of cellulose to react with BTCA at variable temperatures, proving the above conclusion. In addition, the C14- or C11-containing carboxyl of BTCA showed a higher reactivity. Based on calculating reaction kinetics and thermodynamics with Gaussian 09W software, the most likely reaction route between BTCA and cellulose was as follows: BTCA → BTCA C5C14 anhydride → C14O15 ester → C14O15 ester C31C34 anhydride → C14O15C33O ester. American Chemical Society 2021-10-14 /pmc/articles/PMC8552472/ /pubmed/34723036 http://dx.doi.org/10.1021/acsomega.1c04718 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Ji, Bolin Wang, Xiaowen Gong, Shoujia Zhong, Weibing Xie, Ruyi Locating the Reaction Site of 1,2,3,4-Butanetetracarboxylic Acid Carboxyl and Cellulose Hydroxyl in the Esterification Cross-Linking |
title | Locating the Reaction Site of 1,2,3,4-Butanetetracarboxylic
Acid Carboxyl and Cellulose Hydroxyl in the Esterification Cross-Linking |
title_full | Locating the Reaction Site of 1,2,3,4-Butanetetracarboxylic
Acid Carboxyl and Cellulose Hydroxyl in the Esterification Cross-Linking |
title_fullStr | Locating the Reaction Site of 1,2,3,4-Butanetetracarboxylic
Acid Carboxyl and Cellulose Hydroxyl in the Esterification Cross-Linking |
title_full_unstemmed | Locating the Reaction Site of 1,2,3,4-Butanetetracarboxylic
Acid Carboxyl and Cellulose Hydroxyl in the Esterification Cross-Linking |
title_short | Locating the Reaction Site of 1,2,3,4-Butanetetracarboxylic
Acid Carboxyl and Cellulose Hydroxyl in the Esterification Cross-Linking |
title_sort | locating the reaction site of 1,2,3,4-butanetetracarboxylic
acid carboxyl and cellulose hydroxyl in the esterification cross-linking |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552472/ https://www.ncbi.nlm.nih.gov/pubmed/34723036 http://dx.doi.org/10.1021/acsomega.1c04718 |
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