Characteristic activity of phosphorous acid in the dehydration condensation of a chitin-derived nitrogen-containing sugar alcohol
Chitin is a potential resource for the production of renewable organonitrogen compounds, as it contains biologically fixed nitrogen. Hydrolysis of chitin followed by hydrogenation gives the sugar alcohol named 2-acetamido-2-deoxysorbitol (ADS). The dehydration condensation of ADS produces 2-acetamid...
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Veröffentlicht in: | Green chemistry : an international journal and green chemistry resource : GC 2021-09, Vol.23 (18), p.7228-7234 |
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creator | Yang, Cheng Sagawa, Takuya Fukuoka, Atsushi Kobayashi, Hirokazu |
description | Chitin is a potential resource for the production of renewable organonitrogen compounds, as it contains biologically fixed nitrogen. Hydrolysis of chitin followed by hydrogenation gives the sugar alcohol named 2-acetamido-2-deoxysorbitol (ADS). The dehydration condensation of ADS produces 2-acetamido-2-deoxyisosorbide (ADI), which is a prospective precursor of nitrogen-containing polymers. However, the conversion of ADS to ADI in previous works needed a large amount of CF
3
SO
3
H as a superstrong acid catalyst, which is high cost and requires special corrosion-resistant equipment. In this work, we have found that H
3
PO
3
, a weak acid, can convert ADS to ADI. Possibly, H
3
PO
3
alters the reaction mechanism from a simple acid-catalysed dehydration cyclisation to a cyclisation
via
phosphite esters. Density functional theory calculations suggest that the modified pathway
via
the phosphite esters significantly reduces the activation energy. In addition, the reducing ability of the acid likely decreases the formation of condensation by-products.
H
3
PO
3
converts a chitin-derived sugar alcohol to a potential monomer for polymer production by a mechanism different from that for strong acid catalysts. |
doi_str_mv | 10.1039/d1gc02193a |
format | Article |
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3
SO
3
H as a superstrong acid catalyst, which is high cost and requires special corrosion-resistant equipment. In this work, we have found that H
3
PO
3
, a weak acid, can convert ADS to ADI. Possibly, H
3
PO
3
alters the reaction mechanism from a simple acid-catalysed dehydration cyclisation to a cyclisation
via
phosphite esters. Density functional theory calculations suggest that the modified pathway
via
the phosphite esters significantly reduces the activation energy. In addition, the reducing ability of the acid likely decreases the formation of condensation by-products.
H
3
PO
3
converts a chitin-derived sugar alcohol to a potential monomer for polymer production by a mechanism different from that for strong acid catalysts.</description><identifier>ISSN: 1463-9262</identifier><identifier>EISSN: 1463-9270</identifier><identifier>DOI: 10.1039/d1gc02193a</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Acids ; Catalysts ; Chitin ; Condensates ; Corrosion resistance ; Dehydration ; Density functional theory ; Esters ; Green chemistry ; Nitrogen ; Phosphorous acid ; Polymers ; Prepolymers ; Reaction mechanisms ; Triflic acid</subject><ispartof>Green chemistry : an international journal and green chemistry resource : GC, 2021-09, Vol.23 (18), p.7228-7234</ispartof><rights>Copyright Royal Society of Chemistry 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-893fc13155b37348083415b252b2e52662482ac38ec25c42394021dd26496d1b3</citedby><cites>FETCH-LOGICAL-c427t-893fc13155b37348083415b252b2e52662482ac38ec25c42394021dd26496d1b3</cites><orcidid>0000-0002-8468-7721 ; 0000-0001-8559-6509</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Yang, Cheng</creatorcontrib><creatorcontrib>Sagawa, Takuya</creatorcontrib><creatorcontrib>Fukuoka, Atsushi</creatorcontrib><creatorcontrib>Kobayashi, Hirokazu</creatorcontrib><title>Characteristic activity of phosphorous acid in the dehydration condensation of a chitin-derived nitrogen-containing sugar alcohol</title><title>Green chemistry : an international journal and green chemistry resource : GC</title><description>Chitin is a potential resource for the production of renewable organonitrogen compounds, as it contains biologically fixed nitrogen. Hydrolysis of chitin followed by hydrogenation gives the sugar alcohol named 2-acetamido-2-deoxysorbitol (ADS). The dehydration condensation of ADS produces 2-acetamido-2-deoxyisosorbide (ADI), which is a prospective precursor of nitrogen-containing polymers. However, the conversion of ADS to ADI in previous works needed a large amount of CF
3
SO
3
H as a superstrong acid catalyst, which is high cost and requires special corrosion-resistant equipment. In this work, we have found that H
3
PO
3
, a weak acid, can convert ADS to ADI. Possibly, H
3
PO
3
alters the reaction mechanism from a simple acid-catalysed dehydration cyclisation to a cyclisation
via
phosphite esters. Density functional theory calculations suggest that the modified pathway
via
the phosphite esters significantly reduces the activation energy. In addition, the reducing ability of the acid likely decreases the formation of condensation by-products.
H
3
PO
3
converts a chitin-derived sugar alcohol to a potential monomer for polymer production by a mechanism different from that for strong acid catalysts.</description><subject>Acids</subject><subject>Catalysts</subject><subject>Chitin</subject><subject>Condensates</subject><subject>Corrosion resistance</subject><subject>Dehydration</subject><subject>Density functional theory</subject><subject>Esters</subject><subject>Green chemistry</subject><subject>Nitrogen</subject><subject>Phosphorous acid</subject><subject>Polymers</subject><subject>Prepolymers</subject><subject>Reaction mechanisms</subject><subject>Triflic acid</subject><issn>1463-9262</issn><issn>1463-9270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpFkc9LwzAUx4MoOKcX70LAm1DNr6btcdQ5hYEXPZc0SduMmcwkHezof260Mg-P94PP-z74PgCuMbrHiFYPCvcSEVxRcQJmmHGaVaRAp8eak3NwEcIGIYwLzmbgqx6EFzJqb0I0EqbS7E08QNfB3eBCCu_GkOZGQWNhHDRUejgoL6JxFkpnlbZhatKOgHIw0dhMJcW9VtCa6F2vbZbIKIw1todh7IWHYivd4LaX4KwT26Cv_vIcvD8t3-rnbP26eqkX60wyUsSsrGgnMcV53tKCshKVlOG8JTlpic4J54SVREhaaknytEIrloxQinBWcYVbOge3k-7Ou89Rh9hs3OhtOtmQvGCM4LIsEnU3UdK7ELzump03H8IfGoyaH4ubR7yqfy1eJPhmgn2QR-7_BfQbXoF5Ww</recordid><startdate>20210921</startdate><enddate>20210921</enddate><creator>Yang, Cheng</creator><creator>Sagawa, Takuya</creator><creator>Fukuoka, Atsushi</creator><creator>Kobayashi, Hirokazu</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7ST</scope><scope>7U6</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0002-8468-7721</orcidid><orcidid>https://orcid.org/0000-0001-8559-6509</orcidid></search><sort><creationdate>20210921</creationdate><title>Characteristic activity of phosphorous acid in the dehydration condensation of a chitin-derived nitrogen-containing sugar alcohol</title><author>Yang, Cheng ; Sagawa, Takuya ; Fukuoka, Atsushi ; Kobayashi, Hirokazu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-893fc13155b37348083415b252b2e52662482ac38ec25c42394021dd26496d1b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acids</topic><topic>Catalysts</topic><topic>Chitin</topic><topic>Condensates</topic><topic>Corrosion resistance</topic><topic>Dehydration</topic><topic>Density functional theory</topic><topic>Esters</topic><topic>Green chemistry</topic><topic>Nitrogen</topic><topic>Phosphorous acid</topic><topic>Polymers</topic><topic>Prepolymers</topic><topic>Reaction mechanisms</topic><topic>Triflic acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Cheng</creatorcontrib><creatorcontrib>Sagawa, Takuya</creatorcontrib><creatorcontrib>Fukuoka, Atsushi</creatorcontrib><creatorcontrib>Kobayashi, Hirokazu</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Materials Research Database</collection><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Cheng</au><au>Sagawa, Takuya</au><au>Fukuoka, Atsushi</au><au>Kobayashi, Hirokazu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characteristic activity of phosphorous acid in the dehydration condensation of a chitin-derived nitrogen-containing sugar alcohol</atitle><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle><date>2021-09-21</date><risdate>2021</risdate><volume>23</volume><issue>18</issue><spage>7228</spage><epage>7234</epage><pages>7228-7234</pages><issn>1463-9262</issn><eissn>1463-9270</eissn><abstract>Chitin is a potential resource for the production of renewable organonitrogen compounds, as it contains biologically fixed nitrogen. Hydrolysis of chitin followed by hydrogenation gives the sugar alcohol named 2-acetamido-2-deoxysorbitol (ADS). The dehydration condensation of ADS produces 2-acetamido-2-deoxyisosorbide (ADI), which is a prospective precursor of nitrogen-containing polymers. However, the conversion of ADS to ADI in previous works needed a large amount of CF
3
SO
3
H as a superstrong acid catalyst, which is high cost and requires special corrosion-resistant equipment. In this work, we have found that H
3
PO
3
, a weak acid, can convert ADS to ADI. Possibly, H
3
PO
3
alters the reaction mechanism from a simple acid-catalysed dehydration cyclisation to a cyclisation
via
phosphite esters. Density functional theory calculations suggest that the modified pathway
via
the phosphite esters significantly reduces the activation energy. In addition, the reducing ability of the acid likely decreases the formation of condensation by-products.
H
3
PO
3
converts a chitin-derived sugar alcohol to a potential monomer for polymer production by a mechanism different from that for strong acid catalysts.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d1gc02193a</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-8468-7721</orcidid><orcidid>https://orcid.org/0000-0001-8559-6509</orcidid><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Acids Catalysts Chitin Condensates Corrosion resistance Dehydration Density functional theory Esters Green chemistry Nitrogen Phosphorous acid Polymers Prepolymers Reaction mechanisms Triflic acid |
title | Characteristic activity of phosphorous acid in the dehydration condensation of a chitin-derived nitrogen-containing sugar alcohol |
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