Sugar Acetate-based Low Molecular Weight Organogelators
Two novel organogelators that incorporate sugar acetate segments have been identified. One contains a sugar acetate linked directly to an alkyl group, while the second includes an amide linker. We describe the syntheses of both organogelators, as well as their gelation properties in various hydrocar...
Gespeichert in:
Veröffentlicht in: | Chemistry letters 2020-09, Vol.49 (9), p.1026-1029 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1029 |
---|---|
container_issue | 9 |
container_start_page | 1026 |
container_title | Chemistry letters |
container_volume | 49 |
creator | Gentry, Brian M. Perry, Robert Laurie, Tyler Beckman, Eric J. Enick, Robert M. Keith, John A. |
description | Two novel organogelators that incorporate sugar acetate segments have been identified. One contains a sugar acetate linked directly to an alkyl group, while the second includes an amide linker. We describe the syntheses of both organogelators, as well as their gelation properties in various hydrocarbon liquids. We also use molecular modeling with a generic classical force field and Kohn-Sham density functional theory to provide atomic scale insights and physical justification for gelation mechanisms. |
doi_str_mv | 10.1246/cl.200333 |
format | Article |
fullrecord | <record><control><sourceid>proquest_osti_</sourceid><recordid>TN_cdi_osti_scitechconnect_1798989</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2447950500</sourcerecordid><originalsourceid>FETCH-LOGICAL-c401t-a99be6e8b806b04bed820b420a2f4929ac1f2f21b2e73b52e601ec260cd2b5043</originalsourceid><addsrcrecordid>eNplkE1Lw0AQhhdRsFYP_oOgJw-psx_ZJMdS_IJKDyoel93tJE1Js3V3g_TfG0nBg8xhDvO8L8NDyDWFGWVC3tt2xgA45ydkQrkoUshpdkomwKVMc2DsnFyEsAWAouRsQvK3vtY-mVuMOmJqdMB1snTfyatr0fbtcPvEpt7EZOVr3bkaWx2dD5fkrNJtwKvjnpKPx4f3xXO6XD29LObL1AqgMdVlaVBiYQqQBoTBdcHACAaaVaJkpba0YhWjhmHOTcZQAkXLJNg1MxkIPiU3Y68LsVHBNhHtxrquQxsVzctimAG6HaG9d189hqi2rvfd8JdiQuRlBtngZEruRsp6F4LHSu19s9P-oCioX3nKtmqUN7DyyG5w19ihydkG42Gr97r7a_8f_AFYA3JO</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2447950500</pqid></control><display><type>article</type><title>Sugar Acetate-based Low Molecular Weight Organogelators</title><source>Oxford University Press Journals All Titles (1996-Current)</source><creator>Gentry, Brian M. ; Perry, Robert ; Laurie, Tyler ; Beckman, Eric J. ; Enick, Robert M. ; Keith, John A.</creator><creatorcontrib>Gentry, Brian M. ; Perry, Robert ; Laurie, Tyler ; Beckman, Eric J. ; Enick, Robert M. ; Keith, John A. ; Univ. of Pittsburgh, PA (United States)</creatorcontrib><description>Two novel organogelators that incorporate sugar acetate segments have been identified. One contains a sugar acetate linked directly to an alkyl group, while the second includes an amide linker. We describe the syntheses of both organogelators, as well as their gelation properties in various hydrocarbon liquids. We also use molecular modeling with a generic classical force field and Kohn-Sham density functional theory to provide atomic scale insights and physical justification for gelation mechanisms.</description><identifier>ISSN: 0366-7022</identifier><identifier>EISSN: 1348-0715</identifier><identifier>DOI: 10.1246/cl.200333</identifier><language>eng</language><publisher>Tokyo: The Chemical Society of Japan</publisher><subject>Chemistry ; Density functional theory ; Gelation ; Low molecular weights</subject><ispartof>Chemistry letters, 2020-09, Vol.49 (9), p.1026-1029</ispartof><rights>The Chemical Society of Japan</rights><rights>Copyright Chemical Society of Japan 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c401t-a99be6e8b806b04bed820b420a2f4929ac1f2f21b2e73b52e601ec260cd2b5043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/1798989$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Gentry, Brian M.</creatorcontrib><creatorcontrib>Perry, Robert</creatorcontrib><creatorcontrib>Laurie, Tyler</creatorcontrib><creatorcontrib>Beckman, Eric J.</creatorcontrib><creatorcontrib>Enick, Robert M.</creatorcontrib><creatorcontrib>Keith, John A.</creatorcontrib><creatorcontrib>Univ. of Pittsburgh, PA (United States)</creatorcontrib><title>Sugar Acetate-based Low Molecular Weight Organogelators</title><title>Chemistry letters</title><description>Two novel organogelators that incorporate sugar acetate segments have been identified. One contains a sugar acetate linked directly to an alkyl group, while the second includes an amide linker. We describe the syntheses of both organogelators, as well as their gelation properties in various hydrocarbon liquids. We also use molecular modeling with a generic classical force field and Kohn-Sham density functional theory to provide atomic scale insights and physical justification for gelation mechanisms.</description><subject>Chemistry</subject><subject>Density functional theory</subject><subject>Gelation</subject><subject>Low molecular weights</subject><issn>0366-7022</issn><issn>1348-0715</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNplkE1Lw0AQhhdRsFYP_oOgJw-psx_ZJMdS_IJKDyoel93tJE1Js3V3g_TfG0nBg8xhDvO8L8NDyDWFGWVC3tt2xgA45ydkQrkoUshpdkomwKVMc2DsnFyEsAWAouRsQvK3vtY-mVuMOmJqdMB1snTfyatr0fbtcPvEpt7EZOVr3bkaWx2dD5fkrNJtwKvjnpKPx4f3xXO6XD29LObL1AqgMdVlaVBiYQqQBoTBdcHACAaaVaJkpba0YhWjhmHOTcZQAkXLJNg1MxkIPiU3Y68LsVHBNhHtxrquQxsVzctimAG6HaG9d189hqi2rvfd8JdiQuRlBtngZEruRsp6F4LHSu19s9P-oCioX3nKtmqUN7DyyG5w19ihydkG42Gr97r7a_8f_AFYA3JO</recordid><startdate>20200905</startdate><enddate>20200905</enddate><creator>Gentry, Brian M.</creator><creator>Perry, Robert</creator><creator>Laurie, Tyler</creator><creator>Beckman, Eric J.</creator><creator>Enick, Robert M.</creator><creator>Keith, John A.</creator><general>The Chemical Society of Japan</general><general>Chemical Society of Japan</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>OTOTI</scope></search><sort><creationdate>20200905</creationdate><title>Sugar Acetate-based Low Molecular Weight Organogelators</title><author>Gentry, Brian M. ; Perry, Robert ; Laurie, Tyler ; Beckman, Eric J. ; Enick, Robert M. ; Keith, John A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-a99be6e8b806b04bed820b420a2f4929ac1f2f21b2e73b52e601ec260cd2b5043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Chemistry</topic><topic>Density functional theory</topic><topic>Gelation</topic><topic>Low molecular weights</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gentry, Brian M.</creatorcontrib><creatorcontrib>Perry, Robert</creatorcontrib><creatorcontrib>Laurie, Tyler</creatorcontrib><creatorcontrib>Beckman, Eric J.</creatorcontrib><creatorcontrib>Enick, Robert M.</creatorcontrib><creatorcontrib>Keith, John A.</creatorcontrib><creatorcontrib>Univ. of Pittsburgh, PA (United States)</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>OSTI.GOV</collection><jtitle>Chemistry letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gentry, Brian M.</au><au>Perry, Robert</au><au>Laurie, Tyler</au><au>Beckman, Eric J.</au><au>Enick, Robert M.</au><au>Keith, John A.</au><aucorp>Univ. of Pittsburgh, PA (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sugar Acetate-based Low Molecular Weight Organogelators</atitle><jtitle>Chemistry letters</jtitle><date>2020-09-05</date><risdate>2020</risdate><volume>49</volume><issue>9</issue><spage>1026</spage><epage>1029</epage><pages>1026-1029</pages><issn>0366-7022</issn><eissn>1348-0715</eissn><abstract>Two novel organogelators that incorporate sugar acetate segments have been identified. One contains a sugar acetate linked directly to an alkyl group, while the second includes an amide linker. We describe the syntheses of both organogelators, as well as their gelation properties in various hydrocarbon liquids. We also use molecular modeling with a generic classical force field and Kohn-Sham density functional theory to provide atomic scale insights and physical justification for gelation mechanisms.</abstract><cop>Tokyo</cop><pub>The Chemical Society of Japan</pub><doi>10.1246/cl.200333</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0366-7022 |
ispartof | Chemistry letters, 2020-09, Vol.49 (9), p.1026-1029 |
issn | 0366-7022 1348-0715 |
language | eng |
recordid | cdi_osti_scitechconnect_1798989 |
source | Oxford University Press Journals All Titles (1996-Current) |
subjects | Chemistry Density functional theory Gelation Low molecular weights |
title | Sugar Acetate-based Low Molecular Weight Organogelators |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T08%3A23%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Sugar%20Acetate-based%20Low%20Molecular%20Weight%20Organogelators&rft.jtitle=Chemistry%20letters&rft.au=Gentry,%20Brian%20M.&rft.aucorp=Univ.%20of%20Pittsburgh,%20PA%20(United%20States)&rft.date=2020-09-05&rft.volume=49&rft.issue=9&rft.spage=1026&rft.epage=1029&rft.pages=1026-1029&rft.issn=0366-7022&rft.eissn=1348-0715&rft_id=info:doi/10.1246/cl.200333&rft_dat=%3Cproquest_osti_%3E2447950500%3C/proquest_osti_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2447950500&rft_id=info:pmid/&rfr_iscdi=true |