Organogels Resulting from Competing Self-Assembly Units in the Gelator: Structure, Dynamics, and Photophysical Behavior of Gels Formed from Cholesterol−Stilbene and Cholesterol−Squaraine Gelators
Organogels formed from novel organic gelators containing a cholesterol tethered to squaraine dyes or trans-stilbene derivatives have been studied from several different perspectives. The two types of molecules are active toward several organic liquids, gelling in some cases at w/w percentages as low...
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Veröffentlicht in: | Langmuir 1999-03, Vol.15 (7), p.2241-2245 |
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description | Organogels formed from novel organic gelators containing a cholesterol tethered to squaraine dyes or trans-stilbene derivatives have been studied from several different perspectives. The two types of molecules are active toward several organic liquids, gelling in some cases at w/w percentages as low as 0.1. While relatively robust, macroscopically “dry” gels are formed in several cases, studies with a variety of probes indicate that much of the solvent may exist in domains that are essentially liquid-like in terms of their microenvironment. The gels have been imaged by atomic force microscopy and conventional and fluorescence microscopy, monitoring both the gelator fluorescence in the case of the stilbene−cholesterol gels and, the fluorescence of solutes dissolved in the solvent. Remarkably, our findings show that several of the gels are composed of similarly appearing fibrous structures visible at the nano-, micro-, and macroscale. |
doi_str_mv | 10.1021/la981386i |
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The two types of molecules are active toward several organic liquids, gelling in some cases at w/w percentages as low as 0.1. While relatively robust, macroscopically “dry” gels are formed in several cases, studies with a variety of probes indicate that much of the solvent may exist in domains that are essentially liquid-like in terms of their microenvironment. The gels have been imaged by atomic force microscopy and conventional and fluorescence microscopy, monitoring both the gelator fluorescence in the case of the stilbene−cholesterol gels and, the fluorescence of solutes dissolved in the solvent. Remarkably, our findings show that several of the gels are composed of similarly appearing fibrous structures visible at the nano-, micro-, and macroscale.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/la981386i</identifier><identifier>CODEN: LANGD5</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>40 CHEMISTRY ; Atomic force microscopy ; Chemistry ; CHOLESTEROL ; Colloidal gels. Colloidal sols ; Colloidal state and disperse state ; Dyes ; Exact sciences and technology ; FIBERS ; FLUORESCENCE ; GELATION ; GELS ; General and physical chemistry ; Molecular dynamics ; Molecular structure ; MORPHOLOGY ; Solvents ; STILBENE</subject><ispartof>Langmuir, 1999-03, Vol.15 (7), p.2241-2245</ispartof><rights>Copyright © 1999 American Chemical Society</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a447t-75f342a3ea214134e22f14424ab155f9eb8b77ae3e41fbbad38512b3e15fb1d23</citedby><cites>FETCH-LOGICAL-a447t-75f342a3ea214134e22f14424ab155f9eb8b77ae3e41fbbad38512b3e15fb1d23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/la981386i$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/la981386i$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,885,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1758801$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/350235$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Geiger, Cristina</creatorcontrib><creatorcontrib>Stanescu, Marina</creatorcontrib><creatorcontrib>Chen, Liaohai</creatorcontrib><creatorcontrib>Whitten, David G</creatorcontrib><title>Organogels Resulting from Competing Self-Assembly Units in the Gelator: Structure, Dynamics, and Photophysical Behavior of Gels Formed from Cholesterol−Stilbene and Cholesterol−Squaraine Gelators</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>Organogels formed from novel organic gelators containing a cholesterol tethered to squaraine dyes or trans-stilbene derivatives have been studied from several different perspectives. The two types of molecules are active toward several organic liquids, gelling in some cases at w/w percentages as low as 0.1. While relatively robust, macroscopically “dry” gels are formed in several cases, studies with a variety of probes indicate that much of the solvent may exist in domains that are essentially liquid-like in terms of their microenvironment. The gels have been imaged by atomic force microscopy and conventional and fluorescence microscopy, monitoring both the gelator fluorescence in the case of the stilbene−cholesterol gels and, the fluorescence of solutes dissolved in the solvent. Remarkably, our findings show that several of the gels are composed of similarly appearing fibrous structures visible at the nano-, micro-, and macroscale.</description><subject>40 CHEMISTRY</subject><subject>Atomic force microscopy</subject><subject>Chemistry</subject><subject>CHOLESTEROL</subject><subject>Colloidal gels. Colloidal sols</subject><subject>Colloidal state and disperse state</subject><subject>Dyes</subject><subject>Exact sciences and technology</subject><subject>FIBERS</subject><subject>FLUORESCENCE</subject><subject>GELATION</subject><subject>GELS</subject><subject>General and physical chemistry</subject><subject>Molecular dynamics</subject><subject>Molecular structure</subject><subject>MORPHOLOGY</subject><subject>Solvents</subject><subject>STILBENE</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNptkc9qFEEQxgdRcI0efIMWVBAyOv1vZja3uGuiEkjIJghemp7e6p2OPd2b7h5xbx716mP5GHkSJ5llBfFUFPWrrz6-yrKnuHiNC4LfWDmtMa1Lcy-bYE6KnNekup9NiorRvGIlfZg9ivGqKIopZdNJ9vs0rKTzK7ARnUPsbTJuhXTwHZr5bg137QKszg9jhK6xG3TpTIrIOJRaQMdgZfLh4Ob7T7RIoVepD7CP5hsnO6PiPpJuic5an_y63USjpEVvoZVfjQ_I69v1iI586GC5Pdp6CzFB8Pbmx69FMrYBB3cq_4yuexmkcTsL8XH2QEsb4cm27mWXR-8uZu_zk9PjD7PDk1wyVqW84poyIilIghmmDAjRmDHCZIM511No6qaqJFBgWDeNXNKaY9JQwFw3eEnoXvZs1PUxGRGVSaBa5Z0DlQTlBaF8YF6OzDr4635wLToTFVgrHfg-CoJpiUtcDOCrEVTBxxhAi3UwnQwbgQtx-1Gx--jAPt-KyjgEqYN0ysS_CxWv6wIPWD5iZgjr224swxdRVrTi4uJsIeaf59X5p4-lqAf-xchLFcWV74Mb0vvP-T-xZ8KE</recordid><startdate>19990330</startdate><enddate>19990330</enddate><creator>Geiger, Cristina</creator><creator>Stanescu, Marina</creator><creator>Chen, Liaohai</creator><creator>Whitten, David G</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>19990330</creationdate><title>Organogels Resulting from Competing Self-Assembly Units in the Gelator: Structure, Dynamics, and Photophysical Behavior of Gels Formed from Cholesterol−Stilbene and Cholesterol−Squaraine Gelators</title><author>Geiger, Cristina ; Stanescu, Marina ; Chen, Liaohai ; Whitten, David G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a447t-75f342a3ea214134e22f14424ab155f9eb8b77ae3e41fbbad38512b3e15fb1d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>40 CHEMISTRY</topic><topic>Atomic force microscopy</topic><topic>Chemistry</topic><topic>CHOLESTEROL</topic><topic>Colloidal gels. Colloidal sols</topic><topic>Colloidal state and disperse state</topic><topic>Dyes</topic><topic>Exact sciences and technology</topic><topic>FIBERS</topic><topic>FLUORESCENCE</topic><topic>GELATION</topic><topic>GELS</topic><topic>General and physical chemistry</topic><topic>Molecular dynamics</topic><topic>Molecular structure</topic><topic>MORPHOLOGY</topic><topic>Solvents</topic><topic>STILBENE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Geiger, Cristina</creatorcontrib><creatorcontrib>Stanescu, Marina</creatorcontrib><creatorcontrib>Chen, Liaohai</creatorcontrib><creatorcontrib>Whitten, David G</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Geiger, Cristina</au><au>Stanescu, Marina</au><au>Chen, Liaohai</au><au>Whitten, David G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Organogels Resulting from Competing Self-Assembly Units in the Gelator: Structure, Dynamics, and Photophysical Behavior of Gels Formed from Cholesterol−Stilbene and Cholesterol−Squaraine Gelators</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>1999-03-30</date><risdate>1999</risdate><volume>15</volume><issue>7</issue><spage>2241</spage><epage>2245</epage><pages>2241-2245</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>Organogels formed from novel organic gelators containing a cholesterol tethered to squaraine dyes or trans-stilbene derivatives have been studied from several different perspectives. The two types of molecules are active toward several organic liquids, gelling in some cases at w/w percentages as low as 0.1. While relatively robust, macroscopically “dry” gels are formed in several cases, studies with a variety of probes indicate that much of the solvent may exist in domains that are essentially liquid-like in terms of their microenvironment. The gels have been imaged by atomic force microscopy and conventional and fluorescence microscopy, monitoring both the gelator fluorescence in the case of the stilbene−cholesterol gels and, the fluorescence of solutes dissolved in the solvent. Remarkably, our findings show that several of the gels are composed of similarly appearing fibrous structures visible at the nano-, micro-, and macroscale.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/la981386i</doi><tpages>5</tpages></addata></record> |
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subjects | 40 CHEMISTRY Atomic force microscopy Chemistry CHOLESTEROL Colloidal gels. Colloidal sols Colloidal state and disperse state Dyes Exact sciences and technology FIBERS FLUORESCENCE GELATION GELS General and physical chemistry Molecular dynamics Molecular structure MORPHOLOGY Solvents STILBENE |
title | Organogels Resulting from Competing Self-Assembly Units in the Gelator: Structure, Dynamics, and Photophysical Behavior of Gels Formed from Cholesterol−Stilbene and Cholesterol−Squaraine Gelators |
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