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n -alkane adsorption to polar silica surfaces
The structures of medium-length n -alkane species ( C 8 - C 11 ) adsorbed to a hydrophilic silica/vapor interface were examined using vibrational sum frequency spectroscopy. Experiments sampling out-of-plane orientation show a clear pattern in vibrational band intensities that implies chains having...
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Published in: | The Journal of chemical physics 2010-03, Vol.132 (11), p.114701-114701-6 |
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container_end_page | 114701-6 |
container_issue | 11 |
container_start_page | 114701 |
container_title | The Journal of chemical physics |
container_volume | 132 |
creator | Brindza, Michael R. Ding, Feng Fourkas, John T. Walker, Robert A. |
description | The structures of medium-length
n
-alkane species
(
C
8
-
C
11
)
adsorbed to a hydrophilic silica/vapor interface were examined using vibrational sum frequency spectroscopy. Experiments sampling out-of-plane orientation show a clear pattern in vibrational band intensities that implies chains having primarily all-
trans
conformations lying flat along the interface. Further analysis shows that the methylene groups of the alkane chains have their local symmetry axes directed into and away from the surface. Spectra acquired under different polarization conditions interlock to reinforce this picture of interfacial structure and organization. Variation in signal intensities with chain length suggests that correlation between adsorbed monomers weakens with increasing chain length. This result stands in contrast with alkane behavior at neat liquid/vapor interfaces where longer length alkanes show considerably more surface induced ordering than short chain alkanes. |
doi_str_mv | 10.1063/1.3336727 |
format | article |
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n
-alkane species
(
C
8
-
C
11
)
adsorbed to a hydrophilic silica/vapor interface were examined using vibrational sum frequency spectroscopy. Experiments sampling out-of-plane orientation show a clear pattern in vibrational band intensities that implies chains having primarily all-
trans
conformations lying flat along the interface. Further analysis shows that the methylene groups of the alkane chains have their local symmetry axes directed into and away from the surface. Spectra acquired under different polarization conditions interlock to reinforce this picture of interfacial structure and organization. Variation in signal intensities with chain length suggests that correlation between adsorbed monomers weakens with increasing chain length. This result stands in contrast with alkane behavior at neat liquid/vapor interfaces where longer length alkanes show considerably more surface induced ordering than short chain alkanes.</description><identifier>ISSN: 0021-9606</identifier><identifier>EISSN: 1089-7690</identifier><identifier>DOI: 10.1063/1.3336727</identifier><identifier>PMID: 20331310</identifier><identifier>CODEN: JCPSA6</identifier><language>eng</language><publisher>United States: American Institute of Physics</publisher><subject>Adsorption ; Alkanes - chemistry ; Molecular Conformation ; Silicon Dioxide - chemistry ; Spectrum Analysis ; Stereoisomerism ; Surface Properties ; Vibration</subject><ispartof>The Journal of chemical physics, 2010-03, Vol.132 (11), p.114701-114701-6</ispartof><rights>2010 American Institute of Physics</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-17a4653f49405f89d5452cfab2d37042c1bd9e15d8bfabd4b88fd28140a412783</citedby><cites>FETCH-LOGICAL-c401t-17a4653f49405f89d5452cfab2d37042c1bd9e15d8bfabd4b88fd28140a412783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,778,780,791,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20331310$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brindza, Michael R.</creatorcontrib><creatorcontrib>Ding, Feng</creatorcontrib><creatorcontrib>Fourkas, John T.</creatorcontrib><creatorcontrib>Walker, Robert A.</creatorcontrib><title>n -alkane adsorption to polar silica surfaces</title><title>The Journal of chemical physics</title><addtitle>J Chem Phys</addtitle><description>The structures of medium-length
n
-alkane species
(
C
8
-
C
11
)
adsorbed to a hydrophilic silica/vapor interface were examined using vibrational sum frequency spectroscopy. Experiments sampling out-of-plane orientation show a clear pattern in vibrational band intensities that implies chains having primarily all-
trans
conformations lying flat along the interface. Further analysis shows that the methylene groups of the alkane chains have their local symmetry axes directed into and away from the surface. Spectra acquired under different polarization conditions interlock to reinforce this picture of interfacial structure and organization. Variation in signal intensities with chain length suggests that correlation between adsorbed monomers weakens with increasing chain length. This result stands in contrast with alkane behavior at neat liquid/vapor interfaces where longer length alkanes show considerably more surface induced ordering than short chain alkanes.</description><subject>Adsorption</subject><subject>Alkanes - chemistry</subject><subject>Molecular Conformation</subject><subject>Silicon Dioxide - chemistry</subject><subject>Spectrum Analysis</subject><subject>Stereoisomerism</subject><subject>Surface Properties</subject><subject>Vibration</subject><issn>0021-9606</issn><issn>1089-7690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLxDAURoMozji68A9Id-Ki471J2iTuZPAFA250HdI8oNppa9Iu_Pd26OjO1YXL4fBxCLlEWCOU7BbXjLFSUHFElghS5aJUcEyWABRzVUK5IGcpfQAACspPyYICY8gQliRvs9w0n6b1mXGpi_1Qd202dFnfNSZmqW5qa7I0xmCsT-fkJJgm-YvDXZH3x4e3zXO-fX162dxvc8sBhxyF4WXBAlcciiCVK3hBbTAVdUwApxYrpzwWTlbT0_FKyuCoRA6GIxWSrcj17O1j9zX6NOhdnaxvmmlnNyYtGKNKFqqcyJuZtLFLKfqg-1jvTPzWCHofR6M-xJnYq4N1rHbe_ZG_NSbgbgaSrQezL_G_Tbd67qbnbuwHY4lwaQ</recordid><startdate>20100321</startdate><enddate>20100321</enddate><creator>Brindza, Michael R.</creator><creator>Ding, Feng</creator><creator>Fourkas, John T.</creator><creator>Walker, Robert A.</creator><general>American Institute of Physics</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20100321</creationdate><title>n -alkane adsorption to polar silica surfaces</title><author>Brindza, Michael R. ; Ding, Feng ; Fourkas, John T. ; Walker, Robert A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-17a4653f49405f89d5452cfab2d37042c1bd9e15d8bfabd4b88fd28140a412783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adsorption</topic><topic>Alkanes - chemistry</topic><topic>Molecular Conformation</topic><topic>Silicon Dioxide - chemistry</topic><topic>Spectrum Analysis</topic><topic>Stereoisomerism</topic><topic>Surface Properties</topic><topic>Vibration</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brindza, Michael R.</creatorcontrib><creatorcontrib>Ding, Feng</creatorcontrib><creatorcontrib>Fourkas, John T.</creatorcontrib><creatorcontrib>Walker, Robert A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of chemical physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brindza, Michael R.</au><au>Ding, Feng</au><au>Fourkas, John T.</au><au>Walker, Robert A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>n -alkane adsorption to polar silica surfaces</atitle><jtitle>The Journal of chemical physics</jtitle><addtitle>J Chem Phys</addtitle><date>2010-03-21</date><risdate>2010</risdate><volume>132</volume><issue>11</issue><spage>114701</spage><epage>114701-6</epage><pages>114701-114701-6</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><coden>JCPSA6</coden><abstract>The structures of medium-length
n
-alkane species
(
C
8
-
C
11
)
adsorbed to a hydrophilic silica/vapor interface were examined using vibrational sum frequency spectroscopy. Experiments sampling out-of-plane orientation show a clear pattern in vibrational band intensities that implies chains having primarily all-
trans
conformations lying flat along the interface. Further analysis shows that the methylene groups of the alkane chains have their local symmetry axes directed into and away from the surface. Spectra acquired under different polarization conditions interlock to reinforce this picture of interfacial structure and organization. Variation in signal intensities with chain length suggests that correlation between adsorbed monomers weakens with increasing chain length. This result stands in contrast with alkane behavior at neat liquid/vapor interfaces where longer length alkanes show considerably more surface induced ordering than short chain alkanes.</abstract><cop>United States</cop><pub>American Institute of Physics</pub><pmid>20331310</pmid><doi>10.1063/1.3336727</doi><tpages>1</tpages></addata></record> |
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language | eng |
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source | American Institute of Physics:Jisc Collections:Transitional Journals Agreement 2021-23 (Reading list); American Institute of Physics(アメリカ物理学協会) |
subjects | Adsorption Alkanes - chemistry Molecular Conformation Silicon Dioxide - chemistry Spectrum Analysis Stereoisomerism Surface Properties Vibration |
title | n -alkane adsorption to polar silica surfaces |
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