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Kinetics of Formation of Long-Chain n-Alkanethiolate Monolayers on Polycrystalline Gold
The effect of immersion time on the ordering properties of self-assembled docosanethiolate (C22) monolayers has been studied by reflection/absorption infrared spectroscopy (RAIRS). Starting with a chemically cleaned polycrystalline gold surface, we have found that an immersion time of 45 s in microm...
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Published in: | Langmuir 1997-10, Vol.13 (20), p.5335-5340 |
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creator | Bensebaa, Farid Voicu, Raluca Huron, Laurent Ellis, Thomas H Kruus, Erik |
description | The effect of immersion time on the ordering properties of self-assembled docosanethiolate (C22) monolayers has been studied by reflection/absorption infrared spectroscopy (RAIRS). Starting with a chemically cleaned polycrystalline gold surface, we have found that an immersion time of 45 s in micromolar thiol solutions is sufficient to produce ordered “monolayer” films. These films have RAIR spectral features (peak position, line width, and integrated intensity) similar to those obtained with much longer immersion times. Decreasing the immersion time below 45 s gradually increases the disorder. The temperature dependence of the CH2 antisymmetric stretching (d-) peak position of thiol films obtained with an immersion time of 120 s is identical to ones obtained with very long immersion time (0.5 h to several days). In contrast, films obtained with a 5 s immersion time disorder at a lower temperature. Apart from immersion time and temperature, a large solvent effect has been observed based on real-time RAIRS measurements of the continuing film ordering during aging in vacuum. Finally, a new assignment of the shoulder appearing around 2931 cm-1 is proposed. We present arguments suggesting that the generally accepted Fermi resonance assignment of this shoulder should be modified to include a contribution from another vibrational mode. |
doi_str_mv | 10.1021/la970052a |
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We present arguments suggesting that the generally accepted Fermi resonance assignment of this shoulder should be modified to include a contribution from another vibrational mode.</description><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Solid-liquid interface</subject><subject>Surface physical chemistry</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNptkDFPwzAQhS0EEqUw8A8ywMAQOMd2Eo9VoS20iAoKSCzWNU1oWmNXdpDIv8dVUSemu9N9753eEXJO4ZpCQm80ygxAJHhAOlQkEIs8yQ5JBzLO4oyn7JiceL8CAMm47JD3cW3Kpi58ZKtoYN0XNrU122FizWfcX2JtIhP39BoDt6ytxqaMHq0JTVu6IDPR1Oq2cK1vUOvgFg2tXpySowq1L8_-ape8Du5m_VE8eRre93uTGJmEJhYA-ULKlFIKgi6AMVFhxgWXIQcPLUtKmvNKFiKncs6gyOZAMUTN03whkHXJ1c63cNZ7V1Zq4-ovdK2ioLYfUfuPBPZix27QF6grh6ao_V6Q5DwXnAUs3mG1b8qf_RrdWqUZy4SaTV_Ux9sz3I7TBzUK_OWOx8Krlf12JgT-5_wvmEp6PQ</recordid><startdate>19971001</startdate><enddate>19971001</enddate><creator>Bensebaa, Farid</creator><creator>Voicu, Raluca</creator><creator>Huron, Laurent</creator><creator>Ellis, Thomas H</creator><creator>Kruus, Erik</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19971001</creationdate><title>Kinetics of Formation of Long-Chain n-Alkanethiolate Monolayers on Polycrystalline Gold</title><author>Bensebaa, Farid ; Voicu, Raluca ; Huron, Laurent ; Ellis, Thomas H ; Kruus, Erik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a390t-5008d996111051d0335fa74549a974fa732e184f9c5819b30c7b01a102868d5a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Solid-liquid interface</topic><topic>Surface physical chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bensebaa, Farid</creatorcontrib><creatorcontrib>Voicu, Raluca</creatorcontrib><creatorcontrib>Huron, Laurent</creatorcontrib><creatorcontrib>Ellis, Thomas H</creatorcontrib><creatorcontrib>Kruus, Erik</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bensebaa, Farid</au><au>Voicu, Raluca</au><au>Huron, Laurent</au><au>Ellis, Thomas H</au><au>Kruus, Erik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kinetics of Formation of Long-Chain n-Alkanethiolate Monolayers on Polycrystalline Gold</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>1997-10-01</date><risdate>1997</risdate><volume>13</volume><issue>20</issue><spage>5335</spage><epage>5340</epage><pages>5335-5340</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>The effect of immersion time on the ordering properties of self-assembled docosanethiolate (C22) monolayers has been studied by reflection/absorption infrared spectroscopy (RAIRS). Starting with a chemically cleaned polycrystalline gold surface, we have found that an immersion time of 45 s in micromolar thiol solutions is sufficient to produce ordered “monolayer” films. These films have RAIR spectral features (peak position, line width, and integrated intensity) similar to those obtained with much longer immersion times. Decreasing the immersion time below 45 s gradually increases the disorder. The temperature dependence of the CH2 antisymmetric stretching (d-) peak position of thiol films obtained with an immersion time of 120 s is identical to ones obtained with very long immersion time (0.5 h to several days). In contrast, films obtained with a 5 s immersion time disorder at a lower temperature. Apart from immersion time and temperature, a large solvent effect has been observed based on real-time RAIRS measurements of the continuing film ordering during aging in vacuum. Finally, a new assignment of the shoulder appearing around 2931 cm-1 is proposed. We present arguments suggesting that the generally accepted Fermi resonance assignment of this shoulder should be modified to include a contribution from another vibrational mode.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/la970052a</doi><tpages>6</tpages></addata></record> |
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subjects | Chemistry Exact sciences and technology General and physical chemistry Solid-liquid interface Surface physical chemistry |
title | Kinetics of Formation of Long-Chain n-Alkanethiolate Monolayers on Polycrystalline Gold |
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