XAS and XPS Characterization of Monolayers Derived from a Dithiol and Structurally Related Disulfide-Containing Polyamides

X-ray absorption spectroscopy and X-ray photoemission spectroscopy have been used to examine sulfur−gold bond formation in monolayers derived from a dithiol monomer and related disulfide-containing polyamides. These compounds were designed to allow the molecules to adsorb to gold through two termina...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Langmuir 2002-10, Vol.18 (21), p.8123-8128
Hauptverfasser: Vance, Andrew L, Willey, Trevor M, Nelson, A. J, van Buuren, T, Bostedt, C, Terminello, Louis J, Fox, Glenn A, Engelhard, Mark, Baer, Don
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 8128
container_issue 21
container_start_page 8123
container_title Langmuir
container_volume 18
creator Vance, Andrew L
Willey, Trevor M
Nelson, A. J
van Buuren, T
Bostedt, C
Terminello, Louis J
Fox, Glenn A
Engelhard, Mark
Baer, Don
description X-ray absorption spectroscopy and X-ray photoemission spectroscopy have been used to examine sulfur−gold bond formation in monolayers derived from a dithiol monomer and related disulfide-containing polyamides. These compounds were designed to allow the molecules to adsorb to gold through two terminal sulfurs, forming surface-attached loops. Element and site-specific density of unoccupied electronic states were probed by X-ray absorption spectroscopy at the C 1s, N 1s, O 1s (K-edge), and S 2p (L2,3-edge) absorption edges. Photoemission measurements of the C 1s, N 1s, O 1s, and S 2p core lines were also used to estimate relative coverage, to confirm layer formation, and to evaluate chemical bonding of the monomer and polyamide to the gold-coated substrates. In the case of the dithiol monomer, the spectroscopic evidence clearly shows that most of the molecules adsorb through a single thiol end. The disulfide-containing precursors, in contrast to the monomer, attach to the surface through both sulfurs to form the anticipated surface-attached loop.
doi_str_mv 10.1021/la025631g
format Article
fullrecord <record><control><sourceid>acs_osti_</sourceid><recordid>TN_cdi_crossref_primary_10_1021_la025631g</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>b769824778</sourcerecordid><originalsourceid>FETCH-LOGICAL-a389t-d2d4ea2503c4842c667bc65a83ca4680ba6ca3202b2962ebfc31b5e771d6d7193</originalsourceid><addsrcrecordid>eNpt0E1P4zAQBmALLRJd4MA_sIT2sIcs_kjs5IhaPlYqotCCuFkTx6EG10a2i7b8erIUceI00swzI82L0BElfyhh9MQBYZXg9HEHjWjFSFHVTP5AIyJLXshS8D30M6UnQkjDy2aE3h5O5xh8hx9mczxeQgSdTbRvkG3wOPT4KvjgYGNiwpNh8Go63MewwoAnNi9tcB_b8xzXOq8jOLfBt8ZBHtzEprXrbWeKcfAZrLf-Ec-C28BqaKYDtNuDS-bws-6ju_OzxfiymF5f_B2fTgvgdZOLjnWlAVYRrsu6ZFoI2WpRQc01lKImLQgNnBHWskYw0_aa07YyUtJOdJI2fB8db--GlK1K2majlzp4b3RWtCJENFwO6vdW6RhSiqZXL9GuIG4UJep_tOor2sEWW2tTNv--IMRnJSSXlVrM5mp6ezG5v1ycq5vB_9p60Ek9hXX0w7_f3H0HicuH8g</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>XAS and XPS Characterization of Monolayers Derived from a Dithiol and Structurally Related Disulfide-Containing Polyamides</title><source>ACS Publications</source><creator>Vance, Andrew L ; Willey, Trevor M ; Nelson, A. J ; van Buuren, T ; Bostedt, C ; Terminello, Louis J ; Fox, Glenn A ; Engelhard, Mark ; Baer, Don</creator><creatorcontrib>Vance, Andrew L ; Willey, Trevor M ; Nelson, A. J ; van Buuren, T ; Bostedt, C ; Terminello, Louis J ; Fox, Glenn A ; Engelhard, Mark ; Baer, Don ; Pacific Northwest National Lab. (PNNL), Richland, WA (United States)</creatorcontrib><description>X-ray absorption spectroscopy and X-ray photoemission spectroscopy have been used to examine sulfur−gold bond formation in monolayers derived from a dithiol monomer and related disulfide-containing polyamides. These compounds were designed to allow the molecules to adsorb to gold through two terminal sulfurs, forming surface-attached loops. Element and site-specific density of unoccupied electronic states were probed by X-ray absorption spectroscopy at the C 1s, N 1s, O 1s (K-edge), and S 2p (L2,3-edge) absorption edges. Photoemission measurements of the C 1s, N 1s, O 1s, and S 2p core lines were also used to estimate relative coverage, to confirm layer formation, and to evaluate chemical bonding of the monomer and polyamide to the gold-coated substrates. In the case of the dithiol monomer, the spectroscopic evidence clearly shows that most of the molecules adsorb through a single thiol end. The disulfide-containing precursors, in contrast to the monomer, attach to the surface through both sulfurs to form the anticipated surface-attached loop.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/la025631g</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Au ; dithiol ; gold ; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY ; monomer ; photoemission ; polydisulfide self-assembled monolayers ; SAM ; sulfur ; XAS ; XPS</subject><ispartof>Langmuir, 2002-10, Vol.18 (21), p.8123-8128</ispartof><rights>Copyright © 2002 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a389t-d2d4ea2503c4842c667bc65a83ca4680ba6ca3202b2962ebfc31b5e771d6d7193</citedby><cites>FETCH-LOGICAL-a389t-d2d4ea2503c4842c667bc65a83ca4680ba6ca3202b2962ebfc31b5e771d6d7193</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/la025631g$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/la025631g$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,881,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/15006937$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Vance, Andrew L</creatorcontrib><creatorcontrib>Willey, Trevor M</creatorcontrib><creatorcontrib>Nelson, A. J</creatorcontrib><creatorcontrib>van Buuren, T</creatorcontrib><creatorcontrib>Bostedt, C</creatorcontrib><creatorcontrib>Terminello, Louis J</creatorcontrib><creatorcontrib>Fox, Glenn A</creatorcontrib><creatorcontrib>Engelhard, Mark</creatorcontrib><creatorcontrib>Baer, Don</creatorcontrib><creatorcontrib>Pacific Northwest National Lab. (PNNL), Richland, WA (United States)</creatorcontrib><title>XAS and XPS Characterization of Monolayers Derived from a Dithiol and Structurally Related Disulfide-Containing Polyamides</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>X-ray absorption spectroscopy and X-ray photoemission spectroscopy have been used to examine sulfur−gold bond formation in monolayers derived from a dithiol monomer and related disulfide-containing polyamides. These compounds were designed to allow the molecules to adsorb to gold through two terminal sulfurs, forming surface-attached loops. Element and site-specific density of unoccupied electronic states were probed by X-ray absorption spectroscopy at the C 1s, N 1s, O 1s (K-edge), and S 2p (L2,3-edge) absorption edges. Photoemission measurements of the C 1s, N 1s, O 1s, and S 2p core lines were also used to estimate relative coverage, to confirm layer formation, and to evaluate chemical bonding of the monomer and polyamide to the gold-coated substrates. In the case of the dithiol monomer, the spectroscopic evidence clearly shows that most of the molecules adsorb through a single thiol end. The disulfide-containing precursors, in contrast to the monomer, attach to the surface through both sulfurs to form the anticipated surface-attached loop.</description><subject>Au</subject><subject>dithiol</subject><subject>gold</subject><subject>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</subject><subject>monomer</subject><subject>photoemission</subject><subject>polydisulfide self-assembled monolayers</subject><subject>SAM</subject><subject>sulfur</subject><subject>XAS</subject><subject>XPS</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNpt0E1P4zAQBmALLRJd4MA_sIT2sIcs_kjs5IhaPlYqotCCuFkTx6EG10a2i7b8erIUceI00swzI82L0BElfyhh9MQBYZXg9HEHjWjFSFHVTP5AIyJLXshS8D30M6UnQkjDy2aE3h5O5xh8hx9mczxeQgSdTbRvkG3wOPT4KvjgYGNiwpNh8Go63MewwoAnNi9tcB_b8xzXOq8jOLfBt8ZBHtzEprXrbWeKcfAZrLf-Ec-C28BqaKYDtNuDS-bws-6ju_OzxfiymF5f_B2fTgvgdZOLjnWlAVYRrsu6ZFoI2WpRQc01lKImLQgNnBHWskYw0_aa07YyUtJOdJI2fB8db--GlK1K2majlzp4b3RWtCJENFwO6vdW6RhSiqZXL9GuIG4UJep_tOor2sEWW2tTNv--IMRnJSSXlVrM5mp6ezG5v1ycq5vB_9p60Ek9hXX0w7_f3H0HicuH8g</recordid><startdate>20021015</startdate><enddate>20021015</enddate><creator>Vance, Andrew L</creator><creator>Willey, Trevor M</creator><creator>Nelson, A. J</creator><creator>van Buuren, T</creator><creator>Bostedt, C</creator><creator>Terminello, Louis J</creator><creator>Fox, Glenn A</creator><creator>Engelhard, Mark</creator><creator>Baer, Don</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>20021015</creationdate><title>XAS and XPS Characterization of Monolayers Derived from a Dithiol and Structurally Related Disulfide-Containing Polyamides</title><author>Vance, Andrew L ; Willey, Trevor M ; Nelson, A. J ; van Buuren, T ; Bostedt, C ; Terminello, Louis J ; Fox, Glenn A ; Engelhard, Mark ; Baer, Don</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a389t-d2d4ea2503c4842c667bc65a83ca4680ba6ca3202b2962ebfc31b5e771d6d7193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Au</topic><topic>dithiol</topic><topic>gold</topic><topic>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</topic><topic>monomer</topic><topic>photoemission</topic><topic>polydisulfide self-assembled monolayers</topic><topic>SAM</topic><topic>sulfur</topic><topic>XAS</topic><topic>XPS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vance, Andrew L</creatorcontrib><creatorcontrib>Willey, Trevor M</creatorcontrib><creatorcontrib>Nelson, A. J</creatorcontrib><creatorcontrib>van Buuren, T</creatorcontrib><creatorcontrib>Bostedt, C</creatorcontrib><creatorcontrib>Terminello, Louis J</creatorcontrib><creatorcontrib>Fox, Glenn A</creatorcontrib><creatorcontrib>Engelhard, Mark</creatorcontrib><creatorcontrib>Baer, Don</creatorcontrib><creatorcontrib>Pacific Northwest National Lab. (PNNL), Richland, WA (United States)</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vance, Andrew L</au><au>Willey, Trevor M</au><au>Nelson, A. J</au><au>van Buuren, T</au><au>Bostedt, C</au><au>Terminello, Louis J</au><au>Fox, Glenn A</au><au>Engelhard, Mark</au><au>Baer, Don</au><aucorp>Pacific Northwest National Lab. (PNNL), Richland, WA (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>XAS and XPS Characterization of Monolayers Derived from a Dithiol and Structurally Related Disulfide-Containing Polyamides</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2002-10-15</date><risdate>2002</risdate><volume>18</volume><issue>21</issue><spage>8123</spage><epage>8128</epage><pages>8123-8128</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><abstract>X-ray absorption spectroscopy and X-ray photoemission spectroscopy have been used to examine sulfur−gold bond formation in monolayers derived from a dithiol monomer and related disulfide-containing polyamides. These compounds were designed to allow the molecules to adsorb to gold through two terminal sulfurs, forming surface-attached loops. Element and site-specific density of unoccupied electronic states were probed by X-ray absorption spectroscopy at the C 1s, N 1s, O 1s (K-edge), and S 2p (L2,3-edge) absorption edges. Photoemission measurements of the C 1s, N 1s, O 1s, and S 2p core lines were also used to estimate relative coverage, to confirm layer formation, and to evaluate chemical bonding of the monomer and polyamide to the gold-coated substrates. In the case of the dithiol monomer, the spectroscopic evidence clearly shows that most of the molecules adsorb through a single thiol end. The disulfide-containing precursors, in contrast to the monomer, attach to the surface through both sulfurs to form the anticipated surface-attached loop.</abstract><cop>United States</cop><pub>American Chemical Society</pub><doi>10.1021/la025631g</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0743-7463
ispartof Langmuir, 2002-10, Vol.18 (21), p.8123-8128
issn 0743-7463
1520-5827
language eng
recordid cdi_crossref_primary_10_1021_la025631g
source ACS Publications
subjects Au
dithiol
gold
INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY
monomer
photoemission
polydisulfide self-assembled monolayers
SAM
sulfur
XAS
XPS
title XAS and XPS Characterization of Monolayers Derived from a Dithiol and Structurally Related Disulfide-Containing Polyamides
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T06%3A40%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=XAS%20and%20XPS%20Characterization%20of%20Monolayers%20Derived%20from%20a%20Dithiol%20and%20Structurally%20Related%20Disulfide-Containing%20Polyamides&rft.jtitle=Langmuir&rft.au=Vance,%20Andrew%20L&rft.aucorp=Pacific%20Northwest%20National%20Lab.%20(PNNL),%20Richland,%20WA%20(United%20States)&rft.date=2002-10-15&rft.volume=18&rft.issue=21&rft.spage=8123&rft.epage=8128&rft.pages=8123-8128&rft.issn=0743-7463&rft.eissn=1520-5827&rft_id=info:doi/10.1021/la025631g&rft_dat=%3Cacs_osti_%3Eb769824778%3C/acs_osti_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true