Calcium Ion−Calixquinone Complexes Adsorbed on a Silver Electrode
The structures and redox-switching behavior of Ca2+/calix[4]quinone complexes on a Ag surface were investigated by reflection−absorption infrared spectroscopy (RAIRS), Monte Carlo simulation, and voltammetry. RAIRS and Monte Carlo simulation show that the carboxylate groups of calix[4]arene-triacid-...
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Veröffentlicht in: | Journal of physical chemistry. C 2009-11, Vol.113 (46), p.19981-19985 |
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creator | Kang, Sun Kil Lee, One-Sun Chang, Suk-Kyu Chung, Doo Soo Kim, Hasuck Chung, Taek Dong |
description | The structures and redox-switching behavior of Ca2+/calix[4]quinone complexes on a Ag surface were investigated by reflection−absorption infrared spectroscopy (RAIRS), Monte Carlo simulation, and voltammetry. RAIRS and Monte Carlo simulation show that the carboxylate groups of calix[4]arene-triacid-monoquinone (CTAQ) and calix[4]arene-diacid-diquinone (CDAQ) are involved in not only binding with the Ca2+ ions but also spontaneous adsorption of their complexes onto the Ag surface. According to the RAIRS results, the Ca2+ ions in the complexes lie in vicinity to the quinone moieties. Monte Carlo simulation provides more detailed information about the probable conformations of the Ca2+/calix[4]quinone complexes adsorbed on the Ag surface. Voltammetric behavior is consistent with the RAIRS and Monte Carlo simulation results and shows the effect of Ca2+ ions to the redox processes of the CTAQ- or CDAQ-modified Ag electrodes. |
doi_str_mv | 10.1021/jp9067262 |
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RAIRS and Monte Carlo simulation show that the carboxylate groups of calix[4]arene-triacid-monoquinone (CTAQ) and calix[4]arene-diacid-diquinone (CDAQ) are involved in not only binding with the Ca2+ ions but also spontaneous adsorption of their complexes onto the Ag surface. According to the RAIRS results, the Ca2+ ions in the complexes lie in vicinity to the quinone moieties. Monte Carlo simulation provides more detailed information about the probable conformations of the Ca2+/calix[4]quinone complexes adsorbed on the Ag surface. Voltammetric behavior is consistent with the RAIRS and Monte Carlo simulation results and shows the effect of Ca2+ ions to the redox processes of the CTAQ- or CDAQ-modified Ag electrodes.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/jp9067262</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>C: Surfaces, Interfaces, Catalysis</subject><ispartof>Journal of physical chemistry. 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C</title><addtitle>J. Phys. Chem. C</addtitle><description>The structures and redox-switching behavior of Ca2+/calix[4]quinone complexes on a Ag surface were investigated by reflection−absorption infrared spectroscopy (RAIRS), Monte Carlo simulation, and voltammetry. RAIRS and Monte Carlo simulation show that the carboxylate groups of calix[4]arene-triacid-monoquinone (CTAQ) and calix[4]arene-diacid-diquinone (CDAQ) are involved in not only binding with the Ca2+ ions but also spontaneous adsorption of their complexes onto the Ag surface. According to the RAIRS results, the Ca2+ ions in the complexes lie in vicinity to the quinone moieties. Monte Carlo simulation provides more detailed information about the probable conformations of the Ca2+/calix[4]quinone complexes adsorbed on the Ag surface. Voltammetric behavior is consistent with the RAIRS and Monte Carlo simulation results and shows the effect of Ca2+ ions to the redox processes of the CTAQ- or CDAQ-modified Ag electrodes.</description><subject>C: Surfaces, Interfaces, Catalysis</subject><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNptj7FOwzAYhC0EEqUw8AZeGBgCv-3YjscqKqVSJQZgjtzkt5QoiYPdoPIGzDwiT0JQUSemu5M-ne4IuWZwx4Cz-2YwoDRX_ITMmBE80amUp0ef6nNyEWMDIAUwMSN5btuyHju69v3359eU6v3bWPe-R5r7bmhxj5EuqujDFivqe2rpc92-Y6DLFstd8BVekjNn24hXfzonrw_Ll_wx2Tyt1vlik1guzS6xmVHMgVTOAjpA6QwIrmQqmdIZt0JVqCpWaQWGgZ5I41TGJJZa62yrxZzcHnrL4GMM6Ioh1J0NHwWD4vd9cXw_sTcH1paxaPwY-mnZP9wPvdNX_g</recordid><startdate>20091119</startdate><enddate>20091119</enddate><creator>Kang, Sun Kil</creator><creator>Lee, One-Sun</creator><creator>Chang, Suk-Kyu</creator><creator>Chung, Doo Soo</creator><creator>Kim, Hasuck</creator><creator>Chung, Taek Dong</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20091119</creationdate><title>Calcium Ion−Calixquinone Complexes Adsorbed on a Silver Electrode</title><author>Kang, Sun Kil ; Lee, One-Sun ; Chang, Suk-Kyu ; Chung, Doo Soo ; Kim, Hasuck ; Chung, Taek Dong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a259t-a8961f056fa0ef0e5f9032654516782a36de6d1d7609107f059f6815ec7778b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>C: Surfaces, Interfaces, Catalysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kang, Sun Kil</creatorcontrib><creatorcontrib>Lee, One-Sun</creatorcontrib><creatorcontrib>Chang, Suk-Kyu</creatorcontrib><creatorcontrib>Chung, Doo Soo</creatorcontrib><creatorcontrib>Kim, Hasuck</creatorcontrib><creatorcontrib>Chung, Taek Dong</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kang, Sun Kil</au><au>Lee, One-Sun</au><au>Chang, Suk-Kyu</au><au>Chung, Doo Soo</au><au>Kim, Hasuck</au><au>Chung, Taek Dong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Calcium Ion−Calixquinone Complexes Adsorbed on a Silver Electrode</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2009-11-19</date><risdate>2009</risdate><volume>113</volume><issue>46</issue><spage>19981</spage><epage>19985</epage><pages>19981-19985</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>The structures and redox-switching behavior of Ca2+/calix[4]quinone complexes on a Ag surface were investigated by reflection−absorption infrared spectroscopy (RAIRS), Monte Carlo simulation, and voltammetry. RAIRS and Monte Carlo simulation show that the carboxylate groups of calix[4]arene-triacid-monoquinone (CTAQ) and calix[4]arene-diacid-diquinone (CDAQ) are involved in not only binding with the Ca2+ ions but also spontaneous adsorption of their complexes onto the Ag surface. According to the RAIRS results, the Ca2+ ions in the complexes lie in vicinity to the quinone moieties. Monte Carlo simulation provides more detailed information about the probable conformations of the Ca2+/calix[4]quinone complexes adsorbed on the Ag surface. Voltammetric behavior is consistent with the RAIRS and Monte Carlo simulation results and shows the effect of Ca2+ ions to the redox processes of the CTAQ- or CDAQ-modified Ag electrodes.</abstract><pub>American Chemical Society</pub><doi>10.1021/jp9067262</doi><tpages>5</tpages></addata></record> |
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subjects | C: Surfaces, Interfaces, Catalysis |
title | Calcium Ion−Calixquinone Complexes Adsorbed on a Silver Electrode |
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