Dendritic functionalization of monolayer-protected gold nanoparticles
This paper describes the facile synthesis of nanoparticle-cored dendrimers (NCDs) and nanoparticle megamers from monolayer-protected gold clusters using either single or multi-step reactions. First, 11-mercaptoundecanoic acid/hexanethiolate-protected gold clusters were synthesized using the Schiffri...
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Veröffentlicht in: | Materials research bulletin 2007-06, Vol.42 (6), p.1178-1185 |
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creator | Cutler, Erin C. Lundin, Erik Garabato, B. Davis Choi, Daeock Shon, Young-Seok |
description | This paper describes the facile synthesis of nanoparticle-cored dendrimers (NCDs) and nanoparticle megamers from monolayer-protected gold clusters using either single or multi-step reactions. First, 11-mercaptoundecanoic acid/hexanethiolate-protected gold clusters were synthesized using the Schiffrin reaction followed by the ligand place-exchange reaction. A convergent approach for the synthesis of nanoparticle-cored dendrimers uses a single step reaction that is an ester coupling reaction of hydroxy-functionalized dendrons with carboxylic acid-functionalized gold clusters. A divergent approach, which is based on multi-step reactions, employs the repetition of an amide coupling reaction and a Michael addition reaction to build polyamidoamine dendritic architectures around a nanoparticle core. Nanoparticle megamers, which are large dendrimer-induced nanoparticle aggregates with an average diameter of more than 300
nm, were prepared by the amide coupling reaction between polyamiodoamine [G-2] dendrimers and carboxylic acid-functionalized gold clusters.
1H NMR spectroscopy, FT-IR spectroscopy, thermogravimetric analysis (TGA), and transmission electron microscopy (TEM) were used for the characterization of these hybrid nanoparticles. |
doi_str_mv | 10.1016/j.materresbull.2006.08.033 |
format | Article |
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nm, were prepared by the amide coupling reaction between polyamiodoamine [G-2] dendrimers and carboxylic acid-functionalized gold clusters.
1H NMR spectroscopy, FT-IR spectroscopy, thermogravimetric analysis (TGA), and transmission electron microscopy (TEM) were used for the characterization of these hybrid nanoparticles.</description><identifier>ISSN: 0025-5408</identifier><identifier>EISSN: 1873-4227</identifier><identifier>DOI: 10.1016/j.materresbull.2006.08.033</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>A. Metals ; A. Nanostructures ; B. Chemical synthesis ; CARBOXYLIC ACIDS ; CHEMICAL PREPARATION ; COUPLING ; DENDRITES ; ESTERS ; FOURIER TRANSFORMATION ; GOLD ; INFRARED SPECTRA ; LIGANDS ; MATERIALS SCIENCE ; NANOSTRUCTURES ; NUCLEAR MAGNETIC RESONANCE ; SPECTROSCOPY ; THERMAL GRAVIMETRIC ANALYSIS ; TRANSMISSION ELECTRON MICROSCOPY</subject><ispartof>Materials research bulletin, 2007-06, Vol.42 (6), p.1178-1185</ispartof><rights>2006 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-29bd8093812aa215f97ed3796d862ffc1fd6cd65624caec11fd580063f62cb8a3</citedby><cites>FETCH-LOGICAL-c352t-29bd8093812aa215f97ed3796d862ffc1fd6cd65624caec11fd580063f62cb8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.materresbull.2006.08.033$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/21000659$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Cutler, Erin C.</creatorcontrib><creatorcontrib>Lundin, Erik</creatorcontrib><creatorcontrib>Garabato, B. Davis</creatorcontrib><creatorcontrib>Choi, Daeock</creatorcontrib><creatorcontrib>Shon, Young-Seok</creatorcontrib><title>Dendritic functionalization of monolayer-protected gold nanoparticles</title><title>Materials research bulletin</title><description>This paper describes the facile synthesis of nanoparticle-cored dendrimers (NCDs) and nanoparticle megamers from monolayer-protected gold clusters using either single or multi-step reactions. First, 11-mercaptoundecanoic acid/hexanethiolate-protected gold clusters were synthesized using the Schiffrin reaction followed by the ligand place-exchange reaction. A convergent approach for the synthesis of nanoparticle-cored dendrimers uses a single step reaction that is an ester coupling reaction of hydroxy-functionalized dendrons with carboxylic acid-functionalized gold clusters. A divergent approach, which is based on multi-step reactions, employs the repetition of an amide coupling reaction and a Michael addition reaction to build polyamidoamine dendritic architectures around a nanoparticle core. Nanoparticle megamers, which are large dendrimer-induced nanoparticle aggregates with an average diameter of more than 300
nm, were prepared by the amide coupling reaction between polyamiodoamine [G-2] dendrimers and carboxylic acid-functionalized gold clusters.
1H NMR spectroscopy, FT-IR spectroscopy, thermogravimetric analysis (TGA), and transmission electron microscopy (TEM) were used for the characterization of these hybrid nanoparticles.</description><subject>A. Metals</subject><subject>A. Nanostructures</subject><subject>B. Chemical synthesis</subject><subject>CARBOXYLIC ACIDS</subject><subject>CHEMICAL PREPARATION</subject><subject>COUPLING</subject><subject>DENDRITES</subject><subject>ESTERS</subject><subject>FOURIER TRANSFORMATION</subject><subject>GOLD</subject><subject>INFRARED SPECTRA</subject><subject>LIGANDS</subject><subject>MATERIALS SCIENCE</subject><subject>NANOSTRUCTURES</subject><subject>NUCLEAR MAGNETIC RESONANCE</subject><subject>SPECTROSCOPY</subject><subject>THERMAL GRAVIMETRIC ANALYSIS</subject><subject>TRANSMISSION ELECTRON MICROSCOPY</subject><issn>0025-5408</issn><issn>1873-4227</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqNUMtOwzAQtBBIlMI_RHBOWNuJ43BDLS-pEhc4W64f4Cq1K9tFKl-Po3LgyGl3pZnZmUHoGkODAbPbTbOV2cRo0no_jg0BYA3wBig9QTPMe1q3hPSnaAZAurprgZ-ji5Q2ANDyvp-hh6XxOrrsVGX3XmUXvBzdt5yWKthqG3wY5cHEehdDNiobXX2EUVde-rCTsRBHky7RmZVjMle_c47eHx_eFs_16vXpZXG_qhXtSK7JsNYcBsoxkZLgzg690bQfmOaMWKuw1Uxp1jHSKmkULnfHSyRqGVFrLukc3Rx1Q8pOJOWKo08VvC_GBMElFeuGgro7olQMKUVjxS66rYwHgUFMtYmN-FubmGoTwEWprZCXR7IpOb6cidMb45XRLk5fdHD_kfkB3Bd-8w</recordid><startdate>20070605</startdate><enddate>20070605</enddate><creator>Cutler, Erin C.</creator><creator>Lundin, Erik</creator><creator>Garabato, B. Davis</creator><creator>Choi, Daeock</creator><creator>Shon, Young-Seok</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>20070605</creationdate><title>Dendritic functionalization of monolayer-protected gold nanoparticles</title><author>Cutler, Erin C. ; Lundin, Erik ; Garabato, B. Davis ; Choi, Daeock ; Shon, Young-Seok</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-29bd8093812aa215f97ed3796d862ffc1fd6cd65624caec11fd580063f62cb8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>A. Metals</topic><topic>A. Nanostructures</topic><topic>B. Chemical synthesis</topic><topic>CARBOXYLIC ACIDS</topic><topic>CHEMICAL PREPARATION</topic><topic>COUPLING</topic><topic>DENDRITES</topic><topic>ESTERS</topic><topic>FOURIER TRANSFORMATION</topic><topic>GOLD</topic><topic>INFRARED SPECTRA</topic><topic>LIGANDS</topic><topic>MATERIALS SCIENCE</topic><topic>NANOSTRUCTURES</topic><topic>NUCLEAR MAGNETIC RESONANCE</topic><topic>SPECTROSCOPY</topic><topic>THERMAL GRAVIMETRIC ANALYSIS</topic><topic>TRANSMISSION ELECTRON MICROSCOPY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cutler, Erin C.</creatorcontrib><creatorcontrib>Lundin, Erik</creatorcontrib><creatorcontrib>Garabato, B. Davis</creatorcontrib><creatorcontrib>Choi, Daeock</creatorcontrib><creatorcontrib>Shon, Young-Seok</creatorcontrib><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Materials research bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cutler, Erin C.</au><au>Lundin, Erik</au><au>Garabato, B. Davis</au><au>Choi, Daeock</au><au>Shon, Young-Seok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dendritic functionalization of monolayer-protected gold nanoparticles</atitle><jtitle>Materials research bulletin</jtitle><date>2007-06-05</date><risdate>2007</risdate><volume>42</volume><issue>6</issue><spage>1178</spage><epage>1185</epage><pages>1178-1185</pages><issn>0025-5408</issn><eissn>1873-4227</eissn><abstract>This paper describes the facile synthesis of nanoparticle-cored dendrimers (NCDs) and nanoparticle megamers from monolayer-protected gold clusters using either single or multi-step reactions. First, 11-mercaptoundecanoic acid/hexanethiolate-protected gold clusters were synthesized using the Schiffrin reaction followed by the ligand place-exchange reaction. A convergent approach for the synthesis of nanoparticle-cored dendrimers uses a single step reaction that is an ester coupling reaction of hydroxy-functionalized dendrons with carboxylic acid-functionalized gold clusters. A divergent approach, which is based on multi-step reactions, employs the repetition of an amide coupling reaction and a Michael addition reaction to build polyamidoamine dendritic architectures around a nanoparticle core. Nanoparticle megamers, which are large dendrimer-induced nanoparticle aggregates with an average diameter of more than 300
nm, were prepared by the amide coupling reaction between polyamiodoamine [G-2] dendrimers and carboxylic acid-functionalized gold clusters.
1H NMR spectroscopy, FT-IR spectroscopy, thermogravimetric analysis (TGA), and transmission electron microscopy (TEM) were used for the characterization of these hybrid nanoparticles.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.materresbull.2006.08.033</doi><tpages>8</tpages></addata></record> |
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subjects | A. Metals A. Nanostructures B. Chemical synthesis CARBOXYLIC ACIDS CHEMICAL PREPARATION COUPLING DENDRITES ESTERS FOURIER TRANSFORMATION GOLD INFRARED SPECTRA LIGANDS MATERIALS SCIENCE NANOSTRUCTURES NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY THERMAL GRAVIMETRIC ANALYSIS TRANSMISSION ELECTRON MICROSCOPY |
title | Dendritic functionalization of monolayer-protected gold nanoparticles |
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