<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-19T19:50:51Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/35074" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/35074</identifier><datestamp>2022-01-13T07:54:33Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131024</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">Francesco Stellacci.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Bennett, Samantha E</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Materials Science and Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2006-12-18T20:02:32Z</dim:field>
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   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2006</dim:field>
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   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2006.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (leaves 23-24).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Mixed monolayer protected gold nanoparticles were linked using octanedithiol to form aggregates containing hundreds of nanoparticles. These aggregates are an interesting material, posing potential applications in the fields of chemistry, biology and materials science. This study examined the dependence of aggregate size and morphology on temperature of formation, using AFM and TEM imaging. The aggregates formed at 70°C averaged 105nm in width, as compared to 70nm for the room temperature aggregates. The TEM images showed increased density for the 70°C aggregates. In a further study, the room temperature aggregates were functionalized through a place exchange reaction with 1 -mercapto-undecane- l-sodiumsulfonate (MUS), a thiolated ligand with a polar head group. A two-phase test of the water-solubility indicated that the aggregates were fully soluble. TEM images showed a slight increase in size, though similar morphology to the insoluble aggregates. The ability to induce water solubility in the aggregates opens up many potential applications in the field of bionanomaterials.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Samantha E. Bennett.</dim:field>
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   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.</dim:field>
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   <dim:field mdschema="dc" element="subject" lang="en_US">Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Fabrication of water-soluble gold nanoparticle aggregates</dim:field>
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   	&lt;Title>Fabrication of water-soluble gold nanoparticle aggregates&lt;/Title>
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   	&lt;Abstract>Mixed monolayer protected gold nanoparticles were linked using octanedithiol to form aggregates containing hundreds of nanoparticles. These aggregates are an interesting material, posing potential applications in the fields of chemistry, biology and materials science. This study examined the dependence of aggregate size and morphology on temperature of formation, using AFM and TEM imaging. The aggregates formed at 70°C averaged 105nm in width, as compared to 70nm for the room temperature aggregates. The TEM images showed increased density for the 70°C aggregates. In a further study, the room temperature aggregates were functionalized through a place exchange reaction with 1 -mercapto-undecane- l-sodiumsulfonate (MUS), a thiolated ligand with a polar head group. A two-phase test of the water-solubility indicated that the aggregates were fully soluble. TEM images showed a slight increase in size, though similar morphology to the insoluble aggregates. The ability to induce water solubility in the aggregates opens up many potential applications in the field of bionanomaterials.&lt;/Abstract>
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