<?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>2026-09-21T09:43:02Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/43813" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/43813</identifier><datestamp>2022-01-13T07:54:21Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131023</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">Robert Griffin.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Casey, Andrew (Andrew Byron)</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Chemistry.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Chemistry</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2008-12-11T18:31:59Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2008-12-11T18:31:59Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2008</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2008</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/43813</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">262478643</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2008.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (leaves 51-52).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">solid State NMR (SSNMR) can determine molecular as well as supermolecular structure and dynamics. The low signal intensities make many of these experiments prohibitively long. Dynamic Nuclear Polarization provides a method of enhancing signal intensities and reducing experimental time. DNP requires transferring polarization from unpaired electrons to nuclei. Driving this transfer requires irradiation with high power microwaves which are generated with gyrotrons oscillators. We describe a series of modifications are made to an existing 140 GHz gyrotron allows for continuous wave operation and higher power and greater stability. DNP mechanisms are primarily limited to SSNMR. A method of using DNP to enhance liquid state NMR spectra is described. Signal enhancements of over 100 are reported for a solution of glucose. To obtain maximum DNP enhancements microwave irradiation times of up to 40 s are often required. While this increases your signal intensity for a single scan it decreases the gain from signal averaging for a given time. A method of choosing the optimum irradiation time is presented. DNP enhancements in continuous wave experiments exhibit an inverse field dependence. There are several pulsed DNP experiments exhibit no field dependence. To further study these techniques a pulsed 9 GHz EPR spectrometer has been assembled.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Andrew Casey.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">S.M.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">52 leaves</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">eng</dim:field>
   <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>
   <dim:field mdschema="dc" element="rights" qualifier="uri" lang="en_US">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Chemistry.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Dynamic nuclear polarization for NMR : applications and hardware development</dim:field>
   <dim:field mdschema="dc" element="title" qualifier="alternative" lang="en_US">Dynamic nuclear polarization for nuclear magnetic resonance : applications and hardware development</dim:field>
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   	&lt;Title>Dynamic nuclear polarization for NMR : applications and hardware development&lt;/Title>
   	&lt;Subtitle>Dynamic nuclear polarization for nuclear magnetic resonance : applications and hardware development&lt;/Subtitle>
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   	&lt;PublicationDate>2008&lt;/PublicationDate>
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        	&lt;DisplayName>Casey, Andrew (Andrew Byron)&lt;/DisplayName>
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    &lt;Keyword>Chemistry.&lt;/Keyword>
   	&lt;Abstract>solid State NMR (SSNMR) can determine molecular as well as supermolecular structure and dynamics. The low signal intensities make many of these experiments prohibitively long. Dynamic Nuclear Polarization provides a method of enhancing signal intensities and reducing experimental time. DNP requires transferring polarization from unpaired electrons to nuclei. Driving this transfer requires irradiation with high power microwaves which are generated with gyrotrons oscillators. We describe a series of modifications are made to an existing 140 GHz gyrotron allows for continuous wave operation and higher power and greater stability. DNP mechanisms are primarily limited to SSNMR. A method of using DNP to enhance liquid state NMR spectra is described. Signal enhancements of over 100 are reported for a solution of glucose. To obtain maximum DNP enhancements microwave irradiation times of up to 40 s are often required. While this increases your signal intensity for a single scan it decreases the gain from signal averaging for a given time. A method of choosing the optimum irradiation time is presented. DNP enhancements in continuous wave experiments exhibit an inverse field dependence. There are several pulsed DNP experiments exhibit no field dependence. To further study these techniques a pulsed 9 GHz EPR spectrometer has been assembled.&lt;/Abstract>
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