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        <identifier>oai:www.ideals.illinois.edu:2142/23972</identifier>
        <datestamp>2023-07-10</datestamp>
        <setSpec>col_2142_5131</setSpec>
        <setSpec>col_2142_8859</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:contributor>Slichter, C.P.</dc:contributor>
          <dc:creator>Garth, John Campbell</dc:creator>
          <dc:date>2011-05-19T17:03:46Z</dc:date>
          <dc:date>2011-05-19T17:03:46Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1965</dc:date>
          <dc:description>Th.e cubic electron spin resonance spectrum of Fe3+ in
silver chloride has been studied at 1.3°K by the Electron
Nuclear Double Resonance (ENDOR) technique. ENDOR lines
from 6 to 24 megacycles were observed on each of the five
electron spin resonance transitions and have been identified
as lines due to four chlorine nuclei which are nearest
neighbors to the iron ion.
The angular dependence of the crystal field splitting
of the electron resonance, as the orientation of the
applied field is varied, proves that the iron is in a site
of cubic symmetry. The an~ular variation of the ENDOR
spectrum, as the~ield is rotated in a (100) plane, shows
that the iron cannot be in a site of octahedral symmetry and
that it therefore must be in a site of tetrahedral symmetry.
ENDOR lines of both chlorine isotopes were identified.
C135 ENDOR lines, characterized by Ms = +3/2 and Ms = -3/2 0
were studied with the applied field parallel to the (100)
direction, and the best chlorine hyperfine and quadrupole
coupling .constants were determined for both isotopes. It is
found that these constants can be used to predict the
locations'of all observed C135 and C137 ENDOR lines, but
some discrepancies between the predicted spectrum and the
observed lines remain which cannot be accounted for by
effects of the cubic field splitting term in the spin- Hamiltonian.</dc:description>
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  Previous issue date: 1965</dc:description>
          <dc:description>Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Carolyn Mead (cmead2@illinois.edu) on 2011-05-19T17:03:46Z
Item is restricted indefinitely.</dc:description>
          <dc:description>Restriction data tranferred 2014-07-01T11:15:16-05:00
Original Data
Group with Access UIUC Users [automated]
Release Date: none
Reason: Thesis</dc:description>
          <dc:description>Thesis</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:identifier>6195869</dc:identifier>
          <dc:identifier>http://hdl.handle.net/2142/23972</dc:identifier>
          <dc:language>en</dc:language>
          <dc:rights>1965 John Campbell Garth</dc:rights>
          <dc:subject>magnetic resonance</dc:subject>
          <dc:subject>iron</dc:subject>
          <dc:subject>silver chloride</dc:subject>
          <dc:subject>cubic electric spin resonance spectrum</dc:subject>
          <dc:subject>Electron Nuclear Double Resonance (ENDOR) technique</dc:subject>
          <dc:title>A magnetic resonance study of iron in silver chloride</dc:title>
          <dc:type>Dissertation / Thesis</dc:type>
          <dc:type>text</dc:type>
          <degree>
            <department>Physics</department>
            <discipline>Physics</discipline>
            <disciplineCode>University of Illinois at Urbana-Champaign</disciplineCode>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
        </thesis>
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