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        <identifier>oai:www.ideals.illinois.edu:2142/72285</identifier>
        <datestamp>2023-07-11</datestamp>
        <setSpec>col_2142_5131</setSpec>
        <setSpec>col_2142_14789</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>Belford, R. Linn</dc:contributor>
          <dc:creator>Shi, Wenjun</dc:creator>
          <dc:date>2014-12-17T21:29:09Z</dc:date>
          <dc:date>2014-12-17T21:29:09Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1993</dc:date>
          <dc:date>1993</dc:date>
          <dc:description>The conventional electronic magnetic resonance (EMR) spectra of disordered samples often suffer poor resolution due to line-broadening. This thesis describes how a multi-frequency approach applied to the EMR studies of two distinct polycrystalline paramagnetic systems resulted in dramatic resolution improvements.</dc:description>
          <dc:description>The EMR techniques used include continuous wave electron paramagnetic resonance (cw-EPR) and electron spin echo envelope modulation (ESEEM). Performing the cw-EPR experiments at tenfold higher microwave frequency than the conventional X-band (ca. 9 GHz), greatly improved resolution in the field-dependent electronic Zeeman interaction of the nitro-aromatic radicals adsorbed on metal oxide surfaces. In applying the multi-frequency method to ESEEM to reveal weak superhyperfine (shfs, a) and nuclear quadrupole (NQR) interactions, we have established by model calculations a criterion to identify the &amp;quot;exact cancellation&amp;quot; condition, by which the NQR parameters can be determined directly from the multi-frequency ESEEM spectra. This criterion, taking into account the g and a anisotropies, has been verified by ESEEM experiments performed on the remote nitrogen atom of the meta-dinitrobenzene radical on surfaces. The magnetic parameters obtained this way are in excellent agreement with simulations.</dc:description>
          <dc:description>Low-frequency (2-4 GHz) ESEEM spectra of adducts of a copper chelate to an axially coordinated nitrogen-containing Lewis base showed pronounced angle selection patterns. The copper-base systems also provide a large g anisotropy, in which a close approach to cancellation is demonstrated. The nitrogen quadrupole parameters obtained by the pseudo-cancellation method are in reasonably good agreement with those obtained by the orientation-selected ESEEM; the residual discrepancy is discussed.</dc:description>
          <dc:description>Low-frequency ESEEM spectra of oxygen-17, magnesium-25, and aluminum-27 in the metal oxides adsorbed with nitro-aromatic species are also reported and discussed.</dc:description>
          <dc:description>Made available in DSpace on 2014-12-17T21:29:09Z (GMT). No. of bitstreams: 1
9329160.pdf: 6400885 bytes, checksum: f6596ae9d493b2b4398aa49b688cb345 (MD5)
  Previous issue date: 1993</dc:description>
          <dc:description>Embargo set by: Seth Robbins for item 72453
Lift date: Forever
Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:description>237 p.</dc:description>
          <dc:description>Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1993.</dc:description>
          <dc:identifier>http://hdl.handle.net/2142/72285</dc:identifier>
          <dc:identifier>(UMI)AAI9329160</dc:identifier>
          <dc:subject>Chemistry, Physical</dc:subject>
          <dc:title>Multi-Frequency Electronic Magnetic Resonance Studies of Polycrystalline Systems</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Chemistry</department>
            <discipline>Chemistry</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
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