<?xml version="1.0" encoding="UTF-8"?>
<?xml-stylesheet type="text/xsl" href="/oai-pmh.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>2026-09-22T22:11:06Z</responseDate>
  <request identifier="oai:www.ideals.illinois.edu:2142/84219" metadataPrefix="etdms" verb="GetRecord">https://www.ideals.illinois.edu/oai-pmh</request>
  <GetRecord>
    <record>
      <header>
        <identifier>oai:www.ideals.illinois.edu:2142/84219</identifier>
        <datestamp>2023-07-11</datestamp>
        <setSpec>col_2142_5131</setSpec>
        <setSpec>col_2142_14789</setSpec>
        <setSpec>com_2142_5130</setSpec>
        <setSpec>com_2142_14788</setSpec>
        <setSpec>com_2142_8903</setSpec>
      </header>
      <metadata>
        <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>Girolami, G.S.</dc:contributor>
          <dc:creator>Dickinson, Paul W.</dc:creator>
          <dc:date>2015-09-25T22:13:31Z</dc:date>
          <dc:date>2015-09-25T22:13:31Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>2006</dc:date>
          <dc:date>2006</dc:date>
          <dc:description>Treatment of H2OsBr6 with 4 equiv. of tetramethylcyclopentadiene (C5Me4H2) in tert-butanol affords [(C 5Me4H)2OsBr]2[Os2Br 8]. The brown color of the salt suggests that the anion adopts an eclipsed conformation (D4h symmetry) and this conclusion has been confirmed by a single-crystal X-ray diffraction experiment. Treatment of [(C5Me 4H)2OsBr]2[Os2Br8] with excess 1,5-cyclooctadiene (cod) in refluxing ethanol gives (C5Me 4H)2Os and [(C5Me4H)2OsBr][Os 2HBr4(cod)2]. An X-ray crystallographic study of the latter compound indicates that the anion adopts a confacial bioctahedral structure in which the hydride ligand and two bromides bridge between the two osmium centers. This anion is the first example of an anionic diosmium complex containing a bridging hydride.</dc:description>
          <dc:description>Made available in DSpace on 2015-09-25T22:13:31Z (GMT). No. of bitstreams: 2
license.txt: 4848 bytes, checksum: 96035ab3f5e1c23cc7138a224ce498bd (MD5)
3223579.pdf: 4285826 bytes, checksum: 9534c178685f18cbdc6b23f1f56a111f (MD5)
  Previous issue date: 2006</dc:description>
          <dc:description>Embargo set by: Seth Robbins for item 85500
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>132 p.</dc:description>
          <dc:description>Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2006.</dc:description>
          <dc:identifier>http://hdl.handle.net/2142/84219</dc:identifier>
          <dc:identifier>(MiAaPQ)AAI3223579</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:subject>Chemistry, Inorganic</dc:subject>
          <dc:title>Trispyrazolylborate and Tetramethylcyclopentadienyl Osmium Chemistry: Toward Methane Coordination Complexes</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>
        </thesis>
      </metadata>
    </record>
  </GetRecord>
</OAI-PMH>
