  <eprint xmlns="http://eprints.org/ep2/data/2.0">
    <eprintid>2955</eprintid>
    <rev_number>22</rev_number>
    <eprint_status>archive</eprint_status>
    <userid>185</userid>
    <dir>disk0/00/00/29/55</dir>
    <datestamp>2008-02-04 04:55:35</datestamp>
    <lastmod>2008-07-18 10:30:15</lastmod>
    <status_changed>2008-07-16 16:46:05</status_changed>
    <type>article</type>
    <metadata_visibility>show</metadata_visibility>
    <contact_email>allan.canty@utas.edu.au</contact_email>
    <creators>
      <item>
        <name>
          <family>Canty</family>
          <given>AJ</given>
        </name>
        <id>allan.canty@utas.edu.au</id>
      </item>
      <item>
        <name>
          <family>Traill</family>
          <given>PR</given>
        </name>
        <id></id>
      </item>
      <item>
        <name>
          <family>Skelton</family>
          <given>BW</given>
        </name>
        <id></id>
      </item>
      <item>
        <name>
          <family>White</family>
          <given>AH</given>
        </name>
        <id></id>
      </item>
    </creators>
    <title>Synthesis of halogeno, pseudohalogeno, and carboxylatopalladium(IV) complexes by halogen exchange. Crystal structure of azido(2,2’-bipyridyl)benzylpalladium( II), formed on reductive elimination of ethane from Pd(N3)Me2(CH2Ph)(bpy)</title>
    <ispublished>pub</ispublished>
    <for08>
      <item>039904</item>
    </for08>
    <subjects>
      <item>259901</item>
    </subjects>
    <full_text_status>restricted</full_text_status>
    <note>The definitive version is available at http://www.sciencedirect.com</note>
    <abstract>The first examples of fluoro, pseudohalogeno, and carboxylatopalladium(IV) complexes have been obtained by the exchange of the bromo ligand in PdBrMe2(CH2Ph)(bpy) (bpy = 2,2’-bipyridyl) on addition of a silver salt, or silver nitrate and the appropriate anion, in acetonitrile. The syntheses have permitted a study of the effect of groups X on the selectivity in reductive elimination of ethane and ethylbenzene from PdXMe2(CH2Ph)(bpy). For X = Br, N3, SCN, or O2CPh, reductive elimination from the unstable palladium(IV) complexes in acetone gives ethane and PdX(CH2Ph)(bpy) only, but these products together with ca. 10% of ethylbenxene and PdXMe(bpy) are formed from the complexes PdXMe2(CH2Ph)(bpy) (X = F, Cl, I, OCN, SeCN, O2CCF3). The binding mode of the ambidentate pseudohalides OCN-, SCN- and SeCN- has not been determined.</abstract>
    <date>1992</date>
    <date_type>published</date_type>
    <publication>Journal of Organometallic Chemistry</publication>
    <volume>433</volume>
    <number>1-2</number>
    <pagerange>213-222</pagerange>
    <id_number>10.1016/0022-328X(92)80143-L</id_number>
    <refereed>TRUE</refereed>
    <issn>0022-328X</issn>
    <official_url>http://dx.doi.org/10.1016/0022-328X(92)80143-L</official_url>
    <documents>
      <document xmlns="http://eprints.org/ep2/data/2.0">
        <docid>3916</docid>
        <rev_number>4</rev_number>
        <eprintid>2955</eprintid>
        <pos>1</pos>
        <format>application/pdf</format>
        <language>en</language>
        <security>staffonly</security>
        <license>cc_utas</license>
        <main>JOMC1992_2C_213.pdf</main>
        <files>
          <file>
            <filename>JOMC1992_2C_213.pdf</filename>
            <filesize>682365</filesize>
            <url>http://eprints.utas.edu.au/2955/1/JOMC1992_2C_213.pdf</url>
          </file>
        </files>
      </document>
    </documents>
  </eprint>
