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        <dc: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)</dc:title>
        <dc:creator>Canty, AJ</dc:creator>
        <dc:creator>Traill, PR</dc:creator>
        <dc:creator>Skelton, BW</dc:creator>
        <dc:creator>White, AH</dc:creator>
        <dc:subject>259901 Organometallic Chemistry</dc:subject>
        <dc:description>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.</dc:description>
        <dc:date>1992</dc:date>
        <dc:type>Article</dc:type>
        <dc:type>PeerReviewed</dc:type>
        <dc:format>application/pdf</dc:format>
        <dc:identifier>http://eprints.utas.edu.au/2955/1/JOMC1992_2C_213.pdf</dc:identifier>
        <dc:relation>http://dx.doi.org/10.1016/0022-328X(92)80143-L</dc:relation>
        <dc:identifier>Canty, AJ and Traill, PR and Skelton, BW and White, AH (1992) 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). Journal of Organometallic Chemistry, 433 (1-2). pp. 213-222. ISSN 0022-328X</dc:identifier>
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