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        <dc:title>Structural studies of unusually disordered&#13;
diorganoplatinum(IV) complexes containing the cations&#13;
[PtIR2(L-N,N’,N”)]+, where the ligands L are facially coordinated</dc:title>
        <dc:creator>Canty, AJ</dc:creator>
        <dc:creator>Honeyman, RT</dc:creator>
        <dc:creator>Skelton, BW</dc:creator>
        <dc:creator>White, AH</dc:creator>
        <dc:subject>259901 Organometallic Chemistry</dc:subject>
        <dc:description>The reaction of [PtPh2(SEt2)]2 with tris(pyrazol-1-yl)methane [(pz)3CH] and iodine in dichloromethane gives the platinum(lV) complex [PtIPh2{(pz)3CH-N,N’,N”}]2[I][I3] (1). Complex 1, and related complexes of the facially coordinated tridentate ligands (pz)2(mim)CH (mim = N-methylimidazol-2-yl) and (pz)2(py)CH (py = pyridin-2-yl) have octahedral geometry for platinum(IV), “PtIC2N3“, and exhibit unusual disorder in the solid state. Complex 1 has two cations in the asymmetric unit, with one cation well ordered and the other showing disorder between the coordinated iodide and one phenyl group position. The complexes [PtIMe2{(pz)2(mim)CH-N,N’,N”}]I (2a) and&#13;
[PtIMe2{(pz)2(py)CH-N,N’,N”}]I (2b) have coordinated iodide disordered with both methyl groups; in 2a iodine is predominantly trans to the pz groups, and in 2b iodine is predominantly trans to the py group.</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/2958/1/JOMC1992_2C_381.pdf</dc:identifier>
        <dc:relation>http://dx.doi.org/10.1016/0022-328X(92)80012-M</dc:relation>
        <dc:identifier>Canty, AJ and Honeyman, RT and Skelton, BW and White, AH (1992) Structural studies of unusually disordered diorganoplatinum(IV) complexes containing the cations [PtIR2(L-N,N’,N”)]+, where the ligands L are facially coordinated. Journal of Organometallic Chemistry, 424 (3). pp. 381-390. ISSN 0022-328X</dc:identifier>
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