<didl:DIDL xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:didl="urn:mpeg:mpeg21:2002:02-DIDL-NS" xsi:schemaLocation="urn:mpeg:mpeg21:2002:02-DIDL-NS 
			 http://standards.iso.org/ittf/PubliclyAvailableStandards/MPEG-21_schema_files/did/didmodel.xsd"><didl:Item><didl:Descriptior><didl:Statement mimeType="application/xml; charset=utf-8"><dii:Identifier xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="urn:mpeg:mpeg21:2002:01-DII-NS
		 	http://standards.iso.org/ittf/PubliclyAvailableStandards/MPEG-21_schema_files/dii/dii.xsd" xmlns:dii="urn:mpeg:mpeg21:2002:01-DII-NS">http://eprints.utas.edu.au/2957/</dii:Identifier></didl:Statement></didl:Descriptior><didl:Descriptior><didl:Statement mimeType="application/xml; charset=utf-8"><oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/">
        <dc:title>Structural studies of complexes containing cycloplatinated&#13;
tris(pyrazol-1-yl)methane</dc:title>
        <dc:creator>Canty, AJ</dc:creator>
        <dc:creator>Skelton, BW</dc:creator>
        <dc:creator>White, AH</dc:creator>
        <dc:subject>259901 Organometallic Chemistry</dc:subject>
        <dc:description>Cyclometallation at the C(5) position of one ring of tris(pyrazol-1-yl)methane occurs on dissolutionof PtMe2{(pz)3CH} in 3,5-dimethylpyridine, to form the platinum(II) complex PtMe((pz)2(C3H2N2)-CH-N,C)(3,5-Me2py) (lb). Structural studies of lb, and the related complexes PtMe{(pz)3(C3H2N2)-CH-N,C}(N-methylimidazole) (1c) and PtMe{(pz)2(C3H2N2)CH- N,C}{PPh2(o-MeOC6H4)} (ld) show that these complexes have square planar geometry with cis-organic groups, with the cyclometallated group having one pyrazole ring uncoordinated. The complexes PtMe{(pz)2(C3H2N2)CH-C}(L2) (L2 = 2PPh3 (2a), 2PEtPh, (2b), Ph2PCH2CH2PPh2 (2c)] have a similar geometry at platinum(II); the metallated ligand is present as a [C]- donor with two uncoordinated pyrazole rings. In 2a, 2b, and 2c,&#13;
there are short Pt...H contacts at ~2.7 A for the methine proton of the cyclometallated ligand.</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/2957/1/JOMC1992_2C_245.pdf</dc:identifier>
        <dc:relation>http://dx.doi.org/10.1016/0022-328X(92)86011-R</dc:relation>
        <dc:identifier>Canty, AJ and Skelton, BW and White, AH (1992) Structural studies of complexes containing cycloplatinated tris(pyrazol-1-yl)methane. Journal of Organometallic Chemistry, 430 (2). pp. 245-257. ISSN 0022-328X</dc:identifier>
        <dc:relation>http://eprints.utas.edu.au/2957/</dc:relation></oai_dc:dc></didl:Statement></didl:Descriptior><didl:Component><didl:Descriptior><didl:Statement mimeType="application/xml; charset=utf-8"><dii:Identifier xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="urn:mpeg:mpeg21:2002:01-DII-NS
		 	    http://standards.iso.org/ittf/PubliclyAvailableStandards/MPEG-21_schema_files/dii/dii.xsd" xmlns:dii="urn:mpeg:mpeg21:2002:01-DII-NS">http://eprints.utas.edu.au/2957/1/</dii:Identifier></didl:Statement></didl:Descriptior><didl:Resource ref="http://eprints.utas.edu.au/2957/1/JOMC1992_2C_245.pdf"></didl:Resource></didl:Component></didl:Item></didl:DIDL>