Source:http://linkedlifedata.com/resource/pubmed/id/18827937
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
39
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pubmed:dateCreated |
2008-10-1
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pubmed:abstractText |
The nitrile ligands in trans-[PtX2(PhCN)2] (X = Cl, Br, I) undergo sequential 1,3 dipolar cycloadditions with nitrones R1R2C=N+(Me)-O(-) (R1 = H, R2 = Ph; R1 = CO2Et, R2 = CH2CO2Et) to selectively form the Delta4-1,2,4-oxadiazoline complexes trans-[PtX2(PhCN) (N=C(Ph)-O-N(Me)-CR1R2)] or trans-[PtX2(N=C(Ph)-O-N(Me)-CR1R2)2] in high yields. The reactivity of the mixed ligand complexes trans-[PtX2(PhCN)(N=C(Ph)-O-N(Me)-CR1R2)] towards oxidation and ligand substitution was studied in more detail. Oxidation with Cl2 or Br2 provides the Pt(IV) species trans-[PtX2Y2(PhCN)(N=C(Ph)-O-N(Me)-CH(Ph))] (X, Y = Cl, Br). The mixed halide complex (X = Cl, Y = Br) undergoes halide scrambling in solution to form trans-[PtX(4-n)Yn(PhCN)(N=C(Ph)-O-N(Me)-CH(Ph))] as a statistical mixture. Ligand substitution in trans-[PtCl2(PhCN)(N=C(Ph)-O-N(Me)-CR1R2)] allows for selective replacement of the coordinated nitrile by nitrogen heterocycles such as pyridine, DMAP or 1-benzyl-2-methylimidazole to produce mixed ligand Pt(II) complexes of the type trans- [PtX2(heterocycle)(N=C(Ph)-O-N(Me)-CR1R2)]. All compounds were characterised by elemental analysis, mass spectrometry, IR and 1H, 13C and 195Pt NMR spectroscopy. Single-crystal X-ray structural analysis of (R,S)-trans-[PtBr2(N=C(Ph)-O-N(Me)-CH(Ph))2] and trans-[PtCl2(C5H5N)(N=C(Ph)-O-N(Me)-CH(Ph))] confirms the molecular structure and the trans configuration of the heterocycles relative to each other.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Bromine,
http://linkedlifedata.com/resource/pubmed/chemical/Chlorine,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Organoplatinum Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Oxazoles,
http://linkedlifedata.com/resource/pubmed/chemical/Oxygen,
http://linkedlifedata.com/resource/pubmed/chemical/Platinum
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1477-9226
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5302-12
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pubmed:meshHeading |
pubmed-meshheading:18827937-Antineoplastic Agents,
pubmed-meshheading:18827937-Bromine,
pubmed-meshheading:18827937-Chemistry, Pharmaceutical,
pubmed-meshheading:18827937-Chlorine,
pubmed-meshheading:18827937-Drug Design,
pubmed-meshheading:18827937-Ligands,
pubmed-meshheading:18827937-Magnetic Resonance Spectroscopy,
pubmed-meshheading:18827937-Models, Chemical,
pubmed-meshheading:18827937-Molecular Conformation,
pubmed-meshheading:18827937-Molecular Structure,
pubmed-meshheading:18827937-Organoplatinum Compounds,
pubmed-meshheading:18827937-Oxazoles,
pubmed-meshheading:18827937-Oxygen,
pubmed-meshheading:18827937-Platinum,
pubmed-meshheading:18827937-Spectrophotometry, Infrared
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pubmed:year |
2008
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pubmed:articleTitle |
Synthesis and characterisation of mixed ligand Pt(II) and Pt(IV) oxadiazoline complexes.
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pubmed:affiliation |
Chemical Sciences, FHMS, University of Surrey, Guildford, Surrey, UK GU2 7XH.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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