化学
二胺
铂金
立体化学
还原(数学)
药物化学
晶体结构
组合化学
结晶学
高分子化学
有机化学
催化作用
几何学
数学
作者
Trevor W. Hambley,Andrew R. Battle,Glen B. Deacon,Eric T. Lawrenz,Gary D. Fallon,Bryan M. Gatehouse,Lorraine K. Webster,Silvina Rainone
标识
DOI:10.1016/s0162-0134(99)00133-6
摘要
The preparation of a series of novel Pt(IV) complexes containing the anionic polyfluoroaryl ligands, 2,3,5,6-tetrafluorophenyl (p-HC6F4), 2,3,5,6-tetrafluoro-4-methoxyphenyl (p-MeOC6F4) and pentafluorophenyl (C6F5) are described. The crystal structure of a representative complex, [Pt(p-MeOC6F4)2(O2CEt)2(en)] (en = ethane-1,2-diamine) was determined and confirms the trans arrangement of the carboxylato ligands. Reduction potentials of the series of complexes reveal that replacement of equatorial chloro ligands by polyfluoroaryl ligands makes reduction substantially more difficult. They also confirm previously reported trends in that complexes having axial carboxylato ligands are more readily reduced than those having axial hydroxo ligands. Reduction potentials and in vitro activities showed no obvious correlations. Moderate to high activity was observed for many complexes in the series, including some of those that were very difficult to reduce.
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