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1.
Anticancer Potential of (Pentamethylcyclopentadienyl)chloridoiridium(III) Complexes Bearing κP and κP,κS‐Coordinated Ph2PCH2CH2CH2S(O)xPh (x=0–2) Ligands
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Gerd Ludwig Ivan Ranđelović Dr. Danijela Maksimović‐Ivanić Dr. Sanja Mijatović Mirna Z. Bulatović Dr. Djordje Miljković Prof. Marcus Korb Prof. Dr. Heinrich Lang Prof. Dr. Dirk Steinborn Prof. Dr. Goran N. Kaluđerović 《ChemMedChem》2014,9(7):1586-1593
Iridium(III) complexes of the type [Ir(η5‐C5Me5)Cl2{Ph2PCH2CH2CH2S(O)xPh‐κP}] (x=0–2; 1 – 3 ) and [Ir(η5‐C5Me5)Cl{Ph2PCH2CH2CH2S(O)xPh‐κP,κS}][PF6] (x=0–1; 4 and 5 ) with 3‐(diphenylphosphino)propyl phenyl sulfide, sulfoxide, and sulfone ligands Ph2PCH2CH2CH2S(O)xPh were designed, synthesized, and characterized fully, including X‐ray diffraction analyses for complexes 3 and 4 . In vitro studies against human thyroid carcinoma (8505C), submandibular carcinoma (A253), breast adenocarcinoma (MCF‐7), colon adenocarcinoma (SW480), and melanoma (518A2) cell lines provided evidence for the high biological potential of the neutral and cationic iridium(III) complexes. Neutral iridium(III) complex 5 proved to be the most active, with IC50 values up to about 0.1 μM , representing activities of up to one order of magnitude higher than cisplatin. Using 8505C cells, apoptosis was shown to be the main mechanism through which complex 5 exerts its tumoricidal action. The described iridium(III) complexes represent potential leads in the search for novel metal‐based anticancer agents. 相似文献
2.
Victor Sans Anna M. Trzeciak Santiago Luis Józef J. Ziółkowski 《Catalysis Letters》2006,109(1-2):37-41
Efficient cross-coupling and carbonylative coupling of terminal alkynes with aryl iodides catalyzed by PdCl2(P(OPh)3)2 in the presence of NEt3 in toluene and in ionic liquids is described. In imidazolium ionic liquids, [bmim]PF6 or [mokt]PF6 (bmim = 1-butyl-3-methyl imidazolium cation, mokt = 1-methyl-3-octyl imidazolium cation) catalyst was recycled and used in
four concecutive catalytic cycles with high activity. In the absence of aryl iodide the same catalytic system catalyzed head-to-tail
dimerization of phenylacetylene to the 1,3-diphenyl enyne, trans-PhC ≡ C–C(Ph)=CH2, with a yield of 85%. 相似文献