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   <subfield code="a">Antileukemic activity and cellular effects of rhodium(III) crown thiaether complexes</subfield>
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   <subfield code="c">[Ruth Bieda, Igor Kitanovic, Hamed Alborzinia, Andreas Meyer, Ingo Ott, Stefan Wölfl, William Sheldrick]</subfield>
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   <subfield code="a">The cytostatic properties of novel rhodium(III) thiacrown ether complexes [RhCl(LL)([9]aneS3)]n+ with either aromatic κ2 N ligands (n=2) or anionic chelate ligands (n=1) have been investigated for the human cancer cell lines HT-29 and MCF-7 and for immortalized HEK-293 cells. Taken together with literature IC50 values for analogous complexes with polypyridyl ligands or 1,4-dithiane, the in vitro assays indicate that dicationic complexes with soft κ2 N (imino) or κ2 S (thiaether) ligands exhibit significantly higher antiproliferative effects than those with hard κ2 N (amino) ligands. Dicationic complexes are more active than monocationic complexes with similar ligands. Pronounced apoptosis-inducing properties towards Jurkat cells were established for complexes with LL=bpm, dpq, and 1,4-dithiane. The order of activity (bpm&gt;1,4-dithiane&gt;dpq&gt;bpy) contrasts to that observed for adhesive cancer cells (bpm&gt;bpy, 1,4-dithiane&gt;dpq). Necrosis is insignificant in all cases. The percentage of Jurkat cells exhibiting apoptosis after 24 or 48h incubation periods is directly correlated to the percentage of cells exhibiting high levels of reactive oxygen species. As established by online monitoring with a sensor chip system, treatment of MCF-7 cells with the bpm and 1,4-dithiane complexes leads to a significant and permanent concentration-dependent decrease in oxygen consumption and cellular adhesion.</subfield>
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   <subfield code="a">Kitanovic</subfield>
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