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首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >Clusters in bis-tridentate tethered domains of an iron chelating drug
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Clusters in bis-tridentate tethered domains of an iron chelating drug

机译:铁螯合药物的双三齿束缚域中的簇

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The tridentate metal binding domains of iron chelating agents have been tethered via a variable length methylene (CH_2)_n linker (n=1,2,4,6,8,10,14). The single-crystal X-ray structures of monomeric ([Fe(HL~8)].2.5H_2O n=8; H_4L~8 is 1,10-decanedioyl di(salicylaldehyde hydrazone)) and dimeric ([{Fe(H_2PL~4)}_2]Cl_2.2H_2O n=4; H_4PL~4 is 1,6-hexanedioyl di(pyridoxal hydrazone)) iron(III) complexes have been determined. The complexes exhibit oligomerism: with chain lengths of n>=6 monomers are prevalent whereas for shorter chains this is not possible and a series of clusters exist as shown by ESMS and molecular modelling.
机译:铁螯合剂的三齿金属结合域已通过可变长度的亚甲基(CH_2)_n连接子(n = 1,2,4,6,8,10,14)进行束缚。单体([Fe(HL〜8)]。2.5H_2O n = 8; H_4L〜8是1,10-癸二酰二(水杨醛))和二聚体([{Fe(H_2PL〜 4)} _ 2] Cl_2.2H_2O n = 4; H_4PL〜4为1,6-己二酰基二(吡ox)铁(III)配合物。配合物表现出低聚性:链长为n> = 6的单体很普遍,而对于较短的链则不可能,并且存在一系列簇,如ESMS和分子模型所示。

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