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新型半三明治型 Ru(II) 配位化合物,其特征为 fac-Ru(dmso-S)3 片段:面封基团对化学行为和体外抗癌活性的影响。

New half sandwich-type Ru(II) coordination compounds characterized by the fac-Ru(dmso-S)3 fragment: influence of the face-capping group on the chemical behavior and in vitro anticancer activity.

机构信息

Department of Chemical and Pharmaceutical Sciences, Via L. Giorgieri 1, 34127, Trieste, Italy.

出版信息

Dalton Trans. 2011 Oct 7;40(37):9533-43. doi: 10.1039/c1dt11043h. Epub 2011 Aug 19.

Abstract

The Ru(II) complex fac-[RuCl(dmso-S)(3)(dmso-O)(2)][PF(6)] (P2) was found to be an excellent precursor for the facile preparation in high yield of half sandwich-type compounds of the general formula fac-[RuCl(dmso-S)(3)(N)(2)][PF(6)] (e.g. (N)(2) = 1,2-diaminoethane (en, 4), trans-1,2-diaminocyclohexane (dach, 5), or 2 NH(3) (6)). Neutral half sandwich-type compounds of the general formula fac-[RuCl(dmso-S)(3)(N-O)] where N-O is an anionic chelating ligand (e.g. N-O = picolinate (pic, 7)) are best prepared from the universal Ru(II)-dmso precursor cis-[RuCl(2)(dmso)(4)] (P1). These complexes, that were fully characterized in solution and in the solid state, are structurally similar to the anticancer organometallic compounds [Ru(η(6)-arene)(chel)Cl]PF(6) but, in place of a face-capping arene, have the fac-Ru(dmso-S)(3) fragment. In contrast to what observed for the corresponding arene compounds, that rapidly hydrolyze the Cl ligand upon dissolution in water, compounds 4-6 are very stable and inert in aqueous solution. Probably their inertness is the reason why they showed no significant cytotoxicity against the MDA-MB-231 cancer cell line.

摘要

Ru(II) 配合物 fac-[RuCl(dmso-S)(3)(dmso-O)(2)][PF(6)](P2)被发现是一种极好的前体,可以很容易地以高产率制备半三明治型化合物,其通式为 fac-[RuCl(dmso-S)(3)(N)(2)][PF(6)](例如(N)(2)= 1,2-二乙二胺(en,4)、反式-1,2-二氨基环己烷(dach,5)或 2 NH(3)(6))。通式为 fac-[RuCl(dmso-S)(3)(N-O)]的中性半三明治型化合物,其中 N-O 是阴离子螯合配体(例如 N-O = 吡啶甲酸(pic,7))最好由通用的 Ru(II)-dmso 前体 cis-[RuCl(2)(dmso)(4)](P1)制备。这些配合物在溶液中和固态中都得到了充分的表征,它们在结构上与抗癌的有机金属化合物 [Ru(η(6)-芳烃)(chel)Cl]PF(6)相似,但取代面封端的芳烃,而是具有 fac-Ru(dmso-S)(3)片段。与相应的芳烃化合物不同,它们在水中溶解时迅速水解 Cl 配体,化合物 4-6 在水溶液中非常稳定且惰性。它们的惰性可能是它们对 MDA-MB-231 癌细胞系没有显著细胞毒性的原因。

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