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Synthesis, structural and in-vitro functional studies of half-sandwich platinum group metal complexes having various bonding modes of benzhydrazone derivative ligands

机译:具有各种粘合模式的半三明治铂族金属配合物的合成,结构和体外功能研究,具有苯甲酰酮衍生物配体的各种粘合模式

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摘要

Complexes 1-9 were synthesized by reacting metal precursors [(arene)MCl2](2) (arene = p-cymene, Cp*; M = Ru, Rh and Ir) and benzhydrazone derivative ligands L1, L2 and L3 which resulted in the formation of cationic complexes with PF6 as the counter ion. Ruthenium complexes exhibited N boolean AND O bonding mode while rhodium and iridium complexes exhibited N boolean AND N bonding mode with the migration of the N-H proton to the adjacent C=O (keto) group forming enol. Anti-bacterial activity studies (against Gram-positive and Gram-negative bacteria) as well as anti-cancer [HCT116 p53 wild type (p53(+/+)) and HCT116 p53 null (p53(-/-))] were carried out for all the complexes as well as ligands where interestingly, ligand 12 and complex 5 showed high activity potency (in-vitro) for both biological studies. Amongst Ru, Rh and Ir, rhodium complexes showed more anticancer activity. (C) 2019 Elsevier Ltd. All rights reserved.
机译:通过反应金属前体[(芳烃)MCl 2](2)(Arene = P-Cymene,CP *; M = Ru,RH和IR)和苯三唑衍生物配体L1,L2和L3来合成复合物1-9。导致的 用PF6形成阳离子复合物作为反离子。 钌配合物表现出N个布尔和o键合模式,而铑和铱络合物表现出N布尔和N键合模式,并将N-H质子迁移到相邻的C = O(Keto)组形成enol。 进行抗菌活性研究(针对革兰氏阳性和革兰氏阴性细菌)以及抗癌[HCT116 P53野生型(P53(+ / +))和HCT116 P53零(p53( - / - ))] 为所有复合物以及有趣的配体,配体12和复合物5的配体显示出对两个生物学研究的高活性效力(体外)。 在Ru,Rh和IR中,铑综合体显示出更多的抗癌活动。 (c)2019 Elsevier Ltd.保留所有权利。

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