Macrocyclic NHC complexes of group 10 elements with enlarged aromaticity for biological studies

被引:18
作者
Bernd, Marco A. [1 ,2 ]
Bauer, Elisabeth B. [1 ,2 ]
Oberkofler, Jens [1 ,2 ]
Bauer, Andreas [1 ,3 ]
Reich, Robert M. [1 ,2 ]
Kuehn, Fritz E. [1 ,2 ]
机构
[1] Tech Univ Munich, Dept Chem, Lichtenbergstr 4, D-85747 Garching B Munchen, Germany
[2] Tech Univ Munich, Catalysis Res Ctr, Mol Catalysis, Lichtenbergstr 4, D-85747 Garching B Munchen, Germany
[3] Tech Univ Munich, Chair Organ Chem 1, Catalysis Res Ctr, Lichtenbergstr 4, D-85747 Garching B Munchen, Germany
关键词
N-HETEROCYCLIC CARBENE; TRANSITION-METAL-COMPLEXES; ORGANOMETALLIC COMPOUNDS; ANTITUMOR-ACTIVITY; CELLULAR UPTAKE; CANCER-THERAPY; PLATINUM(II); BEARING; ANTIBACTERIAL; CYTOTOXICITY;
D O I
10.1039/d0dt02598d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two sets of macrocyclic, bio-inspired, non-heme ligands are utilized for the synthesis of Ni-II, Pd-II and Pt-II complexes. The ligands consist of a 16-atom macrocycle, formed by four methylene bridged NHC moieties, with imidazole or benzimidazole as building blocks. The complexes exhibit a square planar coordination geometry and are characterized by NMR, ESI-MS, elemental analysis, SC-XRD and UV/Vis. For complexes incorporating benzimidazole, an evaluation of luminescence properties is performed, and is found that phosphorescence is present for the Pd-II derivative and there is fluorescence for the Pt-II derivative. Stability studies in cell culture medium are performed for subsequent MTT assays. Here, the Ni-II complexes show low to no activity, and Pd-II and Pt-II complexes exhibit remarkable low IC50 values in cisplatin resistant A2780cisR cells.
引用
收藏
页码:14106 / 14114
页数:9
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