Palladium(II) N-heterocyclic carbene complexes: synthesis, structures and cytotoxicity potential studies against breast cancer cell line

被引:7
|
作者
Hussaini, Sunusi Y. [1 ,2 ]
Haque, Rosenani A. [1 ]
Fatima, Tabinda [1 ]
Agha, M. Taleb [2 ]
Majid, A. M. S. Abdul [3 ]
Razali, Mohd. R. [1 ]
机构
[1] Univ Sains Malaysia, Sch Chem Sci, George Town, Malaysia
[2] Kano Univ Sci & Technol Wudil, Dept Chem, Kano, Nigeria
[3] Univ Sains Malaysia, Sch Pharm, EMAN Res & Testing Lab, George Town, Malaysia
关键词
N-Heterocyclic carbenes; Ag(I)-NHC; Pd(II)-NHC; benzimidazolium salts; cytotoxicity studies; SUZUKI-MIYAURA; COUPLING REACTION; NHC COMPLEXES; ANTIPROLIFERATIVE ACTIVITY; MEDICINAL APPLICATIONS; PRE-CATALYSTS; COPPER FREE; SILVER; LIGANDS; AGENTS;
D O I
10.1080/00958972.2018.1485901
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Mononuclear trans-Pd(II)-NHC complexes (where NHC = N-heterocyclic carbene) bearing asymmetrically substituted NHC-ligand have been synthesized via transmetalation reaction between Ag(I)-NHC complexes and [Pd(NCCH3)(2)Cl-2]. The NHC precursors are accessible in two steps by N-n-alkyl reactions of benzimidazole. The resultant benzimidazolium salts were deprotonated with Ag2O by in situ deprotonation to facilitate the formation of mononuclear Ag(I)-NHC complexes. Single-crystal structural study for Pd(II)-NHC shows that the palladium(II) ion exhibits a square-planar geometry of two NHC ligands and two chloride ions. The cytotoxicity study was investigated against breast cancer cell line (MCF-7). The Ag(I)-NHC complexes exhibit better activities than their corresponding Pd(II)-NHC complexes, whereas all benzimidazolium salts are inactive toward MCF-7 cancer cell line. [GRAPHICS] .
引用
收藏
页码:2787 / 2799
页数:13
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