Faculty of Chemistry, University of Wrocław, Wrocław, Poland.
Dalton Trans. 2013 May 14;42(18):6572-81. doi: 10.1039/c3dt33026e.
The new series of silver(I) coordination polymers [Ag(N-N)(μ-PTA)]n(X)n (1, 2, 4-8, 10, 11) and discrete monomers Ag(N-N)(PTA)2 (3, 9) {N-N = bpy (1-3), dtbpy (4), neocup (5, 6), phen (7-9), dione (10, 11); X = NO3 (1, 3, 5, 7, 9, 10), PF6 (2, 4, 6, 8, 11)} were generated by self-assembly reactions, in MeOH at ~25 °C, of AgNO3 or AgPF6 with 1,3,5-triaza-7-phosphaadamantane (PTA) and the corresponding polypyridines, namely 2,2'-bipyridine (bpy), 4,4'-di-tert-butyl-2,2'-bipyridine (dtbpy), 1,10-phenanthroline (phen), 2,9-dimethyl-1,10-phenanthroline (neocup) and 1,10-phenanthroline-5,6-dione (dione). The compounds were obtained as air and light stable solids and characterized by IR, (1)H and (31)P{(1)H} NMR spectroscopy, ESI(+)-MS and elemental analyses. The crystal structure of 1 was determined by single crystal X-ray diffraction analysis, revealing infinite one-dimensional (1D) linear chains driven by μ-PTA N,P-linkers. Apart from representing the first examples of the metal-PTA derivatives bearing polypyridine ligands, 1-11 also feature solubility in water (S(25°C) ≈ 4-18 mg mL(-1)). Selected compounds (1, 3, 5, 7, 9 and 10) were thus tested for their biological properties and found to exhibit significant antibacterial and antifungal activities, screened in vitro against the standard strains of Staphylococcus aureus, Staphylococcus pyogenes, Staphylococcus pneumoniae, Staphylococcus sanguinis, Staphylococcus mutans, Enterococcus faecalis, Pseudomonas aeruginosa, Escherichia coli and Candida albicans. Furthermore, the compounds 5, 7, 9 and 10 show a pronounced antiproliferative activity against human malignant melanoma (A375), and the effects on the inhibition of tumor cells in vitro are in agreement with the DNA-binding studies.
新系列的银(I)配位聚合物[Ag(N-N)(μ-PTA)]n(X)n(1、2、4-8、10、11)和离散单体[Ag(N-N)(PTA)2](X)(3、9){N-N = bpy(1-3),dtbpy(4),neocup(5、6),phen(7-9),dione(10、11);X = NO3(1、3、5、7、9、10),PF6(2、4、6、8、11)}是通过自组装反应生成的,在 MeOH 中,AgNO3 或 AgPF6 与 1,3,5-三氮杂-7-磷杂金刚烷(PTA)和相应的多吡啶,即 2,2'-联吡啶(bpy),4,4'-二叔丁基-2,2'-联吡啶(dtbpy),1,10-菲咯啉(phen),2,9-二甲基-1,10-菲咯啉(neocup)和 1,10-菲咯啉-5,6-二酮(dione)。这些化合物作为空气和光稳定的固体获得,并通过 IR、(1)H 和(31)P{(1)H}NMR 光谱、ESI(+)-MS 和元素分析进行了表征。1 的晶体结构通过单晶 X 射线衍射分析确定,揭示了由μ-PTA N,P-配体驱动的无限一维(1D)线性链。除了代表金属-PTA 衍生物与多吡啶配体的第一个例子外,1-11 还具有在水中的溶解度(S(25°C)≈4-18mgmL(-1))。因此,选择了一些化合物(1、3、5、7、9 和 10)进行生物性质测试,发现它们对金黄色葡萄球菌、化脓性链球菌、肺炎链球菌、血链球菌、变异链球菌、粪肠球菌、铜绿假单胞菌、大肠杆菌和白色念珠菌的标准菌株具有显著的抗菌和抗真菌活性。此外,化合物 5、7、9 和 10 对人恶性黑色素瘤(A375)表现出明显的抗增殖活性,体外抑制肿瘤细胞的作用与 DNA 结合研究一致。