首页> 外文OA文献 >Different Rotamer States of Cytosine Nucleobases in Heteronuclear PtPd-, PtPd2, and Pt2Pd2Ag Complexes Derived from Pt(2,2′-bpy)(1-MeC-N3)22+ (1-MeC = 1-Methylcytosine): First Examples of Species with Head–Head Oriented 1-MeC– Ligands
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Different Rotamer States of Cytosine Nucleobases in Heteronuclear PtPd-, PtPd2, and Pt2Pd2Ag Complexes Derived from Pt(2,2′-bpy)(1-MeC-N3)22+ (1-MeC = 1-Methylcytosine): First Examples of Species with Head–Head Oriented 1-MeC– Ligands

机译:Pt(2,2'-bpy)(1-MeC-N3)2 2+(1-MeC = 1-甲基胞嘧啶)衍生的异核PtPd-,PtPd2和Pt2Pd2Ag复合物中胞嘧啶核糖核酸酶的不同旋转状态。头对头1-MeC-配体的物种实例

摘要

[Pt(2,2′-bpy)(1-MeC-N3) 2](NO 3) 2 (1) (2,2′-bpy = 2,2′-bipyridine; 1-MeC = 1-methylcytosine) exists in water in an equilibrium of head-tail and head-head rotamers, with the former exceeding the latter by a factor of ca. 20 at room temperature. Nevertheless, 1 reacts with (en)Pd II (en = ethylenediamine) to give preferentially the dinuclear complex [Pt(2,2′-bpy)(1-MeC --N3,N4) 2Pd(en)](NO 3) 2·5H 2O (2) with head-head arranged 1-methylctosinato (1-MeC -) ligands and Pd being coordinated to two exocyclic N4H - positions. Addition of AgNO 3 to a solution of 2 leads to formation of a pentanuclear chain compound [{Pt(2,2′-bpy)(1-MeC -) 2Pd(en)} 2Ag](NO 3) 5·14H 2O (5) in which Ag + cross-links two cations of 2 via the four available O2 sites of the 1-MeC - ligands. 2 and 5 appear to be the first X-ray structurally characterized examples of di- and multinuclear complexes derived from a Pt II species with two cis-positioned cytosinato ligands adopting a head-head arrangement. (tmeda)Pd II (tmeda = N,N,N′,N′- tetramethylethylenediamine) and (2,2′-bpy)Pd II behave differently toward 1 in that in their derivatives the head-tail orientation of the 1-MeC - nucleobases is retained. In [Pt(2,2′-bpy)(1-MeC -) 2{Pd(2,2′-bpy)} 2](NO 3) 4·10H 2O (4), both (2,2′-bpy)Pd II entities are pairwise bonded to N4H - and O2 sites of the two 1-MeC - rings, whereas in [Pt(2,2′-bpy)(1-MeC -) 2{Pd(tmeda)} 2(NO 3)](NO 3) 3·5H 2O (3) only one of the two (tmeda)Pd II units is chelated to N4H - and O2. The second (tmeda)Pd II is monofunctionally attached to a single N4H - site. On the basis of these established binding patterns, ways to the formation of mixed Pt/Pd complexes and possible intermediates are proposed. The methylene protons of the en ligand in 2 are special in that they display two multiplets separated by 0.64 ppm in the 1H NMR spectrum. © 2012 American Chemical Society.
机译:[Pt(2,2'-bpy)(1-MeC-N3)2](NO 3)2(1)(2,2'-bpy = 2,2'-联吡啶; 1-MeC = 1-甲基胞嘧啶)存在于水中的头尾和头-头旋转器的平衡,前者超过后者约两倍。在室温下为20。然而,1与(en)Pd II(en =乙二胺)反应优先生成双核配合物[Pt(2,2'-bpy)(1-MeC --N3,N4)2Pd(en)](NO 3) 2·5H 2O(2)头-头排列有1-methylctosinato(1-MeC-)配体,Pd配位至两个环外N4H-位置。在2的溶液中添加AgNO 3导致形成五核链化合物[{Pt(2,2'-bpy)(1-MeC-)2Pd(en)} 2Ag](NO 3)5·14H 2O( 5),其中Ag +通过1-MeC-配体的四个可用O2位使2的两个阳离子交联。图2和5似乎是由Pt II物种衍生的双核和多核复合物的首个X射线结构表征的实例,该复合物具有两个采用头-头排列的顺式胞嘧啶配体。 (tmeda)Pd II(tmeda = N,N,N',N'-四甲基乙二胺)和(2,2'-bpy)Pd II对1的行为不同,因为在它们的导数中1-MeC的头尾方向-保留了核碱基。在[Pt(2,2'-bpy)(1-MeC-)2 {Pd(2,2'-bpy)} 2](NO 3)4·10H 2O(4)中,两者(2,2'- bpy)Pd II实体成对键合至两个1-MeC-环的N4H-和O2位,而在[Pt(2,2'-bpy)(1-MeC-)2 {Pd(tmeda)} 2( NO 3)](NO 3)3·5H 2O(3)只有两个(tmeda)Pd II单元之一被螯合到N4H-和O2。第二个(tmeda)Pd II单功能连接到单个N4H-位点。基于这些建立的结合模式,提出了形成混合的Pt / Pd复合物和可能的中间体的方法。 en配体中2的亚甲基质子的特殊之处在于,它们在1H NMR光谱中显示出两个重合峰,相距0.64 ppm。 ©2012美国化学学会。

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    Sanz Miguel Pablo J.;

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  • 年度 2013
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