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首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >Synthesis and solution studies of ruthenium(II) complexes with thiazole and antileukaemic drug thiopurines. Crystal structure of trans-dichlorotris(1,3-thiazole)(triphenylphosphine)ruthenium(II)
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Synthesis and solution studies of ruthenium(II) complexes with thiazole and antileukaemic drug thiopurines. Crystal structure of trans-dichlorotris(1,3-thiazole)(triphenylphosphine)ruthenium(II)

机译:钌(II)与噻唑和抗白血病药物硫嘌呤的配合物的合成和溶液研究。反式二氯三(1,3-噻唑)(三苯基膦)钌(II)的晶体结构

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摘要

The crystalline complexes [RuCl2(PPh3)(2)(thz)(2)] 1, [RuCl2(PPh3)(thz)(3)] 2, [Ru(H(2)tp)(2)(PPh3)(thz)]Cl-2. 2H(2)O 3 . 2H(2)O, [Ru(H(2)tg)(2)(PPh3)(2)]Cl-2. 2H(2)O . EtOH 4 . 2H(2)O . EtOH, [Ru(H(2)tprta)(2)(PPh3)(2)]Cl-2. 3H(2)O 5 . 3H(2)O, [Ru(H(2)tp)(2)(PPh3)(2)][CF3SO3](2). H2O . EtOH 6 . H2O . EtOH, [Ru(H(2)tg)(2)(PPh3)(2)][CF3SO3](2). 3H(2)O 7 . 3H(2)O, [Ru(H(2)tp)(2)(AsPh3)(MeOH)]Cl-2. MeOH 8 . MeOH, [Ru(bzim)(2)Cl-2(PPh3)(2)] 9, and [RuCl2(PPh3)(2)(mpym)(2)] 10 (H(2)tg = purine-2-amino-6-thione, H(2)tp = purine-6-thione, H(2)tprta = purine-6-thione 2',3',5'-tri-O-acetylriboside, thz = 1,3-thiazole, bzim = benzimidazole, mpym = 4-methylpyrimidine) have been prepared from [RuCl2(PPh3)(3)] or [RuCl3(AsPh3)(2)(MeOH)] and the base in alcoholic solution under nitrogen. The structures of the complexes were investigated by X-ray diffraction (2), NMR, conventional spectroscopic techniques and electrochemical methods. All the complex molecules have a pseudo-octahedral co-ordination geometry. The donor set of 2 consists of a phosphorus atom, two chloride anions trans to each other and three thz ligands bound to the metal through nitrogen. The sulfur atom of thz does not show any donor ability. However, the thione function of purine is much more active and in complexes 3-8 the purine base is chelated through S and N(7) atoms. On refluxing a suspension of 2 and H(2)tp in ethanol compound 3 was obtained, which has a slight solubility in water. Electrochemical studies carried out on 7 in acetonitrile revealed a monoelectronic oxidation process at E-1/2 1.02 V. The [Ru-III(H(2)tg)(2)(PPh3)(2)](3+) species which forms at this potential is relatively stable under the experimental conditions [25 degrees C; N-2, 1 bar (10(5) Pa)] can be reversibly reduced to the starting compound which was recovered from the mixture. A molecular mechanics analysis, carried out for 1 and 2, produced a force held for this class of compounds and showed that the trans,trans,trans-[RuCl2(PPh3)(2)(thz)(2)] isomer of 1 is the most stable. [References: 67]
机译:结晶络合物[RuCl2(PPh3)(2)(thz)(2)] 1,[RuCl2(PPh3)(thz)(3)] 2,[Ru(H(2)tp)(2)(PPh3)( thz)] Cl-2。 2H(2)O 3。 2H(2)O,[Ru(H(2)tg)(2)(PPh3)(2)] Cl-2。 2H(2)O。乙醇4。 2H(2)O。 EtOH,[Ru(H(2)tprta)(2)(PPh3)(2)] Cl-2。 3H(2)O 5。 3H(2)O,[Ru(H(2)tp)(2)(PPh3)(2)] [CF3SO3](2)。水乙醇6。水EtOH,[Ru(H(2)tg)(2)(PPh3)(2)] [CF3SO3](2)。 3H(2)O 7。 3H(2)O,[Ru(H(2)tp)(2)(AsPh3)(MeOH)] Cl-2。甲醇8。 MeOH,[Ru(bzim)(2)Cl-2(PPh3)(2)] 9和[RuCl2(PPh3)(2)(mpym)(2)] 10(H(2)tg =嘌呤-2-氨基-6-硫酮,H(2)tp =嘌呤-6-硫酮,H(2)tprta =嘌呤-6-硫酮2',3',5'-三-O-乙酰基核糖苷,thz = 1,3-噻唑,bzim =苯并咪唑,mpym = 4-甲基嘧啶)是由[RuCl2(PPh3)(3)]或[RuCl3(AsPh3)(2)(MeOH)]和碱在乙醇溶液中在氮气下制备的。通过X射线衍射(2),NMR,常规光谱技术和电化学方法研究了配合物的结构。所有复杂分子均具有伪八面体配位几何形状。 2的供体组由一个磷原子,两个相互转化的氯化物阴离子和三个通过氮与金属结合的thz配体组成。 thz的硫原子没有显示任何给体能力。然而,嘌呤的硫酮功能更为活跃,在配合物3-8中,嘌呤碱基通过S和N(7)原子螯合。回流后,获得2-和H(2)tp在乙醇化合物3中的悬浮液,其在水中具有微溶性。在乙腈中的7上进行的电化学研究表明,在E-1 / 2 1.02 V时发生单电子氧化。[Ru-III(H(2)tg)(2)(PPh3)(2)](3+)种类在实验条件下[25摄氏度; N-2,1 bar(10(5)Pa)]可以可逆地还原为从混合物中回收的起始化合物。对1和2进行的分子力学分析产生了针对此类化合物的力,并显示1的反式,反式,反式-[RuCl2(PPh3)(2)(thz)(2)]异构体为最稳定的。 [参考:67]

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