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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >New water-soluble azido- and derived tetrazolato-platinum(II) complexes with PTA. Easy metal-mediated synthesis and isolation of 5-substituted tetrazoles
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New water-soluble azido- and derived tetrazolato-platinum(II) complexes with PTA. Easy metal-mediated synthesis and isolation of 5-substituted tetrazoles

机译:与PTA形成的新型水溶性叠氮基和衍生的四唑并铂(II)配合物。易于金属介导的5取代四唑的合成和分离

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摘要

The water-soluble four- and five-coordinate diazido-platinum(II) complexes cis-[Pt(N-3)(2)(PTA)(2)] (1) (PTA = 1,3,5-triaza-7-phosphaadamantane), cis-[Pt(N-3)(2)(Me-PTA)(2)]I-2 (2) ( Me-PTA = N-methyl-1,3,5-triaza-7-phosphaadamantane cation) and [ Pt( N3) 2( PTA) 3] ( 3) were obtained by reactions of cis-[Pt(N-3)(2)(PPh3)(2)] with PTA or [Me-PTA]I in dichloromethane. [2 + 3] cycloadditions of 1 with organonitriles NCR gave the bis( tetrazolato) complexes trans-[ Pt(N4CR)(2)(PTA)(2)] (R= Ph (4), 4-ClC6H4 (5) or 3-NC5H4 (6)), the reactions being greatly accelerated by microwave irradiation. 5-R-1H-Tetrazoles N4CR (R = Ph, 4-ClC6H4 and 3-NC5H4) were easily liberated from the tetrazolato complexes 4-6 and isolated in high yields, in a single-pot process, upon reaction with aqueous diluted HCl, with concomitant formation of the water soluble cis-[ Pt(Cl)(2)(PTA-H)(2)] complex 7. Alternatively, in a less convenient method, the tetrazoles could be liberated on reaction of 4-6 with propionitrile which also leads to the dicyano trans-[Pt(CN)(2)(PTA)(2)] complex 8. The compounds were characterized by IR, H-1, C-13 and P-31{H-1} NMR spectroscopies, FAB(+)-MS or ESI-MS, elemental analyses and (for 1 and 4) also by X-ray diffraction.
机译:水溶性四坐标和五坐标叠氮基-铂(II)配合物顺式[[Pt(N-3)(2)(PTA)(2)](1)(PTA = 1,3,5-triaza- 7-磷金刚烷),顺-[Pt(N-3)(2)(Me-PTA)(2)] I-2(2)(Me-PTA = N-甲基-1,3,5-triaza-7 -磷酸金刚烷阳离子)和[Pt(N3)2(PTA)3](3)是通过顺式[[Pt(N-3)(2)(PPh3)(2)]与PTA或[Me-PTA]反应制得的我在二氯甲烷中。 [2 + 3] 1与有机腈NCR的环加成反应生成双(四唑酸酯)复合物,反式-[Pt(N4CR)(2)(PTA)(2)](R = Ph(4),4-ClC6H4(5)或3-NC5H4(6)),通过微波辐射大大加速了反应。 5-R-1H-四唑N4CR(R = Ph,4-ClC6H4和3-NC5H4)易于从四唑配合物4-6中释放出来,并通过单锅法与稀释的HCl水溶液反应以高收率分离出,伴随形成水溶性的顺式[[Pt(Cl)(2)(PTA-H)(2)]配合物7。或者,在不太方便的方法中,四唑类化合物在4-6与丙腈也可生成双氰基反式-[Pt(CN)(2)(PTA)(2)]配合物8。化合物的特征在于IR,H-1,C-13和P-31 {H-1} NMR光谱分析,FAB(+)-MS或ESI-MS,元素分析,以及(针对1和4)也通过X射线衍射进行。

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