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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >[n+n]-Heterometallomacrocyclic complexes (n >= 2) prepared from platinum(II)-centred ditopic 2,2 ': 6 ',2 ''-terpyridine ligands: dimensional cataloguing by pulsed-field gradient spin-echo NMR spectroscopy
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[n+n]-Heterometallomacrocyclic complexes (n >= 2) prepared from platinum(II)-centred ditopic 2,2 ': 6 ',2 ''-terpyridine ligands: dimensional cataloguing by pulsed-field gradient spin-echo NMR spectroscopy

机译:由以铂(II)为中心的对位2,2':6',2''-三联吡啶配体制备的[n + n]-超金属大环配合物(n> = 2):通过脉冲场梯度自旋回波NMR光谱进行分类

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摘要

The reaction of 4'-(2-propyn-1-oxy)-2,2':6',2"-terpyridine (HC equivalent to CCH(2)Oterpy) with trans-[PtI2(PR3)(2)] (R = Et, Bu-n, Ph) results in the regioselective formation of the metalloditopic ligands trans-[Pt(C equivalent to CCH(2)Oterpy)(2)(PR3)(2)], crystallographic data for which are presented. Each ditopic ligand reacts with FeCl2 center dot 4H(2)O to give heterometallomacrocycles, the smallest of which is a [2 + 2] macrocycle, confirmed structurally for R = Et. The NMR spectroscopic data confirm the formation of symmetrical species, i.e. macrocyclic and not polymeric species. The distribution of products has been investigated using pulsed-field gradient spin-echo (PGSE) diffusion NMR spectroscopy, and indicates that the kinetic products from the reactions of 1, 2 or 3 (L) with iron(II) are [FenLn](2n+) with n = 2, 3 or 4. For L = 1 and 2, these mixtures of products convert in solution to the thermodynamically favoured [Fe2L2](4+).
机译:4'-(2-丙炔-1-氧基)-2,2':6',2“-吡啶(HC相当于CCH(2)Oterpy)与反式-[PtI2(PR3)(2)]的反应(R = Et,Bu-n,Ph)导致金属对位配体反式-[Pt(C相当于CCH(2)Oterpy)(2)(PR3)(2)]的区域选择性形成,其晶体学数据为每个对位配体与FeCl2中心点4H(2)O反应生成异金属大环,其中最小的是[2 + 2]大环,在结构上证实R =Et。NMR光谱数据证实了对称物质的形成,产物的分布已使用脉冲场梯度自旋回波(PGSE)扩散NMR光谱进行了研究,结果表明,1、2或3(L)与铁( II)是n = 2、3或4的[FenLn](2n +)。对于L = 1和2,这些产物混合物在溶液中转化为热力学上有利的[Fe2L2](4+)。

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