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首页> 外文期刊>Crystal growth & design >Naphthyl amines as novel organoimido ligands for design of POM-based organic-inorganic hybrids: Synthesis, structural characterization, and supramolecular assembly of (Bu4N)(2)[Mo6O18N(Naph-1)]
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Naphthyl amines as novel organoimido ligands for design of POM-based organic-inorganic hybrids: Synthesis, structural characterization, and supramolecular assembly of (Bu4N)(2)[Mo6O18N(Naph-1)]

机译:萘胺作为新颖的有机酰亚胺配体,用于设计基于POM的有机-无机杂化物:(Bu4N)(2)[Mo6O18N(Naph-1)]的合成,结构表征和超分子组装

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摘要

A novel naphthylimido derivative of hexamolybdate, (Bu4N)(2)[Mo6O18N(Naph-1)] ( 1), was synthesized for the first time by the reaction of octamolybdate ion and 1-naphthyl amine hydrochloride with DCC (N, N,-dicyclohexylcarbodiimide) as a dehydrating agent. The ultraviolet-visible absorption spectrum shows the lowest energy electronic transition of 1 occurs at 383 nm, which is dramatically red-shifted compared to that of [Mo6O19](2-) and other monosubstituted phenylimido hexamolybdates reported in the literature. Moreover, cyclic voltammetry studies on compound 1 show the reversible reduction wave at - 0.53 V, which is cathodically shifted relative to that of [Mo6O19](2-). Another interesting characteristic of 1 is that the cluster anions form supramolecular 1D chains via C- H center dot center dot center dot O hydrogen bonding interactions.
机译:八钼酸根离子与1-萘胺盐酸盐与DCC(N,N, -二环己基碳二亚胺)作为脱水剂。紫外可见吸收光谱显示最低的能量电子跃迁1发生在383 nm处,与[Mo6O19](2-)和文献中报道的其他单取代的苯基亚氨基六钼酸盐相比,它发生了显着的红移。此外,对化合物1的循环伏安研究表明,在-0.53 V时可逆还原波相对于[Mo6O19](2-)的还原性阴极移动。 1的另一个有趣特征是,簇状阴离子通过CH-H中心点中心点中心点O的氢键相互作用形成超分子1D链。

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