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首页> 外文期刊>Chemistry of Materials: A Publication of the American Chemistry Society >Metallosupramolecular Side-Chain Polymers and Polyelectrolyte- Metallosupramolecular Surfactant Complexes
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Metallosupramolecular Side-Chain Polymers and Polyelectrolyte- Metallosupramolecular Surfactant Complexes

机译:金属超分子侧链聚合物和聚电解质-金属超表面活性剂复合物

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摘要

Metal coordination has been exploited extensively in supramolecular chemistry, and the creation of supramo-lecular polymeric materials via metal-ligand bonds is an active area of research. Side-chain type supramolecular polymers are of interest because of the ability of these materials to form liquid-crystalline morphologies, with instances of such materials being created via hydrogen bonding, ionic bonding, metal complexation, and combinations thereof. Indeed, the pace of research on polymers with side-chains attached by metal coordination is accelera- ting. In 2005, several of us published the syntheses of metallosupramolecular polymers (MSPs) bearing alkyl-chain decorated dendrons attached to main chains via a terpyridine-Ru-terpyridine (Ru(tpy)2) complexation strategy. More recently, Aamer and Tew reported the synthesis and morphological characterization of two very similar MSPs, also based on polymers bearing pendant tpy groups. The first, in which the polymer was complexed with a simple terpyridine group, showed no mesomorphic structure, whereas the second, in which a C16 alkyl tail was attached to the su-pramolecularly bound terpyridine group, was shown to self-organize into a hexagonal columnar morphology, with some crystallization occurring between the C16 tails. This latter material was also shown to display nematic lyotropic behavior in concentrated solution.
机译:金属配位已经在超分子化学中得到了广泛的利用,并且通过金属-配体键形成超分子聚合物材料是一个活跃的研究领域。侧链型超分子聚合物是令人关注的,因为这些材料具有形成液晶形态的能力,这种材料是通过氢键,离子键,金属络合及其组合形成的。的确,对通过金属配位连接有侧链的聚合物的研究步伐正在加快。在2005年,我们中的一些人发表了通过叔吡啶-Ru-叔吡啶(Ru(tpy)2)络合策略连接主链的烷基链装饰树突的金属超分子聚合物(MSP)的合成。最近,Aamer和Tew报告了两种非常相似的MSP的合成和形态学表征,它们也是基于带有tpy侧基的聚合物。第一种,其中聚合物与简单的三联吡啶基团络合,未显示任何介晶结构,而第二种,其中C16烷基尾部连接至超分子结合的三联吡啶基团,显示出自组织成六边形柱状形态,在C16尾部之间有一些结晶。后一种材料还显示出在浓溶液中显示向列型溶致行为。

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