首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Binding sites on the outside of metallo-supramolecular architectures; engineering coordination polymers from discrete architectures
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Binding sites on the outside of metallo-supramolecular architectures; engineering coordination polymers from discrete architectures

机译:金属-超分子结构外部的结合位点;离散体系结构的工程配位聚合物

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Aggregation of metallo-supramolecular architectures through additional coordination is explored by introducing metal-binding units onto the outside of the supramolecular architectures. This is achieved within the framework of our imine-based approach to supramolecular architecture, by replacing the pyridylimine units with pyrazylketimine units. An advantage of the design is that it retains the ease-of-synthesis which characterises our imine-based approach. Silver(I) complexes of three pyrazylketimine ligand systems are described. The complexes demonstrate that introducing pyrazine donor units does indeed allow higher-order assembly of the distinct supramolecular architectures into engineered coordination polymers. Two distinct types of aggregation are observed. In the first, the donors on the outside of one architecture bind to the metals of another to link the units into a polymeric array. In the second type, the donors on the outside of the architectures bind to separate metal centres which are themselves not part of the architectures, and these separate metal centres link the units to form the macromolecular array. The weaker donor nature of the pyrazine nitrogens (compared to pyridine) also introduces an additional element into the design; higher coordination numbers are favoured and this can lead to arrays with higher connectivity than those observed in the discrete pyridylimine architectures.
机译:通过将金属结合单元引入超分子结构的外部,探索了通过额外配位的金属-超分子结构的聚集。这是在我们基于亚胺的超分子结构方法的框架内实现的,方法是用吡唑基酮亚胺取代吡啶基嘧啶单元。该设计的优点是它保留了易于合成的特征,这是我们基于亚胺的方法的特征。描述了三个吡唑酮亚胺配体系统的银(I)配合物。配合物表明引入吡嗪供体单元确实允许将不同的超分子结构高阶组装为工程配位聚合物。观察到两种不同类型的聚集。首先,一种结构外部的供体与另一种结构的金属结合,从而将单元连接成一个聚合物阵列。在第二种类型中,体系结构外部的供体结合到本身不是体系结构一部分的分离的金属中心,这些分离的金属中心将单元连接起来形成大分子阵列。吡嗪氮的供体性质较弱(与吡啶相比)也为设计引入了其他元素。较高的配位数是有利的,这可以导致阵列具有比在离散的吡啶基嘧啶结构中观察到的阵列更高的连通性。

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