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Noncovalent Synthesis of Nanostructures: Combining Coordination Chemistry and Hydrogen Bonding

机译:纳米结构的非共价合成:配位化学和氢键结合

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摘要

For the synthesis of nanosized particles with structures defined at the molecular level, conventional methods of multistep covalent synthesis have reached their limitations. Consequently, noncovalent synthetic methodologies that equal the precision ofcovalent synthesis but proceed by simple assembly of building blocks are needed. Such methods should be self-correcting under conditions of thermodynamic equilibrium. Zimmerman et al. have exploited hydrogen bonding in the self-assembly of dendrimers centered around a hydrogen-bonded, hexameric nucleus, and we have described a divergent assembly route to dendrimers using coordination chemistry. Hitherto, the combination of two different types of compatible, noncovalent interactions for the assembly offinite nanostructures has not been employed. Here we describe the combined use of hydrogen bonding and coordination chemistry in the assembly of nanosized metallodendrimers with molecular weights of up to. 28 kDa. The combination of three metallodendrimer wedges, constructed by coordination chemistry, into a hydrogen-bonded rosette allows fast and controlled assembly of nanostructures by both divergent and convergent strategies.
机译:对于具有在分子水平上定义的结构的纳米级颗粒的合成,常规的多步共价合成方法已达到其局限性。因此,需要与共价合成的精度相等但通过简单组装构件进行的非共价合成方法。这种方法在热力学平衡条件下应该是自校正的。 Zimmerman等。已经在以氢键结合的六聚体核为中心的树枝状聚合物的自组装中利用了氢键,并且我们已经使用配位化学描述了向树枝状聚合物的发散组装路线。迄今为止,尚未使用两种不同类型的相容性,非共价相互作用的组合来组装有限的纳米结构。在这里,我们描述了氢键结合和配位化学在分子量最大为2的纳米级金属树枝状聚合物组装中的结合使用。 28 kDa。通过配位化学将三个金属树枝状聚合物楔形物结合成氢键玫瑰花结,可以通过发散和收敛策略快速而受控地组装纳米结构。

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