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基于配位驱动的超分子金属环的紧密组装来构筑延展的金属有机堆积超分子组装体。

Coordination-Driven Syntheses of Compact Supramolecular Metallacycles toward Extended Metallo-organic Stacked Supramolecular Assemblies.

机构信息

"Institut des Sciences Chimiques de Rennes", UMR 6226-CNRS, Université de Rennes 1 , Campus de Beaulieu, 35042 Cedex Rennes, France.

INSA de Rennes , 20 Avenue des buttes de Coësmes, 35708 Rennes France.

出版信息

Acc Chem Res. 2017 Apr 18;50(4):885-894. doi: 10.1021/acs.accounts.6b00624. Epub 2017 Mar 6.

Abstract

One important concept associated with supramolecular chemistry is supramolecular self-assembly, which deals with the way discrete individual components interact via intermolecular interactions in order to build, upon their spontaneous association, high order functional assemblies. The accumulation of these very simple and localized noncovalent interactions (such as H-bonding, dipole-dipole, hydrophobic/hydrophilic, van der Waals, π-π, π-CH, etc.) is ubiquitous in the complexity of natural systems (such as DNA, proteins, membranes, micelles, etc.). It can also be transposed to the directed synthesis of intricate artificial scaffolds, which have anticipated geometries and properties. Among the synthetic strategies based on this concept, coordination-driven supramolecular chemistry uses the robust, reversible, and directional metal-to-ligand coordinative bond to build discrete metallo-supramolecular architectures. Within the last two decades, coordination-driven supramolecular chemistry has proved to be one of the most powerful contemporary synthetic approaches and has provided a significant number of increasingly complex supramolecular assemblies, which have predetermined sizes and geometries. While much focus has been devoted to architectures bearing internal cavities for host-guest chemistry or to generate specific reactivity, particular attention can also be paid to compact supramolecular assemblies given that their specific structures are characterized by peculiar synthetic guiding rules as well as by alternative long-range self-assembling properties. This Account describes how a preassembled Cu bimetallic clip bearing short intermetallic distances can be used as a U-shaped molecular clip to give general and versatile access to a large variety of original compact supramolecular metallacycles. When this Cu precursor is reacted with various cyano-capped ditopic linkers that have increasing lengths and complexities, specific effects guiding the selective and straightforward syntheses of such compact supramolecular objects are highlighted. Whereas a subtle compromise between the length of the ditopic linkers and the steric bulk of the molecular clip appears to be a purely stereogeometric preliminary parameter to master, lateral interlinker interactions (π-π stacking interactions or aurophilic interactions depending on the nature of the internal cores of the linkers) can circumvent these constraints regardless of the length of the linkers and allow the selective formation of new compact supramolecular structures. Generally, such derivatives presented a strong tendency to self-assemble in the solid state due to inter-supramolecule interactions. This approach thus opens a new door toward molecular materials having an attractive solid state structure for potential applications related to charge carrier mobility and luminescence properties. These compact supramolecular assemblies can therefore be considered as original secondary binding units directing the predictive preparation of such extended networks. The on-purpose design of original building blocks bearing specific cores allowed the formation of new compact supramolecular metallacycles such as "U-shaped" π-stacked assemblies or "pseudodouble paracyclophanes". Similarly, the control of the secondary structure of one-dimensional coordination polymers alternating π-stacked compact supramolecular metallacycles was also conducted. The results that are discussed in this Account illustrate how the rational design of both preassembled polymetallic precursors bearing short intermetallic distances and ditopic linkers able to induce cumulative lateral weak interactions can implement the general synthetic guiding rules of coordination driven supramolecular chemistry. This opens perspectives to use such compact supramolecular assemblies as secondary building blocks for the design of long-range organized functional molecular materials that have predictable architectures and targeted properties.

摘要

超分子化学的一个重要概念是超分子自组装,它涉及离散的单个组件如何通过分子间相互作用相互作用,以在它们自发缔合的基础上构建高级功能组装体。这些非常简单和局部的非共价相互作用(如氢键、偶极-偶极、疏水/亲水、范德华、π-π、π-CH 等)的积累在复杂的自然系统(如 DNA、蛋白质、膜、胶束等)中无处不在。它也可以转化为复杂人工支架的定向合成,这些支架具有预期的几何形状和性质。在基于这种概念的合成策略中,配位驱动的超分子化学利用坚固、可逆和定向的金属-配体配位键来构建离散的金属超分子结构。在过去的二十年中,配位驱动的超分子化学已被证明是最强大的当代合成方法之一,并提供了越来越多的复杂超分子组装体,这些组装体具有预定的大小和几何形状。虽然人们对具有内部空腔的主体-客体化学的结构或生成特定反应性的结构给予了很大的关注,但也可以特别关注紧凑的超分子组装体,因为它们的特定结构具有独特的合成指导规则以及替代的远程自组装特性。本说明描述了如何使用带有短金属间距离的预组装 Cu 双金属夹作为 U 形分子夹,方便地获得各种原始紧凑的超分子金属环。当将这种 Cu 前体与各种具有增加长度和复杂性的氰基封端的双齿配体反应时,突出了指导这些紧凑的超分子客体选择性和直接合成的特定效应。尽管双齿配体的长度和分子夹的空间位阻之间的细微折衷似乎是一个纯粹的立体几何初步参数,但配体内部核心的性质决定了配体之间的横向相互作用(取决于配体的π-π 堆积相互作用或金相互作用)可以规避这些限制,而不管配体的长度如何,并允许形成新的紧凑超分子结构。通常情况下,这些衍生物由于分子间相互作用,在固态中具有很强的自组装倾向。这种方法为具有吸引力的固态结构的分子材料开辟了新的途径,有望应用于载流子迁移率和发光性能。因此,这些紧凑的超分子组装体可以被视为指导预测制备此类扩展网络的原始次级结合单元。具有特定核心的原始构建块的有目的设计允许形成新的紧凑超分子金属环,例如“U 形”π堆积组装体或“伪双对环芳烃”。同样,还对一维配位聚合物的二级结构进行了控制,这些聚合物交替排列着π堆积的紧凑超分子金属环。本文讨论的结果说明了如何通过合理设计具有短金属间距离的预组装多金属前体和能够诱导累积横向弱相互作用的双齿配体,实现配位驱动超分子化学的一般合成指导规则。这为使用这些紧凑的超分子组装体作为二级构建块来设计具有可预测结构和目标性质的远程组织功能分子材料开辟了前景。

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