EaStCHEM School of Chemistry, University of St Andrews, North Haugh, St Andrews, KY16 9ST, U.K.
J Am Chem Soc. 2022 Aug 10;144(31):14310-14321. doi: 10.1021/jacs.2c05446. Epub 2022 Jul 28.
The future of materials chemistry will be defined by our ability to precisely arrange components that have considerably larger dimensions and more complex compositions than conventional molecular or macromolecular building blocks. However, exerting structural and constitutional control in the assembly of nanoscale entities presents a considerable challenge. Dynamic covalent nanoparticles are emerging as an attractive category of reaction-enabled solution-processable nanosized building block through which the rational principles of molecular synthetic chemistry can be extended into the nanoscale. From a mixture of two hydrazone-based dynamic covalent nanoparticles with complementary reactivity, specific molecular instructions trigger selective assembly of intimately mixed heteromaterial (Au-Pd) aggregates or materials highly enriched in either one of the two core materials. In much the same way as complementary reactivity is exploited in synthetic molecular chemistry, chemospecific nanoparticle-bound reactions dictate building block connectivity; meanwhile, kinetic regioselectivity on the nanoscale regulates the detailed composition of the materials produced. Selectivity, and hence aggregate composition, is sensitive to several system parameters. By characterizing the nanoparticle-bound reactions in isolation, kinetic models of the multiscale assembly network can be constructed. Despite ignoring heterogeneous physical processes such as aggregation and precipitation, these simple kinetic models successfully link the underlying molecular events with the nanoscale assembly outcome, guiding rational optimization to maximize selectivity for each of the three assembly pathways. With such predictive construction strategies, we can anticipate that reaction-enabled nanoparticles can become fully incorporated in the lexicon of synthetic chemistry, ultimately establishing a synthetic science that manipulates molecular and nanoscale components with equal proficiency.
材料化学的未来将取决于我们能否精确地排列具有比传统分子或高分子构建块大得多的尺寸和更复杂组成的组件。然而,在纳米级实体的组装中施加结构和组成控制是一个相当大的挑战。动态共价纳米颗粒作为一类有吸引力的反应型可溶液加工的纳米级构建块出现,通过这种构建块,可以将分子合成化学的合理原理扩展到纳米尺度。从两种具有互补反应性的腙基动态共价纳米颗粒的混合物中,特定的分子指令会触发紧密混合的异质材料(Au-Pd)聚集体或两种核心材料之一高度富集的材料的选择性组装。就像互补反应性在合成分子化学中得到利用一样,化学特异性纳米颗粒结合反应决定了构建块的连接性;同时,纳米尺度上的动力学区域选择性调节了所生成材料的详细组成。选择性,因此聚集组成,对几个系统参数敏感。通过单独表征纳米颗粒结合反应,可以构建多尺度组装网络的动力学模型。尽管忽略了聚集和沉淀等异质物理过程,但这些简单的动力学模型成功地将底层分子事件与纳米级组装结果联系起来,指导合理优化以最大化三种组装途径中的每一种的选择性。通过这种具有预测性的构建策略,我们可以预期反应型纳米颗粒可以完全纳入合成化学的词汇中,最终建立一种能够同等熟练地操纵分子和纳米级组件的合成科学。