Department of Chemistry, UGC Sponsored Centre for Advanced Studies-II, Guru Nanak Dev University, Amritsar, 143005, Punjab, India.
Angew Chem Int Ed Engl. 2019 Nov 4;58(45):16203-16209. doi: 10.1002/anie.201908669. Epub 2019 Sep 25.
The development of synthetic helical structures undergoing stimuli-responsive chirality transformations is important for an understanding of the role of chirality in natural systems. However, controlling supramolecular chirality in entropically driven assemblies in aqueous media is challenging. To develop stimuli-responsive assemblies, we designed and synthesized pyrazine derivatives with l-alanine groups as chiral building blocks. These systems undergo self-assembly in aqueous media to generate helical fibers and the embedded alanine groups transfer their chirality to the assembled structures. Furthermore, these helical fibers undergo a Ni -induced chirality transformation. The study demonstrates the role of intermolecular hydrogen bonding, π-π stacking, and the hydrophobic effect in the Ni -mediated transition of helical fibers to supercoiled helical ensembles which mimic the formation of superstructures in biopolymers.
发展对刺激响应手性转变有响应的合成螺旋结构对于理解手性在自然系统中的作用很重要。然而,在水相中的熵驱动组装中控制超分子手性具有挑战性。为了开发对刺激有响应的组装体,我们设计并合成了具有 l-丙氨酸基团的吡嗪衍生物作为手性构建块。这些体系在水相介质中自组装生成螺旋纤维,并且嵌入的丙氨酸基团将其手性转移到组装结构中。此外,这些螺旋纤维经历 Ni 诱导的手性转变。该研究表明了分子间氢键、π-π 堆积和疏水作用在 Ni 介导的螺旋纤维到超螺旋螺旋聚集体的转变中的作用,这种转变模拟了生物聚合物中超结构的形成。