Gu Zehao, Lu Mengfan, Feng Kai, Jin Zhaoxia
Department of Chemistry, Renmin University of China, Beijing 100872, People's Republic of China.
Nanoscale. 2021 May 7;13(17):8174-8180. doi: 10.1039/d1nr00946j. Epub 2021 Apr 21.
Cellulose nanocrystals (CNCs) are inherently right-handed nanostructures that originate from nature, showing chirality in their fibrils, bundles, and self-assembled films. However, the enantio-specific interaction between CNCs and other chiral molecules has not been explored so far. In this study, we first demonstrated a chirality-related difference in the composite films of cellulose nanocrystals and histidine with a d- or l-configuration. The distinction is not only presented in the self-assembled nanostructures of CNCs, optical properties, and the thermal decomposition of composites but also in the crystallization of the amino acid. We suppose that it might have originated from the packing of amino acids on the twisted surface of CNCs. The knowledge about the enantio-specific interaction between the chiral amino acid and polysaccharide nanostructure is of significant importance for developing a new strategy for enantiomeric separation.
纤维素纳米晶体(CNCs)是天然存在的右旋纳米结构,其原纤维、纤维束和自组装薄膜均表现出手性。然而,迄今为止尚未探索CNCs与其他手性分子之间的对映体特异性相互作用。在本研究中,我们首次证明了具有d-或l-构型的纤维素纳米晶体与组氨酸的复合薄膜中存在与手性相关的差异。这种差异不仅体现在CNCs的自组装纳米结构、光学性质以及复合材料的热分解中,还体现在氨基酸的结晶过程中。我们推测这可能源于氨基酸在CNCs扭曲表面上的堆积。关于手性氨基酸与多糖纳米结构之间对映体特异性相互作用的知识对于开发对映体分离的新策略具有重要意义。