Yu Yang, Yang Guojian, Zhang Shengrui, Liu Mo, Xu Shujue, Wang Chunyu, Li Minjie, Zhang Sean Xiao-An
State Key Lab of Supramolecular Structure and Materials, College of Chemistry, Jilin University, 130012 Changchun, People's Republic of China.
ACS Nano. 2022 Jan 25;16(1):148-159. doi: 10.1021/acsnano.1c04693. Epub 2021 Dec 13.
Circular dichroism (CD) chiral sensing is very promising to meet the ever-increasing demands for high-throughput chiral analysis in asymmetric synthesis. However, it is still very challenging to sensitively quantify the composition of enantiomers in a wide concentration range because the existing sensing systems show either linear CD response resultant from stoichiometric chiral transfer or nonlinear CD response resultant from amplified chiral transfer and thus have the drawbacks of low sensitivity and narrow quantification range, respectively. Herein, we propose a sensing system of two-dimensional (2D) Au(I)-thiolate nanosheets. The disordered interligand interactions on the confined surfaces of nanosheets enable the formation of discrete amplified chiral domains around the adsorbed chiral analytes, resulting in a linearly amplified chiral transfer behavior, which provides a solution for highly sensitive and wide-range quantification of enantiomer compositions. Taking (1, 2)-(-)- and (1, 2)-(+)-1,2-diamino cyclohexanes as example analytes, the concentration and full-range enantiomeric excess (ee) values have been quickly determined by adsorbing them on the surface of Au(I)-MPA (MPA: 3-mercaptopropionic acid) nanosheets in the concentration range of 1.0 × 10 to 4.0 × 10 M. By engineering the surface functional groups, Au(I)-thiolate nanosheets can be extended to sense other types of analytes, and several polyols with multiple chiral centers have been sensed by boronic acid functionalized nanosheets at the 10 M level. The high performances, good extendibility, and one-pot high-yield aqueous synthesis ensure these Au(I)-thiolate nanosheets can be developed as a practical and powerful chiral sensing platform.
圆二色性(CD)手性传感在满足不对称合成中对高通量手性分析不断增长的需求方面非常有前景。然而,在宽浓度范围内灵敏地定量对映体的组成仍然极具挑战性,因为现有的传感系统要么显示出化学计量手性转移导致的线性CD响应,要么显示出放大手性转移导致的非线性CD响应,因此分别存在灵敏度低和定量范围窄的缺点。在此,我们提出了一种二维(2D)金(I)硫醇盐纳米片的传感系统。纳米片受限表面上无序的配体间相互作用能够在吸附的手性分析物周围形成离散的放大手性域,从而产生线性放大的手性转移行为,这为对映体组成的高灵敏度和宽范围定量提供了解决方案。以(1,2)-(-)-和(1,2)-(+)-1,2-二氨基环己烷作为示例分析物,通过将它们吸附在金(I)-MPA(MPA:3-巯基丙酸)纳米片表面,在1.0×10至4.0×10 M的浓度范围内快速测定了浓度和全范围对映体过量(ee)值。通过设计表面官能团,金(I)硫醇盐纳米片可以扩展用于传感其他类型的分析物,硼酸官能化的纳米片已在10 M水平上传感了几种具有多个手性中心的多元醇。这些金(I)硫醇盐纳米片的高性能、良好的可扩展性和一锅法高产率水相合成确保了它们可以被开发成为一个实用且强大的手性传感平台。