多金属氧酸盐
手性(物理)
材料科学
化学物理
螺旋度
非线性光学
结晶学
同种类的
螺旋(腹足类)
超分子手性
级联
质子化
光谱学
分子物理学
发色团
互惠(文化人类学)
纳米技术
衍射
自组装
非线性光学
纳米结构
作者
Zimo Wang,Junjie Ba,Tong Lu,Xinyao Yin,Yingjin Wei,Yizhan Wang
标识
DOI:10.1002/adfm.202531695
摘要
ABSTRACT Efficient, real‐time amplification of molecular chirality into macroscopic helices using inherently symmetric mediators has rarely been demonstrated. Here, we show that highly symmetric inorganic polyoxometalates efficiently direct the hierarchical amplification of chirality from a simple organic chiral precursor into robust, millimeter‐scale helices. Real‐time optical microscopy captures a stepwise cascade with fast axial elongation, subsequent diameter thickening, and progressive pitch tightening. Multiscale spectroscopy and diffraction link the macroscopic helicity to cooperative ion‐pairing between protonated amines and polyoxometalate, together with measurable packing tightening of the organic domain accompanying homogeneous polyoxometalate incorporation. The resulting helices display enhanced chiroptical responses and second‐order nonlinear optical activity. Our results establish inherently symmetric inorganic mediators for chirality amplification and offer design principles for creating advanced chiral materials with tailored optical functionalities.
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