材料科学
发光
超分子化学
非共价相互作用
对映体
肽
光子学
纳米技术
组合化学
氢键
光电子学
结晶学
分子
立体化学
有机化学
化学
晶体结构
生物化学
作者
Na Li,Li‐Mei Chang,Zhi‐Gang Gu,Jian Zhang
标识
DOI:10.1002/adma.202512857
摘要
Abstract Peptide‐based noncovalent glasses exhibit natural origins, green synthesis conditions, and self‐healing properties, representing a promising sustainable alternative to conventional glasses. However, developing chiral noncovalent peptide glasses with highly circularly polarized luminescence (CPL) is still a challenging task. Herein, a supramolecular‐coordination synergistic induced strategy is reported for constructing enantiomeric noncovalent peptide glasses from carnosine (Car) enantiomers and metal ions (Zn 2+ , Eu 3+ , Tb 3+ , Gd 3+ ) under ambient conditions. The resulting chiral Car(M) peptide glasses not only exhibit high optical transparency (>90%), large sizes, easily processable shapes, and high ambient self‐healing performances, but also show programmable multicolor emission, chiral amplification, and full‐spectrum CPL encoding. Due to the synergistic metal coordination and hydrogen‐bonded supramolecular interactions, the obtained chiral Car(M) glasses reveal record‐high and tunable CPL with dissymmetry factors (|g lum |) up to 0.29. Leveraging the high transparency and multicolor chiral emission of Car(M) glasses, an anti‐counterfeiting platform is demonstrated including flexible multicolor QR codes, filter‐resolved patterns, polarization‐sensitive Morse codes, and programmable dot‐array encryption. This work fabricates new chiral noncovalent peptide glasses that exhibit rapid self‐healing capabilities and high, tunable CPL performance, thereby pioneering a novel avenue for chiral photonic applications.
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