光电开关
光致变色
光稳态
材料科学
热的
密度泛函理论
化学物理
热致变色
响应时间
光电子学
双稳态
热稳定性
时间常数
放松(心理学)
纳米技术
光化学
化学
计算化学
计算机科学
热力学
物理
有机化学
心理学
光异构化
催化作用
社会心理学
工程类
异构化
计算机图形学(图像)
电气工程
作者
Simon Ludwanowski,Meral Arı,Karsten Parison,Somar Kalthoum,Paula Straub,Nils Pompe,Stefan Weber,Michael Walter,Andreas Walther
标识
DOI:10.1002/chem.202000659
摘要
Abstract Arylazopyrazoles are an emerging class of photoswitches with redshifted switching wavelength, high photostationary states, long thermal half‐lives and facile synthetic access. Understanding pathways for a simple modulation of the thermal half‐lives, while keeping other parameters of interest constant, is an important aspect for out‐of‐equilibrium systems design and applications. Here, it is demonstrated that the thermal half‐life of a water‐soluble PEG‐tethered arylazo‐bis( o ‐methylated)pyrazole (AAP) can be tuned by more than five orders of magnitude using simple pH adjustment, which is beyond the tunability of azobenzenes. The mechanism of thermal relaxation is investigated by thorough spectroscopic analyses and density functional theory (DFT) calculations. Finally, the concepts of a tunable half‐life are transferred from the molecular scale to the material scale. Based on the photochromic characteristics of E ‐ and Z ‐AAP, transient information storage is showcased in form of light‐written patterns inside films cast from different pH, which in turn leads to different times of storage. With respect to prospective precisely tunable materials and time‐programmed out‐of‐equilibrium systems, an externally tunable half‐life is likely advantageous over changing the entire system by the replacement of the photoswitch.
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