材料科学
准分子
苝
单体
二亚胺
位阻效应
聚合物
吸收(声学)
光化学
聚集诱导发射
吸收光谱法
溶剂
化学工程
化学物理
表征(材料科学)
纳米技术
激子
金属有机骨架
晶体结构
混合材料
Crystal(编程语言)
光子晶体
分子
光电子学
光子学
发射光谱
甲基丙烯酸酯
荧光
作者
Mario de la Hoz Tomás,Taito Hashimoto,Boiko Cohen,Yuzuki Murata,Kazuki Shiga,Ryota Hanyu,Ryusei Oketani,Norimitsu Tohnai,Ichiro Hisaki,Abderrazzak Douhal
摘要
ABSTRACT Perylene diimide (PDI) derivatives exhibit outstanding optical and electronic properties, making them a versatile material for photonic applications. Herein, we report on the synthesis and spectroscopic characterization of a novel PDI‐based hydrogen‐bonded organic framework (HOF, CP‐PDI‐1(DCB) ) and related compounds. The HOF assembles into a layered 2D network with slip‐stacked AB packing mediated by CH···π interactions. The absorption and emission spectra of the studied PDI derivatives in solid state, as well as in polymethyl methacrylate (PMMA) matrices, exhibit monomers, aggregates and excimer contribution. Upon solvent removal, CP‐PDI‐1 shows a red‐shifted emission and an enhanced excimer signal, evidencing that structural reorganization affects its photobehavior. Time‐resolved experiments of CP‐PDI‐1 reveal the coexistence of monomer species (0.32 ns) and H‐type aggregates (0.04 ns) that act as precursors to excimer‐like species (5.60 ns). Additionally, the crystal structure of CP‐PDI‐1 promotes the formation of emissive J‐type aggregates (1.65 ns). While excimer formation occurs slowly in PDI‐boron (220 ps) and CP‐PDI‐ester (130 ps) due to steric hindrance, in unsubstituted PDI and CP‐PDI‐1 it takes place in less than 20 ps (in solid state) and 10 ps in suspension. These findings provide key information for the design of advanced PDI‐based optical materials.
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