Affiliation:
1. Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China
2. University of Chinese Academy of Sciences Beijing 100084 China
Abstract
AbstractAlthough the chemistry of macrocyclic arenes has seen rapid development in recent years, the synthesis of new macrocyclic arenes from aromatic rings with no directing groups remains a challenge. In this work, a new macrocyclic arene, naphth[4]arene (NA[4]A), composed of four naphthalene rings bridged by methylene groups, was synthesized using macrocycle‐to‐macrocycle conversion. NA[4]A shows 1,3‐alternate and 1,2‐alternate conformations in the solid state, which can be selectively obtained. By supramolecular co‐assembly of NA[4]A and 1,2,4,5‐tetracyanobenzene (TCNB) in different concentrations and temperatures, two conformation‐dependent crystalline luminescent co‐assemblies 1,2‐NTC and 1,3‐NTC can be selectively prepared. Interestingly, the two charge‐transfer crystalline assemblies containing NA[4]A with different conformations show bright yellow and green fluorescence, and also display high photoluminescence quantum yields (PLQYs) of 45 % and 43 %. Furthermore, they exhibit color‐tunable two‐photon excited upconversion emission.
Funder
National Natural Science Foundation of China
Youth Innovation Promotion Association of the Chinese Academy of Sciences
Subject
General Chemistry,Catalysis
Cited by
21 articles.
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