Tunable Photoluminescence Including White‐Light Emission Based on Noncovalent Interaction‐Locked N, N′‐Disubstituted Dihydrodibenzo[a, c]phenazines. Issue 12 (16th April 2018)

• Record Type: Journal Article
• Authors: Wang, Jie; Yao, Xuyang; Liu, Yang; Zhou, Haitao; Chen, Wei; Sun, Guangchen; Su, Jianhua; Ma, Xiang; Tian, He
• Is Part Of: Advanced optical materials. Volume 6:Issue 12(2018)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2018-04-16
• Subjects: phenazines -- sulfonatocalixarene -- supramolecular assembly -- vibration‐induced emission; Optical materials -- Periodicals; Photonics -- Periodicals; 620.11295
• DOI: 10.1002/adom.201800074
• Languages: English
• ISSNs: 2195-1071

Abstract

Abstract: Utilizing supramolecular assembling system to achieve tunable photoluminescence emission has become an important method for the development of light‐emitting materials, which could bring out intriguing photophysical properties out of the luminophores themselves without a demanding design and tedious chemical synthesis. In the last few years, vibration‐induced emission (VIE) molecules, with dual photoluminescence emissions and large Stokes shift, have shown their talent in generating tunable fluorescence and potential in fabricating novel light‐emitting materials. However, little attention has been devoted to explore the attractive properties of VIE molecules in supramolecular self‐assembling systems up to now. Herein, the first example of a supramolecular assembling system composed of a water‐soluble VIE molecule N, N ′‐diphenyl‐dihydrodibenzo[ a, c ]phenazines derivative (DPAC‐AB) and bis‐ p ‐sulfonatocalix[4]arene (BSC4 ) is introduced. Based on noncovalent interactions including hydrophobic interaction and host–guest interaction betweenDPAC‐AB andBSC4, tunable fluorescence emissions from orange‐red to white (Commission Internationale de L'éclairage (CIE) coordinates (0.32, 0.37)) to blue are achieved by simple addition of different amounts ofBSC4 to the solution ofDPAC‐AB . Additionally, a competitive guest acetylcholine is utilized to recover the nearly orange‐red fluorescence emission. This strategy to efficiently control the emission of VIE molecules through supramolecular assembling based on reversible noncovalent interactions opens new avenues in developing tunable light‐emitting materials. Abstract : The first example of a supramolecular assembling system with water‐soluble N, N ′‐diphenyl‐dihydrodibenzo[ a, c ]phenazines derivative and bis‐ p ‐sulfonatocalix[4]arene is designed. Based on hydrophobic interaction and host–guest interaction, tunable fluorescent emission color from orange‐red to white (CIE coordinates (0.32, 0.37)) to blue can be obtained. Additionally, a common competitive guest is utilized to recover the fluorescent emission.