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Polymorphism and light conversion properties of anthracene-based isomers

Polymorphism is playing a more important role in revealing the relationships between intermolecular arrangement, stacking and optical properties of luminogens, however, obtaining of polymorphism depends more on luck and accident. Here, two isomers named as 1APPA and 2APPA were designed and synthesiz...

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Published in:Dyes and pigments 2022-01, Vol.197, p.109888, Article 109888
Main Authors: Wang, Yongtao, Qian, Zhean, Li, Xueming, Qin, Anjun, Guo, Yanjun, Tang, Benzhong
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description Polymorphism is playing a more important role in revealing the relationships between intermolecular arrangement, stacking and optical properties of luminogens, however, obtaining of polymorphism depends more on luck and accident. Here, two isomers named as 1APPA and 2APPA were designed and synthesized by furnishing twisted cyanostilbene backbone with planar anthracene unit. The two luminogens show similar solvatochromism and inconspicuous mechanochromism, but different in terms of AIEE activity and polymorphism. Only one crystal is obtained for 1APPA, while needle-like colorless 2APPA-c (kinetic control) and yellow massive 2APPA-y (thermodynamic control) can be obtained for 2APPA in the same solvents, significantly, their crystal growth has good repeatability. Theoretical calculation, solvatochromism combined with crystal analysis further confirm intramolecular charge transfer (ICT) effect from anthracene donor to cyanostilbene acceptor takes responsible for different polymorphism between 1APPA and 2APPA. Crystal analysis indicates that π-π stacking between adjacent anthracene unit leads to red-shifted fluorescence emission for 2APPA-y than 1APPA and 2APPA-c, while twisted molecular configuration, stable crystal phase and high fluorescence quantum yield are attributed to strong intermolecular hydrogen bonds and weak interactions. Besides, 2APPA can be used as potential light conversion agent due to matching fluorescence emission (485 nm), high fluorescence efficiency (0.52) and excellent photostability, and 93.9% of the initial intensity is reserved for 2APPA film after UV radiation of 20 h. •Isomers 1APPA and 2APPA show different polymorphism and AIEE activity.•Crystallization of 2APPA-c and 2APPA-y are kinetic and thermodynamic control in turn.•The internal mechanism of polymorphism is discussed in detail.•Crystal 2APPA-y with intermolecularπ-π stacking show high PLQY (0.72).•2APPA are excellent light conversion agents for agricultural film.
doi_str_mv 10.1016/j.dyepig.2021.109888
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Here, two isomers named as 1APPA and 2APPA were designed and synthesized by furnishing twisted cyanostilbene backbone with planar anthracene unit. The two luminogens show similar solvatochromism and inconspicuous mechanochromism, but different in terms of AIEE activity and polymorphism. Only one crystal is obtained for 1APPA, while needle-like colorless 2APPA-c (kinetic control) and yellow massive 2APPA-y (thermodynamic control) can be obtained for 2APPA in the same solvents, significantly, their crystal growth has good repeatability. Theoretical calculation, solvatochromism combined with crystal analysis further confirm intramolecular charge transfer (ICT) effect from anthracene donor to cyanostilbene acceptor takes responsible for different polymorphism between 1APPA and 2APPA. Crystal analysis indicates that π-π stacking between adjacent anthracene unit leads to red-shifted fluorescence emission for 2APPA-y than 1APPA and 2APPA-c, while twisted molecular configuration, stable crystal phase and high fluorescence quantum yield are attributed to strong intermolecular hydrogen bonds and weak interactions. 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Crystal analysis indicates that π-π stacking between adjacent anthracene unit leads to red-shifted fluorescence emission for 2APPA-y than 1APPA and 2APPA-c, while twisted molecular configuration, stable crystal phase and high fluorescence quantum yield are attributed to strong intermolecular hydrogen bonds and weak interactions. Besides, 2APPA can be used as potential light conversion agent due to matching fluorescence emission (485 nm), high fluorescence efficiency (0.52) and excellent photostability, and 93.9% of the initial intensity is reserved for 2APPA film after UV radiation of 20 h. •Isomers 1APPA and 2APPA show different polymorphism and AIEE activity.•Crystallization of 2APPA-c and 2APPA-y are kinetic and thermodynamic control in turn.•The internal mechanism of polymorphism is discussed in detail.•Crystal 2APPA-y with intermolecularπ-π stacking show high PLQY (0.72).•2APPA are excellent light conversion agents for agricultural film.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.dyepig.2021.109888</doi></addata></record>
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subjects AIEE
Anthracene derivatives
Cyanostilbene derivatives
Isomers
Light conversion agent
Polymorphism
title Polymorphism and light conversion properties of anthracene-based isomers
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