Manipulating noncovalent conformational lock via side‐chain engineering for luminescence at aggregate level
The unfavorable photochemical processes at the molecular level have become a barrier limiting the use of aromatic amides as high‐performance luminescent materials. Herein, we propose a reliable strategy for manipulating noncovalent conformational lock (NCL) via side‐chain engineering to burst out ey...
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| Published in | Aggregate (Hoboken) Vol. 5; no. 4 |
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| Main Authors | , , , , , , , , , |
| Format | Journal Article |
| Language | English |
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01.08.2024
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| Abstract | The unfavorable photochemical processes at the molecular level have become a barrier limiting the use of aromatic amides as high‐performance luminescent materials. Herein, we propose a reliable strategy for manipulating noncovalent conformational lock (NCL) via side‐chain engineering to burst out eye‐catching luminescence at the aggregate level. Contrary to the invisible emission in dilute solutions, dyad OO with a three‐centered H‐bond gave the wondrous crystallization‐induced emission with a quantum yield of 66.8% and clusterization‐triggered emission, which were much brighter than those of isomers. Theoretical calculations demonstrate that crystallization‐induced planarized intramolecular charge transfer (PICT), conformation rigidification, and through‐space conjugation (TSC) are responsible for aggregate‐state luminescence. Robust NCL composed of intramolecular N‐H···O interactions could boost molecular rigidity and planarity, thus greatly facilitating PICT and TSC. This study would inspire researchers to design efficient luminescent materials at the aggregate level via rational conformational control.
The planarized intramolecular charge transfer and through‐space conjugation enabled the wondrous crystallization‐induced and clusterization‐triggered emissions in aromatic amide. Rational manipulating noncovalent conformational lock via side‐chain engineering was proposed to burst out the eye‐catching aggregate‐state luminescence. This study would inspire researchers to acquire strong emission at aggregate level via rational conformational control. |
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| AbstractList | The unfavorable photochemical processes at the molecular level have become a barrier limiting the use of aromatic amides as high‐performance luminescent materials. Herein, we propose a reliable strategy for manipulating noncovalent conformational lock (NCL) via side‐chain engineering to burst out eye‐catching luminescence at the aggregate level. Contrary to the invisible emission in dilute solutions, dyad OO with a three‐centered H‐bond gave the wondrous crystallization‐induced emission with a quantum yield of 66.8% and clusterization‐triggered emission, which were much brighter than those of isomers. Theoretical calculations demonstrate that crystallization‐induced planarized intramolecular charge transfer (PICT), conformation rigidification, and through‐space conjugation (TSC) are responsible for aggregate‐state luminescence. Robust NCL composed of intramolecular N‐H···O interactions could boost molecular rigidity and planarity, thus greatly facilitating PICT and TSC. This study would inspire researchers to design efficient luminescent materials at the aggregate level via rational conformational control.
The planarized intramolecular charge transfer and through‐space conjugation enabled the wondrous crystallization‐induced and clusterization‐triggered emissions in aromatic amide. Rational manipulating noncovalent conformational lock via side‐chain engineering was proposed to burst out the eye‐catching aggregate‐state luminescence. This study would inspire researchers to acquire strong emission at aggregate level via rational conformational control. Abstract The unfavorable photochemical processes at the molecular level have become a barrier limiting the use of aromatic amides as high‐performance luminescent materials. Herein, we propose a reliable strategy for manipulating noncovalent conformational lock (NCL) via side‐chain engineering to burst out eye‐catching luminescence at the aggregate level. Contrary to the invisible emission in dilute solutions, dyad OO with a three‐centered H‐bond gave the wondrous crystallization‐induced emission with a quantum yield of 66.8% and clusterization‐triggered emission, which were much brighter than those of isomers. Theoretical calculations demonstrate that crystallization‐induced planarized intramolecular charge transfer (PICT), conformation rigidification, and through‐space conjugation (TSC) are responsible for aggregate‐state luminescence. Robust NCL composed of intramolecular N‐H···O interactions could boost molecular rigidity and planarity, thus greatly facilitating PICT and TSC. This study would inspire researchers to design efficient luminescent materials at the aggregate level via rational conformational control. |
| Author | Huo, Yanping Zhang, Haoke Mu, Yingxiao Ye, Zecong Lu, Ziying Xiao, Jingping Ji, Shaomin Zhang, Jianyu Lian, Mingbing Tang, Ben Zhong |
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| Notes | Mingbing Lian and Yingxiao Mu contributed equally to this work. |
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| Snippet | The unfavorable photochemical processes at the molecular level have become a barrier limiting the use of aromatic amides as high‐performance luminescent... Abstract The unfavorable photochemical processes at the molecular level have become a barrier limiting the use of aromatic amides as high‐performance... |
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| SubjectTerms | aromatic amide clusterization‐triggered emission crystallization‐induced emission noncovalent conformational lock side‐chain engineering |
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| Title | Manipulating noncovalent conformational lock via side‐chain engineering for luminescence at aggregate level |
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