Self-reversible mechanofluorochromic AIEgens with tunable solid-state fluorescence: effect of acceptors and intermolecular interactions

被引:1
|
作者
Ravi, Sasikala [1 ]
Priyadharsan, R. Rameshbabu [1 ]
Karthikeyan, Subramanian [2 ]
Pannipara, Mehboobali [3 ]
Al-Sehemi, Abdullah G. [4 ,5 ]
Moon, Dohyun [6 ]
Anthony, Savarimuthu Philip [1 ]
机构
[1] SASTRA Deemed Univ, Sch Chem & Biotechnol, Thanjavur 613401, Tamil Nadu, India
[2] Bharathidasan Univ, Khadir Mohideen Coll, PG & Res Dept Chem, Adirampattinam 614701, Tamil Nadu, India
[3] King Khalid Univ, Cent Labs, Abha, Saudi Arabia
[4] King Khalid Univ, Dept Chem, Abha 61413, Saudi Arabia
[5] King Khalid Univ, Res Ctr Adv Mat Sci, Abha 61413, Saudi Arabia
[6] Pohang Accelerator Lab, Beamline Dept, 80 Jigokro 127beongil, Pohang, Gyeongbuk, South Korea
关键词
AGGREGATION-INDUCED EMISSION; FLUOROPHORES;
D O I
10.1039/d4ce00729h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Exploring the organic molecular structural features and supramolecular interactions provide basis for developing stimuli-responsive organic solid-state fluorescent materials. Herein, we have synthesized methoxyphenyl-substituted carbazole-based pi-conjugated derivatives (Cz-MN, Cz-ECA, Cz-CA, Cz-CAA and Cz-NBA) with different acceptor units and investigated their influence on solid-state fluorescence. All five compounds showed aggregation-induced emission (AIE) in the solid state with acceptor-dependent tunable fluorescence from 488 to 602 nm (quantum yield (Phi f) = 7.2 to 1.9%). Cz-ECA exhibited blue-shifted fluorescence, whereas Cz-NBA showed red-shifted fluorescence. Cz-MN, Cz-ECA and Cz-CA revealed relatively strong solid-state fluorescence compared to Cz-CAA and Cz-NBA. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) calculations suggested intramolecular charge transfer (ICT) from the carbazole donor to the acceptor unit. Mechanofluorochromic studies of Cz-MN and Cz-ECA showed self-reversible fluorescence switching but the other three AIEgens did not show any stimuli-response. Single crystal structural analysis of Cz-MN, Cz-ECA and Cz-CA showed twisted molecular conformations with different intermolecular interactions. Both Cz-MN and Cz-ECA did not show any strong intermolecular interactions in the crystal lattice. In contrast, Cz-CA exhibited strong amide-amide complementary H-bonding and an extended network structure. Hence, the twisted molecular conformation and the absence of strong intermolecular interactions in Cz-MN and Cz-ECA contributed to self-reversible mechanofluorochromism (MFC). Thus, the present study is expected to provide further insight to design AIEgens with stimuli-responsive self-reversible fluorescent materials. The intermolecular interacting functionality in the carbazole-based pi-conjugated fluorophores controlled mechano-responsive fluorescence switching.
引用
收藏
页码:5241 / 5248
页数:8
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