Ionic liquid crystals with aggregation-induced emission properties based on pyrrolo[3,2-]pyrrole salt compounds

The present work reports the synthesis, optical properties and mesomorphism of two viologen derivatives DPP-2Py-9 and DPP-2Py-5 of 4,4′-((2,5-diphenylpyrrolo[3,2- b ]pyrrole-1,4-diyl)bis(4,1-phenylene))bis(1-pyridin-1-ium) 4-toluenesulfonate. Both DPP-2Py-5 and DPP-2Py-9 showed aggregation-induced e...

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Veröffentlicht in:Materials chemistry frontiers 2019-07, Vol.3 (7), p.1385-139
Hauptverfasser: Peng, Zhe, Dai, Shuangxiong, Ji, Yingchun, Tong, Bin, Shi, Jianbing, Cai, Zhengxu, Zhi, Junge, Dong, Yuping
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Sprache:eng
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Zusammenfassung:The present work reports the synthesis, optical properties and mesomorphism of two viologen derivatives DPP-2Py-9 and DPP-2Py-5 of 4,4′-((2,5-diphenylpyrrolo[3,2- b ]pyrrole-1,4-diyl)bis(4,1-phenylene))bis(1-pyridin-1-ium) 4-toluenesulfonate. Both DPP-2Py-5 and DPP-2Py-9 showed aggregation-induced emission (AIE) characteristics indicating that the phenyl pyrrolo[3,2- b ]pyrrole core acts as an AIE unit in their salt compounds. DPP-2Py-5 did not show liquid crystalline properties due to the shorter alkoxy chains. DPP-2Py-9 was a liquid crystalline compound with smectic A mesophase, showing marble-like textures observed at 185 °C during the cooling process. DPP-2Py-9 exhibited different emission behaviors in different aggregation states controlled by the change of temperature. The PL intensity of DPP-2Py-9 gradually decreased and the wavelength showed a hypochromic shift as the temperature increased. The most obvious variation of the wavelength occurred in the liquid crystalline range. The liquid crystalline temperature range between 185 and 210 °C determined by the differential curve of PL wavelength vs. temperature was similar to that measured by the DSC technique. Therefore, PL emission spectroscopy could be used as a technical method to characterize the liquid crystalline behaviors. The emission behaviors of AIE-ILC molecules ( DPP-2Py-9 ) in different aggregation states were affected by their molecular stacking arrangements.
ISSN:2052-1537
2052-1537
DOI:10.1039/c9qm00208a