Near‐Infrared and Dual Emissions of Diphenylamino Group‐Substituted Malachite Green Derivatives
Near‐Infrared and Dual Emissions of Diphenylamino Group‐Substituted Malachite Green Derivatives
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二苯氨基取代的孔雀石绿衍生物的近红外和双发射
DOI:
10.1002/ejoc.202200873
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发表时间:
2022
影响因子:
2.8
通讯作者:
Kuninobu Yoichiro
中科院分区:
文献类型:
--
作者:
Mori Toshiaki;Sekine Kohei;Kawashima Kyohei;Mori Toshifumi;Kuninobu Yoichiro
Novel triarylmethanols and triarylmethyl cations with diphenylamino groups were designed and synthesized. The triarylmethyl cations exhibited near‐infrared (NIR) emission in toluene solution, solid film state, and polystyrene (PS) film. The emission intensities of the triarylmethyl cations were strongest in the PS film. The relative quantum yield of the PS film increased as the number of diphenylamino groups increased. In addition, triarylmethanols exhibit dual emission in their aggregated state owing to the intermolecular interactions between triphenyl amine moieties and/or hydroxy groups. These findings are interesting because NIR and dual emissions are not observed in the dimethylamino group‐substituted triarylmethyl cation, which is referred to as the “malachite green,” and the corresponding triarylmethanol, respectively.