In 2020 PHOTOCH PHOTOBIO SCI published article about AGGREGATION-INDUCED EMISSION; MECHANOCHROMIC LUMINESCENCE; FLUORESCENCE; INTERCALATION; ADSORPTION; COMPLEXES; TETRAMETHYLAMMONIUM; DESIGN; MICA; DYE in [Okada, Tomohiko] Shinshu Univ, Res Initiat Supra Mat, Nagano 3808553, Japan; [Okada, Tomohiko; Miyamoto, Yoko; Kurihara, Haruka] Shinshu Univ, Dept Chem & Mat Engn, Nagano 3808553, Japan; [Mochiduki, Yoshifumi; Katsumi, Shiho; Ito, Fuyuki] Shinshu Univ, Inst Educ, Nagano 3808544, Japan in 2020, Cited 48. The Name is Ethyl nicotinate. Through research, I have a further understanding and discovery of 614-18-6. Safety of Ethyl nicotinate
Electrostatic interactions between a quaternary pyridyl-beta-diketonate and anionic charged nanosheets were observed to produce a highly emissive dispersion in a rich water solution. A greater fluorescence quantum yield of approximately 50% was obtained when a luminogenic beta-diketonate, 1-(4-methoxyphenyl)-3-(3-hydroxyethyl-pyridinium bromide)-1,3-propandione (prepared by the Claisen condensation reaction and subsequent quaternization), was molecularly dispersed and enclosed by a couple of atomically flat ultrathin (approximately 1.0 nm) silicate sheets of anionic layered clay. By accommodating beta-diketonate into a narrow interlamellar space (approximately 0.4 nm distance), the molecular motion was suppressed, as confirmed by a smaller non-radiative relaxation rate constant, which was obtained by time-resolved luminescence and quantum yield measurements. Because the dense packing of beta-diketonate quenched the excited state, the isolation of luminogens by the co-adsorption of photochemical inert cations (tetramethylammonium and benzylammonium) was prevented by concentration quenching. A lower quantum yield was obtained by expanding the interlayer distance above 1.0 nm by co-adsorbing a photo-inactive water-soluble polymer, poly(vinylpyrrolidone). Therefore, the fixation and spatial separation of beta-diketonate in the narrow interlayer space was determined to be essential for obtaining strong emission.
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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem