63098-82-8Relevant academic research and scientific papers
Synthesis of azomethines derived from cinnamaldehyde and vanillin: in vitro aetylcholinesterase inhibitory, antioxidant and insilico molecular docking studies
Chigurupati, Sridevi,Selvaraj, Manikandan,Mani, Vasudevan,Mohammad, Jahidul I.,Selvarajan, Kesavanarayanan K.,Akhtar, Shaikh S.,Marikannan, Maharajan,Raj, Suthakaran,Teh, Lay K.,Salleh, Mohd Z.
, p. 807 - 816 (2017/11/16)
In the present study, we report the synthesis of azomethines derived from cinnamaldehyde (C1–C3) and vanillin (V1–V3) using ethanol as a green solvent in the presence of triethyl amine. The synthesized compounds were characterized and investigated for the
Fluorescent probe for identifying superoxide anions, preparation method and application thereof, optical fiber probe and preparation method of optical fiber probe
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Paragraph 0052-0057, (2017/10/07)
The invention relates to a fluorescent probe for identifying superoxide anions, a preparation method and an application thereof, an optical fiber probe and a preparation method of the optical fiber probe, and belongs to the technical field of fluorescent
Synthesis, composition and use of novel therapeutic and cosmetic Schiff base products formed by reaction of a carbonyl containing moeity with a transimination nucleophilic catalyst and the use of transimination nucleophilic catalysts to increase the rate
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Page/Page column 37; 38, (2016/09/26)
The present invention relates to the synthesis, composition and use of novel moieties formed by reacting a transimination nucleophilic catalyst, molecular or polymeric, with carbonyl-containing therapeutic or cosmetic moieties. The resultant Schiff base p
Azo-coupled zinc phthalocyanines: Towards broad absorption and application in dye-sensitized solar cells
Han, Mingliang,Zhang, Xuejun,Zhang, Xiaoxia,Liao, Chaoqiang,Zhu, Baiqing,Li, Qiaoling
, p. 864 - 873 (2015/01/08)
The synthesis of symmetrical azo-coupled zinc phthalocyanines (7, 8, 10 and 11) incorporating two spectrally complementary photogenerators (azo dyes and phthalocyanines) by NN double bonds in a single structure was described. The four sensitizers were fully characterized by Fourier Transform infrared spectroscopy, UV-Vis spectroscopy, proton nuclear magnetic resonance, mass spectrometry, elemental analyses, thermogravimetric analysis and cyclic voltammetry. All the azo-coupled phthalocyanines exhibited broad absorptions covering the range 300-800 nm. The cyclic voltammetry studies indicated that the LUMO and HOMO energy levels of four synthesized azo-coupled phthalocyanines could ensure efficient electron injection and thermodynamically favorable dye regeneration. Thermal stability studies showed that the four sensitizers were stable above 200 °C. The new compounds were tested in dye-sensitized solar cells and compound 8 showed the best photovoltaic performance, yielding 2.7% power conversion efficiency.
