Can You Really Do Chemisty Experiments About 94-41-7

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Formula: C15H12O. Recently I am researching about FACILE SYNTHESIS; BI2MOO6; COMPOSITE; CATALYST, Saw an article supported by the National Natural Science Foundation of China (NSFC)National Natural Science Foundation of China (NSFC) [20567002, 21067007]; Natural Science Fund of Inner Mongolia [2010MS0203, 2014MS0201]; 2013 Annual Grassland Talents Project of the Inner Mongolia Autonomous Region; 2013 Annual Inner Mongolia Talent Development Fund. Published in MDPI in BASEL ,Authors: Li, HY; Yu, XJ; Hao, XL; Zhang, ZY; Wang, Y; Li, JY. The CAS is 94-41-7. Through research, I have a further understanding and discovery of Chalcone

Bi(NO3)(3)center dot 5H(2)O and (NH4)(6)Mo7O24 center dot 4H(2)O were used as precursors to synthesize flaky gamma-Bi2MoO6 samples by a hydrothermal method, and Pt/gamma-Bi2MoO6 samples with different mass fractions were prepared by an NaBH4 reduction method. Alpha alkylation of benzyl alcohol and acetophenone with photocatalysts under visible light irradiation was performed, and the activity of 4 wt % Pt/gamma-Bi2MoO6 (gamma-Bi2MoO6 was prepared by a nitric acid method, pH = 9, and reaction temperature 180 degrees C) was the best. The photocatalytic reaction conditions were optimized by changing various kinds of variables, such as the type of catalyst, solvent, and base, and the amount of base, catalyst, and reactant. The optimal conditions for the organic reaction were 75 mg 4 wt % Pt/gamma-Bi2MoO6, 6 mL n-heptane, 1.2 mmol NaOH, 1 mmol acetophenone, and 3 mmol benzyl alcohol. Under the optimal reaction conditions, the effects of different light wavelengths and light intensities on the reaction were measured, and the cycling ability of the photocatalyst was tested. After five cycles, the photochemical properties of the catalyst were relatively stable. Finally, the active substances were identified (such as electrons (e(-), holes (h(+)), hydroxyl radicals (center dot OH), and superoxide radicals (center dot O-2(-)).

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Reference:
Thiazolidine – Wikipedia,
,Thiazolidine – ScienceDirect.com