Methanol indicator and preparation method thereof
An indicator, methanol technology, used in material analysis by observing the effect of chemical indicators, analysis by chemical reaction of materials, cobalt organic compounds, etc., can solve the problem of expensive, time-consuming and laborious, difficult to distinguish, etc. problem, to achieve the effect of easy operation, simple synthesis, and rapid detection
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Embodiment 1
[0016] Embodiment 1 (NBu 4 )[(Tp)Fe(CN) 3 ]Synthesis:
[0017] Weigh FeCl 2 . 2H 2 O 1.2 g and KTp 4 g, add 30 ml of methanol, stir for 2 h and then filter, discard the filtrate and then add 30 ml of methanol, add 1.36 g of NaCN aqueous solution, and stir overnight at 60 °C. Remove the solvent, dissolve the solid in hot water (70-80°C), filter while it is hot, add NBu after the filtrate is cooled 4 Br (tetrabutylammonium bromide) 7 g, add 30% H 2 o 2 20 ml, after stirring for 10 h, an orange-red solid was produced, which was collected, washed with ether, dried in the air, mixed in methanol solution or diffused with ether for recrystallization to obtain orange-red crystals.
Embodiment 2
[0018] The synthesis of embodiment 2 DCEB
[0019] Weigh 4 g of 2,2'-bipyridine-4,4'-dicarboxylic acid in 30 ml of ethanol, then drop into 4 ml of concentrated sulfuric acid, stir, and heat to reflux for 120 h. The ethanol was removed, and 5 ml of water was added to the residue. After neutralization by sodium carbonate, a white solid was produced. The solid was collected, washed with water, and dried in vacuum to obtain a white powder. Yield: 68%.
Embodiment 3
[0020] Synthesis and characterization of the methanol indicator complex of embodiment 3
[0021] (1) Synthesis: Add Co(ClO 4 ) 2 . 6H 2 O 46 mg and 75 mg of DCEB synthesized above, then add 20 ml of anhydrous methanol, stir until completely dissolved, add (NBu 4 )[(Tp)Fe(CN) 3 ] 70 mg, continued to stir for 2 h, filtered, and the red powder after rotary evaporation to remove the volatile solvent was the target compound. In addition, if the filtrate is allowed to stand for a week, green crystals can be obtained with a yield of 60% (171 mg), which is the methanol adduct of the target product.
[0022] (2) Crystal structure determination of methanol indicator complex methanol adduct
[0023] A green crystal with a size of about 0.08×0.12×0.35 mm was selected, and the Mo Kα ray (λ = 0.71703 ?) monochromated by graphite was used as the light source on the Bruker APEX-II CCD X-ray diffractometer, and the measurement temperature was At 100(2) K, the unit cell parameters were c...
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