Tetrathiomolybdate/1-octanesulfonate/leuh complex and its synthesis method
A technology of tetrathiomolybdate and octane sulfonate, applied in chemical instruments and methods, luminescent materials, etc., can solve the problems of low fluorescence emission intensity of suspensions, and achieve the effect of being environmentally friendly and having application prospects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0027] The present invention also provides a preparation method of the above complex, comprising the following steps:
[0028] Will NO 3 After -LEuH, sodium 1-octanesulfonate and ammonium tetrathiomolybdate are dispersed in water, they are hydrothermally reacted at 70-100°C for 12-24 hours, and after the reaction, the product is post-treated to obtain tetrathiomolybdenum Acid group / 1-octane sulfonate / LEuH complex; Wherein, the molar ratio of described ammonium tetrathiomolybdate and 1-octane sulfonate is 1: (12-18); 1-octane sulfonate sodium and the sum of moles of ammonium tetrathiomolybdate and NO 3 The molar ratio of -LEuH is (5-9):1.
[0029] During specific implementation, preferably, the molar ratio of described ammonium tetrathiomolybdate and 1-octane sulfonate is 1: (14-16); 1-octane sulfonate and tetrathiomolybdic acid The sum of moles of ammonium and NO 3 The molar ratio of -LEuH is (6.5-7.5):1.
[0030] During the synthesis process, the NO can be accelerated by...
Embodiment 1
[0038] Example 1 NO 3 Synthesis and structure characterization of -LEuH
[0039] 0.446g (1mmol) Eu(NO 3 ) 3 ·6H 2 O, 0.846g (10mmol) NaNO 3 , 0.07g (0.5mmol) hexamethylenetetramine was dissolved in 65mL degassed water to obtain an aqueous solution, which was transferred to the reaction kettle and passed into the aqueous solution with N 2 3 minutes, then hydrothermal reaction at 70°C for 18 hours. After the reaction, the obtained product was suction filtered, washed with deionized water, and then suction filtered twice, and then vacuum-dried at 40°C for 24 hours to obtain white powdery NO 3 -LEuH 0.196g.
[0040] The elemental analyzer (model: Vario EL) produced by German Elementar Company was adopted to measure the NO synthesized in the embodiment of the present invention 1. 3 -C, H, N content of LEuH; Adopt the plasma inductively coupled atomic emission spectrometer (ICP) (model: SPECTROARCOSEOP) that German Spike Analytical Instrument Company produces to measure the ...
Embodiment 2
[0044] Example 2 Synthesis and structural characterization of 1-octanesulfonate / LEuH complex
[0045] 0.10g (0.42mmol) NO 3 -LEuH and 0.6488g (3.0mmol) sodium 1-octane sulfonate were added to 80mL deionized water, ultrasonically dispersed, and then placed in a 100mL reactor for hydrothermal reaction at 70°C for 24 hours. After the reaction, cooled to room temperature, suction-filtered the obtained solid product, washed the product with deionized water, and then suction-filtered, repeated 3 times; finally, vacuum-dried at 40°C for 12 hours to obtain a white powdery 1-octanesulfonate / LEuH complex Complex 0.136g.
[0046] The same instrument and test conditions as in Example 1 were used to measure the C, H, N and Eu content of the 1-octanesulfonate / LEuH complex synthesized in this example, thereby calculating the The chemical composition of the 1-octanesulfonate / LEuH complex is
[0047] Eu(OH) 2.41 (C 8 h 17 o 3 S) 0.64 (NO 3 ) 0.01 0.8H 2 O, the relevant data are show...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


