Tetrathiomolybdate radical/1-octane sulfonate radical/LEuH complex and synthesis method thereof
A technology of tetrathiomolybdate and octanesulfonate, applied in chemical instruments and methods, luminescent materials, etc., can solve the problem of low fluorescence emission intensity of suspensions, and achieve the effect of environmental friendliness and promising application prospects
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[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 structural 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 reactor and passed N into the aqueous solution 2 3 minutes, and then hydrothermally reacted at 70°C for 18 hours. After the reaction, the obtained product was suction filtered, washed with deionized water and then suction filtered, repeated twice, and then vacuum-dried at 40 ° C for 24 hours to obtain white powdery NO 3 -LEuH0.196g.
[0040] The NO synthesized in Example 1 of the present invention was measured by using an elemental analyzer (model: Vario EL) produced by Elementar Company in Germany. 3 -C, H, and N contents of LEuH; the NO synthesized in Example 1 of the present invention was measured using a plasma inductively coupled atomic emission spectrometer (ICP) (model: SPECTROARCOSEOP) p...
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 of deionized water, ultrasonicated to make it evenly dispersed, and then placed in a 100mL reactor for hydrothermal reaction at 70 ° C for 24 hours, after the reaction was completed, cooled After reaching room temperature, suction filtration of the obtained solid product, washing the product with deionized water, and then suction filtration, repeated 3 times; finally, vacuum drying at 40 ° C for 12 hours to obtain a white powdery 1-octanesulfonate / LEuH complex Complex 0.136g.
[0046] The C, H, N and Eu contents of the 1-octanesulfonate / LEuH complex synthesized in this example were measured using the same instrument and test conditions as in Example 1, so as to calculate The chemical composition of the 1-octanesulfonate / LEuH complex is
[0047] Eu(OH) 2.41 (C 8 H 17 O 3 S) 0....
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