Method for preparing manganese complex blue fluorescent material in dimer form
A technology of blue fluorescence and manganese in the form of manganese, which is applied in the field of fluorescence emission, can solve the problems that the dimer form has not been reported, and achieve good fluorescence emission performance, good thermal stability, and cheap raw materials
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Embodiment 1
[0019] 1 mmol of 1,6 sodium naphthalene disulfonate, 1 mmol of MnCl 2 4H 2 O and 1 mmol of 1,10-phenanthroline were dissolved in 25 mL of aqueous methanol with a volume ratio of methanol to water of 1:1; the solution obtained in the previous step was transferred to a 30 mL stainless steel reaction vessel lined with polytetrafluoroethylene In 120 ℃ constant temperature condition, reacted for 72 h, slowly cooled to room temperature, filtered to obtain yellow blocky crystals, the product was washed with deionized water, and dried naturally in air, the yield was 65%.
[0020] After elemental analysis, the molecular formula C 142 h 128 mn 4 N 16 o 38 S 8 , measured value % (theoretical value %): C54.43 (54.22), H4.38 (4.07), N7.35 (7.13). Infrared spectrum (cm -1 ): 3458, 1610, 1518, 1205, 1107, 1043, 878, 729, 678.
[0021] It can be known from the accompanying drawings that the fluorescence emission peak of the complex is at 439 nm, and the absorption peak of the ultravi...
Embodiment 2
[0023] 0.85 mmol of 1,6 sodium naphthalene disulfonate, 0.85 mmol of MnCl 2 4H 2 O and 1 mmol of 1,10-phenanthroline were dissolved in 25 mL of aqueous methanol with a volume ratio of methanol to water of 1:1; the solution obtained in the previous step was transferred to a 30 mL Teflon-lined stainless steel reaction After reacting at a constant temperature of 120 °C for 75 h in the kettle, it was slowly cooled to room temperature, filtered to obtain yellow blocky crystals, and the product was washed with deionized water and dried naturally in air.
Embodiment 3
[0025] 0.85 mmol of 1,6 sodium naphthalene disulfonate, 0.85 mmol of MnCl 2 4H 2 O and 1.15 mmol of 1,10-phenanthroline were dissolved in 25 mL of aqueous methanol with a volume ratio of methanol to water of 1:1; the solution obtained in the previous step was transferred to a 30 mL Teflon-lined stainless steel reaction After reacting for 80 h at a constant temperature of 120 °C in the kettle, it was slowly cooled to room temperature, filtered to obtain yellow blocky crystals, and the product was washed with deionized water and dried naturally in air.
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