Photo-induced yellow fluorescent zinc coordination polymer [Zn(HL)(HBPEB)] and method of synthesizing same
A technology of zinc coordination polymers and coordination polymers, applied in the direction of zinc organic compounds, chemical instruments and methods, luminescent materials, etc., to achieve the effects of high energy transfer efficiency, simple operation, and high thermal stability
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Embodiment 1
[0027] The preparation of embodiment 1 complex of the present invention
[0028] Weigh raw materials according to the following molar ratio: H 4 L:BPEB:Zn(NO 3 ) 2 :H 2 O:CH 3 CN=28︰26︰58︰8033︰3480 In a 50mL glass beaker, the mixture was stirred for 0.5 hours (h), then transferred to a 25mL reactor, reacted at 110°C for two days, cooled naturally to room temperature, and yellow crystals were observed , which is the target product, is filtered out from the mother liquor, washed with water and acetonitrile in turn, and then dried naturally.
[0029] The C, H, and N elements in the product [Zn(HL)(HBPEB)] were analyzed for elements, and the calculated values (%): C, 62.25; H, 3.45; N, 4.03. Actually found (%): C, 62.41; H, 3.51; N, 3.97. FT-IR (KBr, cm -1 ): 3231(w), 3067(w), 3014(w), 1682(m), 1614(vs), 1493(m), 1379(vs), 1234(s), 1205(s), 1138(m ), 841(m), 810(m). Note: Elemental analysis values are measured by Perkin-Elmer2400 elemental analyzer; infrared spectrum ...
Embodiment 2
[0033] The preparation of embodiment 2 complexes of the present invention
[0034] Weigh raw materials according to the following molar ratio: H 4 L:BPEB:Zn(NO 3 ) 2 :H 2 O:CH 3 CN=31:28:60:8383:3740 into a 50mL glass beaker, the mixture was stirred for 1 hour (h), then transferred into a 25mL reactor, reacted at 120°C for three days, cooled naturally to room temperature, and yellow crystals were observed , which is the target product, is filtered out from the mother liquor, washed with water and acetonitrile in turn, and then dried naturally.
[0035] The product was characterized by elemental analysis, infrared, fluorescence, and X-ray powder diffraction, and the obtained data were similar to those in Example 1. Illustrate that the crystal structure that makes with embodiment 2 does not change and product is purer (see Figure 7 ), and performance has not changed (see Figure 6 ).
[0036] This example was repeated several times, and the mass of [Zn(HL)(HBPEB)] obtai...
Embodiment 3
[0037] The preparation of embodiment 3 complexes of the present invention
[0038] Weigh raw materials according to the following molar ratio: H 4 L:BPEB:Zn(NO 3 ) 2 :H 2 O:CH 3 CN=34:30:62:8733:3999 Put it in a 50mL glass beaker, stir the mixture for 1.5h, then transfer it into a 25mL reactor, react at 130°C for four days, cool it down to room temperature naturally, and observe yellow crystals, which is the target product, it is filtered out from the mother liquor, washed with water and acetonitrile in turn, and then dried naturally.
[0039] The product was characterized by elemental analysis, infrared, fluorescence, and X-ray powder diffraction, and the obtained data were similar to those in Example 1. Illustrate that the crystal structure that makes with embodiment 3 does not change and product is purer (see Figure 7 ), and performance has not changed (see Figure 6 ).
[0040] This example was repeated several times, and the mass of [Zn(HL)(HBPEB)] obtained accor...
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