Organic metal gel for identifying iodide ions by fluorescence, as well as preparation and applications of organic metal gel
An organometallic and fluorescent recognition technology, applied in the field of anion detection, can solve the problems of expensive instruments, complicated operations, difficult preparation, etc., and achieve the effect of convenient and fast detection
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Embodiment 1
[0036] 1. Synthesis of gelling factor 1-naphthalene-3,4,5-tris(hexadecyloxy)benzoylhydrazone
[0037] Add 30 mL of absolute ethanol, 5.0 mmol of 3,4,5-tris(hexadecyloxy)benzoic hydrazide, 5.0 mmol of 1-naphthaldehyde, and 0.01-0.05 mL of glacial acetic acid into a 50 mL reaction flask, and stir under reflux for 3 ~8h, after cooling, filter with suction and recrystallize with chloroform-ethanol to obtain a white solid product which is 1-naphthalene-3,4,5-tris(hexadecyloxy)benzoylhydrazone.
[0038] Yield: 75%, m.p. 89-91°C, 1 H-NMR (CDCl 3 , 400 MHz) δ 9.59(s, H, -NH), 9.043 (s, H, =CH), 8.691~8.672 (m,8H, -ArH), 7.109(s,2H,-phH), 4.013~3.885 (m, 6H, -OCH 2 ), 1.803~1.030 (m,72H,-C 12 h 24 ), 0.894~0.862 (m, 9H, -CH 2 CH 3 ).IR (KBr, cm -1 ) v : 3449.924(-NH), 1715.631(C=O), 1648.878(CH=N). MS: m / z : 996.1 [C 66 h 110 N 2 o 4 + H + ]; Calcd for C 66 h 110 N 2 o 4 : 995.59.
[0039] 2. Preparation of organogels
[0040] Add 30 mL of absolute ethanol and 1...
Embodiment 2
[0044] 1. Synthesis of gelling factor 1-naphthalene-3,4,5-tris(hexadecyloxy)benzoylhydrazone: same as in Example 1.
[0045] 2. Preparation of organogels
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