Application of 8-hydroxyquinoline manganese, magnesium and nickel complex in preparation of agricultural bactericide
A technology of hydroxyquinoline manganese and nickel complexes, which is applied in the direction of fungicides, chemicals for biological control, biocides, etc. It can solve the problems of increased resistance of pathogenic bacteria, environmental pollution, excessive drug residues, etc., and achieve selectivity High, high bactericidal activity, high product purity
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Embodiment 1
[0025] Synthesis of 2-methyl-8-hydroxyquinoline manganese complex (M-1)
[0026]
[0027] Please refer to the reference method for the synthesis method: Journal of Inorganic Biochemistry 154 (2016) 67-77. The specific synthesis operation is as follows: Synthesis of 2-methyl-8-hydroxyquinoline manganese complex (M-1) (Route IV): Weigh 2-methyl-8-hydroxyquinoline (10mmol) and place it in a 100mL three-necked bottle equipped with a condenser tube and a magnetic stirrer, dissolve it with 50mL of absolute ethanol, heat the solution to 70°C in a water bath, and weigh the chlorine Manganese chloride tetrahydrate (5mmol) was dissolved in 10mL deionized water, and the manganese chloride solution was slowly added dropwise (about 0.5h) to the ethanol solution of 2-methyl-8-hydroxyquinoline with a constant pressure dropping funnel, Magnetic stirring was carried out for 2 hours, and the reaction was stopped. A large amount of yellowish-brown solids precipitated out. After suction filtra...
Embodiment 2
[0030] Synthesis of 5-chloro-8-hydroxyquinoline manganese complex (M-2):
[0031] The experimental procedure is the same as in Example 1, except that 2-methyl-8-hydroxyquinoline is replaced by 5-chloro-8-hydroxyquinoline.
[0032]
[0033] M-2 yellow solid, yield 43.6%; FTIR (KBr) ν / cm -1 :3078.0 (Ar-H), 1576.2, 1536.2, 1496.9, 1460.3 (quinoline ring skeleton vibration), 823.9, 786.2, 739.4 (Ar-H).
Embodiment 3
[0035] Synthesis of 5-bromo-8-hydroxyquinoline manganese complex (M-3):
[0036] The experimental procedure is the same as in Example 1, except that 2-methyl-8-hydroxyquinoline is replaced by 5-bromo-8-hydroxyquinoline.
[0037]
[0038] M-3 yellow solid, yield 40.0%; FTIR (KBr) ν / cm -1:3074.8 (Ar-H), 1625.2, 1574.9, 1493.2, 1457.8 (quinoline ring skeleton vibration), 824.0, 782.5 (Ar-H).
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