共查询到19条相似文献,搜索用时 93 毫秒
1.
研究了新合成的化合物对氟苯甲醛缩乙醇胺席夫碱对枯草杆菌等五种细菌的抑菌作用。抑菌活性实验表明该席夫碱对枯草杆菌、大肠杆菌、大肠杆菌(101)、金黄色葡萄球菌、革兰氏阴性细菌(发荧光Q67)等5种细菌均有较好的抑菌作用,为寻找具有抑菌、抗癌、抗病毒、杀霉等生物活性的药物提供新途径。 相似文献
2.
3.
4.
对氟苯甲醛的合成研究 总被引:2,自引:0,他引:2
醉介绍了用氯化水解法制取对氟苯甲醛的合成路线。以对氟甲苯为原料,在紫外光的作用下进行侧链氯化转化为a,a-二氯对氟甲苯,经95%乙醇催化水解得到高纯度的对氟苯甲醛,总收率达到86.23%。 相似文献
5.
6.
7.
8.
9.
10.
11.
Polyphenols containing Schiff base pendent groups, poly(4-[benzylidene-amino]-phenol) (PBP), and poly(4-[(anthracen-9-ylmethylene)-amino]-phenol)
(PAP) have been synthesized through the combination of Schiff base reaction and enzymatic polymerization using horseradish
peroxidase (HRP) as catalyst. The polymers were characterized by GPC, FTIR, 1H NMR, and UV spectroscopy. It shows that PBP and PAP are composed of polyphenol main chains bearing Schiff base pendent side
groups. The PBP exhibits better solubility than PAP in some common solvents. The PAP has a large red-shift of 86 nm compared
with polyphenols, indicating the Schiff base pendent groups remarkably increase the conjugation lengths of polyphenols. 相似文献
12.
通过乙酰基二茂铁与两种杂环胺(4-氨基安替比林,2-氨基-5-巯基-1,3,4-噻二唑)缩合合成了两种含二茂铁基的Schiff碱(a、b),产率分别为85.8%和72.6%,并通过IR、1HNMR及元素分析对其结构进行了确证。最后,将合成出的两种Schiff碱分别对3种细菌(金黄色葡萄球菌、大肠杆菌、枯草芽孢杆菌)进行了初步抑菌实验,将其结果与非杂环类Schiff碱Fc-C(CH3)NC6H5=(c)的抑菌性能做了比较。结果表明,Schiff碱对上述3种细菌都有抑制作用,且抑菌效果随着Schiff碱浓度的增大而增强。此外,杂环类Schiff碱(a、b)对上述3种细菌的抑菌活性明显优于非杂环类Schiff碱(c)。 相似文献
13.
《Journal of Industrial and Engineering Chemistry》2014,20(6):4227-4232
This study presents a new method in synthesis of nano uranyl Schiff base complexes. In this method slow addition of dilute uranyl(VI) acetate solution to dilute Schiff base solution following the reflux for about 24 h, yields nano uranyl(VI) Schiff base complexes. Characterization of Schiff base ligands and nano uranyl complexes has been done using 1H NMR, IR, UV–vis spectroscopy, elemental analysis. Schiff base ligands were synthesized by the condensation of one mole 3,4-diaminobenzophenone and two moles salicylaldehyde or substituted salicylaldehyde (3-OMe, 4-OMe, 5-OMe, 5-Br, 5-Cl). The electrochemical properties of the uranyl(IV) complexes were investigated by cyclic voltammetry. A good correlation was observed between the oxidation potentials and the electron withdrawing character of the substituents on the Schiff base ligands, according to the following trend: 5-MeO < H < 5-Br ≈ 5-Cl. Also the effect of the position of the substituted groups of Schiff base on the anodic potentials is as follows: 5-OMe < 3-OMe < 4-OMe. 相似文献
14.
15.
16.
A condensation reaction of 2-amino-1,3,4-thiadiazole with 2-pyrrolecarboxaldehyde to form tridentate NNN donor Schiff base has been performed. The prepared Schiff base was further used for the formation of metal complexes having stoichiometry [M(L)(2)]X(n), where M=Cu(II) or Zn(II), L=N-(2-pyrrolylmethylene)-2-amino-1,3,4-thiadiazole, X=SO(4) (2-), NO(3) (-), C(2)O(4) (2-) or CH(3)CO(2-) and n=1 or 2. The new compounds described here have been characterized by their physical, spectral and analytical data, and have been screened against several bacterial strains such as Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. The antibacterial potency of the Schiff base increased upon chelation/complexation, having the same metal ion (cation) but different anions opening up a novel approach in finding new ways to fight against antibiotic resistant strains. 相似文献
17.
报道一种新型含硫席夫碱的合成,结构表征,并测试了它对某些金属离子的配位性。 相似文献
18.
19.
设计、合成吲哚席夫碱类衍生物并研究其抗HIV-1活性。以3-吲哚甲醛衍生物为原料,在碱催化下与芳香胺发生缩合反应合成吲哚席夫碱类化合物,并采用通过 MTT 法测试了目标化合物在MT-4 细胞内的抗 HIV-1病毒株的活性。 合成了32个吲哚席夫碱类衍生物,其结构均通过1H NMR和MS加以确证。初步的生物活性结果测试表明,所合成的吲哚席夫碱类化合物对HIV-1均有优秀的抑制活性,并具有广谱的抗HIV-1活性。其中化合物31 (EC50 = 0.06 mol/L)展现出了最强的抗HIV-1活性,与阳性药物地拉韦啶 (DLV, EC50 = 0.57 mol/L)相当;同时,化合物31具有非常低的毒性,选择指数 (SI)高达2500,明显高于地拉韦啶 (DLV, SI = 1272.9)和依法韦仑 (EFV, SI = 321)。将吲哚和席夫碱两个药效团,能够得到高效、低毒的HIV-1逆转录酶抑制剂,为今后发展新型的HIV-1抑制剂提供了新思路。 相似文献