Sintesis, Karakterisasi, dan Uji Aktivitas Antibakteri Senyawa Organotimah(IV) 4-Nitrobenzoat

Sutopo Hadi, Nova Tri Irianti, Noviany Noviany
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引用次数: 1

Abstract

Dua buah senyawa organotimah(IV) yaitu berupa senyawa trifeniltimah(IV) 4-nitrobenzoat (2) dan difeniltimah(IV) di-4-nitrobenzoat (4) telah berhasil disintesis melalui reaksi antara senyawa trifeniltimah(IV) hidroksida (1) dan difeniltimah(IV) oksida (3) dengan ligan asam 4-nitrobenzoat (HNBA). Senyawa hasil sintesis dikarakterisasi dengan menggunakan spektrofotomer IR, spektrofotomer UV, spektrometer NMR dan microelemental analyzer untuk melihat kemurnian senyawa. Aktivitas biologis senyawa turunan organtotimah(IV) 4-nitrobenzoat telah diuji terhadap bakteri Gram positif Staphylococcus aureus dan Gram negatif Escherichia coli. Hasil uji dengan metode difusi agar menunjukkan senyawa 2 pada konsentrasi 200 ppm (3,87 × 10-4 M) memberikan penghambatan yang lebih efektif dibandingkan senyawa 4, senyawa awal 1 dan 3 serta ligan HNBA.

Synthesis, Characterization, and Antibacterial Activity Test of Organotin(IV) 4-nitrobenzoate. Two organotin(IV) compounds, namely triphenyltin(IV) 4-nitrobenzoate (2) and diphenyltin(IV) di-4-nitrobenzoate (4) compounds have been successfully synthesized through a reaction between triphenyltin(IV) hydroxide (1) and diphenyltin(IV) oxide (3) with 4-nitrobenzoic acid (HNBA) The synthesized compounds were characterized using IR, UV, NMR spectrometer, and a microelemental analyzer to check the compound purity. The biological activity of the organotin(IV) 4-nitrobenzoate derivative was tested against Gram-positive bacteria S. aureus and Gram-negative bacteria E. coli. The test results with the agar diffusion method showed that compound 2 at a concentration of 200 ppm (3.87 x 10-4 M) provide more effective inhibition than compound 4, the starting materials 1 and 3, and the ligand HNBA.

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合成、分类和测试抗菌化合物(IV) 4-硝基苯甲酸盐的活性
两种由三氧化二氮(四)和二氧化二氮(四)的二氮苯甲酸化合物(四)和二氮苯胺(四)的二氮苯甲酸化合物(四)和二氧化二氮(三)与一根酸4- nitrobezoat (HNBA)混合而成的有机化合物(四)。合成材料通过红外光谱仪、紫外线光谱仪、NMR光谱仪和微元素分析仪进行分类,以观察化合物的纯度。4 . nitrobezoat已在杆菌样呈阳性的菌根物质(IV)和大肠杆菌样呈阴性。扩散的方法,以便测试显示化合物浓度200 mtc(3.87 2×10 M)提供了更有效的抑制化合物4相比,化合物1和3 HNBA配体开始。合成、作用和抑制微生物活性测试(IV) 4-硝基苯唑。二organotin (IV) compounds, namely triphenyltin (IV) 4-nitrobenzoate(2)和diphenyltin (IV) di-4-nitrobenzoate (4) compounds已被successfully synthesized triphenyltin (IV) hydroxide之间通过a反应(1)和diphenyltin (IV)氮和4-nitrobenzoic酸(HNBA)(3)《synthesized compounds是characterized用IR、UV、NMR全量程和a microelemental分析仪检查迎化合物purity。4 .氮气菌株的生物活性是对大肠杆菌正阳性和大肠杆菌负抑制的。根据不同的方法进行的试验,这种化合物在200 ppm(3.87×10-4米)的集中作用下呈2倍于化合物的强度,1和3的基本材料,以及ligand HNBA。
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