{"title":"合成、分类和测试抗菌化合物(IV) 4-硝基苯甲酸盐的活性","authors":"Sutopo Hadi, Nova Tri Irianti, Noviany Noviany","doi":"10.20961/alchemy.18.1.47872.19-29","DOIUrl":null,"url":null,"abstract":"<p>Dua buah senyawa organotimah(IV) yaitu berupa senyawa trifeniltimah(IV) 4-nitrobenzoat (<strong>2</strong>) dan difeniltimah(IV) di-4-nitrobenzoat (<strong>4</strong>) telah berhasil disintesis melalui reaksi antara senyawa trifeniltimah(IV) hidroksida (<strong>1</strong>) dan difeniltimah(IV) oksida (<strong>3</strong>) dengan ligan asam 4-nitrobenzoat (HNBA). Senyawa hasil sintesis dikarakterisasi dengan menggunakan spektrofotomer IR, spektrofotomer UV, spektrometer NMR dan <em>microelemental analyzer</em> untuk melihat kemurnian senyawa<em>. </em>Aktivitas biologis senyawa turunan organtotimah(IV) 4-nitrobenzoat telah diuji terhadap bakteri Gram positif <em>Staphylococcus aureus</em> dan Gram negatif <em>Escherichia coli</em>. Hasil uji dengan metode difusi agar menunjukkan senyawa <strong>2</strong> pada konsentrasi 200 ppm (3,87 × 10<sup>-4 </sup>M) memberikan penghambatan yang lebih efektif dibandingkan senyawa <strong>4, </strong>senyawa awal<strong> 1 </strong>dan<strong> 3 </strong>serta ligan HNBA.</p><p><strong>Synthesis, Characterization, and Antibacterial Activity Test of Organotin(IV) 4-nitrobenzoate.</strong> Two organotin(IV) compounds, namely triphenyltin(IV) 4-nitrobenzoate (<strong>2</strong>) and diphenyltin(IV) di-4-nitrobenzoate (<strong>4</strong>) compounds have been successfully synthesized through a reaction between triphenyltin(IV) hydroxide (<strong>1</strong>) and diphenyltin(IV) oxide (<strong>3</strong>) 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 <em>S. aureus</em> and Gram-negative bacteria <em>E. coli</em>. The test results with the agar diffusion method showed that compound <strong>2</strong> at a concentration of 200 ppm (3.87 x 10<sup>-4</sup> M) provide more effective inhibition than compound <strong>4</strong>, the starting materials<strong> 1 </strong>and<strong> 3</strong>, and<strong> </strong>the ligand HNBA.</p>","PeriodicalId":7926,"journal":{"name":"Alchemy: Jurnal Penelitian Kimia","volume":"2 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Sintesis, Karakterisasi, dan Uji Aktivitas Antibakteri Senyawa Organotimah(IV) 4-Nitrobenzoat\",\"authors\":\"Sutopo Hadi, Nova Tri Irianti, Noviany Noviany\",\"doi\":\"10.20961/alchemy.18.1.47872.19-29\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Dua buah senyawa organotimah(IV) yaitu berupa senyawa trifeniltimah(IV) 4-nitrobenzoat (<strong>2</strong>) dan difeniltimah(IV) di-4-nitrobenzoat (<strong>4</strong>) telah berhasil disintesis melalui reaksi antara senyawa trifeniltimah(IV) hidroksida (<strong>1</strong>) dan difeniltimah(IV) oksida (<strong>3</strong>) dengan ligan asam 4-nitrobenzoat (HNBA). Senyawa hasil sintesis dikarakterisasi dengan menggunakan spektrofotomer IR, spektrofotomer UV, spektrometer NMR dan <em>microelemental analyzer</em> untuk melihat kemurnian senyawa<em>. </em>Aktivitas biologis senyawa turunan organtotimah(IV) 4-nitrobenzoat telah diuji terhadap bakteri Gram positif <em>Staphylococcus aureus</em> dan Gram negatif <em>Escherichia coli</em>. Hasil uji dengan metode difusi agar menunjukkan senyawa <strong>2</strong> pada konsentrasi 200 ppm (3,87 × 10<sup>-4 </sup>M) memberikan penghambatan yang lebih efektif dibandingkan senyawa <strong>4, </strong>senyawa awal<strong> 1 </strong>dan<strong> 3 </strong>serta ligan HNBA.</p><p><strong>Synthesis, Characterization, and Antibacterial Activity Test of Organotin(IV) 4-nitrobenzoate.</strong> Two organotin(IV) compounds, namely triphenyltin(IV) 4-nitrobenzoate (<strong>2</strong>) and diphenyltin(IV) di-4-nitrobenzoate (<strong>4</strong>) compounds have been successfully synthesized through a reaction between triphenyltin(IV) hydroxide (<strong>1</strong>) and diphenyltin(IV) oxide (<strong>3</strong>) 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 <em>S. aureus</em> and Gram-negative bacteria <em>E. coli</em>. The test results with the agar diffusion method showed that compound <strong>2</strong> at a concentration of 200 ppm (3.87 x 10<sup>-4</sup> M) provide more effective inhibition than compound <strong>4</strong>, the starting materials<strong> 1 </strong>and<strong> 3</strong>, and<strong> </strong>the ligand HNBA.</p>\",\"PeriodicalId\":7926,\"journal\":{\"name\":\"Alchemy: Jurnal Penelitian Kimia\",\"volume\":\"2 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-02-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Alchemy: Jurnal Penelitian Kimia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.20961/alchemy.18.1.47872.19-29\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alchemy: Jurnal Penelitian Kimia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20961/alchemy.18.1.47872.19-29","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Sintesis, Karakterisasi, dan Uji Aktivitas Antibakteri Senyawa Organotimah(IV) 4-Nitrobenzoat
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, andthe ligand HNBA.