{"title":"带有丁基化氧杂茴香醚基团的新型螺-(2,2′-二氧联苯)-环三磷嗪衍生物的合成和表征及其抗氧化和抗菌活性","authors":"Efe Bilal Sönmez , Şule Şahin Ün , Ceylan Mutlu Balcı , Devrim Atilla , Mine Gül Şeker , Hanife İbişoğlu","doi":"10.1016/j.poly.2024.117252","DOIUrl":null,"url":null,"abstract":"<div><div>In this study, novel cyclotriphosphazene derivatives, {[N<sub>3</sub>P<sub>3</sub>(biph)(BA)<sub>2</sub>] (<strong>6a/b</strong>), [N<sub>3</sub>P<sub>3</sub>(biph)(BA)<sub>3</sub>] (<strong>7</strong>), [N<sub>3</sub>P<sub>3</sub>(biph)<sub>2</sub>(BA)Cl (<strong>8</strong>) and [N<sub>3</sub>P<sub>3</sub>(biph)<sub>2</sub>(BA)<sub>2</sub> (<strong>9</strong>)]}, (biph = 2′,2′′-dioxy-1′,1′′- biphenyl, BA = butylated oxyanisole}, were synthesized from the nucleophilic substitution reactions of butylated hydroxyanisole (BHA) (<strong>5</strong>) with [N<sub>3</sub>P<sub>3</sub>(biph)Cl<sub>4</sub>] (<strong>3</strong>) and [N<sub>3</sub>P<sub>3</sub>(biph)<sub>2</sub>Cl<sub>2</sub>] (<strong>4</strong>), respectively. The structures of all the products (<strong>6a/b</strong>, <strong>7</strong>, <strong>8</strong> and <strong>9</strong>) were determined -using elemental analysis, mass and (<sup>1</sup>H and <sup>31</sup>P) NMR spectroscopic techniques. The molecular and crystal structure of compound <strong>9</strong> was also determined by single crystal X-ray crystallography. At the same time, the compounds (<strong>3</strong>, <strong>4</strong>, <strong>7</strong>, <strong>8</strong> and <strong>9</strong>) were tested for their antimicrobial and antioxidant (free radical scavenging) activities. Of all, compounds <strong>8</strong> and <strong>9</strong> showed relatively significant antimicrobial activity against the control strains <em>Bacillus cereus</em> DSMZ 4312 (16,5 and 18,25 mm) and against <em>Staphylococcus aureus</em> ATCC 29213 (25 and 22,5 mm) compared to their positive controls. The MIC<sub>50</sub> values of compounds <strong>8</strong> and <strong>9</strong> against <em>Bacillus cereus</em> were determined at 125 µg/mL and < 325 µg/mL, respectively, and <em>Staphylococcus aureus</em> at 125 µg/ mL for both compounds. While the other compounds (<strong>3</strong>, <strong>4</strong> and <strong>7</strong>) did not possess antimicrobial properties, they showed strong antioxidant activity. In the antioxidant assay based on the EC<sub>50</sub> value of BHA used as a control, compound <strong>7</strong> showed antioxidant activity even at low concentrations such as 9,37 µg/ mL (83 %), while compounds <strong>3</strong> and <strong>4</strong> showed antioxidant properties even at relatively low concentrations such as 18,75 µg/mL. Compounds <strong>8</strong> and <strong>9</strong>, two antimicrobial compounds, did not exhibit antioxidant properties.</div></div>","PeriodicalId":20278,"journal":{"name":"Polyhedron","volume":"265 ","pages":"Article 117252"},"PeriodicalIF":2.4000,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and characterization of novel spiro-(2,2′-dioxybiphenyl)-cyclotriphosphazene derivatives bearing butylated oxyanisole groups and their antioxidant and antimicrobial activities\",\"authors\":\"Efe Bilal Sönmez , Şule Şahin Ün , Ceylan Mutlu Balcı , Devrim Atilla , Mine Gül Şeker , Hanife İbişoğlu\",\"doi\":\"10.1016/j.poly.2024.117252\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In this study, novel cyclotriphosphazene derivatives, {[N<sub>3</sub>P<sub>3</sub>(biph)(BA)<sub>2</sub>] (<strong>6a/b</strong>), [N<sub>3</sub>P<sub>3</sub>(biph)(BA)<sub>3</sub>] (<strong>7</strong>), [N<sub>3</sub>P<sub>3</sub>(biph)<sub>2</sub>(BA)Cl (<strong>8</strong>) and [N<sub>3</sub>P<sub>3</sub>(biph)<sub>2</sub>(BA)<sub>2</sub> (<strong>9</strong>)]}, (biph = 2′,2′′-dioxy-1′,1′′- biphenyl, BA = butylated oxyanisole}, were synthesized from the nucleophilic substitution reactions of butylated hydroxyanisole (BHA) (<strong>5</strong>) with [N<sub>3</sub>P<sub>3</sub>(biph)Cl<sub>4</sub>] (<strong>3</strong>) and [N<sub>3</sub>P<sub>3</sub>(biph)<sub>2</sub>Cl<sub>2</sub>] (<strong>4</strong>), respectively. The structures of all the products (<strong>6a/b</strong>, <strong>7</strong>, <strong>8</strong> and <strong>9</strong>) were determined -using elemental analysis, mass and (<sup>1</sup>H and <sup>31</sup>P) NMR spectroscopic techniques. The molecular and crystal structure of compound <strong>9</strong> was also determined by single crystal X-ray crystallography. At the same time, the compounds (<strong>3</strong>, <strong>4</strong>, <strong>7</strong>, <strong>8</strong> and <strong>9</strong>) were tested for their antimicrobial and antioxidant (free radical scavenging) activities. Of all, compounds <strong>8</strong> and <strong>9</strong> showed relatively significant antimicrobial activity against the control strains <em>Bacillus cereus</em> DSMZ 4312 (16,5 and 18,25 mm) and against <em>Staphylococcus aureus</em> ATCC 29213 (25 and 22,5 mm) compared to their positive controls. The MIC<sub>50</sub> values of compounds <strong>8</strong> and <strong>9</strong> against <em>Bacillus cereus</em> were determined at 125 µg/mL and < 325 µg/mL, respectively, and <em>Staphylococcus aureus</em> at 125 µg/ mL for both compounds. While the other compounds (<strong>3</strong>, <strong>4</strong> and <strong>7</strong>) did not possess antimicrobial properties, they showed strong antioxidant activity. In the antioxidant assay based on the EC<sub>50</sub> value of BHA used as a control, compound <strong>7</strong> showed antioxidant activity even at low concentrations such as 9,37 µg/ mL (83 %), while compounds <strong>3</strong> and <strong>4</strong> showed antioxidant properties even at relatively low concentrations such as 18,75 µg/mL. Compounds <strong>8</strong> and <strong>9</strong>, two antimicrobial compounds, did not exhibit antioxidant properties.</div></div>\",\"PeriodicalId\":20278,\"journal\":{\"name\":\"Polyhedron\",\"volume\":\"265 \",\"pages\":\"Article 117252\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2024-10-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polyhedron\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0277538724004285\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polyhedron","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0277538724004285","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Synthesis and characterization of novel spiro-(2,2′-dioxybiphenyl)-cyclotriphosphazene derivatives bearing butylated oxyanisole groups and their antioxidant and antimicrobial activities
In this study, novel cyclotriphosphazene derivatives, {[N3P3(biph)(BA)2] (6a/b), [N3P3(biph)(BA)3] (7), [N3P3(biph)2(BA)Cl (8) and [N3P3(biph)2(BA)2 (9)]}, (biph = 2′,2′′-dioxy-1′,1′′- biphenyl, BA = butylated oxyanisole}, were synthesized from the nucleophilic substitution reactions of butylated hydroxyanisole (BHA) (5) with [N3P3(biph)Cl4] (3) and [N3P3(biph)2Cl2] (4), respectively. The structures of all the products (6a/b, 7, 8 and 9) were determined -using elemental analysis, mass and (1H and 31P) NMR spectroscopic techniques. The molecular and crystal structure of compound 9 was also determined by single crystal X-ray crystallography. At the same time, the compounds (3, 4, 7, 8 and 9) were tested for their antimicrobial and antioxidant (free radical scavenging) activities. Of all, compounds 8 and 9 showed relatively significant antimicrobial activity against the control strains Bacillus cereus DSMZ 4312 (16,5 and 18,25 mm) and against Staphylococcus aureus ATCC 29213 (25 and 22,5 mm) compared to their positive controls. The MIC50 values of compounds 8 and 9 against Bacillus cereus were determined at 125 µg/mL and < 325 µg/mL, respectively, and Staphylococcus aureus at 125 µg/ mL for both compounds. While the other compounds (3, 4 and 7) did not possess antimicrobial properties, they showed strong antioxidant activity. In the antioxidant assay based on the EC50 value of BHA used as a control, compound 7 showed antioxidant activity even at low concentrations such as 9,37 µg/ mL (83 %), while compounds 3 and 4 showed antioxidant properties even at relatively low concentrations such as 18,75 µg/mL. Compounds 8 and 9, two antimicrobial compounds, did not exhibit antioxidant properties.
期刊介绍:
Polyhedron publishes original, fundamental, experimental and theoretical work of the highest quality in all the major areas of inorganic chemistry. This includes synthetic chemistry, coordination chemistry, organometallic chemistry, bioinorganic chemistry, and solid-state and materials chemistry.
Papers should be significant pieces of work, and all new compounds must be appropriately characterized. The inclusion of single-crystal X-ray structural data is strongly encouraged, but papers reporting only the X-ray structure determination of a single compound will usually not be considered. Papers on solid-state or materials chemistry will be expected to have a significant molecular chemistry component (such as the synthesis and characterization of the molecular precursors and/or a systematic study of the use of different precursors or reaction conditions) or demonstrate a cutting-edge application (for example inorganic materials for energy applications). Papers dealing only with stability constants are not considered.