Ayoub Abarkan , Nafea Achalhi , Ridouan El Yousfi , Sara Moumnassi , Zoubida Aissaoui , Abdeslam Asehraou , Abderrahman El Idrissi
{"title":"通过绿色自由基介导的 \"点击 \"反应途径对水溶性烯丙基纤维素进行最先进的磷酸化处理,增强抗真菌活性","authors":"Ayoub Abarkan , Nafea Achalhi , Ridouan El Yousfi , Sara Moumnassi , Zoubida Aissaoui , Abdeslam Asehraou , Abderrahman El Idrissi","doi":"10.1016/j.carbpol.2024.123014","DOIUrl":null,"url":null,"abstract":"<div><div>Allyl Cellulose (AC) was synthesized using allyl bromide in sodium hydroxide (NaOH)/urea aqueous solution. By employing a molar ratio of 6:1 of allyl bromide/cellulose, low-degree of substitution (DS) water-soluble AC (AC<sub>1</sub>) was obtained (DS = 0.67). Then, radical-mediated “click” reactions of AC<sub>1</sub> with diethyl phosphite (DEP) and dibutyl phosphite (DBP) were carried out in deionized water as green reaction medium, using 4,4′-azobis(4-cyanovaleric acid) (ACVA) as a radical initiator. The synthesized AC<sub>1</sub>-DEP and AC<sub>1</sub>-DBP showed high conversion percentages of 84 % and 87 %, respectively. Fourier-transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) techniques were used to validate the structure of the products and confirm the successful radical-mediated “click” reactions of AC<sub>1</sub> with dialkyl phosphite (DAP) in water. X-ray diffraction (XRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), static contact angle, and scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDX) analyses were used to investigate structural, thermal, and surface properties, revealing an increase in flexibility and hydrophobicity upon phosphorylation. AC<sub>1</sub>-diethyl phosphite (AC<sub>1</sub>-DEP) and AC<sub>1</sub>-dibutyl phosphite (AC<sub>1</sub>-DBP) exhibited efficient antifungal activities with inhibition zone ranges from 14 to 27 mm.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"349 ","pages":"Article 123014"},"PeriodicalIF":10.7000,"publicationDate":"2024-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"State-of-the-art phosphorylation of water-soluble allyl cellulose via a green radical-mediated “click” reaction pathway with enhanced antifungal activity\",\"authors\":\"Ayoub Abarkan , Nafea Achalhi , Ridouan El Yousfi , Sara Moumnassi , Zoubida Aissaoui , Abdeslam Asehraou , Abderrahman El Idrissi\",\"doi\":\"10.1016/j.carbpol.2024.123014\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Allyl Cellulose (AC) was synthesized using allyl bromide in sodium hydroxide (NaOH)/urea aqueous solution. By employing a molar ratio of 6:1 of allyl bromide/cellulose, low-degree of substitution (DS) water-soluble AC (AC<sub>1</sub>) was obtained (DS = 0.67). Then, radical-mediated “click” reactions of AC<sub>1</sub> with diethyl phosphite (DEP) and dibutyl phosphite (DBP) were carried out in deionized water as green reaction medium, using 4,4′-azobis(4-cyanovaleric acid) (ACVA) as a radical initiator. The synthesized AC<sub>1</sub>-DEP and AC<sub>1</sub>-DBP showed high conversion percentages of 84 % and 87 %, respectively. Fourier-transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) techniques were used to validate the structure of the products and confirm the successful radical-mediated “click” reactions of AC<sub>1</sub> with dialkyl phosphite (DAP) in water. X-ray diffraction (XRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), static contact angle, and scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDX) analyses were used to investigate structural, thermal, and surface properties, revealing an increase in flexibility and hydrophobicity upon phosphorylation. AC<sub>1</sub>-diethyl phosphite (AC<sub>1</sub>-DEP) and AC<sub>1</sub>-dibutyl phosphite (AC<sub>1</sub>-DBP) exhibited efficient antifungal activities with inhibition zone ranges from 14 to 27 mm.</div></div>\",\"PeriodicalId\":261,\"journal\":{\"name\":\"Carbohydrate Polymers\",\"volume\":\"349 \",\"pages\":\"Article 123014\"},\"PeriodicalIF\":10.7000,\"publicationDate\":\"2024-11-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Carbohydrate Polymers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0144861724012402\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbohydrate Polymers","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0144861724012402","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
State-of-the-art phosphorylation of water-soluble allyl cellulose via a green radical-mediated “click” reaction pathway with enhanced antifungal activity
Allyl Cellulose (AC) was synthesized using allyl bromide in sodium hydroxide (NaOH)/urea aqueous solution. By employing a molar ratio of 6:1 of allyl bromide/cellulose, low-degree of substitution (DS) water-soluble AC (AC1) was obtained (DS = 0.67). Then, radical-mediated “click” reactions of AC1 with diethyl phosphite (DEP) and dibutyl phosphite (DBP) were carried out in deionized water as green reaction medium, using 4,4′-azobis(4-cyanovaleric acid) (ACVA) as a radical initiator. The synthesized AC1-DEP and AC1-DBP showed high conversion percentages of 84 % and 87 %, respectively. Fourier-transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) techniques were used to validate the structure of the products and confirm the successful radical-mediated “click” reactions of AC1 with dialkyl phosphite (DAP) in water. X-ray diffraction (XRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), static contact angle, and scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDX) analyses were used to investigate structural, thermal, and surface properties, revealing an increase in flexibility and hydrophobicity upon phosphorylation. AC1-diethyl phosphite (AC1-DEP) and AC1-dibutyl phosphite (AC1-DBP) exhibited efficient antifungal activities with inhibition zone ranges from 14 to 27 mm.
期刊介绍:
Carbohydrate Polymers stands as a prominent journal in the glycoscience field, dedicated to exploring and harnessing the potential of polysaccharides with applications spanning bioenergy, bioplastics, biomaterials, biorefining, chemistry, drug delivery, food, health, nanotechnology, packaging, paper, pharmaceuticals, medicine, oil recovery, textiles, tissue engineering, wood, and various aspects of glycoscience.
The journal emphasizes the central role of well-characterized carbohydrate polymers, highlighting their significance as the primary focus rather than a peripheral topic. Each paper must prominently feature at least one named carbohydrate polymer, evident in both citation and title, with a commitment to innovative research that advances scientific knowledge.