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dc.rights.licenseopenen_US
hal.structure.identifierLaboratoire de Chimie des Substances Naturelles [LCSN]
dc.contributor.authorKHALDI, Zineb
hal.structure.identifierLaboratoire de Chimie des Substances Naturelles [LCSN]
dc.contributor.authorBESSE, Claire
hal.structure.identifierLaboratoire de Chimie des Substances Naturelles [LCSN]
dc.contributor.authorNZAMBE TA KEKI, Jean Kerim
hal.structure.identifierLaboratoire de Chimie des Substances Naturelles [LCSN]
dc.contributor.authorOUK, Tan-Sothéa
hal.structure.identifierLaboratoire de Chimie des Substances Naturelles [LCSN]
dc.contributor.authorGLOAGUEN, Vincent
hal.structure.identifierLaboratoire de Chimie des Substances Naturelles [LCSN]
dc.contributor.authorZERROUKI, Rachida
dc.date.accessioned2019
dc.date.available2019
dc.date.issued2019
dc.identifier.issn10427147en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/3831
dc.description.abstractEnContamination of surfaces by bacteria and the emergence of antimicrobial resistantstrains are very worrying issues. One of ways to limit the bacterial proliferation is todevelop antimicrobial materials. We reported herein the development of new antimi-crobial support by grafting different aryl azide onto propargylated Kraft Pulp, usingthe copper (I)–catalyzed alkyne‐azide 1,3‐dipolar cycloaddition (CuAAC) reaction,forming 1,2,3‐triazole aryl. These novel materials have been investigated for theirantibacterial properties againstEscherichia coliandStaphylococcus aureus. The devel-oped materials acquire its antimicrobial potential only after grafting via triazole link.Depending on the substituent of the grafted aryl, the elaborated materials showeda bacteriostatic or even bactericidal activity.
dc.language.isoENen_US
dc.subject.en1
dc.subject.en2
dc.subject.en3‐triazoles
dc.subject.enantibacterial material
dc.subject.encellulosic fibers
dc.subject.enclick chemistry
dc.subject.enfunctionalization of polymers
dc.title.enSynthesis, characterization, and antibacterial activities of a new lignocellulosic material carrying aryl triazole moiety
dc.title.alternativePolym Adv Technolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/pat.4471en_US
dc.subject.halChimie/Matériauxen_US
bordeaux.journalPolymers for Advanced Technologiesen_US
bordeaux.page344-350en_US
bordeaux.volume30en_US
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN) - UMR 5248
bordeaux.issue2en_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03182004
hal.version1
hal.date.transferred2021-03-26T08:40:46Z
hal.exporttrue
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Polymers%20for%20Advanced%20Technologies&rft.date=2019&rft.volume=30&rft.issue=2&rft.spage=344-350&rft.epage=344-350&rft.eissn=10427147&rft.issn=10427147&rft.au=KHALDI,%20Zineb&BESSE,%20Claire&NZAMBE%20TA%20KEKI,%20Jean%20Kerim&OUK,%20Tan-Soth%C3%A9a&GLOAGUEN,%20Vincent&rft.genre=article


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