简介：Tetradecyldimethylbenzylammoniumsalt(TDMBA)cationswereintercalatedintosodiummontmorillonite(Na-MMT)byanionexchangereaction.TheresultingTDMBA-MMTwascharacterizedbyFourier-transforminfraredspectroscopy(FTIR),thermogravimetricanalysis(TGA),andX-raydiffraction(XRD).Moreover,theantibacterialactivityandwater-resistanceofTDMBA-MMTwereinvestigated.TheresultsshowthatTDMBAcationsareintercalatedintotheNa-MMT.TheonsettemperatureofdecompositionofTDMBAcationsinTDMBA-MMTisraisedabout60℃higherthanthatoftetradecyldimethylbenzylammoniumchloride(TDMBACl),andthed_((001))spacingenlargedfrom1.23nmto2.10nm.0.1mg/mLTDMBA-MMTisfullyenoughtokillalltheStaphylococciaureus(S.aureus)andmorethan99.99%oftheEscherichiacoli(E.coli)inasamplesolutionwithin6.0htouch,andtheTDMBA-MMTalsoshowslongactingproperties.

简介：Anewmethacrylamidemonomer,hexylaminemethacrylamide(MAHA),wassynthesizedandusedinpolymerizations.ThehomopolymerofMAHAanditscopolymersweresynthesizedbyfreeradicalpolymerizationtechniqueswithN-isopropylacrylamide(NIPAAm)intwodifferentcompositions.Thequaternizationofthehomopolymerandcopolymerswerecarriedoutusing1-bromopropane.ThecopolymerswithNIPAAmandalowMAHAcontentshowedtemperature-responsivebehaviorinanaqueousenvironment.Thelowercriticalsolutiontemperatures(LCSTs)ofthesepolymersvariedbetween32℃and44℃.TheLCSTsofquaternizedcopolymerswerehigherthanthoseofneutralcopolymersbecausetheyweremorehydrophilic.TheobtainedhomopolymersandcopolymersweretestedforantibacterialactivitiesagainstS.aureusandE.coli.Thequaternizedwater-solublecopolymersshowedantibacterialactivitiesagainstS.aureus.Thequaternizationresultedinthesynthesisofbothantibacterialandtemperature-responsivecopolymers.

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简介：Fivenewcephalosporincompoundsweredesignedandsynthesized,andtheantibacterialactivitieswereevaluatedbythestandardserial2-foldagardilutionmethodinvitro.TheresultsshowedthattheactivitiesofthecompoundsⅠaandⅠbagainstESBLE.coliandK.pneumoniaearecomparabletothoseofCefepime.

简介：Severalkindsofactivatedcarbonfiber(ACF),GranuleActivatedcarbon(AC)containingsilverionorfinesilverparticle(Ag-ACF/AC)havebeenpreparedbysoakingACForACinthesaltsolutionofsilver.Ag,AgClandAgIcompoundshavebeenloadedontothefibers:Thestuctureofthefiberswasmeasuredbyscanningelectronmicroscopy(SEM)andpowerX-raydiffraction(XRD),THeAgcontentinthefiberwasobtainedbyanAtomicabsorptionspectroscopy(AAS),TheAg^+contentinwateraftertheantibacterialtestwasmeasuredbyanInductivelyCoupledplasma(ICP)emissionspectroscopy.AntibacterialtestwascarriedoutagainstEscherichiacoli(E.coli)andStaphylococcusaureus(S.aureus).TheresultsshowthatAg-ACF/AChavestrongantibacterialactivityagainstE.ColiandS.aureus.AfterdealtwithACF/ACloadingAg,AgCl,AgI,noE.coliandS.aureusaliveinsolutioncanbedetected.TheanalysisofAgcontentinwaterafterantibacterialtestshowedthatthecontentofAgmeetthequalityrequirementoftheNationalPotableWaterStandrd,ItisindicatedthatACF/AC-Aginthisexperimentwouldbeasafeantibacterialagent.

简介：Polymersupportedalkyldimethylbenzylammoniumchlorideresindisinfectantusedforthedisinfectionofdrinkingwaterhasbeensynthesized,anditsantibacterialactivitieshavebeendetermined,comparedwiththecommerciallyusedtriiodinedisinfectantresin.Theresindisinfectantwasgeneratedsuccessfullywhenusethecombinationofsurfaceactiveagentsandultrosonic.

简介：Severalkindsofactivatedcarbonfibers,usingsisalfiberasprecursors,werepreparedwithsteamactivationorwithZnCl2activation.Zincoritscompoundsweredispersedinthem.Theantibacterialactivitiesoftheseactivatedcarbonfibersweredeterminedandcompared.TheresearchresultsshowedthatthesesisalbasedactivatedcarbonfiberssupportingzinchavestrongerantibacterialactivityagainstEscherichiacoliandS.aureus.Theantibacterialactivityisrelatedtotheprecursors,thepyrolysistemperature,andthezinccontent.Inaddition,smallquantityofsilversupportedonzinc-containingACFswillgreatlyenhancetheantibacterialactivityofACFs.

简介：我们为把坚持、有效的抗菌剂性质合并到广泛地使用的聚合物报导灵巧的策略，poly(甲基methacrylate)(PMMA)，由异分子聚合有2-(tert-butylamino)的甲基methacrylate(MMA)在经由原子转移基聚合(ATRP)的一个壶的乙醇methacrylate(TA)。随后自己组装结果poly(甲基methacrylate)-block-poly[(2-tert-butylamino)ethylmethacrylate](PMMA20-b-PTA15)diblock共聚物负担得起明确的水可分散的泡，它能轻易地为有效抑制在医院里在墙上被喷洒并且细菌杀死。1H-NMR和胶化浸透层析(GPC)研究证实了良好共聚物的成功的合成。传播电子显微镜学(TEM)，原子力量显微镜学(AFM)和散布的动态光(DLS)学习与狭窄的尺寸分发证明了泡的形成。DLS研究在各种各样的温度揭示了泡的优秀稳定性。抗菌剂测试对克积极、克否定的细菌显示出聚合物泡的有效抗菌剂活动。而且，这策略可以为在许多领域里为灵巧的抗菌剂应用准备大量聚合材料被扩大。

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简介：Antibacterialpoly(D,L-lactide)(PDLLA)fibrousmembranesweredevelopedviaelectrospinning,followedbysurfacemodificationwhichinvolvedplasmapretreatment,UV-inducedgraftcopolymerizationof4-vinylpyridine(4VP)andquaternizationofthegraftedpyridinegroupswithhexylbromide.ThesuccessofmodificationwithquatemizedpyridiniumgroupsonthePDLLAfibrousmembraneswasascertainedbyX-rayphotoelectronspectroscopy(XPS).TheantibacterialactivitiesofthesemembraneswereassessedagainstGram-positiveStaphylococcusaureus(S.aureus)andGram-negativeEscherichiacoli(E.coli).ThePDLLAfibrousmembranesmodifiedwithquaternizedpyridiniumgroupsshowedantibacterialefficiencyagainstbothbacteriaashighas99.999%.Theresultsdemonstratedthattheantibacterialactivitywasbasedontheinteractionofthepositivechargeofpyridiniumgroupandnegativelychargedcellmembraneofbacteria,resultinginlossofmembranepermeabilityandcellleakage.

简介：Asystematicstudyonthesynthesisandantibacterialactivityofthequaternary"onium"saltsgraftedonaninsoluble"gel-type"stryene-7%divinylbenzenecopolymerbypolymer-analogousreactionsisshowed.Antibacterialactivityofquaternaryammoniumand/orphosphoniumsaltsgraftedonpolymer-supportshasbeenstudiedagainststaphylococcusaureusandEscherichiacoli.Awidevarietyof"onium"saltsboundtomacromolecularsupportswithdifferentquaternarygroupsanddifferentquaternarychainlengthsubstituentswereexamined.Theantibacterialactivityofmixed"onium"saltsincreasesasaconsequenceoftheassociationofammoniumandphosphoniumsaltsgraftedonthesamepolymericsupport.

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简介：6/3-(4-Chlorophenyl)-s-triazolo[3,4-b][1,3,4]thiadiazoles(2a-e)and(5a-e)weresynthesizedrespectivelybyintermolecularcyclizationof5-aryl/4-chlorophenyl-4-amino-3-mercapto-1,2,4-triazoles(1a-e)and(4)with4-chlorobenzoicacid/arylacids,whichwerecondensedwithpiperazineunderphasetransfercatalystTBABtoyieldthecorrespondingfreebasesofmonopiperazinederivativesandfollowedtoformwater-solublesalts(3a-e)and(6a-e)withhydrochloricacidingoodyields.Theinvitrobiologicalresultsshowedthatpiperazinegroupconjugatedwiththeabovefusedheterocyclesplayedanimportantroleinantibacterialactivity.ThestructuresofnovelcompoundswereconfirmedbyIR,1HNMR,MSandelementalanalysis.

简介：Treatmentof4-amino-3-(1-aryl-5-methyl-1,2,3-triazol-4-yl)-5-mercapto-1,2,4-triazoles/2-amino-5-(1-aryl-5-methyl-1,2,3-triazole-4-yl)-1,3,4-thiadiazoleswithbenzaldehyde,acetoneandω-bromoacetophenonewastestedandcompared.ThetitlecompoundsSchiffbases,amides,imidazolo[2,1-b]-1,3,4-thiadiazolesand7H-s-triazolo[3,4-b]-1,3,4-thiadiazineshavebeenconfirmedbyelementalanalyses,^1HNMR,IRandMSspectra.AllthecompoundshavealsobeenscreenedfortheirantibacterialactivitiesagainstB.subtilis,S.aureusandE.coli.