简介：Amild,regioselective1,3-dipolarcycloadditionprotocolforthepreparationofphenylselenomethylisoxazolinesthroughsubstitutedallylphenylselenidesandnitrileoxideswasreported.

简介：没有明显的形态学损坏的一条直接decarbonation线路为大测微计规模被开发分层的双氢氧化物(LDH)。首先，我们综合了有由最近报导的脲水解作用方法的测微计尺寸的侧面的尺寸的纯、六角形形状的LDH。然后，使用HNO3NaNO3混合了答案，有在夹层(LDH_CO3)的碳酸盐阴离子的获得的LDH直接被使除去碳酸到它的硝酸盐形式，LDH_NO3，它的形态学和粒子尺寸仍然是未改变的。与最近出版的二拍子的圆舞decarbonation方法相比，此处报导的直接decarbonation是很方便的。

简介：Three—layerback—propagationneuralnetworkswereusedforprocessingtheinformationprovidedbytheultravioletspectraoffive—componentmixtures,affectingthesimultaneousdeterminationofthecomponentswithsatisfactoryresults.

简介：Poly(vinylidenefluoride)(PVDF)/multi-walledcarbonnanotube(MWCNT)nanocompositeswerepreparedbymeansofultrasonicdispersionmethod.X-raydiffraction(XRD)resultsindicatethatincorporatingMWCNTsintoPVDFcausedtheformationofβphase.Athermalannealingat130°Cconfirmedthattheβphasewasstableinthenanocomposites.Differentialscanningcalorimetry(DSC)resultsindicatethatthemeltingtemperatureslightlyincreasedwhiletheheatoffusionmarkedlydecreasedwithincreasingMWCNTcontent.ThetensilestrengthandmodulusofPVDFwereimprovedbyloadingtheMWCNTs.Thescanningelectronmicroscopy(SEM)observationsshowedthatMWCNTswereuniformlydispersedinthePVDFmatrixandaninterfacialadhesionbetweenMWCNTandPVDFwasachieved,whichwasresponsiblefortheenhancementinthetensilestrengthandmodulusofPVDF.

简介：Polyamide/acrylonitrile-butadiene-styrenecopolymer(PA/ABS)blendshavedrawnconsiderableattentionfrombothacademiaandindustryfortheirimportantapplicationsinautomotiveandelectronicareas.DuetopoormiscibilityofPAandABS,developinganeffectivecompatibilizationstrategyhasbeenanurgentchallengetoachieveprominentmechanicalproperties.Inthisstudy,wecreateasetofmechanicallyenhancedPA6/ABSblendsusingtwomulti-monomermelt-graftedcompatibilizers,SEBSg-(MAH-co-St)andABS-g-(MAH-co-St).Thedisperseddomainsizeissignificantlydecreasedandmeanwhiletheunique“softshell-encapsulating-hardcore”structuresforminthepresenceofcompatibilizers.Theoptimummechanicalperformancesmanifestanincreaseof36%intensilestrengthandanincreaseof1300%inimpactstrength,comparedwiththeneatPA6/ABSbinaryblend.

简介：Inthisworkamulti-objectivequantitativestructure-propertyrelationship(QSPR)analysisapproachwasreportedbasedonthestudyonthreepartitionpropertiesof50aromaticsulfur-containingcarboxylates.Heremulti-objectives(properties)weretakenasavectorforQSPRmodeling.Thequantitativecorrelationsforpartitionpropertiesweredevelopedusingage-neticalgorithm-basedvariable-selectionapproachwithquantumdescriptors,derivedfromAM1-basedcalculations.WiththeQSPRmodels,theaqueoussolubmty,octanol/waterpartitioncoefficientsandreversed-phaseHPLCcapacityfactorsofsulfur-contalningcompoundswereestimatedandpredicted.UsingGA-basedmultivariatelinearregressionwithcross-vali-dationprocedure,asetofthemostpromisingdescriptorswasselegtedfromapoolof28quantumchemicalsemi-empiricalde-scriptors,inclodingstericandelectronictypes,tointegrallybuildQSPRmodels.Theselectedmoleculardescriptorsinclud-edthenetchargesoncarboxylgroup(Qoc),the2ndpowerofnetehnrgesonnitrogenatoms(QN^2),thenetatomicchargeonthesulfuratoms(Qs),thevanderWaalsvolumeofmolecule(V),themostpositivenetatomicchargeonhydrogenatoms(QH)andthemeasureofpolarityandpolarizability(π),whichweremainfactorsaffectingthedistributionprocessesofthecompoundsunderstudy.ThestatisticallybestQSPRmodelsofsixdescriptorsweresimultaneouslyobtainedbyGA-basedlinearregressionanalysis.WiththeselecteddescriptorsandtheQSPRequations,mechanismsofpartitionactionoftheSulfur-containingcarboxylateswereabletobeinvestigatedandinter-preted.

简介：

简介：Inthiswork,acidfunctionalizedmulti-wallcarbonnanotubes(MWCNTs)weremodifiedwithimidazolium-basedionicliquids.Theselectiveoxidationofvariousalcoholswithhydrogenperoxidecatalyzedby[PZnMo_2W_9O_(39)]~(5-),ZnPOM,supportedonionicliquids-modifiedwithMWCNTs,MWCNTAPIB,isreported.Thiscatalyst[ZnPOM@APIB-MWCNT],wascharacterizedbyX-raydiffraction,scanningelectronmicroscopy(SEM)andFT-IRspectroscopicmethods.Thisheterogeneouscatalystexhibitedhighstabilityandreusabilityintheoxidationreactionwithoutlossofitscatalyticperformance.

简介：3,4,5代用品furan-2(5H)的灵巧的一个壶合成从在用象催化剂的tetra-n-butylammonium重硫酸盐的温和条件下面的苯胺衍生物，dialkylacetylenedicarboxylates和芳香的醛的三部件的反应的一衍生物被开发了。