简介:The1,1'-binaphtholbasedoligomers3and7with3,3'-acetylene-phenylene-acetylenespacerwerepreparedfromBINOL1.ThehighopticalrotationvalueandCDspectrademonstratedthemainchainchiralityoftheoligomermolecule.TheUV-VISandfluorescentspectraevidencethecharacteristicsofconjugatedstructure.Incomparisonwitholigomer2bearing3,3'-acetylenespacer,theoligomers3and7havelongerefficientconjugationsegment,andtheirfluorescentquantumyields(φ)increased(0.60-0.65versus0.14).Extendingtheeffectiveconjugationsegmentwouldimprovethephotophysicalpropertiesofchiralconjugatedpolymers.``
简介:Thepolymerizationof1-octeneinitiatedbymethylalumoxane(MAO)-activatedNi(Ⅱ)-based-α-diiminecomplexes[(2,6-i-Pr)_2C_6H_3-DAB(An)]NiBr_2wasinvestigated.Usingthiscatalyst,poly(1-octene)swithmolecularweightbetween100×10~3and400×10~3andpolydispersity(M_w/M_n)between1.3and1.5weresynthesizedsuccessfullybyvaryingreactiontimeatroomtemperature.Thepoly(1-octene)swereamorphouspolymersandcouldbewellsolubleintetrahydrofuran(THF).Afterfractionalprecipitation,poly(1-octene)swithnarrowmolecularweightdistributions(M_w/M_n≤1.12)wereobtained.Theirweight-averagemolecularweightsweremeasuredbygelpermeationchromatography(GPC)inconjunctionwithonlinemodelBI-MwAmultianglelaserlightscattering(MALLS),andtheirintrinsicviscositiesweremeasuredbyMaron'ssingle-pointmethod.ThekandavaluesinMark-Houwinkequation[η]=KM~αinTHFat40℃were0.089mL/gand0.61respectively.
简介:Theinsertionof1,1-bis(1′-naphthyl)ethylenemonomerunitintotheactivepolystyrenechainendgreatlydecreasedthereactivityoftheactivechainendtothecarbonylgroup,andallowedthepolymericchainendtoreactonlywiththedoublebondinN-methacryloylcaprolactam,resultinginN-acylcaprolactamfunctionalizedpolystyrenein100%conversion.Newdiblockcopolymerofpolystyrenewithpolycaprolactamwassynthesizedbydirectreactionofthefunctionalizedpolymerwithcaprolactamwithoutaddingadditionalalkalimetalortheircaprolactamsalts.
简介:Thestructureofpolyimidefrom1,4-bis(3’,4’-dicarboxyphenoxy)benzeneand4,4’-oxydianilinefilmspecimensbeforeandafterhotstretchinghasbeeninvestigatedbyWAXD,DSCandFTIR.AsevidencedbyboththeWAXDandDSCresults,itcouldbebelievedthatstraininducedcrystallizationdidtakeplaceafterhotstretching.Meanwhile,shiftingpositionandsplittingofsomebandpeaksexistedontheFTIRspectrogramswereexplainedintermsoftheclosepackingofchainsandthechangesofinter-molecularcharge-transferinteractionbetweenimidegroupsandaromaticgroupsuponcrystallization.
简介:Theefficiencyofthepoly(3-hexylthiophene)(P3HT)and[6,6]-phenylC61-butyricacidmethylester(PC61BM)basedorganicsolarcellswasenhancedbyusing1,2,4-trichlorobenzene(TCB)asaprocessingadditivetocontroltheblendmorphology.TheadditionofTCBimprovedthearrangementofP3HTwhichresultedingoodphaseseparatedblendfilms.Correspondingly,theoptimizedsolarcellsshowedapowerconversionefficiency(PCE)of4.17%withafillfactor(FF)of0.69,whichwerehigherthanthoseofcommonthermalannealingdevices(PCE3.84%,FF0.67).Theefficiencywasfurtherimprovedto4.74%bythermalannealingat150°Cfor10minwithahigherFFof0.74.
简介:1-Ethoxycarbonylalkyldiphenylpolystyrylphosphoniumtriflatescanbeeasilypreparedbyquaternizingdiphenylpolystyrylphosphinewithethyl2-trifloxyalkanoates;basetreatmentofthesepolymer-supportedphosphoniumtriflatesaffords1-ethoxycarbonylalkylidenephosphoraneswhicharestableandundergosatisfactoryWittigreactions.
简介:Newmodelcompound1H,1′H-Bis(benz-Δ^4-imidazoline)2,2′-spiro-titaniumdichloridewaspreparedandthestructureofthecompoundwasdeterminedby1R,MSandelementaryanalysis.
简介:在这个工作,综合体新热地稳定(amide-imide)poly,有在n丁基甲基imidazolium溴化物的悬挂的2-pyridyl-1,3,4-oxadiazole单位的s作为反应媒介被报导了。新二羟基的酸从肼的反应被导出,2-(5-(3,5-diaminophenyl)-1,3,4-oxadiazole-2-yl)pyridine(POBD),和trimellitic酸酐。聚合物在丁基甲基imidazolium溴化物从diimide二酸(DIDA)和不同的芳香的肼的反应被准备,[bmim][Br],面对triphenyl亚磷酸盐(TPP)作为没有需要任何额外的部件的压缩代理人。poly准备了(amide-imide)s被FTIR描绘,元素的分析,并且通过模型混合物的合成。准备聚合物是可溶的在极并且aprotic溶剂例如DMF,DMSO,NMP和DMAc。聚合物答案的固有的粘性在在0.125g/dL的集中在集中的H2SO4测量在的0.521.33dL/g的范围(25
简介:Anovelpolymercontainingthesucrosegroupwassynthesizedbyradicalpolymerizationfromanenzymaticallypreparedmonomer,1′-O-vinyladipoyl-sucrose(VAS).TransesterificationreactionofsucrosewithdivinyladipateinanhydrouspyridinecatalyzedbyanalkalineproteasefromBacillussubtilisat60℃for7daysgaveVAS(yield55%)withoutanyblocking/deblockingsteps.ThevinylsucroseestercouldbepolymerizedwithpotassiumpersulfateandH2O2asinitiatortogivepoly(1′-O-vinyladipoyl-sucrose)withMn=33,000andMw=53,200,Mw/Mn=1.61.Thepolymerwasbiodegradable.After6daysinaqueousbuffer(pH7),thisalkalineproteasecoulddegradepoly(1′-O-vinyladipoyl-sucrose)toMnofca.1080,Mw/Mn=3.30(37℃),andMnofca.5200,Mw/Mn=2.44(4℃).Thepolymercontainingthesucrosebranchwouldbeafunctionalmaterialinvariousapplicationfields.
简介:Thecopolymerizationofl-octenewithstyrenecatalyzedbyrareearthcoordinationcatalystshasbeenstudiedforthefirsttime.Somefeaturesandkineticbehavioraredescribed.Theoverallactivationenergyofthecopolymerizationwas22.2KJ/molandthecopolymerizationratecouldbeexpressedasRp=Kp[Nd][M]2.(=1.68×10-3L2/mol2.S,50℃,[Oct]/[St]=1).ThecatalyticactivityofvariousrareearthelementsinLn(naph)3forthecopolymerizationwascomparedandshowsthefollowingsequence:Dy,Y,Yb>Ho>Sm,Gd,Nd>Pr>Ce>La>Tm.Bothmonomersofl-octeneandstyreneinthecopolymerizationbyNd(naph)3-AlEt3havethetendencyofconstantproportioncopolymerization.Thestructureofthecopolymerswasstudiedby1H-NMR.
简介:ThephysicalandchemicalpropertiesofFFA-1ionexchangefiberhavebeencharacterizedwithIRspectrum,thermalanalysisandSEMmeans.ThepHtitrationcurve,swellingrate,mechanicalproperties,resistancedropoffilterlayeraswellasthedynamicadsorptionforSO2wasdetermined.TheseexperimentsprovidedtheessentialparametersforthepracticalapplicationofFFA-1materialinadsorptionoftoxicgases.
简介:Aseriesof1-naphthylmethylmethacrylate(NMMA)-methylmethacrylate(MMA)copolymersweresynthesizedonfreeradicalmechanism.ThereactivityratiosofNMMA(r1)andMMA(r2)werereportedtobe0.83and0.89,respectively.ThecharacterizationofthecopolymersbyusingIR,NMR,GPC,UVandfiuorescencespectrometrywasdescribedinthispaper.
简介:Opticallyactive(R)-(+)-2,2’-bis(2-trifluoro-4-aminophenoxy)-1,1’-binaphthylwaspreparedfrom1,1’-bi-2-naphthol.Theopticallyactivearomaticpolyimidewasalsosuccessfullysynthesized.Thisnewpolymerhasgoodsolubility,thermalstabilityetc.Itsspecificrotationwasfoundtobe+174°,anditschiropticalpropertywasalsostudied.