简介：Theinsertionof1,1-bis(1′-naphthyl)ethylenemonomerunitintotheactivepolystyrenechainendgreatlydecreasedthereactivityoftheactivechainendtothecarbonylgroup,andallowedthepolymericchainendtoreactonlywiththedoublebondinN-methacryloylcaprolactam,resultinginN-acylcaprolactamfunctionalizedpolystyrenein100%conversion.Newdiblockcopolymerofpolystyrenewithpolycaprolactamwassynthesizedbydirectreactionofthefunctionalizedpolymerwithcaprolactamwithoutaddingadditionalalkalimetalortheircaprolactamsalts.

简介：1－Ethoxycarbonylalkyldiphenylpolystyrylphosphoniumtriflatescanbeeasilypreparedbyquaternizingdiphenylpolystyrylphosphinewithethyl2-trifloxyalkanoates;basetreatmentofthesepolymer-supportedphosphoniumtriflatesaffords1-ethoxycarbonylalkylidenephosphoraneswhicharestableandundergosatisfactoryWittigreactions.

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：Newmodelcompound1H,1′H-Bis（benz-Δ^4-imidazoline)2,2′-spiro-titaniumdichloridewaspreparedandthestructureofthecompoundwasdeterminedby1R,MSandelementaryanalysis.

简介：Ｍｅｔａｔｈｅｓｉｓｏｆ１－ＨｅｐｔｅｎｅｏｖｅｒＴｕｎｇｓｔｅｎＣａｔａｌｙｓｔＩｍｍｏｂｉｌｉｚｅｄｏｎＰｏｌｙｍｅｒｓＹａｏＪｉｎｓｈｕｌ；ＬｉＨｏｎｇ；ＳｕｎＪｕｎｔａｎ；ＨｅＢｉｎｇｌｉｎ（ＩｎｓｔｉｔｕｔｅｏｆＰｏｌｙｍｅｒＣｈｅｍｉｓｔ...

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.

简介：Animprovedmethodisdevelopedbyusingstronglyacidiccationexchangeresin(001×1，H^+form)asacatalystforthesynthesisofdiphenyl1-(N-benzyloxycarbonyl-amino)alkanephosphonatesand1-(N-benzyloxycarbonylamino)alkanephenylphosphinicacidsinhighyields.

简介：

简介：Anovelpolymer-bound1,2-diol,3-polystyrylsulfonyl-1,2-propanediol(6)hadbeenpreparedbythereactionofsodiumpolystyrylsulfinatewithallylbromide,followedbyoxidationand.hydrolysisordirectlywith3-chloro-1,2-propanediolinthepresenceofaphasetransfercatalyst,n-tetrabutylammoniumiodide.Thecapacityofresin6forterephthaidehydereached1.43mmol/g.Thealdehydicgroupsattachedtopolymer6reactedwithhydroxylaminehydrochlorideorreducedbysodiumborohydridegivingp-formylbenzaldoxime(yield:89%)andp-formyl-benzalcohol(yield:734%),respectively.Thehighyieldsofthesepolymer-supportedreactionsshowedthatthepolymer6possessedtheeffectiveisolationofitsreactivesites.

简介：

简介：Theadsorptiondynamicsforphenolinaqueoussolutionoftheadsorbentbasedonpolystyrenewasstudied.InordertodistinguishwiththeBoydquasi-homogeneousmodeloftheinnerstructureofion-exchanger,theparticlediffusionmodelincludingsurfacediffustionmodelandporediffusionmodelwassuggestedwhichissuitabletothemacroporousadsorbent.Thediffusiondeterminationstepoftheadsorptionpocesswasestablishedandtheeffectivediffusioncoefficientwasalsodetermined.Theinfluenceofsurfacediffusionandporedifusionontheparticlediffusionratewasinvestigatedqualitatively.Allofthesewereveryimportanttoimprovethestructureofthemacroporousadsorbentinordertoimprovethemass-transferrate.

简介：Fluorescencepropertiesofaseriesofstyrene/p-divinylbenzene(St/p-DVB)copolymerbeadswereinvestigatedbysteady-statefluorescencespectra.Inadditiontothefluorescenceofthephenylringexcimer,anewemissionbandatca395nmappearswhenp-DVBcontentinfeedishigherthan13%(wt).Theintensityofthisnewemissionwasfoundtochangewithp-DVBcontentandtodecreasewithswollenbeads.Theoriginofthisnewemissionisconsideredtobeamulti-ringexcimerformation.

简介：Polymer-supportedRCpCpTiCl2(Cp=η^5-C5H4;RCp=η^5-RC5H4)havebeenpreparedandreducedbyi-C3H7MgBrinsitu，thenusedincatalyticisomerizationof1,5-hexadiene.Theisomerizationof1,5-hexadieneleadstoamixtureofcyclicandlinearproducts.Theratioofcyclictolinearproductdependsonthenatureofthesupporterandthesubstituentonthecyclopentadienylring.Theformercontributesthemost,forexample,silicasupportedCp2TiCl2gavecyclic-linearratioof99/1,whileforpolymer-supportedCp2TiCl2species,linearcompoundsarethemajorproductsandtheratioofcyclictolinearproductchangeswithdifferentRgroupsonthecyclopentadienylring.

简介：Thetreatmentandresourcereuseof1,2,4-acidproducingwastewaterbyself-mademacroporousadsorptionresinND,A-107wasstudiedinthispaper.Optimumadsorptionanddesorptionprocessparameterswereacquiredbysystematicallystudy.ThepolymericresinNDA-107indicatedgoodadsorption&desorptionof1,2,4-acidinthewastewater.Theremovalefficiencyof1,2,4-acid,CODerisabout78%,72%respectively.Itisevidentthatthisadsorptionprocessisanefficienttreatmentmethodfor1,2,4-acidproducingwastewater.Atthesametime,theaccumulationandresourcereuseofl,2,4-acidcanberealizedinthisprocess.

简介：Transesterificationbetweenmethyl-butyrateand1-butanolinnonaqueoussystemswascatalyzedbyporcinepancreaticlipasewhichwasimmobilizedoncross-linkedpolystyrene.Organicsolvents,substrateconcentration,contentsofwaterandotherparameterswhichaffecttheimmobilizedenzymeactivitywerestudied.Lipaseimmobilizedonhydrophobiccrosslinkedpolystyrenecanreduceitsdiffusionlimitinthereaction.Itwasfoundthattheactivityofimmobilizedlipaseinorganicsystemswastwotimesashighasthatoffreelipase.

简介：Fluorescencespectraofladderlikepolyphenylsilsesquioxane(LPPS)andladderlike1,4-phenylene-bridgedpolyvinylsiloxane(LPPVS)havebeenmeasuredasafunctionoftemperature(4-55℃),indilutetetrahydrofuransolution.Theexcimer(IE)tomonomer(IM)intensityratio(IE/IM)ofLPPSdilutesolutionshowsadoublelinearArrheniusplotwithabreakpointascribabletoatransitiontemperatureTr.Thisbehaviorhasnotbeenfoundforsinglechainpolyorganosiloxanes.WhenIn/EofLPPSwasplottedagainst1/T,italsogaveadoublelinearplotwithonebreakpoint,whichwasfoundinsinglechainpolyorganosiloxanes.ThedifferentbehaviorsbetweenLPPSandsinglechainpolyorganosiloxanesmaybemainlyattributedtotherelativelyrigiddouble-chainmacromolecularbackboneofLPPS.However,theln(IE/IM)ofdiluteLPPVSsolutionversus1/Tshowsasimplelinearvariationwithapositiveslopewhichconfirmsourproposition.ThedifferencebetweenthefluorescenceresultsofLPPSandthoseofLPPVSmaypossiblyderivefromtheirstructuredifferencesandcooperativemotioninbackbonechainbonds.