简介：Highlyselectivedimerizationofα-methylstyrene(AMS)waseffectedusingaBroenstedacidicionicliquid,[Hmim]^+BF4^-,assolventaswellascatalyst,providingtheindustrialhigh-valueolefin,2,4-diphenyl-4-methyl-1-pentene(1-PT).Thedesireddimer1-PTcouldbeobtainedin90%yieldat96%conversioninthedimerizationofAMSunderoptimizedconditions.Featuresoftheprocedureincludeuseofreadilyavailableionicliquid-catalyst,exclusionofvolatileorganicsolvents,higherselectivityandefficiencyfor1-PT.

简介：AnefficientroutetoprepareL-glucoseandL-galactoseisdescribed.TheL-sugarsareachievedbyusingthestrategyofswitchingthefunctionalgroupsatC1andC5ofD-glucoseandD-mannose.TheoxidationandreductionofthesilylenoletheratC1andthelead(IV)tetraacetatemediatedoxidativedecarboxylationatC5arethekeysteps.L-GlucoseandL-galactosearepreparedinaconvenientandinexpensiveway.

简介：［1］BASFUSP4479906［2］BASFBP1443541［3］BASFDE3618265［4］WangL.,WuZ.,ChinaLeather,26(8),11,(1997)［5］YuanL.,DinY.,ChineseChemistryBulletin,(2),19(1988)［6］KurokiH.,ChemistryofDyeingTheory(ChineseTranslation),TextileIndustryPress,Beijing,89(1982)［7］WangS.,LiP.,WuZ.DyestuffIndustry(Chinese),34(4),1,(1997)［8］Tian,Y.,Wu,Z.,Wang,G.,Zhang,S.J.ChineseChem.Eng.,46,156(1995)［9］Tian,Y.,Wang,G.,Wu,Z.,J.ChineseChem.Eng.,47,75(1996)［10］Lycka,A.,DyesandPigment,32,11(1996)［11］Griffith,J.,ColourandConstitutionofOrganicMolecules,AcademicPress,London,191(1976)

简介：ThecomplexK3H4GeW9V3O40·8H2OcrystallizedinamonocliiniesystemwithspacegroupP2,Mr=2784.67,a=11.099（3）,b=16.452（4）,c=13.534（4）,β=108.14°,Z=2,V=2348.493,F（000）:2456,μ=239.7cm-1,De=3.932g/cm3.ThefinalR=0.083for4528non-zeroreflexions.ThestructureofanionsGeW9V3O40andGeW9O34belongstoA--type.

简介：Poly(4-vinylpyridine)supportednanoparticleofcopper(Ⅰ)iodideisreportedasagreenandrecyclablecatalystfortheregioselectivesynthesisof1,4-disubstituted-1H-1,2,3-triazolesfrombenzylhalides,sodiumazideandterminalalkynesinwater.Thiscatalystcanberecoveredbysimplefiltrationandrecycledupto8consecutiverunswithoutanylossofitsefficiency.

简介：Sixnewopticallyactivepoly(amide-imide)s(5a-f)weresynthesizedthroughthedirectpolycondensationreactionofN,N'-(4,4'-diphthaloyl)-bis-L-leucine(3)withsixhydantoinderivatives(4a-f).Triphenylphosphite(TPP)/pyridineinthepresenceofcalciumchloride(CaCl_2)andN-methyl-2-pyrrolidone(NMP)weresuccessfullyappliedfordirectpolycondensation.Thepolycondensationreactionsproduceaseriesofnewpoly(amide-imide)s(5a-f)inhighyields,andinherentviscositybetween0.42and0.55dL/g.Theresultingpoly(amide-imide)s(5a-f)werecharacterizedbyelementalanalysis,viscositymeasurements,thermalgravimetricanalysis(TGAandDTG),solubilitytestandFT-IRspectroscopy.

简介：NineteenL-N-2-hydroxyethylaminoacidsandL-N,N-bis(2-hydroxyethyl)aminoacidswerepreparedfromthereactionofchlorohydrinwithL-alanine,L-valine,L-leucine,L-isoleucine,L-phenylalanine,L-serine,L-thrcunine,L-glutamicacid,L-asparticacidandglycine.L-N,N,N’,N’-tetra(2-hydroxyethyl)cystinewaspreparedbythereactionofL-cystinewithchlorohydrin.

简介：采用电感耦合等离子体原子发射光谱法测定钛合金TC4中Fe、Al、V含量。使用硝酸与氢氟酸溶解试样，大幅缩短了溶样时间；确定了Fe、Al、V分析线分别为238.204、309.271、292.402nm。精密度实验表明，待测组分的相对标准偏差(RSD，n=10)均低于1.3%，能满足钛合金TC4中Fe、Al、V含量的检测要求。

简介：Dibromobiphenylreactedwithcynomethylanioninammoniaunderirradiationtoformnucleophilicbis-substitutedproductinhighyieldwithoutsubstantialmonosubstitutedproduct.Quantumyieldsfortheformationsofbis-andmonosubstitutedproductswerefoundtobe85.6and2.3×10-6respectively,whilethecorrespondingpseudo-first-orderrateswere6.9×10-3and5.2×10-10mol.L-1.S-1.Blockupthepossibleelectrontransferof4-brome-4’-cyanomethylbiphenylylradicalanionto4-cyanometbyl-biphenylylradicalandbromineion.

简介：Anewbiflavonoid,stelleranol,wasisolatedfromtherootsofStellerachamaejasmeL..ItsstructurewasdeterminedbytheanalysisofMSandNMRdata,especially2DNMRspectra.

简介：

简介：新奇sesquiterpenoid，pterisemipol，从PterissemipinnataL被孤立。它的骨骼，也就是pterisane，被认为从protoilludane被重排，它的结构根据分光镜的分析被阐明。

简介：Ahomologousseriesof4’-methylphenyl4"-[(4-alkoxy-2,3,5,6-tetrafluorophenyl)ethynyl]-benzoateshavebeensynthesized.Polarizingmicroscopictexturalobservationshowsthatsuchcompoundsexhibitenantiotropicnematicphase.

简介：

简介：Thesynthesisofopen-fiameworkmetalphosphateshasbeenasubjectofintenseresearchowingtotheirinterestingstructuralchemistryandpotentialapplicationsasionexchangers,catalystsandadsorbents.Alargenumberofthesematerialsaresynthesizedinthepresenceoforganicaminesasstructure-directingagents.Recently,manyresearchactivitieshavefocusedonthesynthesisofinorganic-organichybridframeworks.Ascomparedwithinorganicligands,theadvantageofusingorganicmultidentateligandsistheefficacyofrationaldesignofcrystallinesolidsthroughtheircoordinatingpropensitiesandgeometries.

简介：Thesynthesisandphasebehaviorofaseriesof4’-alkyloxy-4-hydroxybiphenylswerediscribed.Theeffectsofreactionconditionsontheyieldsofproductswereinvestigated.Thecharacterizationsofthermotropicliquidcrystallineproductsforthetypeandthermalpropertiesarediscussedthroughtheuseofdifferentialscanningcalorimetry,polarizingmicroscopy.

简介：Reactionsofthe6-hydroxy-thiopyrano[3,4-c]pyridine-5-carbonitrilederivative1withα-halo-carbonylcompoundsgavetheortho-substitutedintermediates2a-cwhichwereconvertedintofuro[2,3-b]thiopyrano[4,3-d]pyridines3a-cbyfusionofafuranmoietyunderbasicconditions.Furthercyclizationof3a-cledtoafusionofapyrimidinering,yieldingthetetracyclicproducts6,7and8.Inaddition,condensationof6withvariousaromaticaldehydesaffordedthecorrespondingimines9a,b.Mannichreactionof7gaveproducts10a,b.

简介：3,5,6,8-Tetrahydro-4H-thiopyrano[4′,3′:4,5]thieno[2,3-d]pyrimidin-4-ones(7)weresynthesizedviathebasecatalyticreactionsofaminesorphenolswithcarbodiimides(5),whichwereobtainedfromtheaza-Wittigreactionsofiminophosphoranes(4)witharomaticisocyanates.

简介：ByusingOH-terminatedpolyaryletherdendrimerandN-Fmoc-glycineasrawmaterials,thedendriticpolyarylether2-aminoacetate(G3-NH2)wassynthesizedviatwostepreactions.G3-NH2asamacroinitiatorforthering-openingpolymerizationofγ-benzylL-glutamateN-carboxyanhydridewasinvestigated.Itisfoundthattheresultingcopolymerspossessedrelativelyhighmolecularweightandnarrowmolecularweightdistribution(1.12

简介：ConformationofL-lysineinaqueoussolutionwasinvestigatedbylanthanideshiftprobes（Dy,Ho,Er,TmandYb）.Reilley’smethodwasemployedtoseparatethecontactanddipolarcom-ponentsofthe13Cparamagneticshifts.ThisstudyrevealsthatCαshifthasthelargestcontactcon-tributionwhiletheothercarbonshiftsaredominatedbythedipolarcontribution.TheaverageoverallconformationofL-lysineinaqueoussolutionisextendedwiththemolecularbackboneintransform.Inthecomplex,lanthanideioncoordinatestothecarboxylgroupwithLn—Obondlength2.2/nandthewholeligandislocatedoutsidethezero-dipolarshiftconeofthelanthanideion.Theelectronicspindensitydistributionontheligandnucleishowsthatthespinpolarizationisthepredominantmech-anismofthecontactinteractionfornucleiincloseproximitytotheboundlanthanideion.