简介：标题化合物（C24H16N4S）以噻吩-2-甲醛、苯甲酰乙腈和3-甲基-1-苯基-1H-吡唑-5-胺为原料,在离子液体[bmim]Br溶剂中,在80℃搅拌合成得到.其结构通过单晶X射线衍射法确定,晶体属于三斜晶系,空间群P-1,相对分子质量Mr=392.47,晶胞参数a=0.93612（8）nm,b=1.03063（12）nm,c=1.16624（16）nm,V=0.96853（19）nm3,Z=2,晶胞密度Dc=1.346g/cm3,吸收系数μ=0.185mm-1,单胞中电子的数目F（000）=408.晶体结构用直接法解出,经全矩阵最小二乘法对原子参数进行修正,最终的偏离因子R=0.0585,wR=0.1337.在晶体结构中新形成的吡啶环与吡唑环近似于共平面结构.
简介：AsimpleandefficientcascadeMichael/cyclizationreactionof3-aminoindolin-2-oneswithenones/enalswasidentifiedforthesynthesisofpotentiallybiologicallyactive3’,4’-dihydrospiro[pyrrol-3,2’-oxindoles],usingDBUasanefficientcatalystandethyleneglycolasanenvironmentallybenignsolvent.Morediverse3’,4’-dihydrospiro[pyrrol-3,2’-oxindoles]analoglibrarieswerepreparedingoodyields(upto97%).Thestructureof3’,4’-dihydrospiro[pyrrol-3,2’-oxindoles]wasconfirmedbymassspectrometryanalysis,NMRanalysisandsinglecrystalX-raydiffraction.Themainadvantagesofthismethodincludetheavailabilityofstartingmaterials,simpleexperimentaloperation,shortreactiontime,aswellashighyieldsobserved.
简介：Wehavefoundthattheexcitedenergyfromthegroundstatewith1f7=2configurationtothefirstexcitedstatewith2p3=2configurationin37SisobviouslylowercomparedwiththatinnearbyN=21isotones35Si,39Arand41Ca(seeFig.1,Theinsertindicatestherelevantsingle-particleorbitsofprotonandneutron).ThisinterestingphenomenonmayresultfromthecollapseofN=28closure,whichgivesthesufficientvalencespaceforcollectivedeformationwhichcanbeenrevealedfromtheB(E2)value.Therefore,toobtaintheB(E2),weperformtheexperimentsformeasuringthelifetimeofthefirstexcitedstatein37S.
简介：Wereporteddiversesolitonoperationsinathulium/holmium-dopedfiberlaserbytakingadvantageofataperedfiber-basedtopologicalinsulator（TI）Bi2Te3saturableabsorber（SA）.TheSAhadanonsaturablelossof53.5%andamodulationdepthof9.8%.Stablefundamentallymode-lockedsolitonsat1909.5nmwithdistinctKellysidebandsontheoutputspectrum,apulserepetitionrateof21.5MHz,andameasuredpulsewidthof1.26pswereobservedinthework.Byincreasingthepumppower,bothbunchedsolitonswithsolitonnumberupto15andharmonicallymode-lockedsolitonswithharmonicorderupto10wereobtained.Toourknowledge,thisisthefirstreportofbothbunchedsolitonsandharmonicallymode-lockedsolitonsinafiberlaserat2μmregionincorporatedwithTIs.
简介：AgraphGiscalledchromatic-choosableifitschoicenumberisequaltoitschromaticnumber,namelych(G)=χ(G).Ohba’sconjecturestatesthateverygraphGwith2χ(G)+1orfewerverticesischromaticchoosable.ItisclearthatOhba’sconjectureistrueifandonlyifitistrueforcompletemultipartitegraphs.Recently,Kostochka,StiebitzandWoodallshowedthatOhba’sconjectureholdsforcompletemultipartitegraphswithpartitesizeatmostfive.Butthecompletemultipartitegraphswithnorestrictionontheirpartitesize,forwhichOhba’sconjecturehasbeenverifiedarenothingmorethanthegraphsKt+3,2*(k-t-1),1*tbyEnotomoetal.,andKt+2,3,2*(k-t-2),1*tfort≤4byShenetal..Inthispaper,usingtheconceptoff-choosable(orL0-size-choosable)ofgraphs,weshowthatOhba’sconjectureisalsotrueforthegraphsKt+2,3,2*(k-t-2),1*twhent≥5.Thus,Ohba’sconjectureistrueforgraphsKt+2,3,2*(k-t-2),1*tforallintegerst≥1.
简介：Thispaperreportsonthelongevityofglycerol-dry(CO2)reformingoverthelanthanum(La)promotedNi/Al2O3catalysts.TheXRDresultsshowedthattheNiparticlewaswell-dispersedinthepresenceofLapromoter.Inaddition,viatheNH3-TPDanalysis,itwasfoundthattheLapromoterhasreducedtheacidityofNicatalystwhichmayhaveexplainedthemitigationofcarbonlaydown.Itwasdeterminedthatthe3.0wt%La-promotedNi/Al2O3catalystpossessedthelargestBETspecificsurfaceareaof97m2g-1.Consequently,ityieldedthebestcatalyticlongevityperformancewithconversionattainedmorethan90%,evenafter72hofreactionduration.Significantly,itcanbeconfirmedthatthepresenceofCO2duringtheglyceroldryreformingwasessentialinreducingcarbondeposition,mostlikelyviagasificationpathway.Thishasensuredastabilityofcatalyticactivityforalongreactionperiod(72h).
简介：Inthispaper,wereportedamultiwavelengthpassivelyQ-switchedYb3+:GdAl3（BO3）4solid-statelaserwithtopologicalinsulatorBi2Te3asasaturableabsorber（SA）forthefirsttime,tothebestofourknowledge.Bi2Te3nanosheetswerepreparedbythefacilesolvothermalmethod.TheinfluenceofthreeBi2Te3densitiesonthelaseroperationwascompared.Themaximumaverageoutputpowerwasupto57mWwithapulseenergyof511.7nJ.Theshortestpulsewidthwasmeasuredtobe370nswith110kHzpulserepetitionrateand40mWaveragepower.Thelaseroperatedatthreewavelengthssimultaneouslyat1043.7,1045.3,and1046.2nm,ofwhichthefrequencydifferenceswerewithintheterahertzwaveband.OurworksuggeststhatsolvothermalsynthesizedBi2Te3isapromisingSAforsimultaneouslymultiwavelengthlaseroperation.
简介：PlanarringresonatorwaveguidesarefabricatedinthinfilmsofAs2S3chalcogenideglass,depositedonsilicaon-siliconsubstrates.WaveguidecoresaredirectlywrittenbyscanningthefocusedilluminationofafemtosecondTi:sapphirelaseratacentralwavelengthof810nm,throughatwo-photonphoto-darkeningprocess.Alargephotoinducedindexchangeof0.3–0.4refractiveindexunitsisobtained.Theradiusoftheringresonatoris1.9mm,correspondingtoatransmissionfreespectralrangeof9.1GHz.Ahighloaded（intrinsic）Qvalueof110,000（180,000）isachieved.Thethermaldependenceoftheresonatortransferfunctionischaracterized.Theresultsprovidethefirstreport,tothebestofourknowledge,ofdirectlywrittenhigh-Qringresonatorsinchalcogenideglassfilms,anddemonstratethepotentialofthissimpletechniquetowardsthefabricationofplanarlightguidecircuitsinthesematerials.
简介：PureAl2O3-2SiO2powderswerepreparedbysol-gelandcoprecipitationmethods,andtheiralkaliactivationreactivitieswerecompared.Thealkali-activationreactivityofthepowderpreparedbythesol-gelmethodwashigherthanthatofthepowderpreparedbythecoprecipitationmethod.Thepowderswereinvestigatedby27AIand29Simagic-anglespinningnuclearmagneticresonancespectroscopy（MASNMR）tounderstandtherelationshipbetweentheirstructureandalkali-activationreactivity.The27AlMASNMRdatashowedthatthefive-coordinateAIcontentofthepowderpreparedbythesol-gelmethodwashigherthanthatofthepowderpreparedbycoprecipitation.Thehighercontentoffive-coordinateAlcorrespondedtohigheralkali-activationreactivity.The29SiMASNMRdatashowedthatforthepowderpreparedbythesol-gelmethod,siliconwasreplacedbyaluminumatsecondarycoordinationsitesofthecentralSiatomsduringcalcination.However,forthepowderpreparedbysingle-batchcoprecipitation,themainchangewasfromalowdegreeofpolycondensationtoahighdegreeofpolycondensation.
简介：Inthisarticle,nano-scaleAl/Fe2O3compositeswithdifferentmorphologiesweresuccessfullyobtainedbyasimpleelectrospinningtechnique,whichisbasedonasurfactant（polyvinylpyridine,PVP）inamixtureofN,N-dimethylformamide（DMF）and2-propanol.TheelectrospunAl/Fe2O3compositesexhibitedacrystalstructureandphasecompositionbyX-raydiffractionanalysis.ThedifferentmorphologiesoftheAl/Fe2O3compositeswerealsoobservedthroughscanningelectronmicroscopyandtransmissionelectronmicroscopy.Itwasfoundthattherathersimpleelectrospinningmethodusedtopreparethemorphology-controlledAl/Fe2O3compositesmayhavethepotentialforpreparationofpropellants,explosives,andpyrotechnicsinthefuture.
简介：Nanostructuredtransitionmetaloxidesarepromisingalternativeanodesforlithiumionbatteries.Li-ionstorageperformanceisexpectedtoimproveifhighpackingdensityenergyparticlesareavailable.Herein,Mn2O3microsphereswithaca.18μmdiameterandatappeddensityof1.33g/cm3weresynthesizedbyafacilesolvothermal-thermalcoversionroute.SphericalMnCO3precursorswereobtainedthroughsolvothermaltreatmentandtheydecomposedandconvertedintoMn2O3microspheresatanannealingtemperatureof700C.TheMn2O3microspheresconsistedofMn2O3nanoparticleswithanaverage40nmdiameter.TheseporousMn2O3microspheresallowgoodelectrolytepenetrationandprovideanionbufferreservoirtoensureaconstantelectrolytesupply.TheMn2O3microsphereshavereversiblecapacitiesof590and320mAh/gat50and400mA/g,respectively.Wethusreportanefficientrouteforthefabricationofenergyparticlesforadvancedenergystorage.
简介：Thenatureofresistivetransitionofhigh-qualitycrystallinethinfilmsofYBa2Cu3O7-δhasbeenstudiedundermagneticfields(H)appliedalongthecdirectionoverawiderangeofdopedholes,p,intheCuO2planes.Thefield-andtemperature-dependentin-planeresistivity,ρab(T,H),hasbeenanalyzedwithinthethermallyassistedflux-flow(TAFF)formalism.Thefluxactivationenergy,U(T,H),hasbeenextractedfromthisanalysis.Thelow-Tpartoftheρab(T,H)datacanbedescribedbyanactivationenergyhavingthefunctionalformofU(T,H)=(1-t)m(H-0/H)β,wheret=T/Tc(reducedtemperature),andH0isafieldscalethatprimarilydeterminesthemagnitudeofU(T,H).Thetemperatureexponent,m,showsasystematicvariationwithp,whereasthefieldexponent,β,isinsensitivetothepvaluesandisclosetounity.TheH0,ontheotherhand,changesrapidlyaspisvaried.U(T,H)islinkedtothepinningpotentialandconsequentlyonthesuperconductingcondensationenergy.Sincethenormalstatepseudogapdirectlyaffectssuperconductingcondensationenergy,aclearcorrespondencebetweenH0andthePGenergyscale,εg,isfound.Possibleimplicationsoftheseresultsarediscussed.
简介：Onenovelorganic-inorganichybridsupramolecularassemblies|（NDPA）（18-crown-6）]2+（DMA）+·3ClO4-（1）,hasbeensuccessfullyconstructedthroughtheprominentstrategiesofcrystalengineering（NDPA=N,N-dimethyI-1,4-phenylenediamine,DMA=dimethylamine）,andcharacterizedbyIR,powderXRDandsinglecrystalX-raydiffraction.Inthestructure,thesupramolecularorganiccationsandinorganicClO4-anionsarearrangedalternatelyandlinkedbyN-O…Hhydrogenbonds.ItisworthytonotethattheClO4-arelinkedtoformone-dimensionalinorganicchainthroughstrongNH…Ohydrogenbondsalongb-axis.Thereisnodistinctdielectricanomalyinthetemperaturedependentandfrequency-dependentdielectricconstantcurves,suggestingthatnophasetransitionexistswithinthemeasuredtemperaturerange（120-420K）.Therelativedisplacementofcationsandanions,theturnedpolarizationofmolecularelectricmomentandmacrocyclicmoleculerotatorarethemainfactorstodeterminethetrendofdielectricconstant.
简介：目的：探索燃料富氧燃烧过程中不同浓度CO2的稀释作用对NOx生成的影响，为探索Nx在O2／CO2气氛中生成机理研究提供理论基础。创新点：提出一种无分支链式反应解释说明CO2在还原性粒子环境中对反应的影响。方法：通过ChemkinPro中塞流式反应器模块对混入NH3的CH4燃料在O2／CO2气氛中反应进行数值模拟，同时改变CO2的稀释程度来探索CO2浓度对NOx生成的影响，并比较不同反应机理下的模拟结果，探索此环境中NOx的生成机理（表1）。结论：1．无支链反应机理可用于解释CO2在还原性粒子环境中对Nq生成与还原的影响；2．随着C02浓度的升高，无支链反应和支链反应相互竞争H，进而抑制NO的生成；3．在对NH，转化效率的影响方面，CO2浓度增加引发的无支链反应和支链反应对H的竞争，在富燃料条件下从促进转化变为抑制转化，在化学当量和贫燃料条件下从无影响变为抑制转化。
简介：Liquid-phase-exfoliationtechnologywasutilizedtopreparelayeredMoS2,WS2,andMoSe2nanosheetsincyclohexylpyrrolidone.Thenonlinearopticalresponseofthesenanosheetsindispersionswasinvestigatedbyobservingspatialself-phasemodulation（SSPM）usinga488nmcontinuouswavelaserbeam.ThediffractionringpatternsofSSPMwerefoundtobedistortedalongtheverticaldirectionrightafterthelasertraversingthenanosheetdispersions.Thenonlinearrefractiveindexofthethreetransitionmetaldichalcogenidesdispersionsn2wasmeasuredtobe10-7cm2W-1,andthethird-ordernonlinearsusceptibilityχ（3）10-9esu.TherelativechangeofeffectivenonlinearrefractiveindexΔn2e∕n（2e）oftheMoS2,WS2,andMoSe2dispersionscanbemodulated0.012–0.240,0.029–0.154,and0.091–0.304,respectively,bychangingtheincidentintensities.Ourexperimentalresultsimplynovelpotentialapplicationoftwo-dimensionaltransitionmetaldichalcogenidesinnonlinearphasemodulationdevices.
简介：Inthiswork,theinfluenceofCO2onthestructuralvariationandcatalyticperformanceofNa2WO4/Mn/SiO2foroxidativecouplingofmethanetoethylenewasinvestigated.ThecatalystwaspreparedbyimpregnationmethodandcharacterizedbyXRD,RamanandXPStechniques.AppropriateamountofCO2inthereactantgasesenhancedtheformationofsurfacetetrahedralNa2WO4speciesandpromotedthemigrationofOinMOx,Na,Wfromthecatalystbulktosurface,whichwerefavorableforoxidativecouplingofmethane.WhenthemolarratioofCH4/O2/CO2was3/1/2,enrichedsurfacetetrahedralNa2WO4speciesandhighsurfaceconcentrationofOinMOx,Na,Wweredetected,andthenhighCH4conversionof33.1%andhighC2H4selectivityof56.2%wereobtained.WithfurtherincreaseofCO2inthereagentgases,thecontentofactivesurfacetetrahedralNa2WO4speciesandsurfaceconcentrationofOinMOx,Na,Wdecreased,whilethatofinactivespecies(MnWO4andMn2O3)increaseddramatically,leadingtolowCH4conversionandlowC2H4selectivity.ItcouldbespeculatedthatNa2WO4crystalwastransformedintoMnWO4crystalwithexcessiveCO2addedunderthereactionconditions.PretreatmentofNa2WO4/Mn/SiO2catalystbymoderateamountofCO2beforeOCMalsopromotedtheformationofNa2WO4species.
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![<b style='color:red'>3</b><b style='color:red'>-</b>甲基-1,6-二<b style='color:red'>苯基</b>-4-（噻吩-<b style='color:red'>2</b><b style='color:red'>-</b>基）-1H-吡唑并[<b style='color:red'>3</b>,4-b]吡啶-5-甲腈的绿色合成和结构表征](/image/thesis0 "<b style='color:red'>3</b><b style='color:red'>-</b>甲基-1,6-二<b style='color:red'>苯基</b>-4-（噻吩-<b style='color:red'>2</b><b style='color:red'>-</b>基）-1H-吡唑并[<b style='color:red'>3</b>,4-b]吡啶-5-甲腈的绿色合成和结构表征")
![Direct construction of <b style='color:red'>3</b>＇,4＇-dihydrospiro[pyrrol-3,<b style='color:red'>2</b>＇-oxindoles]through a cascade Michael/cyclization reaction of <b style='color:red'>3</b>-aminoindolin-<b style='color:red'>2</b>-ones with enones/enals](/image/thesis2 "Direct construction of <b style='color:red'>3</b>＇,4＇-dihydrospiro[pyrrol-3,<b style='color:red'>2</b>＇-oxindoles]through a cascade Michael/cyclization reaction of <b style='color:red'>3</b>-aminoindolin-<b style='color:red'>2</b>-ones with enones/enals")
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