简介：AnewlayeredCu-basedoxychalcogenideBa3Fe2O5Cu2S2hasbeensynthesizedanditsmagneticandelectronicpropertieswererevealed.Ba3Fe2O5Cu2S2isbuiltupbyalternativelystacking[Cu2S2]2-layersandironperovskiteoxide[（FeO2）（BaO）（FeO2）]2-layersalongthecaxisthatareseparatedbybariumionswithFe3+fivefoldcoordinatedbyasquare-pyramidalarrangementofoxygen.Fromthebondvalencearguments,weinferredthatinlayeredCuCh-based（Ch=S,Se,Te）compoundsthe+3cationinperovskiteoxidesheetprefersasquarepyramidalsite,whilethelowervalencecationprefersthesquareplanarsites.Thestudiesonsusceptibility,transport,andopticalreflectivityindicatethatBa3Fe2O5Cu2S2isanantiferromagneticsemiconductorwithaNe′eltemperatureof121Kandanopticalbandgapof1.03eV.Themeasurementofheatcapacityfrom10Ktoroomtemperatureshowsnoanomalyat121K.TheDebyetemperatureisdeterminedtobe113K.TheoreticalcalculationsindicatethattheconductionbandminimumispredominantlycontributedbyO2pand3dstatesofFeionsthatantiferromagneticallyarrangedinFeO2layers.TheFe3dstatesarelocatedatlowerenergyandresultinanarrowbandgapincomparisonwiththatoftheisostructuralSr3Sc2O5Cu2S2.
简介：利用水热合成方法合成了2个新的苯并咪唑修饰的Keggin型多酸基化合物[（C_7H_6N_2）_3（H_3PMo_（12）O_（40））]·H_2O（1）和[KNa_2（C_7H_5N_2）_2（H_（2.5）SiW_（12）O_（40））_2]·6（C_7H_6N_2）（2）（C_7H_6N_2=苯并咪唑）.化合物1为超分子结构,化合物2为2种碱金属钾和钠与多酸配位形成链状多酸基化合物,并通过元素分析和X-射线单晶衍射方法确定了2种化合物的晶体结构.单晶结构分析表明化合物1属于三斜晶系,P-1空间群,晶胞参数a=1.1580（7）nm,b=1.3159（8）nm,c=1.8254（12）nm,α=84.418（10）°,β=88.958（10）°,γ=65.852（10）°,V=2.5255（3）nm3,Z=2;化合物2也属于三斜晶系,P-1空间群,晶胞参数a=1.3586（9）nm,b=1.4403（10）nm,c=1.8365（13）nm,α=109.509（10）°,β=90.755（10）°,γ=114.864（10）°,V=3.0236（4）nm3,Z=1.
简介：Inthisarticle,theSm-dopingsinglecrystalsCa1-xSmxFe2As2（x=00.2）werepreparedbytheCaAsfluxmethod,andfollowedbyarapidquenchingtreatmentafterthehightemperaturegrowth.Thesampleswerecharacterizedbystructural,resistive,andmagneticmeasurements.ThesuccessfulSm-substitutionwasrevealedbythereductionofthelatticeparameterc,duetothesmallerionicradiusofSm3+thanCa2+.SuperconductivitywasobservedinallsampleswithonsetTcvaryingfrom27Kto44KuponSm-doping.ThecoexistenceofacollapsedphasetransitionandthesuperconductingtransitionwasfoundforthelowerSm-dopingsamples.ZeroresistivityandsubstantialsuperconductingvolumefractiononlyhappeninhigherSm-dopingcrystalswiththenominalx>0.10.Thedopingdependencesofthec-axislengthandonsetTcweresummarized.Thehigh-TcobservedinthesequenchedcrystalsmaybeattributedtosimultaneoustuningofelectroncarriersdopingandstraineffectcausedbylatticereductionofSm-substitution.
简介：TostudytheintramolecularDiels-Aldercycloadditonof2H-chromen-2-oneasadiene,aseriesofchiralN-allyl-N-benzylamidesthatcontaina2H-chromen-2-onemoietyweredesignedforthesynthesisofbenzo[f]isoindol-l-onesviaanintramolecularDiels-Alderandasubsequentretro-Diels-AldercycloadditionwiththeexpulsionofCO2.Boththeyield（80%-89%）andabsolutestereocontrolofthetandemreactionwerehighwhenanelectron-withdrawinggroupwasattachedtothedienophile.Thedoublebondinthestyrenesubstructureremainedintheproductscouldbefurtherderivatizedbydihydroxylation.
简介：Takingadvantageofthelargeγ-detectorarrayGammasphereandtherecoilmassseparatorFMA,highspinstatesin117Bawereinvestigatedthroughtherecoil-β-delayedprotondecaytaggingtechniqueviatheheavy-ioninducedfusion-evaporationreaction64Zn(58Ni,2p3n)117Ba,atabeamenergyof305MeV.Promptγraysbelongingto117Bahavebeenidentifiedfurthermore,arotationalbandhasbeenidentifiedforthefirsttimeandpresentedasbandAinFig.1.
简介：Anewmethodforfabricatingorderedporoussiliconisreported.Atwo-dimensionalsilicananospherearrayisusedasatemplatewithahydrofluoricacid-hydrogenperoxidesolutionforetchingthenanospheres.Theinitialdiameteranddistributionoftheholesintheresultingporoussiliconlayeraredeterminedbythesizeanddistributionofthesilicananospheres.Thecorrosiontimecanbeusedtocontrolthedepthsoftheholes.ItisfoundthatthepresenceofaSiO_2layer,formedbytheoxidationoftheroughinternalsurfaceofthehole,istheprimaryreasonallowingthecorrosiontoproceed.Ultravioletreflectionandthermalconductivitymeasurementsshowthatthediameteranddistributionoftheholeshaveagreatinfluenceonpropertiesoftheporoussilicon.
简介：我们揭示并且解释thermopowerS/T的可伸缩的行为展出了由典型重费米子(HF)金属YbRh2在在温度T的磁场B的申请下面的Si2。我们证明一样的可伸缩被不同HF混合物例如表明?-YbAlB4和强烈相关的分层的钴氧化物[BiBa0.66K0.36O2]CoO2。用YbRh2是的Si2一个例子，，我们证明S/T的可伸缩的行为在antiferromagnetic阶段转变被违背剩余抵抗力0和状态的密度，N，经验在阶段转变跳，引起thermopower做二跳并且改变它的符号。我们的说明基于深刻地影响0和N的单个粒子的光谱变平。描绘S/T行为的主要特征，我们构造TBYbRh2Si2。我们为HF混合物的计算S/T在对试验性的事实的好同意并且支持我们的观察。
简介：Twofamiliesofcatalysts,basedonPdnanoparticlessupportedonceramicasymmetrictubularaluminamembranes,arestudiesinthedirectsynthesisofH_2O_2.TheyarepreparedbydepositingPdintwoways:(i)reductionwithN_2H_4inanultrasonicbathand(ii)byimpregnation-deposition.Thefirstpreparationleadstolargerparticles,withaveragesizeofaround11nm,whilethesecondpreparationleadstosmallerparticles,withaveragesizearound4nm.Thecatalyticmembranesweretestedasprepared,afterthermaltreatmentinairandafterfurtherpre-reductionwithH_2inmild(100℃)conditions.SampleswerecharacterizedbyTEM,CO-chemisorptionmonitoredbyDRIFTSmethodandTPR,whilecatalytictestshavebeenperformedinasemi-batchrecirculationmembranereactor.Experimentalcatalyticresultswereanalysedusingtwokineticsmodelstoderivethereactionconstantsfortheparallelandconsecutivereactionsofthekineticnetwork.SmallerparticlesofPdshowlowerselectivityduetothehigherrateofparallelcombustion,evenifthebetterdispersionofPdandthushighermetalsurfaceareainthesampleleadtoaproductivityinH_2O_2similarorevenhigherthanthesamplewiththelargerPdparticles.IndependentlyonthepresenceofsmallerorlargerPdnanoparticles,anoxidationtreatmentleadstoasignificantenhancementintheproductivity,althoughthecatalystprogressivelyreducesduringthecatalyticprocess.Theinhibitionoftheparallelcombustionreaction(towater)inducedfromthecalcinationtreatmentremainsafterthein-situreductionoftheoxidizedPdspeciesformedduringthepre-treatment.Thisislikelyduetotheeliminationofdefectsiteswhichdissociativelyactivateoxygen,andtentativelyattributedtoPdsitesabletogivethree-andfour-foldcoordinationofCO.
简介：对化合物[Na_2（H_2O）_（10）][Cu_4（H_2O）_（12）（H_2W_（12）O_（42））]·15H_2O（简称Na_2Cu_4W_（12））进行了体外抗肿瘤活性研究.应用四甲基偶氮唑盐（3-[4,5-dimethylthiazo-2-y]-2,5-diphenyltetrazoliumbromide,MTT）比色法分析Na_2Cu_4W_（12）对人肝癌细胞（HepG2）、人神经母细胞瘤细胞（SHY5Y）增殖抑制活性.采用光学显微镜观察肿瘤细胞的凋亡形态变化,用流式细胞术分析细胞周期和细胞凋亡,计算各期细胞比例及细胞凋亡率.结果表明,Na_2Cu_4W_（12）对HepG2和SHY5Y2种肿瘤细胞增殖半数抑制浓度IC_（50）值分别为5.3和10.2μmol·L~（-1）,且呈剂量依赖性.光学显微镜下处理组细胞出现皱缩、变圆、缩小等形态变化,不同浓度Na_2Cu_4W_（12）处理12h早期凋亡细胞所占的百分比显著增加且呈剂量依赖性.综上所述,Na_2Cu_4W_（12）能够抑制胞瘤细胞增殖,诱导细胞凋亡.
简介：Nuclearmassisoneofthefundamentalquantityofatomicnucleus.Thetotalbindingenergyofanucleusderivedfromtherelatedmassvaluesreflectsalltheinteractionsamongtheconstitutingnucleons.Massesofshort-livedA=2Z+3nucleiof112SnprojectilefragmentshavebeenmeasuredattheexperimentalcoolerstorageringCSRe,employingtheIsochronousmassspectrometry(IMS).TheexperimentwasconductedattheHeavyIonResearchFacilityinLanzhouatthebeginningof2016.Theprimarybeamof112Sn35+wasaccumulatedinthesynchrotronCSRmandacceleratedto467.91MeV/u.Secondarybeamwereproducedbyimpingingthehighintensity112Sn35+beamontoa10mmberylliumtargetwhichwaslocatedattheentranceoftheradioactivebeamlineRIBLL2.Theprojectilefragmentsof112Snemergedfromthetargetwerethentransmitted,separatedinflightthroughRIBLL2andfinallyinjectedintoCSRe.
简介：Lifetimemeasurementsoflow-lyingexcitedstatesin^87Zrhavebeenperformedviaβ-γcoincidences.The127MeV^32SbeamwasdeliveredfromtheSector-FocusingCyclotron(SFC)oftheHeavyIonResearchFacilityinLanzhou(HIRFL).Theparentnuclei^87Nbwereproducedbythereaction58Ni(32S,2p1n),atabeamenergy127MeVthrougha8umAldegrader.A200ug/cm^2layerof58Nievaporatedontoa200ug/cm^2thickcarbonfoilwasemployedasthetarget.Afterevaporationresidueswereseparatedfromtheprojectilebeamsbythegas-filledrecoilseparatorSHANS[1],thenucleiofinterest87Zrcanbeobtainedwithahigherpurityandthenwereimplantedintoa300umsilicondetector.
简介：New[1+1]and62-membered[2+2]Schiffbasemacrocyclescontaininga2,6-diamidopyridinesubunithavebeensynthesizedbycondensationreactionoftheprecursorspyridine-2,6-dicarboxamideand1,10-bis(20-formylphenyloxy)decaneinthepresenceofphosphoricacidviaaone-potprocess.Thecyclocondensedproductswereeffectivelyisolatedbygelcolumnchromatographyandcharacterizedby~1HNMR,FTIR,massspectrometryandX-rayanalysis.Thetwomacrocycleshaveatwistedstructure,andnotanopen‘circular’conformationinthesolidstate.
简介：WehavestudiedtheangularmagnetoresistanceofironpnictidesBaFe2-xNixAs2,whichshowsclear180degreeperiodicityasfittedbyacosinefunction.Inthex=0.065sample,thephaseofthetwo-foldsymmetrychanges90degreesabovethetetragonal-to-orthorhombicstructuraltransitiontemperatureTs.Sincethephaseatlowtemperatureisassociatedwiththerotationoforthorhombicdomainsbymagneticfield,weshowthatevenvacuumgreasecanpushthepresenceoforthorhombicdomainsattemperaturesmuchhigherthanTs.Ourresultssuggestthatresidualstressmayhavesignificanteffectsinstudyingthenematicordersanditsfluctuationsinironpnictides.
简介：TheapplicationofLanthanumBromide(LaBr3)detectorsprovidesauniqueopportunitytomeasurelifetimeofexcitedstatesinpicosecond-nanosecondregion.Reducingthebackgroundisofcriticalimportancetogetpreciseresults.Forsomeexcitedstatesfeedingfromisomerswithlifetimelongerthan1μs,itcanbeachievedbytheSpectrometerforHeavyAtomandNuclearStructure(SHANS)[1].143Eunucleiwerepopulatedviathe123Sb(24Mg,4n)fusion-evaporationreaction.Mostoftheevaporationresiduesatgroundstateorlong-livedisomersweretransferredtodetectionterminalafteraflightofabout1.4μsinSHANS.Inthecaseof143Eu,threetransitionshavebeenobserved(Fig.1).
简介：ThecapacitytocaptureCO2wasdeterminedinseveralstoichiometriccompositionsintheLi2O–Bi2O3system.Thecompounds（Li7BiO6,Li5BiO5,Li3BiO4andLiBiO2phases）weresynthesizedviasolid-statereactionandcharacterizedbyX-raydiffraction,scanningelectronmicroscopyandN2adsorptiontechniques.Thesampleswereheat-treatedattemperaturesfrom40to750°CundertheCO2atmospheretoevaluatethecarbonateformation,whichisindicativeofthecapacityofCO2capture.Moreover,Li7BiO6showsanexcellentCO2capturecapacityof7.1mmol/g,whichisconsiderablyhigherthanthoseofotherpreviouslyreportedceramics.Li7BiO6isabletoreactwithCO2from240°Ctoapproximately660°CshowingahighkineticreactionevenatCO2partialpressurevaluesaslowas0.05.
简介：DigitaldecayspectroscopyofactinideisotopesatthegasfilledseparatorSHANSAlloverthechartofnuclides,theregiontothe“north-east”of208Pb,withZ≥84andN=128~130,hoststheshortest-livedαradioactivities,withhalf-livesintherangeofnanosecondstomicroseconds.Synthesisanddetectionofneutron-deficientisotopesabovethoriuminthisregionarechallengingduetotheirlowproductioncrosssectionsandshorthalf-lives.
简介：Thescientificprogramofthegroupcoversbigbangnucleosynthesis,hydrostaticburninginstarsandexplosivenucleosynthesisinsupernova.Byconsideringnon-equilibriumstatistics,wesuggestapossiblewaytosolvetheLiprobleminbigbangnucleosynthesis.The13C(α,n)16Oisthemajorneutronsourceforthes-processhappeninginAGBstars.The19F(p,α)16Oisrelevanttotheproductionoffluorine.WearedevelopingexperimentalplatformstostudytheimportantreactionforthefirsttimedirectlyattheirstellarenergiesinJinpingUndergroundLaboratory.The59Festellardecayrateisimportantfortheproductionof60Fe,animportantisotopewhosegammarayhasbeenobservedbysatellites.WedetermineitsstellardecayrateforthefirsttimeusingexperimentalB(GT)strength.Thenewratereducesthediscrepancyofthe60Feyieldsbetweenthemodelpredictionsandtheobservations.Theundergroundexperimentisexpectedtobeginin2018.
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![新型仲钨酸盐-B化合物[Na_<b style='color:red'>2</b>（H_<b style='color:red'>2</b>O）_（10）][Cu_4（H_<b style='color:red'>2</b>O）_（12）（H_<b style='color:red'>2</b>W_（12）O_（42））]·15H_<b style='color:red'>2</b>O体外抗肿瘤活性研究](/image/thesis9 "新型仲钨酸盐-B化合物[Na_<b style='color:red'>2</b>（H_<b style='color:red'>2</b>O）_（10）][Cu_4（H_<b style='color:red'>2</b>O）_（12）（H_<b style='color:red'>2</b>W_（12）O_（42））]·15H_<b style='color:red'>2</b>O体外抗肿瘤活性研究")
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