简介：Thecrystalandmolecularstructuresof[(C3H7O)2PS2]2(CCDCNo.217201)weredeterminedbymeansofX-raycrystallography.ItcrystallizedinatriclinicsystemwithspacegroupP1^-andlatticeparametersa=0.82794(3)nm,b=0.84764(2)nm,c=0.85034(3)nm,α=97.78(3)°β=110.77(3)°,γ=94.95(3)°,V=0.54701(9)nm^3,Z=1.Inthismolecule,thetwodiisopropyldithiophosphategroups,[(C3H7O)2PS2]2,whichareparalleltoeachother,arelinkedbyanS--Sbondandthereexistinversioncentersinthemolecule,Inthestructure,theP=Sbondsinthetwodithiophosphateunitsaretrans-orientedtoeachother.
简介：TheinfluencesofboththevolumeofPS/toluenesolutionintheUbbelohdeviscometerandtheprecisionofthetimemeasuringontheviscositybehaviorindiluteandextremelydiluteconcentrationregionareinvestigatedItwasfoundthattheinfluenceoftheformercanneglect,butthatofthelatterissoprominentthatthedatafluctuatebitterlyandlinearityofthecurveofthereducedviscosityvs.Concentration(ηsp/c～c)becomestoobadtoobeytheHugginsequationdowntotheextremelydiluteregion,despitetheerroroftheflowtimes△t≤0.2s,whichispermittedbytheconventionalmethodofviscositymeasurement.Throughstrictmathematicalanalyses,itwasfoundthatthcerror(E)ofthereducedviscosityisinproportionandinverseproportionto△tandconcentrationc,respectively.Sothelesstheconcentration,themoretheerroris.Consequently,alowestconcentrationlimitcLcorrespondingtogivenexperimentalerrormayexistanditwillbemeaninglessforfurtheroperationbelowcLbecauseofthegreatfluctuationofthedata.Therefore,itneedstoseriouslyreconsidertheapplicationoftheconventionalmethodofUbbelohdeviscositymeasurementintheextremelydilutepolymersolutionundertraditionalconditionsbecauseofthegreatinfluenceoftheexperimentalerror.
简介：ThelasersystemPALS,asadriverofabroad-beamionsource,delivereddeuteronswhichgeneratedneutronswithenergieshigherthan14MeVthroughthe7Li(d,n)8Bereaction.Deuteronswithsub-MeVenergywereacceleratedfromthefrontsurfaceofamassiveCD2targetinthebackwarddirectionwithrespecttothelaserbeamvector.Simultaneously,neutronswereemittedfromtheprimaryCD2targetandasecondaryLiFcatcher.Thetotalmaximummeasuredneutronyieldfrom2D(d,n)3He,7Li(d,n)8Be,12C(d,n)13Nreactionswas～3.5(±0.5)×108neutrons/shot.
简介：AseriesofPS-PPACwasdevelopedandthepositionresolutionwassuccessivelyimprovedbyusinordertomeettheneedofheavyionphysicsresearch.ThePS-PPACmaybedividedintotwogroups.1PS-PPACusedforstable(ion)bearna)Doublegridpositionsensitiveavalanchechamber(DGAC)~[1].DGACconsistsof4electrodes:anodeA,cathodeC,gridsKandG,whicharemadeofwireplanes.Thesensitiveareawas25×20cm~2.Aposition
简介：这篇文章介绍一条灵巧的途径给聚苯乙烯/银(PS/Ag)的准备不对称的混合粒子。在这个方法，polystyrene/polyglycidylmethacrylate(PS/PGMA)Janus粒子经由dichloromethane(DCM)的蒸发从PS/PGMA/DCM-in水乳剂微滴触发的内部阶段分离被综合。然后，Janus粒子是aminated并且顺序获得PS/PGMA-NH2和PS/PGMA-COOH粒子的carboxylated。在由与amine/carboxyl协调的functionalizedPS/PGMA粒子的PGMA半球的表面上自我装配的Ag+。有Ag的7.29wt%的PS/Ag不对称的混合粒子被Ag+的减小获得。扫描电子显微镜学，精力散的X光检查光谱学和传播电子显微镜学结果证实Ag在聚合物粒子的表面上是不均匀地分布式的。
简介：Thehybridstructuresofpolystyrene-b-poly(ethyleneoxide)(PS-b-PEO)blockcopolymerandinorganicnanoparticleswithgoodstabilityandbiocompatibilityhavepotentialapplicationsindrugdeliveryandbioimaging.Sphericalco-assembliesofPS120-b-PEO318andoleylamine-cappedCdSquantumdots(QDs)areproducedsuccessfullyinthisworkbyaddingwatertoamixedcommonsolvent,suchasN,N-dimethylmethanamide(DMF)/chloroform,DMF/tetrahydrofuran(THF),orDMF/toluene.TheenergydispersiveX-ray(EDX)spectrumindicatesthatQDsarelocatedattheinterfacebetweenthecoreandshellofthesphericalco-assemblies.Theco-assemblyprocessduringwateradditionistracedbytransmissionelectronmicroscopy(TEM)andturbiditymeasurement.Sphericalco-assembliesareformedthroughbuddingfrombilayersoftheblockcopolymerandQDs.Themorphologyoftheco-assembliesisrelatedtothemiscibilityoftheQD-dispersingsolventswithwaterandthemorphologychangesfromasphericaltoavesicle-likestructurewithDMF/toluene.IncreasingTHFcontentinthemixedsolventcausesmorphologicaltransitionsfromsphericalco-assembliestomulti-branchedcylindersandmicelleswhereQDsarelocatedinthecentralcore.Increasingchloroformcontentyieldsvesicle-likestructureswithprotrudingrodsonthesurface.Themechanismofthemorphologicaltransitionsisalsodiscussedindetail.
简介：嵌段共聚物聚苯乙烯-b-聚氧化乙烯（PS-b-PEO）甲苯溶液在室温下陈化2个月可形成中间是PEO单晶上下表面为PS具有＂三明治＂结构的方形片层,并且既能形成单层方形片层,也能形成多层方形片层.采用透射电子显微镜手段观察了这种结构在不同水含量的水/甲苯混合溶剂蒸汽诱导后形成的结构形貌.结果证明在甲苯和水蒸汽中,方形片层结构均能稳定存在,不能进行结构重构;而随着混合蒸汽中水含量的增加,单晶溶解、消失,在甲苯和水的共同作用下,可通过结构重构形成新的垂直或平行于表面的柱状相结构.
简介：Twonewdicyanamidecoordinationpolymers,{Mn(dmpz)[N(CN)2]2}2(1)and{Cu(dmpz)[N(CN)2]2}2(2)(dmpz=3,5-dimethylpyrazole),weresynthesizedandcharacterizedbysinglecrystalX-raydiffractionanalysisandIRspectroscopy.In1and2themetalionshavetwodifferentcoordinationmodes,whereoneiscoordinatedtofourdicyanamideanionsandtwomonodentatedmpzmoleculestoformaslightlydistortedoctahedralgeometry,whiletheotheradoptsoctahedralgeometry,surroundedbyfournitrileNatomsandtwoamideNatomsofthedicyanamideanions.Bothcomplexescontaintwoalternatingchainsthatareparalleltoeachother.
简介：Hypersubstitutions是印射操作符号到相应arities的术语的地图砰。他们作为使ahyperidentity和归纳的概念精确到M-hyperidentities的一个方法被介绍。每身份作为亢奋的身份在满足的一个变化被称为固体。如果每身份是为子集Mof的M-hyperidentity所有亢奋的替换的集合，变化被称为M固体。在亢奋的替换的单音的标志和一种给定的类型的代数学的所有变化的格子的潜水艇格子之间有一个Galois连接。因此，知道怎么有趣、有用半组或在到M固体变化的相应格子的性质的这个Galois连接下面的亢奋的替换转移的单音的标志性质ofmonoids。在这篇论文，我们学习类型(2,2)的eachhypersubsfitution的顺序，即，周期的subsemigroup的顺序由类型的所有亢奋的替换的单音的标志的thathypersubstitution产生了(2，2)。主要结果是顺序是1，2，3，4或无限。
简介：ThesplittingofpotentialenergylevelsforgroundstateX2ΠgofOx2(x=+1,1)underspin–orbitcoupling(SOC)hasbeencalculatedbyusingthespin–orbit(SO)multi-configurationquasi-degenerateperturbationtheory(SO-MCQDPT).TheirMurrell–Sorbie(M–S)potentialfunctionsaregained,andthenthespectroscopicconstantsforelectronicstates2Π1/2and2Π3/2arederivedfromtheM–Sfunction.TheverticalexcitationenergiesforOx2(x=+1,1)areν[O+12(2Π3/2→X2Π1/2)]=195.652cm1,andν[O12(2Π1/2→X2Π3/2)]=182.568cm1,respectively.Allthespectroscopicdataforelectronicstates2Π1/2and2Π3/2aregivenforthefirsttime.
简介：ThecrystalstructureofDi-nitratobis（ethylcaprolactam）uranyl（Ⅱ）UO2[CH2（CH2）4CONC2H5]2（NO3）2wasestablishedbyasingle-crystalX-raydiffractionstudy.Itistriclinie,spacegroupP1,witha=7.171（2）,b=8.655（3）,c=10.182（5）A,α=78.27（3）,β=70.63（3）,γ=81.76（3）°,V=581.7（4）A3,Z=l,Dc=1.94g.cm-3.FinalRvalueis0.0218.Theresultrevealsthaturanylioniscoordinatedtosixoxygenatoms,twoofthemarefromtwocarbonylgroupsofethylcaprolactamandtheotherfourarefromtwonitrategroups.
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![Crystal Structure of Bis （0, O＇-diisopropyl dithiophosphate） ： [（C3H7O）<b style='color:red'>2</b><b style='color:red'>PS</b><b style='color:red'>2</b>]<b style='color:red'>2</b>](/image/thesis0 "Crystal Structure of Bis （0, O＇-diisopropyl dithiophosphate） ： [（C3H7O）<b style='color:red'>2</b><b style='color:red'>PS</b><b style='color:red'>2</b>]<b style='color:red'>2</b>")
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![CRYSTAL STRUCTURE OF DI - NITRATOBIS（ETHYLCAPROLACTAM）URANYL（Ⅱ） UO<b style='color:red'>2</b>[CH<b style='color:red'>2</b>（CH<b style='color:red'>2</b>）4CONC<b style='color:red'>2</b>H5]<b style='color:red'>2</b>（NO3）<b style='color:red'>2</b>](/image/thesis18 "CRYSTAL STRUCTURE OF DI - NITRATOBIS（ETHYLCAPROLACTAM）URANYL（Ⅱ） UO<b style='color:red'>2</b>[CH<b style='color:red'>2</b>（CH<b style='color:red'>2</b>）4CONC<b style='color:red'>2</b>H5]<b style='color:red'>2</b>（NO3）<b style='color:red'>2</b>")
