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简介：Geant4LowEnergyElectromagneticpackageProvidesaprecisetreatmentofelectromagneticinterationsofparticleswithmatterdowntoverylowenergies(250oVforelectronsandphotons,<1keVforhadronsandions),Itincludesaverietyofmodelsfortheelectromagneticprocessesofelectrons,photons,hadronsandions,takingintoaccountadvancefeatures,suchasshelleffectsandeffectsduetochargedependence.Thecomprehensivesetofparticletypesitcanhandle,thevarietyofmodelingapproachesandtheextendedcoverageofenergyrangemakethispackageauniquetoolamongMonteCarlocodesonthemarket,andofrelevancetoserveralexperimentaldomainsinHIEP,astroparticlephysics,spacescienceandbiomedicalstudies.

简介：AseriesofcarboxylicacidswasesterifiedtothecorrespondingesterswithTiCl_4ascatalystatroomtemperature,inhighyields.Thiscatalystwashighlyeffectivefortheselectiveesterificationofprimaryalcoholswithcarboxylicacids,inthepresenceofsecondaryalcohols,andfortheselectiveesterificationofsaturatedacidwithalcoholinthepresenceofconjugatedacidoraromaticacid.Onaccountofthehighyield,highchemoselectivity,mildcondition,andbeingfreeofotherdehydrants,thisisanefficientmethod.

简介：<正>InthispaperwestudysurfacesinS~4andtheirtwistorGaussmaps.SomenecessaryandsufficientconditionsthatthetwistorGaussmapisharmonicaregiven.Wefindmanyexamplesofnonisotropicharmonicmapsfromasurfaceto(?)P~3.

简介：Newboronoalkoxycalix[4]arenesweresynthesizedbyallylation,alkylation,hydroborationandhydrolysisof25,26,27,28-tetrahydroxycalix[4]arene,andidentifiedbyelementalanalysis,IR,1HNMR,13CNMR,11BNMR,MSandUVspectra.ThedataofUVandfluorescencespectrashowedthattctrapropoxycalix-[4]arenetriboronicacidcouldcoordinatesignificantlywithmonosaccharides.

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简介：Duetotheirsize-dependentpropertiesandflexibleprocessingchemistry(Alivisatos,1996),monodispersednanocrystalshaveattractedconsiderableattentionfortheirdistinguishedroleinfundamentalstudiesandtechnicalapplications.AlthoughmuchhasbeenreportedonfabricationofmonodispersedinorganicnanocrystalssuchasFe2O3,CdSe,PbSeandZrO2(Peng&Peng,2002;Zhuetal.,2002;Niederbergeretal.,2002;Pangetal.,2001),littlepublishedonthepreparationofBaSO4nanocrystalsandtheircrystalsizeandmorphologywhichaffecttheirperformanceinapplication.PolymeradditiveswithcomplexfunctionshavebeenusedastemplatestodirectorientednucleationandgrowthofBaSO4(Xiaoetal.,2001;Yuetal.,2002;Summersetal.,2002),asanewclassoffunctionalpolymers,theso-calleddouble-hydrophilicblockcopolymers,designedtocontrolthemorphologyofBaSO4(Colfenetal.,2002),includingtheirnanofiberssynthesizedinAOTmicroemulsion(Li&Mann,2000).ThoughsomuchresearchhasbeendevotedtocontrollingtheBaSO4morphologies,thepresentnotewillreportonthesynthesisofBaSO4nanocrystalswithsizecontrolling.

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简介：Thecombinationofboth4,4′-bipyridine(4,4′-bipy)anddihydrogenphosphateanionligandswithcopper(Ⅱ)resultsintheformationofanovellayeredcompoundCu(4,4′-bipy)2(H2PO4)2(H2O)2.ThecrystalstructurecomprisesdiscreteneutralCu(4,4′-bipy)2(H2PO4)2(H2O)2units.Thecopperatom,locatedonthecrystallographictwofoldaxis,iscoordinatedwithtwonitrogenatomsofterminal4,4′-bipyligandsandtwowatermoleculesattheequatorialpositions,andtwodihydrogenphosphateoxygenatomsattheaxialpositions,forminganelongatedoctahedron.Thecomplexisatwo-dimensionaldistortedrhomboidalnetworkpossessingtwokindsofrhomboidswithdimensionsofca.1.6792nm×0.3203nmand1.2778nm×0.3198nm,respectively.Thetwo-dimensionalnetworksarestackedparallellyoneachotheralongc-axistogiveanextendedthree-dimensionalchannelnetworkwithaninterlayerdistanceofca.0.5030nm.Crystaldata:triclinic,spacegroupP-1,a=1.0253(2)nm,b=1.4501(3)nm,c=0.79715(16)nm,α=97.91(3)°,β=90.99(3)°,γ=85.54(3)°,V=1.1703(4)nm3,Z=2,R=0.0892,wR=0.2451.

简介：在有ArSSAr的THF的SmI2的反应生产了二binuclear钐thiolate建筑群[(THF)3I2-Sm(-SAr)]2[Ar=Ph(1)，4-Me2NC6H4(2)]在高收益。2的结构被单个水晶X光检查晶体学描绘。2的水晶与空格组和a=0.95705(13)一起属于三斜晶系的系统nm，b=1.22287(14)nm，c=1.26450(14)nm，=64.194(11)??匭吗？？v？？

简介：用多光子光电效应理论简要分析了多光子光电效应实验,指出多光子光电效应满足nhν=12mv20+φ(hν0)且nν/ν0=4/3。同时用微扰法及单光子光电效应理论分析了H原子电离问题,结果表明也是当ω/ω0=4/3时电离几率最大

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简介：SrMoO4nanoplatesweresynthesizedbyafacilereversemicroemulsionmethodatroomtemperature.Energyevolutionofthisinsitugrowthprocesswasmonitoredbymeansofamicrocalorimeter.Asharpexothermicpeakfortheinitialreactionandtwodiscontinuousrelativelyweakexothermicpeaksforthesubsequentcrystalgrowthemergedonthemicrocalorimetricheatflowcurve.Basedontheinsituthermokineticdata,therateconstantsofthenucleationprocessandcrystallizationprocessat298.15Kwerecalculatedtobe4.078×10-3and5.033×10-4s-1,respectively.Thegrowthmechanismandenergyevolutionwereinvestigated.

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简介：Theacylationof3-pentanoneenaminewasstudiedandanovelformationof4-pyronesfromβ-diketoneenolesterswasfoundinvolvinganintramolecularO-toC-acylshiftfollowedbycyclization.