简介：Metalion-imprintedlycrosslinkedchitosanresin1andresin2werepreparedbytheuseofCu^2+andNi^2+astemplateionsandglutaraldehydeascrosslinkingagent,respectively,ThroughinvestigationontheadsorptioncapactiesandbindingconstantsforCu^2+,Ni^2+andCo^2+ionsonchitosanresins,resin1andresin2exhibittheadsorptionselectivityforthemixturesolutionof1L1Cu^2+andNi^2+ions.Theadsorptionselectivityofmetalion-imprintedresinsfortheirtemplateionsinmuchhigherthanthatofuncrosslinkedchitosanresin.

简介：N复杂的Cu2+的相互作用，有DNA的N二度(2-aminoethyl)-2,6-pyridinedicarboxamide(BAP)被agarose胶化电气泳动分析学习。结果显示BAP-Cu2+建筑群能以生理的状况支持supercoiledDNA的phosphodiester债券的劈开，哪个是3.2畤瑣潩?牯杩湩漠?敧杯慲桰捩漠楲楧?景眠湩獥吗？？

简介：用微波高温固相法合成了Er^3+单掺Lu2O3,Li^+与Er^3+共掺Lu2O3及Li^+,Zn^2+,Mg^2+掺杂Lu2O3∶Er^3+的荧光粉。实验表明金属离子Li^+、Zn^2+、Mg^2+、Er^3+掺杂Lu2O3,不影响Lu2O3的立方晶相。扫描电子显微镜测量表明,Li^+掺杂可以有效改善粉体的分散性和形貌,Li^+,Zn^2+,Mg^2+共掺杂获得的粉体颗粒分布更加均匀,粒径范围为80~100nm。379nm激发下,Li^+与Er^3+共掺样品发光较单掺Er^3+样品在565nm处的发光增强了4.5倍,而Li^+、Zn^2+、Mg^2+与Er^3+共掺样品较其发光增强5.3倍。980nm激发下,Li^+与Er^3+共掺样品,Li^+、Zn^2+、Mg^2+与Er^3+共掺样品的发光分别比单掺Er^3+样品在565nm处发光增强23倍与39倍,在662nm处发光强度分别增强20倍与43倍。379nm激发下,较单掺Er3+的样品,掺杂Li^+的样品和Li^+,Zn^2+,Mg^2+和Er^3+共掺的样品荧光寿命均有所增加,而Zn^2+、Er^3+共掺及Mg^2+、Er^3+共掺样品的荧光寿命则有所缩短。

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简介：Emissionquenchingof[Ru(bpy)2(4,4’-dcbpy)](PF6)2(1)bybenzenamine,4-[2-[5-[4-[4-dimethylamino]phenyl]-4,5-di-hydro-1-phenyl-1H-pyrazol-3-yl]-ethenyl]-N,N-dimetyl(2)or1,5-diphenyl-3-(2-phenothiazine)-2-pyrazoline(3)wasobserved.Measurementsoftheemissiondecayof1beforeandafteradditionof2or3bysinglephotoncountingtechniquecon-finnedtheobservations.Theemissionquenchingof1by2or3wassubmittedtoStern-Volmerequation.Itwascalculatedthatthequenchingrateconstants(kq)are5.5×109(mol/L)-1s-1for2and4.0×109(mol/L)-1s-1for3,respectively.Theseresultsindicatedacharacterofdynamicquenchingprocess.Thesinglet-stateof2or3wasalsoquenchedby1.ThequenchingbehaviorsdidnotconformtotheStern-Volmerequationandinvolvedbothstaticanddynamicquenchingprocesses.Theapparentquenchingrateconstant(kapp)wascalculatedtobe3×109(mol/L)-1fortheinteractionofexcited2with1,and1.2×109(mol/L)-1forthatofexcited3wit

简介：TheroleoftemperatureontheoxidationdynamicsofCu2OonZnO(0001)wasinvestigatedduringtheoxidationofCu(111)/ZnO(0001)byusingoxygenplasmaastheoxidant.AtransitionfromsinglecrystallineCu2O(111)orientationtomicro-zonephaseseparationwithmultipleorientationswasrevealedwhentheoxidationtemperatureincreasedabove300°C.TheexperimentalresultsclearlyshowtheeffectoftheoxidationtemperaturewiththeassistanceofoxygenplasmaonchangingthemorphologyofCu(111)filmandenhancingthelateralnucleationandmigrationabilitiesofcuprousoxides.Averticaltop-downoxidationmodeandalateralmigrationmodelwereproposedtoexplainthedifferentnucleationandgrowthdynamicsofthetemperature-dependentoxidationprocessintheoxidationofCu(111)/ZnO(0001).

简介：theAlternatingSegmentCrank-Nicolsonschemeforone-dimensionaldiffusionequationhasbeendevelopedin[1],andtheAlternatingBlockCrank-Nicolsonmethodfortwo-dimensionalproblemin[2].Themethodshavetheadvantagesofparallelcomputing,stabilityandgoodaccuracy.Inthispaperforthetwo-dimensionaldiffusionequation,thenetregionisdividedintobands,aspecialkindofblock.ThismethodiscalledthealternatingBandCrank-Nicolsonmethod.

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简介：描述表面在nanocrystals熄灭孤立的离子中心的一个模型基于在做的离子和熄灭中心的nanocrystalline表面之间的精力转移被建议。熄灭的率在nanocrystal取决于离子的位置，在非选择的刺激下面的因此腐烂曲线通常是非指数的。与这个模型一起计算的腐烂曲线在对T-4(1)的好同意>(6)在ZnS的A(1)排放:Mn2+nanocrystals。

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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：Three-dimensional(3D)flowerlikehierarchicalZn2GeO4andMn2+-dopedZn2GeO4microstructureshavebeenpreparedbyafacilehydrothermalapproach.X-Raydiffraction(XRD),fieldemissionscanningelectronmicro-scopy(FESEM),transmissionelectronmicroscopy(TEM)andphotoluminescence(PL)spectrometrywereemployedtocharacterizethesamples.SuchflowerlikehierarchicalZn2GeO4microstructureswithanaveragediameterof3―4μmwerefoundtobeconstructedbyabundantsinglecrystallinenanorodsofabout90nmindiameter.TheluminescentpropertiesofZn2GeO4:xMnphosphorswithdifferentcontentsofMn2+asanactivatorwereinvestigated.TheMn2+-dopedsamplesshowedgreenluminescencecorrespondingtothed-dtransitionofMn2+undertheirradiationofUVlight.Theredshift(from531nmto538nm)inλemwithincreasingMn2+contentwasobservedintheluminescentspectra,whichshouldbeattributedtoaweakcrystalfieldbecauseofthesubstitutionofZn2+byMn2+atadistortedtetrahedrallatticesite.

简介：用离子交换法将具有Keggin结构TBA4H3PW7Mo3Cu2O38（H2O）2（M=Fe2＋，Co2＋，Cu2＋，Ni2＋和Mn2＋）嵌入到Zn2A1黏土中，得到层状化合物LDH-PW7Mo3Cu2O38（H2O）2（M=Fe2＋，Co2＋，Cu2＋，Ni2＋和Mn2＋），并用XRD，IR，uV对其进行了表征．结果表明：杂多阴离子进入黏土后，仍保留了其Keggin结构．利用合成的层状化合物为催化剂，以顺丁烯二酸与HzO。的环氧化反应为模型反应考察其催化活性，结果表明：层状化合物在环氧化反应中显示优良的催化性能．

简介：研究了ＹＢａＣｕ３Ｏ６～７超导催化剂上ＣＯ２的加氢制醇反应。考察了温度、压力和空速等条件对催化剂反应性能的影响。反应的主要产物是甲醇、ＣＯ和少量甲醚。利用ＸＰＳ、ＸＲＤ和ＡＦＭ等技术对催化剂的结构、铜的存在状态和反应活性位进行表征发现，在反应过程中，ＹＢａ２Ｃｕ３Ｏ６～７由ｏｒｔｈｏｍｂｉｃ相转变为ｔｅｔｒａｇｏｎａｌ相。反应活性位可能是Ｃｕ（Ｉ）物种。反应后催化剂颗粒的分散程度明显提高

简介：TheternaryCu(Ⅱ）complexwith2,2′-bipyridyl(bipy)andL-methioninte(L-Met)hasbeensynthesizedandcharacterizedbyelementalanalysis,molarconductivity,UV-Visspectra,IRspectraandpH-potentiometrictitrationmethods.Thestructureofthecomplex[Cu(L-Met)(bipy)(H2O)]ClO4·3/8H2OwascharacterizedbytheX-raydiffractionanalysis.Itcrystallizesinthetriclinicsystem,spacegroupP1withfourmoleculesinaunitcellofdimensions,a=0.7656(2)nm,b=1.3142(3)nm,c=2.0596(4)nm,α=97.70(3)°,β=97.96(3)°,γ=94.33(3)°，V=2.0244(8)nm^3,R1=0.0441andwR2=0.0678,Thecrystalcontainsfourcrystallographicallyindependent[Cu(L-Met)(bipy)(H2O)]^+complexes(Cu1-Cu4),havingadistortedsquare-pyramidalgeometrywiththesamecoordinatedatomsaroundeachcoppercenter.Thebaseplaneisoccupiedbytwonitrogenatomsofonebipy,theaminonitrogenatomandonecarboxylateoxygenatomfromeachindependentL-Metmoiety,andonewateroxygenatanaxialposition.CulandCu3areessentiallyenantiomersofCu2andCu4.Thefourmoleculesarepackedwitheachotherbyintermolecularhydrogen-bondingandaromatic-ringstackinginteractions.

简介：［1］G.C.Chinchen,P.J.Denny,J.R.Jennings,M.S.Spencer,K.C.Waugh,Appl.Catal.,1988,36,1.［2］R.A.Koppel,A.Baiker,Appl.Catal.,1992,84,77.［3］M.Satio,T.Fujitani,M.Takeuchi,T.Watanabe,Appl.Catal.,1996,138,311.［4］J.A.Brown,N.Homs,A.T.Bell,J.Catal.,1990,124,73.［5］J.S.Lee,K.Moon,S.H.Lee,S.Y.Lee,Y.G.Kim,Catal.Lett.,1995,34,93.［6］C.Frohlich,R.A.Koppel,A.Baiker,M.Kilo,A.Wokaun,Appl.Catal.,1993,106,275.［7］J.F.Deng,Q.Sun,Y.L.Zhang,D.Wu,S.Y.Chen,Appl.Catal.,1996,139,75.［8］K.K.Bando,K.Sayama,H.Kusama,K.Okabe,H.Arakawa,Appl.Catal.,1997,165,391.［9］G.C.Chinchen,K.C.Waugh,D.A.Whan.Appl.Catal.,1986,25,101.［10］B.Denise,R.P.A.Sneeden,B.Beguin,O.Cherifi.Appl.Catal.,1987,30,353.［11］G.C.Chinchen,K.C.Waugh.J.Catal.,1986,97,280.［12］T.H.Fleisch,R.L.Mieville.J.Catal.,1984,90,165.［13］K.Klier,V.Chatikavanij,R.G.Herman,G.W.Simmons.J.Catal.,1982,74,343.［14］R.Burch,R.J.Chappel.Appl.Catal.,1992,45,65.［15］H.Berndt,V.Briehn,S.Evert.Appl.Catal.,B,1992,86,65.［16］W.P.Dow,Y.P.Wang,T.J.Huang.J.Catal,1996,160,155.

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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：AnefficientprocessfortheconversionofdimethyloxalateintoethyleneglycolwithhighselectivityandhighyieldoverCu2Owasinvestigated.InsituformedCuasatruecatalyticallyactivespeciesshowedagoodcatalyticperformanceforDMOconversiontoproduceEGin95%yield.