简介：Anewμ3-Otriiron（Ⅲ）complex[Fe3O（OBz）6（CH3OH）3]（NO3）（CH3OH）2（HOBZ=benzoicacid）hasbeensynthesized,itsstructurehasbeendeterminedandvariabletemperaturemagneticsusceptilityhasalsobeenmeasured.Inthemolecule,threeironatomsformedanequilateraltrianglewithu3-Oincenter.ThefittingtothemagneticsusceptibilityshowedthatanintramolecularantiferromagneticexchangeinteractionoccurredbetweenironatomswithJ=-25.51cm-1,andaweakerintermolecularantiferromagneticexchangeinteractionoccurredwithzJ’=-2.30cm-1.
简介：Pureandneodymium-dopedgadoliniumcalciumoxoboratecrystalsofhighqualityweregrownbytheCzochralskimethod.Theorientationofcrystalwaspreciselydetermined,andthesamplesformeasurementswereprepared.Throughsynchrotronx-raytopographyandhigh-resolutionx-raydiffractometry,thetwinstructurewasdiscovered.Somepropertiessuchasthefigureofmeritvalue,anddielectric,piezoelectric,andelasticconstantsweremeausuredalongwithadiscussionoftheanisotropyofthelaserproperties.
简介：At-hyperwheel(t≥3)oflengthl(orW(t)lforbrevity)isat-uniformhypergraph(V,E),whereE={e1,e2,...,el}andv1,v2,...,vlaredistinctverticesofV=∪eii=1lsuchthatfori=1,...,l,vi,vi+1∈eiandei∩ej=P,j∈/{i1,i,i+1},wheretheoperationonthesubscriptsismodulolandPisavertexofVwhichisdifferentfromvi,1≤i≤l.Inthispaper,theminimumcoveringproblemofMCλ(3,W(3)4,v)isinvestigated.DirectandrecursiveconstructionsonMCλ(3,W(3)4,v)arepresented.Thecoveringnumbercλ(3,W(3)4,v)isfinallydeterminedforanypositiveintegersv≥5andλ.
简介：Europium（Ⅲ）-dopedYF3ispreparedbyahydrothermalprocessat200℃.X-raydiffraction（XRD）patternidentifiestheformationofYF3phasewithoutdetectableimpurity.Environmentscanningelectronmicroscopy（ESEM）imageshowstheevensizedistributionofthesampleswithcubicmorphology.TheexcitationandemissionspectraoftherareearthionsdopedYF3areinvestigatedbyfluorescencespectrophotometer.Theexcitationspectrumfor591nmemissionhasseveralexcitationbandsat320,365,386,397and467nm,andthemainpeakvaluewas397nm.TypicalEu3+emissionpeaksat591nm（5D0→7F1）and612nm（5D0→7F2）areobservedwhenexcitedby397nm,andthestrongestemissionis591nm,demonstratingthattherareearthionsoccupythecentrosymmetricalsitesinYF3.
简介：Ca3Y2(BO3)(4):Eu3+黄磷被高温度solid-statereaction方法综合，并且光特征被调查。排放光谱在相应于电的dipoleD-5(0)的613和621nm展出二强壮的红排出物在365nm刺激下面的Eu3+的-F-7(2)转变，原因是Eu3+代替forY3+在Ca3Y2(BO3)(4)的水晶结构占据非中心对称的位置。为613nm的Theexcitation光谱显示黄磷能是有效地激动的由紫外(紫外)(254nm，365nm和400nm)并且蓝色(470nm)光。Ca3Y2(BO3)(4)的排放紧张上的Eu3+集中的效果:Eu3+黄磷被测量，排放紧张与增加Eu3+集中增加的结果表演，然后减少。Ca3Y2(BO3)(4)的CIE颜色坐标:Eu3+黄磷是(0.639，0.357)在15mol%Eu3+。
简介：[Co3(1,2-S2C6H4)3(PPh3)3][CoBr3(DMF)].sol(1,sol=CHCl3,O(C2H5)2,H2O)wasobtainedfromthereactionofCoBr(PPh3)3withNa2(S2C6H4)inchloroform.TheCo3coreinthecationof1exhibitsametal-metalbondedisoscelestriangle,inwhichthetwolongerCo-CobondsarebothbridgedbyS2C6H4ligandsontwosidesofthetriangleplanerespectively,whilethebottomshortCo-CobondisbridgedbythethirdbidentateS2C6H4ligand.Aseriesofpolynu-clearcobaltclustercompoundswithphosphine,thiolateand/orsulphurligandswerepreparedbylowoxidationstateCo+withthiolatesinorganicsolvents.Thesetri-,tetra-,hexa-,heptanuclearclustercompounds1-8withvarioustypesofcrystalstructurescanbeviewedasthecondensedpolynuclearcobaltcomplexesthatthecobaltatomframeworkswithsulphurbridgedwerebuiltthroughthesmalltriangularunitsof[Co3S3nL3](n=1,2)withorwithout[CoL](L=PR3,Br,Cl,5-C5H5)fragments.
简介：Asanimportantmulti-functionalmaterialappliedinsurfaceacousticwavedevices,opticalcommunications,laserandoptoelectronicsduetoitsgoodphotoelectricandpiezoelectricproperties,lithiumtantalate(LiTaO3)hasdrawnextensiveinterests[1].NumerousphysicalpropertiesofLiTaO3,suchasacoustical,electronicstructures,opticalpropertiesandeffectivemass,thermodynamicproperties,havebeenreportedinseveralpapers.Pointdefectswillaffecttheelectronicstructurewhichshouldberesponsibleformanyphysicalproperties,especiallyopticalproperties.
简介：Reactionsofthe6-hydroxy-thiopyrano[3,4-c]pyridine-5-carbonitrilederivative1withα-halo-carbonylcompoundsgavetheortho-substitutedintermediates2a-cwhichwereconvertedintofuro[2,3-b]thiopyrano[4,3-d]pyridines3a-cbyfusionofafuranmoietyunderbasicconditions.Furthercyclizationof3a-cledtoafusionofapyrimidinering,yieldingthetetracyclicproducts6,7and8.Inaddition,condensationof6withvariousaromaticaldehydesaffordedthecorrespondingimines9a,b.Mannichreactionof7gaveproducts10a,b.
简介：Poly(3-hydroxybutyrate-co-3-hydroxyvalerate)/Organophilicmontmorillonite(PHBV/OMMT)nanocompositeswerepreparedandthebiodegradabilityofthePHBV/OMMTnanocompositeswasstudiedbyacultivationdegradingmethodinsoilsuspension.TherelationshipbetweenstructureandbiodegradabilityofPHBV/OMMTnanocompositeswasinvestigated.TheresultsshowedthatthebiodegradabilityofPHBV/OMMTnanocompositesdecreasedwithincreasingamountofOMMTanditwasrelatedtothenumberofPHBVdegradingmicroorganismsindegradationenvironment,theanti-microbialpropertyofOMMTandthedegreeofcrystallinityofthenanocomposites.
简介：DrugsSPD-304(6,7-dimethyl-3-{[methyl-(2-{methyl-[1-(3-trifluoromethyl-phenyl)-1H-indol-3-ylmethyl]-amino}-ethyl)-amino]-methyl}-chromen-4-one)andzafirlukastcontainacommonstructuralelementof3-substitutedindolemoietywhichcloselyrelatestoadehydrogenatedreactioncatalyzedbycytochromeP450s(CYPs).ItwasreportedthatthedehydrogenationcanproduceareactiveelectrophilicintermediatewhichcausetoxicitiesandinactivateCYPs.DrugL-745,870(3-{[4-(4-chlorophenyl)piperazin-1-yl]-methyl}-1H-pyrrolo2,3-β-pyridine)mighthavesimilareffectsinceitcontainsthesamestructuralelement.Weusedmoleculardockingapproachcombinedwithmoleculardynamics(MD)simulationtomodelthree-dimensional(3D)complexstructuresofSPD-304,zafirlukastandL-745,870intoCYP3A4,respectively.Theresultsshowthatthesethreedrugscanstablybindintotheactivesiteandthe3-methylenecarbonsofthedrugskeepareasonablereactivedistancefromthehemeiron.ThecomplexstructureofSPD-304-CYP3A4isinagreementwithexperimentaldata.Forzafirlukast,thecalculationresultsindicatethat3-methylenecarbonmightbethedehydrogenationreactionsite.DockingmodelofL-745,870-CYP3A4showsapotentialpossibilityofL-745,870dehydrogenatedbyCYP3A4at3-methylenecarbonwhichisinagreementwithexperimentinvivo.Inaddition,residuesinthephenylalanineclusteraswellasS119andR212playacriticalroleintheligandsbindingbasedonourcalculations.ThedockingmodelscouldprovidesomecluestounderstandthemetabolicmechanismofthedrugsbyCYP3A4.
简介：以化学沉淀法制备单相的铕离子掺杂硼铝酸盐红色荧光粉YAl3（BO3）4：Eu3＋，考察了焙烧温度、掺铕量等因素对材料性能的影响，用X射线衍射、扫描电镜、激发光谱和发射光谱对荧光粉的结构、形貌和发光性能进行了表征．以尿素为沉淀剂，900℃焙烧沉淀前驱体可得到单相荧光粉YAl3（BO3）4：Eu3＋，反应温度比传统高温固相法降低了300℃；沉淀法制备的荧光粉粒径分布范围小，无团聚现象，粒径约300nm．掺铕量为10％（物质的量比）时发光强度最大．在260nIn的紫外光激发下，Eu3＋的5D0→F72的电偶极跃迁最强，发射光为618nm的红光．
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![The structure and magnetic properties of μ<b style='color:red'>3</b>-oxotriiron（Ⅲ） complex [Fe<b style='color:red'>3</b>O（OBz）6（CH<b style='color:red'>3</b>OH）<b style='color:red'>3</b>]（NO<b style='color:red'>3</b>）（CH<b style='color:red'>3</b>OH）2](/image/thesis0 "The structure and magnetic properties of μ<b style='color:red'>3</b>-oxotriiron（Ⅲ） complex [Fe<b style='color:red'>3</b>O（OBz）6（CH<b style='color:red'>3</b>OH）<b style='color:red'>3</b>]（NO<b style='color:red'>3</b>）（CH<b style='color:red'>3</b>OH）2")
![[Co<b style='color:red'>3</b>（1,2-S2C6H4）<b style='color:red'>3</b>（PPh<b style='color:red'>3</b>）<b style='color:red'>3</b>]+, A basic triangle unit of some polynuclear molecules](/image/thesis10 "[Co<b style='color:red'>3</b>（1,2-S2C6H4）<b style='color:red'>3</b>（PPh<b style='color:red'>3</b>）<b style='color:red'>3</b>]+, A basic triangle unit of some polynuclear molecules")
![Synthesis of thiopyrano[4',<b style='color:red'>3</b>':4',5']pyrido[<b style='color:red'>3</b>',2':4, 5]furo[<b style='color:red'>3</b>,2-d]pyrimidines](/image/thesis12 "Synthesis of thiopyrano[4',<b style='color:red'>3</b>':4',5']pyrido[<b style='color:red'>3</b>',2':4, 5]furo[<b style='color:red'>3</b>,2-d]pyrimidines")
