简介:HeteroatomM-ZSM-12zeolites(M=B,Al,Ge,Ga,Fe)arehydrothermallysynthesizedanditisprovedthattheheteroatomMisinvolvedintheframeworkofsynthesizedmolecularsievesbymeansofXRD,IRspectra.TheresultsofadsorptionanddiffusionexperimentsindicatethattheheteroatomMmodifiestheporevolume,specificsurfacearea,andthechannelofZSM-12molecularsieves.
简介:Thetitlecomplex[NH_3CH_2CH(NH_2)CH_3]_2[M(Ⅵ)O_2(OC_6H_4O)_2](M=Mo_(0.6)W_(0.4))wassynthesizedviaasimplesolution-phasechemicalroute.ThedeterminationofsinglecrystalX-raydiffractionrevealedthatthetitlecompoundiscrystallizedinamonoclinicsystemwithP2(1)/nspacegroup,a=1.0913(10)nm,b=1.0442(10)nm,c=1.8842(19)nm,α=90°,β=96.530(17)°,γ=90°,Z=4,andV=2.133(4)nm3.Themononuclearanionicunit[M(Ⅵ)O2(OC6H4O)2]2-displayschiralpseudo-octahedral[MO_6]coordinationgeometryandislinkedbychiralcationsviahydrogenbondandπ…πstackinginteraction.Thetransmissionelectronmicroscopyimagesshowthatthetitlecomplexiscomprisedofnano-particleswithdiametersrangingfrom20to50nm.TheNMRstudyshowsthe1Hdownfieldchemicalshiftsof[NH_3CHaHbCH(NH_2)CH_3]+cationsinthetitlecomplexwhenitismixedwithadenosine-triphosphate(ATP),andthechemicalshiftdifferencebetweenHaandHbisincreasedgreatly,andmostofthecatecholateligandsdissociatefromthecentralmetalatoms.TheDNAcleavageactivityexperimentrevealsthatDNAcleavagepromotedbythetitlecomplexislowerthanthatbyNa_2MoO_4whichpossessesantitumorpro-perty,buthigherthanthatbyNa_2WO_4.
简介:Bytheadditionalreactionofbinuclearcompounds(Me4N)2M2S4(TDT)2(M=Mo,W;H2TDT=H2CH3C6H3S2)withmononuclearcuprouscomplex,twonewM-Cu-SclustersMo2Cu2S4(TDT)2-(PPh3)2·CH3CH2OH(1)andW2Cu2S4(TDT)2(PPh3)2·0.5CH3CH2OH-0.5H2O(2)havebeenpreparedandcharacterizedbyIR,UV-Vis,31PNMRspectroscopy,cyclicvoltammetryandsinglecrystalX-raystructureanalysis.BothcompoundscrystallizeinspacegroupP21/nwithlatticeparametersa=1.0956(3),b=2.2072(3),c=2.4340(3)nm,β=100.36(2)°,V=5.790(3)nm3andZ=4for1anda=1.0965(9),b=2.2135(3),c=2.4317(4)nm,β=99.63(8)°,V=5.819(8)nm3andZ=4for2.Bothmolecularstructurescontainacubane-likeclustercore[M2Cu2S4](M=Mo,W)andtheirskeletonsarealmostthesameexceptforMatoms.Thesyntheses,structuresandspectrumcharacterizationsofthesetwoclustersarediscussed.Thethird-ordernonlinearoptical(NLO)propertyofthetwoclusterswasstudiedbythetechniqueofforwarddegeneratefour
简介:利用电介质的平均能带模型计算了PrBa2Cu3O7的化学键参数,得到Cu(1)-O键的人价性为0.41,Cu(2)-O键的平均共价性为0.28,应用由共价性和要化率定义的化学环境因子计算了^57Fe在PrBa2Cu3O7中的Mossbauer同质异能位移,确定了^57Fe在PrBa2Cu3O7中的价态和占位情况。
简介:Theoptimalconditionsforthecomplexationreactionofmeso-tetra(3-methoxy-4-hy-droxyphenyl)porphineT(3-M-4HP)Pwithplatinumandrhodiumarepresented.Beer’sLawisobeyedwhentheconcentrationofrhodiumisintherangeof0.45-1.15μg/25mL.Themolarabsorptivityofrhodiumwasfoundtobe1.99×106L·mol-1·cm-1at460nm.ThevalueofεPtwasfoundtobe6.28×105L·mol-1·cm-1bylinearregressionmethod.TheKcoefficientmethodandcompensatingcoefficientwereusedtodetermineplatinumandrhodiumsimultaneoulywithoutremovalormaskingoftheinterferentsinthesample.Theresultsforthedeterminationofplatinumandrhodiuminthemixedsolutionofplatinumandrhodiumaresatisfactory.
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:Threenewcomplexes[Ni(H2L)][Fe(CN)5(NO)]2·6H2O(1),[Ni(H2L)][Fe(CN)5(NO)]2·4H2O(2)and[Cu(H2L)][Fe-(CN)5(NO)]2·4H2O(3)(L=3,10-bis(2-aminoethyl)-1,3,5,8,10,12-hexaazacyotetradecane)arepreparedandcharacter-izedbyIR,elementalanalysesandsingle-crystalX-rayanaly-ses,indicatingthattheyarethefirstexamplesoftrinurlearni-troprnsside-bridgedMFe2(M=CuandHi)complexes.Inthethreecomplexes,thecentralmetalatoms(M)areallsix-coor-dinatedbythenitrogenatomsfromthemacroeyclicligandandtwocyano-bridgesatthetrans-positionstoformdistortedocta-hedralconfigurations.TheaxialN—M—NlinkageisnearlyverticaltotheequatorialplanedefinedbyfourcoordinatingNatomsofmcroeyclicligand.TheC≡N—Nibondangleof172.6°incompleox1isapparentlylargerthanthoseincom-plexes2and3(152.57°and136.37°,respectively).Thethreecomplexesareallconnectedbyhydrogenbondsinto3Dnet-works.Thisstudyshowsthatthecyano-bridgedtrinuclearspeciescouldbegeneratedviathecontrolofthechargeofthebuildingblocks.
简介:FiveC3/C3fluoroquinolonedimerstetheredwithafusedheterocyclicringofs-triazolo[2,1-b][1,3,4]thiadiazolederivedfromantibacterialquinolonesweresynthesizedandcharacterized,andtheirinvitroantitumoractivityagainstL1210,CHOcelllineswasevaluatedviatherespectiveIC50values.
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.
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简介:Anumberofnaphthalenedonorcompoundsthatpossessanadamantanaminebindingmoietyandan(OCH2CH2)n(nn1,2,3,4,6,8)spacerweresynthesized.Thefluorescencequenchingbetweenthesedonorsubstratesandmono-6-O-p-nitrobenzoyl-β-cyclodextrin(pNBCD)andmono-6-O-m-nitrobenzoyl-β-cyclodextrin(mNBCD)wasstudiedindetail.Itwasfoundthatveryefficientfluorescencequenchingcouldoccurinthesesupramolecularsystems.Thisquenchingwasattributedtothephotoinducedelectrontransferinsidethesupramolecularassemblybetweenthenaphthalenedonorsandcyclodextrinacceptors.DetailedStern-VolmerconstantsweremeasuredandtheywerepartitionedintodynamicStern-Volmerquenchingconstantsandstaticbindingconstants.Itwasdemonstratedthatthebindingconstantsbetweenallthenaphthalenecompoundsandcyclodextrinsarethesameastheypossessthesamebindingsite,i.e.,adamantanamine.