简介:ELECTRON TRANSFER BETWEEN Eu3+ AND Ce3+ IN SrMgF4 MATRIXELECTRONTRANSFERBETWEENEu3+ANDCe3+INSrMgF4MATRIX¥YingWU;Ch...
简介:Lophenol,cholest-4α-methyl-7-en-3β-ol(1),obtainedfromDracaenacochinchinensis(Lour.)S.C.Chen,wasstructurallymodified.Itwasacetylatedtoprotect3β-hydroxylgroup,andthenoxidisedbyseleniumdioxideinaceticacidtogivecholest-4a-methyl-8-en-3β,Ta-dioldiacetate(3).Thiscompound3isunstableinchloroformsolutionorwhenheatedandeasilyconvertedtoadienecompound,cholest-4a-methyl-7,14-dien-3β-olacetate(4).Thestructuresof3and4wereelucidatedbymeansofIR,^1HNMR,^13CNMRandMS,andtheabsoluteconfigurationof3wasestablishedbyX-raycrystallography.Thepropertyof3wasalsodiscussedinthispaper.Both3and4arenewcompoundsandwerereportedforthefirsttime.
简介:3-(2-Hydroxyphenyl)-6-(4-nitrophenyl)-7H-1,2,4-triazolo[3,4-b][1,3,4]thiadiazine,C16H11N5O3S,waspreparedbythecyclizationof3-(2-hydroxyphenyl)-4-amino-5-mercapto-1,2,4-triazolewith2-bromo-4-nitroacetophenone.Thecompoundwascharacterizedbymeansofelementalanalysis,IR,1HNMR,13CNMR,massspectrometry,andX-raydiffraction.ThecompoundcrystallizesinamonoclinicsystemwithspacegroupCc,a=2.1853(4)nm,b=2.1192(5)nm,c=1.3526(3)nm,β=95.21(2)°,V=6.238(2)nm3,Dcalcd.=1.505Mg/m3,Z=16,F(000)=2916,R1=0.0501,wR2=0.0427.Acomparisonbetweenthecrystalstructuresof1,2,4-triazolo[3,4-b][1,3,4]thiadiazineand1,2,4-triazolo[3,4-b][1,3,4]thiadiazolewasmadeinthestructuralview.Atwo-dimensionalnetworkisformedbyhydrogenbondsandπ-πstackinginteractions.
简介:Ionothermalsynthesiswasusedtoprepareanovelaminoacidcontaininghybridzincophosphatemonomer,[Zn(HPO4)(H2PO4)][C6H10N3O2](denotedasZnPO-CJ58).Theinorganicframeworkof[Zn(HPO4)(H2PO4)]·[C6H10N3O2]consistsof4-memberedringsformedbyZnO3OHisandPO2(OH)2tetrahedra.TheHPO4andaminoacidmoietieshangontheZncenter.Suchaframeworkisstabilizedbyextensivemultipointhydrogenbondsinvolvingthephosphateunitsandhistidinemoleculestoformapseudo-3Dsupramolecularstructure.ItisnoteworthythatZnPO-CJ58isthefirstzincphosphateclusterwithaminoacidactingastheligand.Itexhibitsphotoluminescenceexcitedatawavelengthof220nm.Interestingly,ZnPO-CJ58cantransformintoalayeredstructure(C6H10N3O2)Zn2·(HPO4)(PO4)·H2O(ZnPO-CJ36)throughfurtherreactingwithwaterorzincacetatedihydrateinwaterat85℃for1h.Thisworkwillbehelpfulforthesynthesisofcrystallineinorganic-organichybridmaterialswithbiofunctionalmolecules.
简介:标题化合物C22H29N3O3以简单易得的试剂为原料,在乙醇溶剂中,微波辐射下经两步多组分反应合成得到.其结构通过单晶X射线衍射法确定,晶体属三斜晶系,空间群P-1,相对分子质量Mr=383.48,晶胞参数a=1.14770(12)nm,b=2.0657(2)nm,c=1.00780(12)nm,V=2.1841(4)nm3,Z=4,晶胞密度Dc=1.166mg/m3,吸收系数μ=0.078mm-1,单胞中电子的数目F(000)=824.晶体结构用直接法解出,经全矩阵最小二乘法对原子参数进行修正,最终的偏离因子为R1=0.0709,wR2=0.1405.在晶体结构中新形成的噌啉环为近似于共平面结构,而其中的哒嗪环则为船式构象.
简介:2-Phenyl-1,2,3-triazole-4-formylhydrazine(2)waspreparedbyhydrazinolysisofthecorrespondingester1.Reactionof2withCS2/KOHgavetheoxadiazolederivatives(3)whichvia,Mannichreactionwithdifferentdialkylaminesfurnished3-N,N-dialkylderivatives(4a-c).Also,condensationof2withappropriatearomaticacidinPOCl3yieldedoxadiazolederivatives(5a-c),orwithaldehydesandketonesaffordedhydrazones(6a-c).Cyclizationof(6a-c)withaceticanhydridegavethedesireddihydroxadiazolederivatives(7a-c).Ontheotherhand,reactionofdithiocarbazate(8)withhydrazinehydrategavethecorrespondingtriazolederivative(9)whichontreatmentwithcarboxylicacidsinrefluxingPOCl3yieldeds-triazole[3,4-b]-1,3,4-thiadiazolederivatives(10a-b).ThestructuresofalltheabovecompoundswereconfirmedbymeansofIR,1HNMR,MSandelementalanalysis.
简介:Asimpleeffectivesynthesisofbis(dihydropyrimidinone-4-yl)benzenederivatives,usingboricacidascatalyst,fromisophthalicaldehydeorterephthalicaldehyde,1,3-dicarbonylcompoundsandureaorthioureainglacialaceticacidwasdescribed.AstheexpansionoftheclassicalBiginellireaction,thismethodhastheadvantageofexcellentyields83%-94%andshortreactiontime0.5-1.5h.
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简介:ThespinelferritesMnFe2O4nanowiresweresynthesizedbyhydrothermalroute,porousMnFe2O4andnanoparticlesmorphologiesweresynthesizedbysol-gelmethodwitheggwhite.Thestructures,morphologies,magneticpropertiesandadsorptionpropertiesoftheseobtainedferriteswithdifferentmorphologieswerestudiedcontrastively.Resultsshowthattheobtainedsamplesexhibitferromagneticproperties.Thisrealizesconvenientmagneticseparationfromsolutionwhentheyareusedinthetreatmentoforganicdyeswastewater.However,thecontrastivestudiesshowthatthesaturationmagnetizations(Ms)ofMnFe2O4withdifferentmorphologiesaredifferentandtheMsfollowstheorder:Ms(porous)
简介:WiththedecreaseofpHvaluefrom8.45to–1.0,theUV-Visabsorptionandfluorescentspectraof1,2-bis(4-pyridyl)ethylene(BPE)tookonthesamechangingtrendatfourdifferentsuccessivepHstages:8.45―7.20,7.20―5.62,5.62―2.60,and2.60―-1.0,namely,nochange,decrease,increase,anddecreaseagain.Amongthese,inarangeof7.20―5.62,thefluorescencewavelengthblueshiftedfrom418to359nm,buttheUV-Visabsorptionwavelength,incontrast,redshiftedfrom285to298nm.ThefluorescenceintensityofBPEhadadropeventoquenchuponadeclineinthepHvaluefrom2.60to–1.0probablyowingtoitscation-πinteractiontoreducetheπelectronclouddensityofBPE.Twodissociationconstants,pKa1(4.30±0.01)andpKa2(5.65±0.04),wereobtainedbasedonfluorescencedata.ThechangesoffluorescencespectraindicatethatBPEhas'off-on-off'switchbehavior.ThefluorescentspectraofBPEwerenearlyindependentonthepresenceofα-andβ-cyclodextrins.