简介：

简介：Anovelquaternarymetalselenide,K_2CdSnSe_4,wassynthesizedviaamolten-saltreactionat550℃.Thecompoundhasaone-dimensionalstructurecontainingachainof_∞~1[CdSnSe_4]~(2-)anionsseparatedbyK~+cations.ThecrystalbelongstothespacegroupI-42m,withtheunitcellparametersa=0.80298(11)nm,b=0.80298(11)nm,c=0.69217(14)nm,α=β=γ=90°.Areflectancespectroscopystudyrevealsthenatureofthesemiconductorwithanenergygapof1.7eVforthecompoundandithasastrongopticalabsorptioninarangeof2—5eV.

简介：N酰--hydroxy-4-phenyl-oxazolidinethiones能被处理很快在高收益变换成他们的乙醇thiol酉旨与在0è的EtSH

简介：［1］BASFUSP4479906［2］BASFBP1443541［3］BASFDE3618265［4］WangL.,WuZ.,ChinaLeather,26(8),11,(1997)［5］YuanL.,DinY.,ChineseChemistryBulletin,(2),19(1988)［6］KurokiH.,ChemistryofDyeingTheory(ChineseTranslation),TextileIndustryPress,Beijing,89(1982)［7］WangS.,LiP.,WuZ.DyestuffIndustry(Chinese),34(4),1,(1997)［8］Tian,Y.,Wu,Z.,Wang,G.,Zhang,S.J.ChineseChem.Eng.,46,156(1995)［9］Tian,Y.,Wang,G.,Wu,Z.,J.ChineseChem.Eng.,47,75(1996)［10］Lycka,A.,DyesandPigment,32,11(1996)［11］Griffith,J.,ColourandConstitutionofOrganicMolecules,AcademicPress,London,191(1976)

简介：ThecomplexK3H4GeW9V3O40·8H2OcrystallizedinamonocliiniesystemwithspacegroupP2,Mr=2784.67,a=11.099（3）,b=16.452（4）,c=13.534（4）,β=108.14°,Z=2,V=2348.493,F（000）:2456,μ=239.7cm-1,De=3.932g/cm3.ThefinalR=0.083for4528non-zeroreflexions.ThestructureofanionsGeW9V3O40andGeW9O34belongstoA--type.

简介：Dibromobiphenylreactedwithcynomethylanioninammoniaunderirradiationtoformnucleophilicbis-substitutedproductinhighyieldwithoutsubstantialmonosubstitutedproduct.Quantumyieldsfortheformationsofbis-andmonosubstitutedproductswerefoundtobe85.6and2.3×10-6respectively,whilethecorrespondingpseudo-first-orderrateswere6.9×10-3and5.2×10-10mol.L-1.S-1.Blockupthepossibleelectrontransferof4-brome-4’-cyanomethylbiphenylylradicalanionto4-cyanometbyl-biphenylylradicalandbromineion.

简介：Twocalix[4]arenederivativescontaining1,2,3-triazolemoietyweresynthesizedviaK2CO3-catalyzed1,3-dipolarcycloadditionreactionbetweencalix[4]arene-basedazideandactivemethylenecompoundsingoodyields.Thestructuresofthetwocompoundssynthesizedhereinwerefullyconfirmedby1HNMR,,13CNMR,andMS（ESI）.Thethermalanalysisshowedthatthemasslossesofthesynthesizedcompounds4and5containing1,2,3-triazolegroupsaresimilartoeachother.

简介：Ahomologousseriesof4’-methylphenyl4"-[(4-alkoxy-2,3,5,6-tetrafluorophenyl)ethynyl]-benzoateshavebeensynthesized.Polarizingmicroscopictexturalobservationshowsthatsuchcompoundsexhibitenantiotropicnematicphase.

简介：

简介：Thesynthesisofopen-fiameworkmetalphosphateshasbeenasubjectofintenseresearchowingtotheirinterestingstructuralchemistryandpotentialapplicationsasionexchangers,catalystsandadsorbents.Alargenumberofthesematerialsaresynthesizedinthepresenceoforganicaminesasstructure-directingagents.Recently,manyresearchactivitieshavefocusedonthesynthesisofinorganic-organichybridframeworks.Ascomparedwithinorganicligands,theadvantageofusingorganicmultidentateligandsistheefficacyofrationaldesignofcrystallinesolidsthroughtheircoordinatingpropensitiesandgeometries.

简介：Thesynthesisandphasebehaviorofaseriesof4’-alkyloxy-4-hydroxybiphenylswerediscribed.Theeffectsofreactionconditionsontheyieldsofproductswereinvestigated.Thecharacterizationsofthermotropicliquidcrystallineproductsforthetypeandthermalpropertiesarediscussedthroughtheuseofdifferentialscanningcalorimetry,polarizingmicroscopy.

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：3,5,6,8-Tetrahydro-4H-thiopyrano[4′,3′:4,5]thieno[2,3-d]pyrimidin-4-ones(7)weresynthesizedviathebasecatalyticreactionsofaminesorphenolswithcarbodiimides(5),whichwereobtainedfromtheaza-Wittigreactionsofiminophosphoranes(4)witharomaticisocyanates.

简介：Excessmolarvolume(VE)dataonbinaryliquidmixturesofmethylheptenone(MHO)withmethanol,ethanol,n-propanolorn-butanolhavebeendeterminedfromthedensitymeasurementsat298.15Kandatmosphericpressure.ThevaluesofVEinallthesystemsovertheentirecompositionrangearequantifiedbytheRedlich-Kisterequation.TheeffectsofthechainlengthofalkanolsonVEarediscussed.

简介：

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：Poly(4-vinylpyridine)(P4-VP)nanofiberandfluoresentpoly(4-vinylpyridine)/porphyrin(P4-VP/TPPA)nanofiberwererespectivelypreparedbyelectrospinning.TheeffectoftheconcentrationofP4-VP/dimethylformamide(DMF)electrospinningsolutionsonthemorphologyofP4-VPnanofiberwasinvestigatedanditwasfoundthattheaveragediameterofthenanofiberofP4-VP/DMFincreasedwiththeincreaseoftheconcentrationofthespinningsolution.AftertheadditionofTPPAtotheP4-VP/DMFspinningsolution,thediameterofP4-VP/TPPAnanofiberbecameevenduetotheincreaseoftheconductivityoftheP4-VP/DMF-TPPAsolution.Thephotoluminescent(PL)spectralanalysisindicatesthattheemissionpeakpositionofP4-VP/TPPAnanofiberisalmostthesameasthatofpureTPPAatabout650nmwithoutpeakshift,andwhenitwasstoredfor20days,theemissionpeakofP4-VP/TPPAnanofiberisalsoat650nm,indicatingthatthefluorescentpropertyofP4-VP/TPPAnanofiberisstable.Fourier-transforminfrared(FTIR)spectrumconfirmsthechemicalcompositionoftheresultingP4-VP/TPPAcompositenanofiber.

简介：Treatmentof4-amino-3-(1-aryl-5-methyl-1,2,3-triazol-4-yl)-5-mercapto-1,2,4-triazoles/2-amino-5-(1-aryl-5-methyl-1,2,3-triazole-4-yl)-1,3,4-thiadiazoleswithbenzaldehyde,acetoneandω-bromoacetophenonewastestedandcompared.ThetitlecompoundsSchiffbases,amides,imidazolo[2,1-b]-1,3,4-thiadiazolesand7H-s-triazolo[3,4-b]-1,3,4-thiadiazineshavebeenconfirmedbyelementalanalyses,^1HNMR,IRandMSspectra.AllthecompoundshavealsobeenscreenedfortheirantibacterialactivitiesagainstB.subtilis,S.aureusandE.coli.

简介：Ahighlysensitiveelectrochemiluminescence-polymerasechainreaction(ECL-PCR)methodforK-raspointmutationdetectionisdeveloped.Briefly,K-rasoncogenewasamplifiedbyaRu(bpy)32+(TBR)-labeledforwardandabiotin-labeledreverseprimer,andfollowedbydigestionwithMvaIrestrictionenzyme,whichonlycutthewild-typeampliconcontainingitscuttingsite.Thedigestedproductwasthenadsorbedtothestreptavidin-coatedmicrobeadthroughthebiotinlabelanddetectedbyECLassay.TheexperimentresultsshowedthatthedifferentgenotypescanbeclearlydiscriminatedbyECL-PCRmethod.Itisusefulinpointmutationdetection,duetoitssensitivity,safety,andsimplicity.

简介：过量音量(VE)，超声的速度(u)，isentropic压缩的可能性(K)和粘性()为有在303.15点的1,2-dichlorobenzene，1,3-dichlorobenzene，1,2,4-trichlorobenzene，o-chlorotoluene，m-chlorotoluene，p-chlorotoluene，o硝基甲苯和m硝基甲苯的dimethylformamide(DMF)的二进制混合物，K被学习。过量卷数据展览在为有1,2-dichlorobenzenes和1,3-dichlorobenzenes和性质的dimethylformamide的混合物的符号的倒置在为有1,2,4-trichlorobenzene，o硝基甲苯和m硝基甲苯的dimethylformamide的混合物的全部作文范围上是完全积极的。在另一方面，数量为有chlorotoluenes的dimethylformamide的混合物是否定的。Isentropic压缩的可能性(K)从精确健全速度和密度数据为一样的系统被计算了。进一步，从理想的行为的isentropic压缩的可能性(K)的偏差也是计算的。K值在在所有二进制混合物的全部音量部分范围上是否定的。试验性的健全速度数据以免费长度理论(FLT)和碰撞因素理论(CFT)被分析。粘性数据根据相应州的途径被分析。测量数据根据在不同分子之间的分子间的相互作用被讨论。