简介：采用水热方法合成一种新型钼-氧簇化合物Ni(en)3MoO4,并通过X射线单晶结构分析、红外光谱分析、元素分析、差热热重分析对该化合物进行了表征.结构分析数据表明:该化合物属三方晶系,P-31c空间群,晶胞参数a=0.9226(13)nm,b=0.9226(13)nm,c=0.9959(2)cm,α=90°,β=90°,γ=120°,V=0.7342(2)nm3,Z=2,Dc=1.805mg/m3,μ=2.153mm-1,F(000)=408,R=00553,Rw=0.1732;该化合物是分立结构,是由MoO4四面体簇和Ni(en)3八面体簇形成,其中MoO4四面体簇和Ni(en)3八面体簇交替排列,存在较强的氢键作用,结构中分立的手性配合物Ni(en)3的两种对映体构象以MoO4簇为中心对称排布.

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简介：多代替的dihydrofurans是为自然产品和药品的合成的珍贵中介。可观的注意集中于发展有效并且为他们的准备的regioselective方法。把K2CO3用作一个底，与fur-2-oylmethyltriphenylarsonium溴化物1的反应和乙醇2-acetyl-3-arylacrylate2在在房间温度的tetrahydrofuran，我们发现一个有效协议被完成综合trans-3-aryl-4-carbethoxy-2,3-dihydro-2-fur-2-oyl-5-methylfurans3在有高stereoselectivity的好产量。化合物3的结构被红外，1HNMR，MS和HRMS证实。为3的形成的机制被建议。

简介：Onenovelorganic-inorganichybridsupramolecularassemblies|（NDPA）（18-crown-6）]2+（DMA）+·3ClO4-（1）,hasbeensuccessfullyconstructedthroughtheprominentstrategiesofcrystalengineering（NDPA=N,N-dimethyI-1,4-phenylenediamine,DMA=dimethylamine）,andcharacterizedbyIR,powderXRDandsinglecrystalX-raydiffraction.Inthestructure,thesupramolecularorganiccationsandinorganicClO4-anionsarearrangedalternatelyandlinkedbyN-O…Hhydrogenbonds.ItisworthytonotethattheClO4-arelinkedtoformone-dimensionalinorganicchainthroughstrongNH…Ohydrogenbondsalongb-axis.Thereisnodistinctdielectricanomalyinthetemperaturedependentandfrequency-dependentdielectricconstantcurves,suggestingthatnophasetransitionexistswithinthemeasuredtemperaturerange（120-420K）.Therelativedisplacementofcationsandanions,theturnedpolarizationofmolecularelectricmomentandmacrocyclicmoleculerotatorarethemainfactorstodeterminethetrendofdielectricconstant.

简介：磁性的支持nanoparticle的Pd/Fe3O4乐意地被准备并且证明了是为在温和条件(汽球H2压力和房间温度)下面的nitroarenes的有效铃木跨coupling反应，和减小的万用的催化剂。催化剂能方便地与持续催化活动若干次被恢复并且再使用。

简介：归纳了从钛铁矿中分离铁和二氧化钛的方法,包括亚熔盐法、预氧化法、还原锈蚀法;其次,初步总结了目前国内外制备Fe3O4磁性纳米颗粒和TiO2纳米粒子的方法。最后,对Fe3O4/TiO2复合材料的制备方法包括溶胶-凝胶法、微乳液法、均匀沉淀法作了梳理。Fe3O4/TiO2复合纳米材料很好地解决了单独使用TiO2作为废水处理催化剂,在实际应用过程中易随水流失,难以回收利用的问题,具有一定的实用性。

简介：在有ArSSAr的THF的SmI2的反应生产了二binuclear钐thiolate建筑群[(THF)3I2-Sm(-SAr)]2[Ar=Ph(1)，4-Me2NC6H4(2)]在高收益。2的结构被单个水晶X光检查晶体学描绘。2的水晶与空格组和a=0.95705(13)一起属于三斜晶系的系统nm，b=1.22287(14)nm，c=1.26450(14)nm，=64.194(11)??匭吗？？v？？

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：在这研究，一新(乙烯基氯化物)(PVC)poly，为Ho3+离子的膜传感器作为ionophore基于N-phenyl-2-(thiophen-2-ylmethylene)hydrazinecarbothioamide(PHC)被准备。这个传感器与阳离子的变化比较向钬离子表明了好选择和敏感，包括碱，碱的地球，转变和重金属离子。电极的反应性质上的膜作文和pH的效果被调查。详细，建议传感器展出了Nernstian行为(与20.4的一个斜坡??洀????x

简介：采用一步法合成了氨基化四氧化三铁（NH2-Fe3O4）磁性纳米材料,并以XRD,IR等手段对其进行了表征.将NH2-Fe3O4组装到磁性玻碳电极表面,得了NH2-Fe3O4修饰的磁玻碳电极,并以该修饰电极为工作电极,研究了其电化学性能.利用差分脉冲溶出伏安法研究了铅（Ⅱ）离子和铜（Ⅱ）离子在该修饰电极上的电化学行为.结果表明：NH2-Fe3O4纳米粒子可显著提高Pb2＋和Cu2＋在电极表面的富集量,提高溶出峰电流.由于差分脉冲溶出伏安曲线中Pb2＋和Cu2＋的溶出峰电位差较大,且没有相互干扰,所以该电极可用于Pb2＋和Cu2＋的同时测定.

简介：RemanspectroscopyisusedasatooltomonitorthereactionbetweenN,N’-di（pmethyl）monothioxamidesand1,3-diaminetrimethyleneandtodetectthereactionintermediate.Byobservingchangesof1024cm-1C=Sbandandappearanceofanewbendataround1720cm-1,thereactionmechanismisdiscussed.

简介：AseriesofnovelN-（3-furan-2-yl-1-phenyl-1H-pyrazol-5-yl）amidesderivativesweredesignedandsynthesized.Theirstructureswereconfirmedby1HNMR,13CNMRandHRMS.Alltitlecompoundswereevaluatedfortheirherbicidalandantifungalactivities.Preliminarybioassayresultsindicatedthatthetitlecompoundsshowedgoodtomoderateherbicidalactivityat1000mg/L.Compound6qpresentedthebestactivityagainstDigitariasanguinalis（L）Scop.,AmaranthusretroflexusL.andArabidopsisthalianawithaninhibitiondegreeoffive.Compound6dalsoshowedaninhibitiondegreeoffiveagainstD.sanguinalis.Inaddition,at50mg/L,mostcompoundsexhibitedgoodinvitroantifungalactivityagainstSclerotiniasclerotiorum,withcompound6cshowingover90%antifungalactivityagainstS.sclerotiorumandPelliculariasasakii.

简介：TwonewintercalationcompoundsFe0.90PS3(phen)0.41(1)(phenstandsfor1,10-phenanthrolineincludingapartof1,10-phenanthrolineH+)andFe0.83PS3(bipy)0.34(2)(bipystandsfor2,2’-bipyridineH+)weresynthesizedbythereactionofthelayeredFePS,with1,10-phenanthrolineor2,2’-bipyridineinthepresenceofaniliniumchloride.Theywerecharacterizedbyelementalanalyses,powderX-raydiffraction(XRD),infraredspectroscopy.Thelatticespacingoftheintercalatewasexpandedby0.90nmforFe0.90PS3(phen)0.41and0.57nmforFe0.83PS3(bipy)0.34withrespecttothepristineFePS3,indicatingthattheringplaneoftheguestsisperpendiculartothelayerofthehost.TheUV-visabsorptionspectraofthefiltrateinpreparationoftheintercalatesindicatethat1,10-phenanthrolineor2,2’-bipyridinealsoactsasacomplexingagenttoremoveintralamellarFe2+ionsintothesolutionduringintercalation.Themagneticpropertiesof1and2werestudied.

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简介：Startedfrom5-hydroxy-2-pentanone,(R)(E)-3,7-dimethyl-2-octene-1,8-dioicacid,callosobruchusicacid,wassynthesizedviafivestepswithD-(-)-camphorsultamasthechiralauxiliary.Itwasofgoodopticalpurityandyield.

简介：存取2-substituted-N1-carbethoxy-2,3-dihydro-4(1H)的一条灵巧、有效、新奇的途径-quinazolinones是被代替的N-carbethoxyanthranilamide的冷凝作用用p-toluenesulfonic酸在refluxing2,2,2-trifluoroethanol或hexafluoroisopropanol与烷基，aromatic或异种aromatic醛开发催化剂。

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.

简介：有代替的吲哚的o-alkynylbenzaldehydes或o-alkynylbenzaldimines的催化双人脚踏车反应由羰基或imine组的吲哚的分子间的增加开始了的Pd(II)由intramolecular炔属羟的nucleopalladation列在后面，由protonolysis熄灭碳钯契约改革Pd(II)种类被开发。没有一个氧化还原作用系统的必要性，反应能在温和条件下面被执行。

简介：0.5%Pt-K/γ-Al2O3catalystsforthesynthesisofo-phenylphenol(OPP)fromo-cyclohexenyl-cyclohexanone(dimer)dehydrogenationwerepreparedbymeansofatwosubsequentimpregnationmethod.Theeffectsofcatalystpreparationparameters,suchasKpromoters,calcination,andreductionconditions,wereinvestigated.TheresultsshowedthattheadditionofK2SO4toPt/γ-Al2O3catalystnotablypromotedtheselectivityofOPP,anditsoptimumcontentwasfoundtobe6%inmassfraction.ThehigheractivitywasobtainedwhenPt/γ-Al2O3catalystwascalcinedinnitrogenatmosphereat400―500°Candthenreducedatthesametemperaturefor3hinhydrogenatmosphere.TheconversionofthedimerandtheselectivityofOPPwerealwaysabove99%and90%,respectively,over0.5%Pt-6%K2SO4/γ-Al2O3catalystduringthepilotscaletestof8000h.