简介：ＳＹＮＴＨＥＳＩＳ　ＡＮＤ　１８３Ｗ　ＮＭＲ　ＣＨＡＲＡＣＴＥＲＩＺＡＴＩＯＮ　ＯＦ　Ｐ４Ｗ３０Ａｌ４（Ｈ２Ｏ）２Ｏ１１２２０－　ＨＥＴＥＲＯＰＯＬＹＡＮＩＯＮＳＹＮＴＨＥＳＩＳＡＮＤ１８３ＷＮＭＲＣＨＡＲＡＣＴＥＲＩＺ?..

简介：有N-(2-propionic酸)的新奇金轧(III)建筑群-salicyloylhydrazone(C10H10N2O4，H3L)并且1,10-phenanthroline(C12H8N2，phen)被准备并且描绘。水晶结构[Gd(H2L)(HL)-(H2O)3]2潲楰湯捩???慳楬祣潬汹?票牤穡湯??ㄠ??桰湥湡桴潲楬敮???????楢慯瑣癩瑩？

简介：Afacilesyntheticroutetotwoseco-eudesmane,4,5-dioxo-10-epi-4,5-seco-γeudesmane(1)and4,5-dioxo-10-epi-4,5-seco-γ-eudesmol(2)from(+)-dihydrocarvonehasbeendescribed.Avoidingexpensivereagents,thishighlyeconomicmethodespeciallysuitsforthesynthesisof4,5-seco-eudesman-typeandophianon-typesesquiterpeneswithadoublebondatposition11and12.

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简介：Anovelclassoffulgimide,(Z)-4-oxazolylfulgimide((Z)-1-benzyl-4-isopropylidene-3-[1-(2-aryl-5-methyloxazolyl)ethylidene]tetrahydropyrrole-2,5-dione),wassynthesizedbythereactionof(Z)-4-oxazolylfulgide(4-isopropylidene-3-[1-(2-aryl-5-methyloxazolyl)ethylidene]tetrahydrofuran-2,5-dione)withbenzylamine.Photochromicpropertyof(Z)-4-oxazolylfulgimidewasstudied.Comparedwith(Z)-4-oxazolylfulgide,theabsorptionmaximumofthecoloredformof(Z)-4-oxazolylfulgimideisbathochromic-shifted.Substituentsonthearylringaffecttheabsorptionmaximumoftheopenformandthecoloredformof(Z)-4-oxazolylfulgimide.

简介：Thenon-isothermaldecompositionoflead2,4,6-trinitroresorcinatemonohydrate,Pb(TNR)·H2O,wasinvestigatedbymeansofTG-DTA,DSCandIR.Thethermaldecompositionmechanismandthedissociatedkineticswerealsoinvestigated.ThekineticparameterswereobtainedfromtheanalysisoftheDSCcurvesbyintegralanddifferentialmethods.ThemostprobablekineticmodelfunctionofthedehydrationreactionofPb(TNR)·H2Owassuggestedbythecomparisonofthekineticparameters.

简介：Itiswellknownthatelectrochemicaloxidationofanilinedissolvedinelectrolytesolutionsisaveryusefulmethodforpreparingpolyanilinefilmsonelectrodes’.However,itisverydifficultforthismethodtoprepareauniformmonolayerpolymersincelocalnucleationandgrowthofpolyme...

简介：本文探讨（CH3Li）4中键的作用,通过计算,发现（CH3Li）4分子的面甲基结构比顶甲基结构要稳定;指出Li—Li间的成键作用相当强,约为Li2分子中键作用的40%左右,估计（CH3Li）4中的J7Li-6Li值约为1Hz。

简介：4-(Succinimido)-1-butanesulfonicacidasanefficientandreusableBronstedacidcatalyzedthesynthesisofpyrano[4,3-b]pyranderivativesundersolvent-freeconditions.Thecatalystcanbepreparedbymixingsuccinimideand1,4-butanesultonethatismoresimpleandsaferthanthepreparationofsuccinimidesulfonicacid.Thismethodhastheadvantagesofhighyield,cleanreaction,simplemethodologyandshortreactiontime.Thecatalystcouldberecycledwithoutsignificantlossofactivity.

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简介：Thesynthesisof(S)-2-(3-arylacrylamido)-3-{4-[2-(5-methyl-2-phenyloxazol-4-yl)ethoxy]phenyl}propanoicacidsisdescribed.TheirstructureswereconfirmedbyH-NMR.

简介：新奇pyridopyrazolopyrimidinone衍生物作为潜在的PDE5禁止者被设计并且综合。目标混合物比sildenafil对人的血小板PDE5，而是更少的有势力表明了重要禁止的活动。

简介：Anovelsupportedliquidphasefilmcatalyst:SupportedPdCl2-(n-C4H9)4N+Cl-moltensaltswasfoundtobeaneffectivecatalystwithgoodstabilityforselectivehydrodechlorinationofCCl2F2(CFC-12)toitsalternativesCH2F2andCHClF2.AdditionofCoCl2,GaCl3andCuCl2toPdCl2-(n-C4H9)4N+Cl-modifiesthecatalyticperformanceofsupportedmoltensalts.

简介：在水热条件下,制备了一种基于Keggin型多金属氧酸盐的银配合物[Ag（10）（NCA）4（PW9ⅥW3ⅤO（40））（H2O）4].通过元素分析、红外光谱和X-射线单晶衍射方法确定了该配合物的晶体结构.在合成过程中,3-（2-吡啶羧酸）酰胺-吡嗪配体（L）分解成烟酸NCA.结构分析表明：该化合物属于三斜晶系,P1空间群,晶胞参数a=1.18874（9）nm,b=1.24950nm,c=1.41103（10）nm,α=73.712（2）°,β=66.720（2）°,γ=83.467（2）°,V=1.8479（2）nm3,Z=1,R1=0.0731,ωR2=0.1974.配合物中含有一种六核银亚单元[Ag6（NCA）4]（2＋）,不同亚单元间通过配位水的氧原子连接形成一维双链结构,而一维双链进一步通过Ag—N键连接形成二维层状结构,二维层则通过[PW9ⅥW3ⅤO（40）]（6-）多阴离子形成最终的三维金属有机框架.标题配合物修饰的碳糊电极对H2O2和KNO2还原有好的电催化活性,而且该配合物对降解亚甲基蓝、罗丹明B分子有较高的光催化效率.

简介：“开火的复合真空”和熄灭的水技术在LiFePO4的合成被介绍阴极粉末。样品被加热在真空石英试管封上的预先分解的先锋混合物准备，走水路在sintering温度熄灭跟随。结果显示使用“快熄灭”的处理能成功控制最后的产品的谷物尺寸的增生并且改进它活跃材料的利用比率。样品由这种技术综合了有高可逆的分泌物特定的能力和好周期的电气化学的性能。

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简介：Two-armedneutralanionreceptors(4,5),calix[4]arenesbeatingthioureaandamidebindingsites,werepreparedandexaminedtheiranion-bindingabilitybytheUV-visspectra.Theresultsofnon-linearcurvefittingandJobplotindicatethat4or5forms1：1stoichiometrycomplexwithfluoridebyhydrogenbondinginteractions.Receptors4and5haveanexcellentselectivityforfluoridebuthavenobindingabilitywithacetate,dihydrogenphosphateandthehalogenanions(Cl^-,Br^-,I^-).

简介：Threepairsofnovel2-aryl-3,4,5-trihydroxypiperidines(6–8andtheirenantiomers),thepiperidineanaloguesofthepyrrolidinealkaloidsradicamineAandradicamineB,werepreparedfromsixmemberedcyclicnitronesthroughaconcisetwo-stepprocedure,i.e.,Grignardreagentadditionanddeprotection.Thesenovelpolyhydroxylatedpiperidineiminosugarswereassayedagainst10typesofenzymes.Onlycompound8exhibitedweakinhibition(IC501080mmol/L)againstb-galactosidasefromratintestinallactases.

简介：毛状的电气泳动(CE)能分开收费并且有高速度和效率的中立物质。在这篇论文，利用meso-octamethylcalix[4]吡咯，meso-tetraspirocyclohexylcalix[4]是的吡咯，bimethyl双性人(2-pyrryl)甲烷和1,1双性人(2-pyrryl)环己烷在毛状的地区电气泳动(CZE)的添加剂电解质，他们无机的阴离子的识别能力被讨论。dipyrrylmethanes比其它有更好的识别能力。他们由CZE的七个正常无机的阴离子的分离上的效果被学习。

简介：Anovelflower-likehydratedmagnesiumcarbonatehydroxide,Mg_5(CO_3)_4(OH)_2·4H_2O,withmicro-structurecomposedofindividualthinnano-sheetswassynthesizedusingafacilesolutionroutewithouttheuseoftemplateororganicsurfactant.Reactiontimehasanimportanteffectonthefinalmorphologyoftheproduct.Themicro-structureandmorphologyofMg_5(CO_3)_4(OH)_2·4H_2OwerecharacterizedbymeansofX-raydiffractometry(XRD),field-emissionscanningelectronmicroscopy(FE-SEM).Brunauer-Emmett-Teller(BET)surfaceareasofthesampleswerealsomeasured.Theprobableformationmechanismofflower-likemicro-structurewasdiscussed.ItwasfoundthatMg_5(CO_3)_4(OH)_2·4H_2Owithflower-likemicro-structurewasanovelandefficientcatalystforthesynthesisofdiphenylcarbonate(DPC)bytransesterificationofdimethylcarbonate(DMC)withphenol.