简介：Anovelpolymercontainingthesucrosegroupwassynthesizedbyradicalpolymerizationfromanenzymaticallypreparedmonomer,1′-O-vinyladipoyl-sucrose(VAS).TransesterificationreactionofsucrosewithdivinyladipateinanhydrouspyridinecatalyzedbyanalkalineproteasefromBacillussubtilisat60℃for7daysgaveVAS(yield55%)withoutanyblocking/deblockingsteps.ThevinylsucroseestercouldbepolymerizedwithpotassiumpersulfateandH2O2asinitiatortogivepoly(1′-O-vinyladipoyl-sucrose)withMn＝33,000andMw＝53,200,Mw/Mn＝1.61.Thepolymerwasbiodegradable.After6daysinaqueousbuffer(pH7),thisalkalineproteasecoulddegradepoly(1′-O-vinyladipoyl-sucrose)toMnofca.1080,Mw/Mn＝3.30(37℃),andMnofca.5200,Mw/Mn＝2.44(4℃).Thepolymercontainingthesucrosebranchwouldbeafunctionalmaterialinvariousapplicationfields.

简介：ThesplittingofpotentialenergylevelsforgroundstateX2ΠgofOx2(x=+1,1)underspin–orbitcoupling(SOC)hasbeencalculatedbyusingthespin–orbit(SO)multi-configurationquasi-degenerateperturbationtheory(SO-MCQDPT).TheirMurrell–Sorbie(M–S)potentialfunctionsaregained,andthenthespectroscopicconstantsforelectronicstates2Π1/2and2Π3/2arederivedfromtheM–Sfunction.TheverticalexcitationenergiesforOx2(x=+1,1)areν[O+12(2Π3/2→X2Π1/2)]=195.652cm1,andν[O12(2Π1/2→X2Π3/2)]=182.568cm1,respectively.Allthespectroscopicdataforelectronicstates2Π1/2and2Π3/2aregivenforthefirsttime.

简介：Anewsyntheticapproachto1,4,6-tri-O-benzylmyo-inositolwasdescribedonthebasisoftheregioselectivebenzylationof1,2-O-isopropylidene-4,6-di-O-benzylmyo-inositol,subsequentacidhydrolysis,phosphorylationwithtetrabenazylpyrophosphateandappropriatedeprotec-tion.

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简介：Ithasbeenproposedthatfusionreactionsbetweenneutron-richlightnuclei,forexample24C,24Oand28Ne,maycontributetoachievingtheignitiontemperatureforexplosivecarbonburningprocessduringsuperbusrsts[1,2].Studiesoffusionreactionsinvolvingneutron-richnucleiarebeyondordinaryexperimentaltechniques,sincetheintensityofradioactivebeambecomelowforthesemeasurements[3].TheactivetargettechniqueusingTPC(TimeProjectionChamber),withpropertiesofmulti-sampling,highefficiencyandlowbackground,isasuitablesolutiontotheproblem.

简介：Thesolidaddofthefirstprotonatedzincoborophosphate,(H3O)Zn(H2O)2BP2O8·H2O(1),wassoventothermallysyn-thesizedbythereactionofZn(NO3)2·6H2OandH3BO3withH3PO4inamixedsolvent,andstructurallycharacterizedbysingle-ystalX-raydiffractionanalysis.ItcrystallizesinthehexagonalP6122,a=0.9604(4)nm,c=1.5297(6)nm,V=1.2218(8)nm^3,Dc=2.921g/cm^3,Z=6,F(000)=1080,μ=3.495mm^-1.Thestmchwefeaturesthatthetetrahedra-te-trahedrahdlcesinterconnectedbyoctahedraandstronghydro-gembondinteractionsformathree-dimensionalframework.Theprotonatedwatermoleculesarelocatedatuniquepositions.othercharacterizationsbyIRandthermalanalysisarealsode-scribed.

简介：利用水热方法制备了一个新的过渡金属镉配合物[Cd（1，3-BDC）（L）（H2O）2]·H2O（1，3-H2BDC=间苯二甲酸，L=2-（3-吡啶基）-1H-苯并咪唑），并通过元素分析、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．结构分析表明该配合物属于单斜晶系，P21／c空间群，晶胞参数a=1．01641（6）nm，b=2．08842（12）nm，C=1．00l38（6）nm，β=106．3360（10）°，V=2．0398（2）nm3，Z=4，R1=0．0207，wR2=0．494．配合物中CdⅡ“离子与L配体的1个吡啶N原子、1，3-BDC的4个氧原子和2个配位水的O原子配位，形成七配位的扭曲十面体结构．配体1，3-BDC的桥连相邻的CdⅡ离子形成一维聚合物链，相邻链间通过氢键和π…π作用形成三维超分子网络，并对该配合物的热稳定性和荧光性质进行了研究．

简介：Aseriesofbenzo-fusedheteroaromaticcompoundswith5-,6-and7-memberedtings,suchasbenzimidazole,quinoxalineand1H-1,5-benzodiazepinederivatives,weresynthesizedthroughcondensationreactionofo-pheny1-enediaminewithary1aldehydesorketones.Theexperimentalconditionswerecarefullyexamined,andtheproductswerecharacterizedby^1HNMR,^13CNMR,MS,IRandelementalanalyses.Inaddition,thestructureofabenzodiazaepinederivativewith7-memberedringwasconfirmedbysinglecrystalX-raydiffractionanalysis.

简介：Theobjectinthispaperistoconsidertheproblemofexistence,uniqueness,explicilrepresentationof（0,2）-interpolationonthezerosof（1-x2）P_{n-1（x）/xwhennisodd,wherePn-1denotesLegendrepolynomialofdegreen-1,andtheproblemofconvergenceofinterpolatorypolynomials.}

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.

简介：阴极材料李[CoxNiyMn1?x?y]为锂的O2第二等的电池被一条新线路作为一位先锋用分层的双氢氧化物(LDH)准备了。结果有-NaFeO2结构的分层的阶段在菱形的系统结晶，与有到0.47nm的夹层间距结束的空格组R-3m。X光检查光电子光谱学(XPS)被用来测量公司，Ni和Mn的氧化状态。在结构和李的电气化学的性质上改变Co/Ni/Mn比率的效果[CoxNiyMn1?x?y]O2被X光检查衍射和电气化学的测试调查了。产品表明了相当稳定的骑车行为，与为有Co/Ni/Mn=1/1/1的分层的材料的118mAh/g的一个可逆能力。

简介：WeuseMnforthesetofalln×nrealmatrices;（n）for{1,…,n};Snforthesymmetricgroupon〈n〉;A[α]α∈

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简介：Theenantiomersofthirty-nineO-ethylO-phenylN-isopropylphosphoroamidothioateshavebeenseparatedbyhighperformanceliquidchromatographyonaPirklemodelchiralstationaryphaseusingtenmobilephase.Chromatographicdataarepresentedfortheseparationoftheseorganicphosphorusenantiomersonthechiralphase.Theinfluencesofmolecularstructuresandcompositionsofmobilephaseshavebeendescribed.

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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：建立了非线性热力学模型,定性分析了外加应力和外加温度对外延生长在正交基底上的Pb（Zr1-xTix）O3（PZT）薄膜相变的影响。在外力场下,固定其中一个方向失配应变e1=0.005,模拟得到了不同组分的PZT薄膜的失配应变一外加应力的相图。研究发现,随着Ti组分的减少,出现了新相正交a1c相和四方相a1相,且新相区域也会随Ti组分的不同而变化。在外加拉应力下,c相是薄膜较易出现的相,而在外加压应力下薄膜易处于a1a2相。在不同温度场下,模拟非等轴失配应变的PZT薄膜得到不同组分的PZT薄膜的失配应变一外加温度相图。当组分x≤0.7时,相图中出现了正交a1c相,由于非等轴失配应变的存在,使得从顺电相向r相发生相变的过程中,多出了正交a1a2相;同时另一新的四方a1相也出现在沿失配应变正方向e2被拉伸的区域。随着Ti组分的增加,单斜r相的面积缩小且位置下移。之前存在的四相点也变为了三相点,而正交相a1a2相则向相图的中心位置移动。模拟结果对研究外场下铁电薄膜微器件的性能变化具有一定的指导意义。

简介：伪-芳基nitrone是nitrones的最有用的类型之一并且广泛地在最近的年里被探索了。然而，糖一半以前没被介绍进这些分子。我们这里在苯经由代替N的hydroxylamine和芳基醛glycosides的冷凝作用介绍了伪-芳基nitroneO-glycosides的有效合成。

简介：利用直接法合成未见文献报道的K8[ZnMg（H2O）W11O39]·15H2O，通过ICP，IR和XRD等方法对其结构进行表征，结果表明所合成的配合物具有Keggin结构．采用化学热扩渗法对合成配合物进行稀土扩渗实验，经XPS测试表明，有微量的钆渗进配合物的体相，并与组成元素存在键合作用，导电性测试结果表明，扩渗后试样的导电率提高10^5倍，是一种优良的固体电解质，有望成为具有实用价值的功能材料．

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