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简介：在现在的纸，我们声明有关为非卷绕旋转的一个类的pointwise集中和它的率的一些近似定理打形式的非线性的不可分的操作员：

简介：Four1,2,3-trisubstitutedimidazoliniumiodideswhichwereusedas5,10-+CPh-THFmodel（7-10）atformicacidoxidationlevelweresynthesized.Thebenzylidynegroup（phenyl-substitutedonecarbonunit）transferreactionsfromthesecompoundstoGrignardreagentwerein-vestigated,andthereactionsofthesecompoundswithKBH4andNaOHwerealsostudied.

简介：Aseriesofnovel1H-benzimidazol-1-ylacetatesand1H-benzimidazol-1-ylpropionatescontaining1H-1,2,4-triazolemoietyweresynthesizedundermicrowaveirradiationbymulti-stepreactions,inyieldsof87-94%.TheirinvitroantifungalactivitiesagainstBotrytiscinereaandSclerotiniasclerotiorumwereevaluatedbymycelialgrowthratemethod.AllthetargetcompoundsexhibithighactivitiesagainstB.cinereawiththeEC50valuesof7.96-21.74μg/mL,higherthanthatofcarbendazim.

简介：Poly(4-vinylpyridine)supportednanoparticleofcopper(Ⅰ)iodideisreportedasagreenandrecyclablecatalystfortheregioselectivesynthesisof1,4-disubstituted-1H-1,2,3-triazolesfrombenzylhalides,sodiumazideandterminalalkynesinwater.Thiscatalystcanberecoveredbysimplefiltrationandrecycledupto8consecutiverunswithoutanylossofitsefficiency.

简介：Novelsulfur-containingcompounds(3a–3c,4a–4c)wereobtainedinethanolwith1,3-diphenyl-2-propanoneasthestartingmaterial.Theadvantagesofthisprocedureweremildreactionconditions,simpleprotocol,andhighyields.ThestructuresoftheproductswerecharacterizedbyIR,1HNMR,MSandelementaryanalysis.Thecrystalofthenewcompound4abelongstomonoclinic,spacegroupC2witha=18.727(3),b=6.5179(9),c=13.7576(18),b=131.0610(10)°,V=1266.2(3)A3,Z=2,Dc=2.136g/cm3,μ=1.078mm-1,F(000)=843,R=0.0490andwR=0.1247for3211observedreflectionwithI>2δ(I).X-rayanalysisrevealsthatthemoleculeisnotsymmetrical,themolecularstructureisstabilizedbyweakp–pstackinginteractions,andnoclassicalhydrogenbondscanbeobserved.

简介：Sixnewopticallyactivepoly(amide-imide)s(5a-f)weresynthesizedthroughthedirectpolycondensationreactionofN,N'-(4,4'-diphthaloyl)-bis-L-leucine(3)withsixhydantoinderivatives(4a-f).Triphenylphosphite(TPP)/pyridineinthepresenceofcalciumchloride(CaCl_2)andN-methyl-2-pyrrolidone(NMP)weresuccessfullyappliedfordirectpolycondensation.Thepolycondensationreactionsproduceaseriesofnewpoly(amide-imide)s(5a-f)inhighyields,andinherentviscositybetween0.42and0.55dL/g.Theresultingpoly(amide-imide)s(5a-f)werecharacterizedbyelementalanalysis,viscositymeasurements,thermalgravimetricanalysis(TGAandDTG),solubilitytestandFT-IRspectroscopy.

简介：采用噻吩-2-甲醛分别与邻氨基苯硫酚和硫代氨基脲合成了2种噻吩-2-甲醛杂环席夫碱.利用红外光谱、紫外-可见光谱、荧光光谱、X-射线单晶衍射分析、热重分析和核磁共振氢谱等检测方法对2种目标新型杂环类席夫碱产物的结构和性质进行了表征与分析.采用量子化学中常用的密度泛函方法（DFT）对2种新席夫碱化合物进行几何优化,采用单激发组态相互作用（CIS）和含时密度泛函方法（TD-DFT）进一步优化,比较计算光谱与实际测试光谱之间的误差,探究了2种席夫碱化合物荧光发光机制,为这类席夫碱分子结构设计提供了理论依据.

简介：The2-C,methylenegroupof1-aroyl-1,2-dihydro-3H-naphtho[2,1-b]pyran-3-ones(2)havebeenshowedtopossessasuperiorreactivitytowardsmanyoforganicreagents.Thena-phthopyrones(2)condensedwitharomaticaldehydestogivethe2-arylidinederivatives(3).Bromin-ationof2gave1,2-dibromo(4)or5-bromo(5)derivativesdependingonthereactionconditions.Thebasecatalyzedadditionorcycloadditionofnaphthopyrones(2)to4-methoxybenzalacetophenonegavetheexpectedMichaeladduct(6)orthecyclicadducts(7-9)dependingonthetypeofcatalyticbaseandreactionconditions.Structuresoftheproductshavebeenestablishedbyelementalanalyses,IRand~1HNMRspectroscopicmethods.

简介：在非紧L-凸空间中建立了一个新的GLKKM定理。作为应用,获得了带上下界的广义平衡问题的解的存在定理.

简介：六新光学地活跃并且flame-retardant(amide-imide)poly，在主要的链作为一个flame-retardant单位包含磷化氢氧化物一半的s白族5a鈥?f从六chiralN的直接polycondensation反应被综合，有二度(3-aminophenyl)的N鈥?(pyromellitoyl)-bis-L-amino酸3a鈥?f在中等在于的苯基磷化氢氧化物4N-methyl-2-pyrrolidone(NMP)，triphenyl亚磷酸盐(TPP)，钙氯化物(CaCl2)和pyridine。生产的聚合反应一系列光学地活跃poly(amide-imide)有好产量和0.34鈥?.70dLg的好固有的粘性的s?1。结果的聚合物充分借助于FTIR和1H-NMR光谱学，胶化浸透层析(GPC)，元素的分析，固有的粘性和溶解度测试被描绘。热性质和白族5a鈥?f的flame-retardant行为被调查使用热gravimetric分析(TGA和DTG)并且限制氧索引(LOI)。热分析(TGA和DTG)获得的数据表明这些聚合物显示出好热稳定性。而且，在TGA的高字符产量和好LOI值显示产生聚合物能够展出好火焰retardant性质。N，N鈥?(pyromellitoyl)-bis-L-amino酸3a鈥?f被pyromelliticdianhydride(1,2,4,5-benzenetetracarboxylicacid-1,2,4,5-dianhydride)的冷凝作用反应在量的收益准备1与L丙氨酸2a，L缬氨酸2b，L白氨酸2c，L异白氨酸2d，L苯基丙氨酸2e和L-2-aminobutyric在醋酸的酸2f答案。关键词光学地活跃-Flame-retardant聚合物-Poly(amide-imide)s-限制氧索引

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．

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简介：Inthispaper,weshowthatnewmodifieddoublecosinetrigonometricsumsintroducedin[1]areinappropriate,theclassofdoublesequencesJdintroducedthereisunusableforsuchsumsandconsequentlytheresultsobtainedinitarecompletelyincorrect.WehereintroduceappropriatemodifieddoublecosinetrigonometricsumsmakingtheclassJdusableconsideringaparticulardoublecosinetrigonometricseries.

简介：本文通过电化学测量（循环伏安法）和量子化学计算（CNDO/2法）对几种原子簇化合物[（MoS4）2FeL]3-（其中配位体L为O2CH3CN,O2,O）的氧化还原活性进行了研究.实验测量与理论计算所得结果相符.研究结果表明这几种阴离子的还原皆为不可逆的单电子转移过程.它们接受电子的能力按如下次序递增:[（MoS4）2FeO2CH3CN]3-<[（MoS4）2FeO2]3-<[（MoS4）2FeO]3-

简介：8,8′-Dibromo-6,6′,7,7′-tetramethoxy-5,5′-diisopropyl-3,3′-oxydimethylenedinaphtho[2,1-b:2′,1′-d]furan,C32H30Br2O;M.W.=670;triclinic;spacegroupP1;a=8.896（2）,b=10.216（1）,c=10.423（1）A,α=108.48（1）,β=119.36（1）,γ=99.26（1）;V=723.5A3;Z=1,Dcal.=1.479g.cm-3.MoKα=28.11cm-1,F（000）=326,T=293K.Thestructurewassolvedbydirectmethodandfull-matrixleast-squaresrefinementconvergedatR=0.034for2377observedreflections.Theoxygenatominseven-memberedringexistsinadisorderedarrangement.Bothbisnaphthaleneandoxygen-containingfive-memberedringhaveplanarconformationswithdihedralangle6°,showingmarkedaromaticfeature.

简介：Themononuclearcomplex,[NtCl2(trzCHzCHzCOPh)4]·6H2O(trz=1,2,4-triazole),wassynthesizedanditsstructurewasdeterminedbysinglecrystalX-raydetermination.Itcrystallizesinthemonoclinicsystem,spacegroupP21/c,withlatticepa-rameters:a=0.80391(2)nm,b=1.06215(2)nm,c=2.90133(2)nm,β=94.792(1)°andZ=2.EachnickelatomiscoordinatedbyfourNatomsoftriazolefromfourβ-(1,2,4-IriHole-1-yl)propiophenoneligandsandtwochlorideanionsinarrangementwithoctahedralcoordinationgeometry.Inadditiontothecoordinatingnickelcomplex,therearesixunco-ordinatedwatermolecules.TheNi—Ndistanceis0.24865(8)nmandtheNi—Ndistaneesareintherangeof0.2072(2)to0.2099(2)nm,respectively.Inthesolidstate,theUtiecom-poundformsthreedimensionalnetworkstructurethroughhy-drogenbonds.Theintermolecularhydrogenbondsconnectthe[NiCl2(C2H2N3CH2CH2COPh)4]andH2Omoieties.Thedeepgreencrystalswerealsoexaminedbyelementalanalysis,FT-IRandUVspectra,whichareinagreementwiththestructuralda-ta.

简介：标题化合物C26H26O5以2,3-萘二甲醛和5-甲基-1,3-环己二酮为原料,在醋酸溶剂中,室温下经搅拌多组分一锅法合成得到.其结构通过单晶X-射线衍射法确定,晶体属单斜晶系,空间群P21,相对分子质量Mr=418.47,晶胞参数a=0.99004（8）nm,b=1.09098（9）nm,c=1.04246（11）nm,V=1.08753（17）nm3,Z=2,晶胞密度Dc=1.278g/cm3,吸收系数μ=0.088mm-1,单胞中电子的数目F（000）=444.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=0.0533,wR2=0.1293.在晶体结构中新形成的吡喃环为半椅式构象,而茚中五元环则为信封式构象.