有机磷化合物的质谱研究(Ⅶ)——二氮二磷杂环戊烷衍生物的化学电离质谱

本文报道了七种4.5-二氧代-2-硫代-1,3,2,4-二氮二磷杂环戊烷衍生物的化学电离质谱(CIMS,甲烷为反应气),结果表明:CIMS中准分子离子MH~+为基峰离子;MH~+离子易发生失去H_2S,CO,C_3H_6等小分子的裂解,(M+C_2H_5)~+离子存在再断裂。     

超声波作用下羰基化合物的还原偶联反应

超声波在一些有机反应中有明显的促进作用「“，Luche等认为超声波的作用有两种主要类型［’j．一类是涉及电子转移的自由基或离子一自由基型反应，由于超声波的空化作用所产生的局部高温高压可以促进电子转移，从而明显地加快反应速度；对大多数离子型反应，超声波只能起到机械的物理作用．我们曾报道偕二卤化合物在Li、Na、Mg等金属作用下产生卡宾的反应是单电子转移过程，该反应可由于超声辐射而大大加速［‘］；而在芳基叔脚的断裂反应中，超声波可以促进三苯基俄与金属馊反应生成二苯基脚负离子，但对它进一步的亲核取代反应却没有明…     

羰基过渡金属异核原子簇(PPh3)2CuFe2Co(CO)8(μ3-S)和(PPh3)3AuFe2Co(CO)7(μ3-S)的合成与表征

本文利用高压法制备HFe₂Co(CO)₉(μ₃-S),作为原料,经脱质子化作用,再分别与(PPh₃)₂Cu(NO₃)和PPh₃AuCl反应,将Ph₃Cu-或Ph₃Au-联接到原始簇合物的中心骨架上,使簇核扩大,得到了组成为(PPh₃)₂CuFe₂Co(CO)₈(μ₃-S)和(PPh₃)₃AuFe₂Co(CO)₇(μ₃-S)的化合物.文中对此两个新化合物进行了IR,UV,¹H和³¹P NMR.元素分析、熔点测定等性质表征,并对(PPh₃)₂CuFe₂Co(CO)₇(μ₃-S)进行了单晶X-射线衍射分析.两个化合物具有类似的中心骨架,在Fe₂和Co原子三角形的上面和下面分别键联着Cu和S,或Au和S原子,构成了三角双锥结构.其中一个簇合物由二个三苯基膦和八个羰基配位,另一个则由三个三苯基膦和七个羰基配位.     

Asymmetric michael addition of aromatic thiols to 2-cyclohexenone and maleic acid esters via formation of crystalline cyclodextrin complexes

The asymmetric Michael addition of aromatic thiols to 2-cyclohexenone and maleic acid esters has been carried out by utilizing their crystalline cyclodextrin complexes suspended in water. The best chiral induction, 30% enantiomeric excess (ee), was achieved in combinations of 2-cyclohexenone and octyl maleate with the crystalline -cyclodextrin complex of benzenethiol (method A) to afford (S)-3-phenylthiocyclohexanone and (S)-octyl-2-phenylthiosuccinate, respectively, whereas the reaction of benzenethiol with 2-cyclohexenone included in -cyclodextrin (method B) inversely induced the chiral recognition to give the (R)-adduct with 4–9% ee.     

Hydrothermal Synthesis and Crystal Structure of a Cadmium（Ⅱ） Polymer with One-dimensional Chain Structure： [Cd（MDPPz）（BDC）（H2O）]n

A metal-organic coordination compound formulated as [Cd(MDPPz)(BDC)(H2O)]n 1 (MDPPz=11-methyldipyrido[3,2-a:2',3'-c]phenazine,BDC=1,4-benzenedicarboxylate) has been hydrothermally synthesized and structurally characterized by elemental analysis,IR spectrum,fluorescence spectrum and single-crystal X-ray diffraction. The title compound crystallizes in the monoclinic system,space group C2/c,with a=30.673(8),b=9.623(3),c=20.784(6) ,β=98.646(3)o,V=6065(3)3,C27H17CdN4O5,Mr=589.85,Dc=1.292 g/cm3,μ(MoKα)=0.757 mm-1,F(000)=2360,Z=8,the final R=0.0381 and wR=0.0855 for 4191 observed reflections (I>2σ(I)). 1 exhibits blue fluorescence property at room temperature.     

三价铟化合物在有机合成中的应用

综述了近年来三价铟化合物促进的多种有机反应及其在有机合成中的应用,其中重点讨论了三价铟化合物促进下的碳-碳键和碳-杂原子键的形成反应.     

Pd(PPh3)2Cl2-CuCl体系催化有机高价碘杂环化合物与末端炔烃的化学选择性交叉偶联反应

以有机高价碘杂环化合物1,2为底物,在Pd(PPh3)2Cl2-CuCl催化剂存在下与末端炔烃进行交叉偶联反应,实验发现该反应为--化学选择性反应,控制反应体系的物料比、温度及反应时间可以分别得到单偶联或双偶联产物,从而证实了有机高价碘杂环化合物的碘盐在进行交叉偶联反应时的反应活性比sp2的碘化物高.     

Solid state synthesis and structure of two novel polyoxometalates [(n-Bu)4N]4[M6O19][Ag2I4](M?Mo,W)†

The reaction of [NH₄]₂[MO₂S₂], AgI and (n-Bu)₄NBr in solid state produced the polyoxometalates [(n-Bu)₄N]₄[M₆O₁₉][Ag₂I₄] (1, M? Mo; 2, M? W) which were structurally determined. The crystals of 1 and 2 are isomorphous, monoclinic, space group P2₁/c. 1, a = l.6624(2), b=1.6699(3), c=l.7217(2) nm, β=98.29(1)°, V=4.729(1) nm³, Z=2, R=0.040, R_w“0.037; 2, a = 1.6636(3), b = 1.6733(3), c = 1.7190(3) nm, β=98.25(1)°, V=4.736(l) nm³, Z = 2, R = 0.038, R_w = 0.047. The results of the structure determination showed that the two compounds had the same structures whose skeletons are composed of [Ag₂I₄]². and [M₆O₁₉]^2-. The difference of them and heteropolymetalate compounds synthesized in solution is that the title compounds contain cluster. ion, heteropolymetalate and organic cations, while the latter is only composed of heteropolymetalate and organic cations.     

Thermal properties of sodium acetylacetonate

Sodium acetylacetonate was prepared by the interaction of acetyl acetone with sodium hydroxide. The thermal conductivity, phonon velocity, mean free path, Yong's modulus, and the thermal expansion coefficient were studied. The thermal conductivity of the material decreases with increasing temperature due to the thermal lattice scattering of phonons. The velocity of phonons is also decreased due to the perturbation of thermal phonons. The linear thermal expansion coefficient increases with temperature due to the weakness of the attractive forces between the small Na⁺ cations and bulkier acetylacetonate anions in the lattice.

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Zusammenfassung Natriumacetylacetonat wurde durch die Wechselwirkung zwischen Acetylaceton und Natriumhydroxid gewonnen. Es wurde die Wärmeleitfähigkeit, die Phononengeschwindigkeit, die mittlere freie Wegstrecke, das Elastizitätsmodul und der Wärmeausdehnungskoeffizient untersucht. Die Wärmeleitfähigkeit der Substanz nimmt wegen der thermischen Gitterstreuung der Phononen mit steigender Temparatur ab. Die Geschwindigkeit der Phononen nimmt auf Grund der Perturbierung der thermischen Phononen ebenfalls ab. Der lineare Wärmeausdehnungskoeffizient steigt mit zunehmender Temperatur an, was auf die schwachen Anziehungskräfte zwischen den kleinen Na⁺ Ionen und den massigen Acetylacetonat-Anionen im Gitter zurückzuführen ist.

     

Reactivity in the solid state between CoWO4 and RE2WO6 where RE = Sm, Eu, Gd

Reactivity in the solid state between CoWO₄ and some rare-earth metal tungstates RE₂WO₆ (RE = Sm, Eu, Gd) was investigated by the XRD method. Two families of new isostructural cobalt and rare-earth metal tungstates, Co₂RE₂W₃O₁₄ and CoRE₄W₃O₁₆, were synthesized. The Co₂RE₂W₃O₁₄ phases are formed by heating in air the CoWO₄ and RE₂WO₆ compounds mixed at the molar ratio 2:1, while the CoRE₄W₃O₁₆ phases are synthesized at the molar ratio of CoWO₄/RE₂WO₆ equals to 1:2. The Co₂RE₂W₃O₁₄ phases as well as the CoRE₄W₃O₁₆ compounds crystallize in the orthorhombic system. The Co₂RE₂W₃O₁₄ and CoRE₄W₃O₁₆ compound melt above 1150 °C. A melting manner of the Co₂RE₂W₃O₁₄ and CoRE₄W₃O₁₆ compounds was determined in an inert atmosphere. The formation of CoWO_4−x phase was observed during heating in an inert atmosphere.