Nucleophilic reactivity of the peroxide anion in aqueous-alcoholic solutions in the presence of detergents

The reactivity of hydroxide and peroxide anions with 4-nitrophenyl N,N-dimethylcarbamate in aqueous-alcoholic detergent media and in “oil in water” microemulsions has been studied. Aqueous-alcoholic solutions of cationic (CTAB) and neutral (Triton X-100) surface active substances have promise for decomposition of substrates by a nucleophilic mechanism. __________ Translated from Teoreticheskaya i éksperimental’naya Khimiya, Vol. 43, No. 6, pp. 358–363, November–December, 2007.     

Synthesis and Crystal Structure of a Novel Three-dimensional Cu(II) Compound {[Cu(2,2''-bipy)(C7H4O5S)(H2O)2]·(H2O}n

The title compound, {[Cu(2,2'-bipy)(C7H4O5S)(H2O)2](H2O}n (2,2'-bipy = 2,2'- bipyridine), was synthesized by the hydrothermal reaction of Cu(NO3)2(3H2O, 2,2'-bipyridine and 2-sulphobenzoic acid, and structurally characterized by single-crystal X-ray diffraction analysis. The crystal is of triclinic, space group P with a = 9.21(3), b = 10.17(3), c = 10.77(3) (A), α = 77.017(16), β = 89.80(8), γ = 68.46(7)°, V = 911(5) (A)3, Z = 2, (D/s)max = 0.001, Mr = 473.94, Dc = 1.728 g/cm3, μ(MoKα) = 1.365 mm-1, F(000) = 486, the final R = 0.0246 and wR = 0.0628 for 3809 observed reflections with I > 2σ(I). The mononuclear crystal structure extends into a two-dimensional net- work via hydrogen-bonding interactions and a three-dimensional framework is further formed by means of π-π stacking interactions.     

以金属硫酸氢盐为催化剂在无溶剂条件下高效合成3,4-二氢嘧啶-2(1H)-酮

以金属硫酸氢盐M(HSO4)n(Ca(HSO4)2,Zn(HSO4)2和过硫酸氢钾制剂oxone○R)为催化剂催化醛、1,3-二羰基化合物和尿素进行缩合反应,在90℃及无溶剂的条件下高收率、一锅法合成了3,4-二氢嘧啶-2(1H)-酮.     

离子液体［bmim］HSO4中合成的苯胺与环氧丙烷共聚物的电催化性能

 采用恒电流电解法,在1-丁基-3-甲基咪唑硫酸氢盐(［bmim］HSO4)离子液体中合成了苯胺与环氧丙烷共聚物(PAN-PPO). 扫描电镜观察表明, PAN-PPO由直径小于80 nm的纳米纤维组成. PAN-PPO对草酸氧化具有较好的电催化活性. 采用电化学原位红外光谱技术对草酸的电催化氧化进行了简单的分析.     

富镧和富铈混合稀土贮氢电极的性能

富镧和富铈混合稀土贮氢电极的性能＊赵东江马松艳（黑龙江省绥化师专化学系绥化市１５２０６１）关键词混合稀土贮氢电极性能中图分类号Ｏ６４６．５４混合稀土贮氢合金具有良好的电化学特性和较低的价格，成为贮氢电极研究的主要对象，已经开发出许多实用的电极材料［１...     

电沉积镍钨注钼电极的析氢反应

在所有电极过程中研究最多的是析氢反应,其重要性一直为化学界所关注。提高电极活性的各种方法中,普遍采用电沉积法,它价廉简便、效果明显。但涂层不够牢固,在使用过程中易脱落,使用寿命短。为了克服上述缺点,作者将电沉积和离子注入技术联合使用,即在Ni、W镀层上注入Mo离子,利用Mo离子的能量将Ni、W打入表面内层,进行离子束混合。这既     

Thermodynamics of the dissociation of 2-aminopyridinium ion in synthetic seawater and a standard for pH in marine systems

Buffer solutions composed of 2-aminopyridinium chloride and 2-aminopyridine in synthetic seawater are useful as a supplement to buffers of Tris (pH 8.2) and Bis (pH 8.8) in standardizing measurements of hydrogen ion concentration (pm _H or pH(SWS)) in oceanography. The dissociation constant of 2-amino-pyridinium ion over the range of salinities (S) from 30 to 40 has now been determined from the emf of cells without liquid junction at eight temperatures (T) from 278.15 to 313.15 K. The results fit the equation pK=2498.31/T–15.3274+2.4050 lnT+S(0.012928–2.9417×10^–5T) with a standard deviation of 0.0023. Thermodynamic constants for the dissociation process and standard reference values of pm _H and pH(SWS) were derived from the data. The pm _H of the buffer consisting of 2-aminopyridinium chloride and 2-aminopyridine (each 0.04 molal) in synthetic seawater of salinity 35 varies from 7.356 at 278.15 K to 6.601 at 313.15 K.     

New Aspects of Cyclodextrin Chemistry Induced by Outside Type Complex Formation; Asymmetric Reduction of Indol-3-Pyruvic Acid with NaBH4 in Aqueous Solution

Asymmetric reduction of indol-3-pyruvic acid (IPA) with NaBH₄ in aqueous solution in the presence of various cyclodextrins (α-, β-, γ-, mono-6-amino-6-deoxy-β- and di-6^ABamino-6^AB-deoxy-β-cyclodextrin) was investigated. From the NMR and circular dichroism spectral studies, the conformation of the CyD–substrate complexes is suggested; the part of carboxylic group stay in the cavity of α-CyD, whole of IPA in β-CyD, two molecules in a γ-CyD cavity, and IPA(s) is/are on the rim of the cavity of mono-6-amino-6-deoxy-β- and di-6^ABamino-6^AB-deoxy-β-CyD (AβCyD, DAβCyD) with electrostatic interaction between amino group and carboxylic group. This conformational difference provides in the difference in the optical selectivity of reduction.