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91.
The reaction of Os3(CO)10(NCMe)[Si(OMe)3](-H),1, with PMe2Ph yielded the new complex Os3(CO)10(PMe2Ph)[Si(OMe)3](-H),2 by substitution of the MeCn ligand with the phosphine ligand. When heated to 125°C compound2 was decarbonylated and transformed into the new unsaturated cluster complex Os3(CO)8[-PMe2(C6H4)][Si(OMe)3](-H)2,3 in 54% yield. Compound3 was characterized by a single crystal X-ray diffraction analysis, osmium bonds. The phenyl ring of the phosphine ligand has undergoneortho-metallation by a neighboring metal atom. A terminally coordinated Si(OMe)3 ligand is coordinated to the third osmium atom. The cluster is unsaturated by the amount of 2 electrons, and there is an open coordination site on the siloxyl substituted osmium atom that is partially filled by a weak interaction with one of the -bonds of theortho-metalled phenyl ring. Complex3 reacts with CO at 1 atm to reform compound2 in 85% yield in 5 h at 40°C. Crystal Data: for3: space group = P21/n,a = 9.911(2) Å,b = 18.451(6) Å,c = 14.872(2) Å, = 95.64(2)°,Z = 4, 1994 reflections,R = 0.028. 相似文献
92.
Gy. Marosi R. Lágner Gy. Bertalan P. Anna A. Tohl 《Journal of Thermal Analysis and Calorimetry》1996,47(4):1155-1161
Nucleating and transcrystallization behaviour of additives in engineering PP composites and the effect of modified interfacial structure is the subject of this series of papers. The first part concentrates on polypropylene/liquid crystalline polyester blends. Increased crystallisation temperature and degree of crystallinity of polypropylene is characteristic to the blends containing different amount of LCP additive. Transcrystallization process governs the formation of crystalline structure in these systems in course of isothermal crystallisation at 132C. The nucleating effect of LCP gives rise to more uniform crystalline structure in the polypropylene phase.The financial support of the OTKA 014194 is acknowledged with gratitude. 相似文献
93.
94.
H2PtCl6可被一系列的酸处理定形聚偕胺肟树脂所吸附,吸附容量的大小与处理树脂的质子酸的Pka值有关.认为是解高度低的酸所处理的树脂上的伯胺基成盐的机会较少,即树脂的吸附中心保留着较多的空穴,有利于H2PtCl6的接近而被吸附下来.吸附动力学的研究表明化学反应是吸附速度的控制因素。 相似文献
95.
LING Daren LIU Bing WU Guoqi Department of Applied Chemistry Jiangsu Institute of Petrochemical Technology Changzhou China 《Chinese Journal of Reactive Polymers》2002,(1)
1. INTRODUCTION When investigating contaminated sites it is often essential to determine specific pollutants in a large number of ambient air samples. Amongst these sites, polycylic aromatic hydrocarbons (PAHs) are a major class of compounds that hav… 相似文献
96.
螯合树脂交换——光度法测定氯化钠溶液中微量镁 总被引:3,自引:1,他引:3
研究了用螯合树脂交换分离富集氯化钠溶液中微量镁及吸光光度法测定镁含量的方法。回收率为96.0-101.0%,在PH10的硼砂-氢氧化钠介质中,镁含量在0-12μg/25ml范围内符合比耳定律。方法稳定性高、重现性好。 相似文献
97.
Narisawa Masaki Okabe Yoshio Iguchi Masahiro Okamura Kiyohito Kurachi Yasuo 《Journal of Sol-Gel Science and Technology》1998,12(3):143-152
Inorganic-organic hybrid gels were prepared by simultaneous condensation of the liquid mixture of ethyl silicate, ethyl borate and water soluble phenol resin with low molecular weight. The liquid mixtures were changed into lightly colored transparent gels after a catalyst addition and stirring. The obtained gels were crushed, dried and fired in controlled conditions to yield the inorganic precursors. Since the tailored inorganic precursors mainly consisted of SiO2 and carbon, silicon carbide was formed with the heat treatments in an Ar atmosphere beyond 1773 K with carbothermic reduction. The properties and morphology of the formed silicon carbide powders in terms of the starting precursor compositions and the conditions of the carbothermic reduction were investigated with SEM, XRD and TG-DTA analysis. 相似文献
98.
Sergei V. Levchik Giovanni Camino Maria Paola Luda Luigi Costa Bruno Costes Yves Henry Emile Morel George Muller 《先进技术聚合物》1995,6(2):53-62
Tetraglycidyl 4,4′-diaminodiphenylmethane (TGDDM) undergoes homopolymerization on heating. Intramolecular reactions which compete with crosslinking favor the formation of cyclic structures with increasing thermal and fire resistance of the resin, whereas physical mechanical properties tend to decrease. The mechanism of thermal decomposition of TGDDM is studied by thermogravimetry, differential scanning calorimetry and thermal volatilization analysis with characterization of volatiles evolved and residue left. Thermal degradation of poly-(TGDDM) starts at 260°C with elimination of water from secondary alcoholic groups which is a typical pathway for epoxy resin degradation. Resulting unsaturations weaken bonds in the β-position and provoke the first chain breaking at allyl–amine and allyl–either bonds. With increasing temperature, saturated alkyl–ether bonds and alkyl carbon–carbon bonds are broken first, followed by the most stable alkyl–aryl bonds at T>365°C. The combustion performance of TGDDM is discussed on the basis of the thermal degradation behavior. 相似文献
99.
D. Beigzadeh S. Sajjadi F. Afshar Taromi 《Journal of polymer science. Part A, Polymer chemistry》1995,33(9):1505-1510
Synthesis of unsaturated polyesters using adipic acid, ethylene glycol, and fumaric acid in the absence and presence of a foreign acid (phosphoric acid) as catalyst was carried out by a two-stage method under constant reaction temperatures of 160–180°C and at different ratios of diol to diacid. The experimental data fit the Chen–Wu rate equations for self-catalyzed and acid-catalyzed reactions. The reaction rate constants and activation energies for both systems were calculated. The rate constants of fumaric acid–ethylene glycol systems were found to be nearly constant and had negligible variations with increasing chain length of polymer. © 1995 John Wiley & Sons, Inc. 相似文献
100.
A mild and efficient two-step synthesis of a polystyrene thiol resin is reported. Firstly, a polystyrene resin was reacted with an activated sulfoxide to afford the resin bound bis-(2-methoxy-carbonylethyl)-sulfonium trifluoromethanesulfonate. Smooth β-elimination based dealkylations afforded the polystyrene thiol resin with good and controlled loading. Its reactivity was assessed through a derivatisation step. 相似文献