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951.
Kebing Wang Jie Yao Yue Wang Gongying Wang 《天然气化学杂志》2007,16(3):286-292
The coupling reaction of formaldehyde(FA)and methyl formate(MF)to form methyl glycolate(MG)and methyl methoxy acetate(MMAc),catalyzed by p-toluenesulfonic acid(p-TsOH)as well as assisted by different kinds of solvents or Ni-containing compounds,had been investigated.The results showed that when the reaction was carried out at 140℃,with a molar ratio of FA to MF of 0.65:1, molar fraction of p-TsOH to total feedstock of 11.0%,and reaction time of 3 h,the yield of MG and MMAc was 31.1% and 17.1%,respectively,p-TsOH catalyzed the coupling reaction by means of the synergistic catalysis of protonic acidity and soft basicity.Adding extra solvents to the reaction system was unfavorable for the reaction.The composite catalytic system consisting of p-TsOH and NiX_2(X=Cl,Br,I)exhibited a high catalytic performance for the coupling reaction,and NiX_2 acted as a promoter in the reaction,whose promotion for the catalysis increased in the following order:NiCl_2相似文献
952.
Milaeva E. R. Shpakovsky D. B. Gracheva Yu. A. Berberova N. T. Egorov M. P. 《Russian Chemical Bulletin》2001,50(6):1097-1100
2,6-Di-tert-butylphenols containing the Pt—SnCl3 and Pt—GeCl3 groups in the para position exert a dual effect on the oxidation of methyl oleate by molecular oxygen. Initially, these compounds act as antioxidants producing the corresponding phenoxyl radicals whose decomposition is accompanied by elimination of SnCl2 and GeCl2, which are oxidation promoters. 相似文献
953.
A universally significant method,which combines the anionic polymerization with photoinduced charge transfer polymerization,for preparation of soluble star ABC triblock copolymer of ethylene oxide,styrene and methyl methacrylate,was described.The poly(ethylene oxide) (PEO) block was formed by initiation of phenoxy an-ions using p-aminophenol protected by Schiff's base as the parent compound Then the charge transfer system composed of PEO chains with deprotected-amino end groups and benzophenone initiated the polymerization of styrene and methyl metnacrylate sequentially under UV irradiation.The formed star triblock copolymer of styrene,ethylene oxide and methyl methacrylate could be purified by thin-layer chromatography (TLC) and characterized by IR,1H NMR,GPC (gel permeation chromatogrphy) and PGC (pyrolysis gas chromatography). 相似文献
954.
150×3 mm I.D. columns, packed with 1-μm non-porous spherical silica particles, were used to separate soluble synthetic polymers by hydrodynamic chromatography. The columns exhibited a plate height of about 1.4 μm allowing very fast and efficient separations of polymers in the molecular mass range 103−2·106 g/mol. The migration behaviour of polymers could be well described by a simple theoretical model. The applicability of packed bed HDC for the fast separation of polymers was illustrated with separations of polystyrene and poly(methyl methacrylate) mixtures. 相似文献
955.
Methyl trifluoropyruvate (1) enters into reductive dimerization during UV irradiation in the presence of isopropyl alcohol or of a sensitizer and during reaction with sodium in the presence of trimethyldichlorosilane, giving dimethyl 2,3-bis(trifluoromethyl)-2,3-dihydroxysuccinate. Unlike hexafluoroacetone, compound 1 does not form the reductive dimerization product after prolonged standing over sodium but is converted into the cyclic dimer 2-methoxycarbonyl-4-methoxy-2,4-bis(trifluoromethyl)-1,3-dioxolan-5-one.A. N. Nesmeyanov Institute of Heteroorganic Compounds, Russian Academy of Sciences, 117813 Moscow. Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 6, pp. 1408–1411, June, 1992. 相似文献
956.
The fabrication and application of a novel electrochemical detection (ED) system with the platinum/poly(methyl violet) (Pt/MV) chemically modified electrode (CME) for high performance liquid chromatography (HPLC) were described. The Pt particles deposited on the poly-MV film were characterized by atomic force microscope (AFM). It was found that the Pt/MV CME exhibited efficiently electrocatalytic effect on the current responses of cysteine (Cys), homocysteine (Hcy) and methionine (Met) with relatively high sensitivity, stability and long-life of activity. In HPLC-ED, these three amino acids had good and stable current responses at the CME and their linear ranges were over three orders of magnitude (R ≥ 0.9996) with the detection limits being 7.5 × 10−8 mol L−1 for Cys, 1.0 × 10−7 mol L−1 for Hcy, 5.0 × 10−7 mol L−1 for Met. The application of this method coupled with microdialysis sampling for the determination of Cys, Hcy and Met in plasma from patients with hypothyroidism was satisfactory. 相似文献
957.
The 4-chloromethyl styrene (CMS) was copolymerized with different styrenic monomers such as methyl styrene, 4-methoxy styrene and α-methyl styrene by free radical polymerization method at 70 ± 1 °C using α,α′-azobis(isobutyronitrile) (AIBN) as an initiator and the copolymers I, II and III collected respectively. The very bulky tris(trimethylsilyl)methyl {trisyl} substituents were covalently attached to the obtained copolymers with replacement of all the chlorine atoms in CMS units. The polymers, obtained in quantitative yields, were characterized by FT-IR, 1H NMR and 13C NMR spectroscopy; differential scanning calorimetry (DSC) and GPC studies. All the polymers containing trisyl groups showed a high glass transition temperature (in the range 150-190 °C) in comparison with copolymers I-III (in the range 90-95 °C). The increase of the glass transition temperature reflects the substantial increase in rigidity of new polymers bearing very bulky substituents in side chains. 相似文献
958.
Simultaneous and sequential poly(N-isopropyl acrylamide) (PNIPAAm)/poly(dimethyl siloxane) (PDMS) semi-interpenetrating polymer networks (IPNs) with different linear PDMS contents were prepared by free radical polymerization method. Their phase morphologies have been characterized by FTIR, DSC and SEM. The simultaneous semi-IPNs exhibited phase transition temperatures (Tpt) shifted higher temperature from glass transition temperatures (Tg) of their respective homopolymers, suggesting a heterophase morphology and only physical entanglement between the PNIPAAm network and linear PDMS with high molecular weight (Mn≈9000 g/mol). For sequential semi-IPNs, the shift of Tpts towards lower temperature suggested that the chemical interaction between the constituents of the IPNs increased with increasing PDMS content in the network. In addition, these semi-IPNs were characterized for their thermo-sensitive behaviour by equilibrium swelling studies. The results showed that incorporation of hydrophobic PDMS polymer into the thermo- and pH-sensitive PNIPAAm and P(NIPAAm-co-IA) (itaconic acid) hydrogels by semi-IPN formation decreased swelling degrees of IPNs without affecting their LCSTs whereas addition of acrylated PDMS (Tegomer V-Si 2250) as crosslinker instead of N,N′-methylenebisacrylamide (BIS) into the structures of these hydrogels changed their LCSTs along with their swelling degrees. 相似文献
959.
本文以樟脑衍生物(-)-莰烷磺内酰胺(2)为原料,经N-烷酰基莰烷-2,10-磺内酚胺(3)与碘代烷的不对称烷基化反应,用二锂代乙基苯基砜取代磺内酰胺助剂以及铝汞还原性脱硫反应等三步合成(S)和(R)一切叶蚁警戒信息素(1),其光学纯度高达95%e.e以上。 相似文献
960.
用Hg(Ⅱ)-SCN~- -甲基紫三元络合物光度法测定牛奶中痕量的汞,该法灵敏度高,络合物的摩尔吸光系数ε=5.015×10~5 L/(mol·cm),汞浓度在0~8μg(50 mL)时与吸光度呈线性关系,线性回归方程为A=0.04693c 0.01816,相关系数r=0.9928,汞的回收率为97.0%~98.5%,检出限为0.0068μg/mL。 相似文献