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81.
《Journal of Coordination Chemistry》2012,65(9):985-990
The crystal of pentaqua (catena-pyridine-3,5-dicarboxylato-O,O) calcium(II) contain zigzag molecular chains composed of Ca ions linked by two bridging oxygen atoms, each donated by one carboxylate group [Ca-O1 2.353(2) Å, Ca-O3III 2.334(1) Å]. The Ca ions, the ligand molecules and one water oxygen atom coordinated by each metal ion [Ca-O5 2.410(2) Å] are coplanar. The coordination of the Ca ion is completed by four other water oxygen atoms situated above and below the plane of the chain [Ca-O6 2.475(1) Å, Ca-O7 2.371(2) Å]. The coordination number of the calcium(II) ion is seven. The water molecules act as donors in a system of hydrogen bonds. 相似文献
82.
83.
Bungo Ochiai Haruka Kojima Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2014,52(8):1113-1118
Polyhydroxyurethane bearing silicone backbone was prepared by polyaddition of silicone diamines with a bifunctional five‐membered cyclic carbonate prepared from the corresponding diepoxide and CO2. Polymerization in propylene glycol methyl ether acetate proceeded smoothly, and polymers could be obtained in high yields under appropriate conditions. The introduced silicone moieties improved the hydrophobicity and lowered the glass transition temperature keeping thermal stability. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1113–1118 相似文献
84.
Lian-Hua Fu Yan-Yan Dong Ming-Guo Ma Wen Yue Shao-Long Sun Run-Cang Sun 《Ultrasonics sonochemistry》2013,20(5):1188-1193
Vaterite is an important biomedical material due to its features such as high specific surface area, high solubility, high dispersion, and small specific gravity. The purposes of this article were to explore the growth mechanism of vaterite on the cellulose matrix via sonochmistry process. In the work reported herein, the influences of experimental parameters on the polymorph of calcium carbonate were investigated in detail. The calcium carbonate crystals on the cellulose matrix were characterized by means of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). Experimental results revealed that all the reactants, solvent, and synthesis method played an important role in the polymorph of calcium carbonate. The pure phase of vaterite polymorph was obtained using Na2CO3 as reactant in ethylene glycol on the cellulose matrix via sonochmistry process. Based on the experimental results, one can conclude that the synthesis of vaterite polymorph is a system process. 相似文献
85.
A series of polystyrene-divinylbenzene cross-linked resin (PS)–supported zinc chloride catalysts were prepared in this study. They can efficiently catalyze the solventless cycloaddition of cyclohexene oxide with carbon dioxide in the presence of tetrabutylammonium bromide (TBAB) as cocatalyst under relatively mild reaction conditions. The catalyst is composed of carrier, connecting arm, ligand, and active ingredient. The connecting arms of different lengths can significantly affect the catalytic activity. Among these catalysts, the one using diethylene glycol as connecting arm and 2-aminopyridine as ligand, named PS-DEG-2ap-ZnCl2, showed the optimal catalytic performance. The yield of cyclohexene carbonate was 95.18% calculated by gas chromatographic analysis under the optimal conditions (393 K, 5 MPa, 6 h). Moreover, the catalyst showed good stability and reusability. From the viewpoint of industrial application, the catalyst is attractive because of its excellent catalytic efficiency on the synthesis of cyclohexene carbonate. 相似文献
86.
Cedric Samuel Yvan Chalamet Fernande Boisson Jean‐Charles Majesté Frédéric Becquart Etienne Fleury 《Journal of polymer science. Part A, Polymer chemistry》2014,52(4):493-503
A one‐step process is reported to directly synthesize blends of poly(trimethylene carbonate) (PTMC) with a modified granular starch. Trimethylene Carbonate (TMC) ring‐opening polymerization is performed in the presence of native starch particles in bulk conditions at 150 °C and the efficiency of metal‐free organic catalysts (TBD and phosphazene superbases P1‐t‐Oct, P2‐t‐bu, and P4‐t‐bu) are investigated to replace the organo‐metallic stannous octanoate initiator. TMC monomer is successively converted into PTMC and the robustness of organic catalysts is highlighted with significant activities at very low concentrations (<100 ppm), where stannous octanoate is inefficient. Reactivity of starch toward TMC ROP is deeply investigated by NMR techniques and a starch‐graft‐PTMC is indirectly evidenced. Starch substitution degree reaches 0.9% indicating that PTMC grafting only occurs at the surface of swollen granular starch. PTMC graft length from the starch surface remained low in the range 2–12 and model ROP reactions highlight the role of TMC hydrolysis on PTMC graft length. Despite low PTMC grafts, a fine dispersion of intact starch particles into the PTMC matrix is evidenced. Consequently, metal‐free organic catalysts at low concentrations are promising candidates for synthesizing blends of PTMC with high loadings of surface‐modified starch (32% by weight) in 2 min within a one‐step process. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 493–503 相似文献
87.
《Analytical letters》2012,45(12):933-946
Abstract A simple d.c. are emission spectrographic method is described for the determination of 12 trace impurities in phosphor grade CaWO4 in the range 5 to 250 ppm. A charge of 25 mgs containing sample mixed with graphite in the ratio 1:3 is excited in a 10 amp d.c. arc. Scandium is used as the internal standard. The precision of the method is ± 15%. Detailed discussion on the selection of the final parameters has been given with supporting data. 相似文献
88.
Single crystals of a new silicate carbonate, K2Ca[Si2O5](CO3), have been synthesized in a multi-components hydrothermal solution with a pH value close to neutral and a high concentration of a carbonate mineralizer. The new compound has an axial structure (s.g. P6322) with unit cell parameters a = 5.04789 (15), c = 17.8668 (6) Å. Pseudosymmetry of the structure corresponds to s.g. P63/mmc which is broken only by one oxygen position. The structure consists of two layered fragments: one of the type of the mineral kalsilite (KAlSiO4) and the other of the high-temperature soda-like α-Na2CO3, Ca substituting for Na. The electro-neutral layer K2[Si2O5] (denoted K) as well as the layer Ca(CO3) (denoted S) may separately correspond to individual structures. In K2Ca[Si2O5](CO3) the S-K layers are connected together via Ca-O interactions between Ca atoms from the carbonate layer and apical O atoms from the silicate one, and also via K-O interlayer interactions. A hypothetical acentric structure, sp.gr. P-62c, is predicted on the basis of the order-disorder theory. It presents another symmetrical option for the arrangement of K-layers relative to S-layers. The K,Ca-silicate-carbonate powder produces a moderate SHG signal that is two times larger that of the α-quartz powder standard and close to other silicates with acentric structures and low electronic polarizability. 相似文献
89.
Carbon K‐edge X‐ray spectroscopy has been applied to the study of a wide range of organic samples, from polymers and coals to interstellar dust particles. Identification of carbonaceous materials within these samples is accomplished by the pattern of resonances in the 280–320 eV energy region. Carbonate minerals are often encountered in the study of natural samples, and have been identified by a distinctive resonance at 290.3 eV. Here C K‐edge and Ca L‐edge spectra from a range of carbonate minerals are presented. Although all carbonates exhibit a sharp 290 eV resonance, both the precise position of this resonance and the positions of other resonances vary among minerals. The relative strengths of the different carbonate resonances also vary with crystal orientation to the linearly polarized X‐ray beam. Intriguingly, several carbonate minerals also exhibit a strong 288.6 eV resonance, consistent with the position of a carbonyl resonance rather than carbonate. Calcite and aragonite, although indistinguishable spectrally at the C K‐edge, exhibited significantly different spectra at the Ca L‐edge. The distinctive spectral fingerprints of carbonates provide an identification tool, allowing for the examination of such processes as carbon sequestration in minerals, Mn substitution in marine calcium carbonates (dolomitization) and serpentinization of basalts. 相似文献
90.
Qingmin Wang Runqiu Huang 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1):173-179
Abstract 1-Oxo-4-chlorocarbony1-1-phospha-2,6,7-trioxabicyclo[2.2.2]octane (5) was obtained from phosphorus oxychloride. Benzyl chloroformate was synthesized by the reaction of benzyl alcohol and triphosgene in good yield for the first time. N-r-Butyl-N-benzoylhydrazine(II) was prepared in a new and convenivent procedure with good yield. The reaction of 5 and II proceeded smoothly in the presence of sodium carbonate and afforded the desired compound 13 in good yield, while in the presence of triethylamine, the elimination of butyl was observed and afforded the compound 12. 相似文献