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71.
Bretonnière Y Mazzanti M Pécaut J Olmstead MM 《Journal of the American Chemical Society》2002,124(31):9012-9013
The simple asymmetric tetradentate ligand 2,2':6',2' '-terpyridine-6-carboxylic acid leads to the self-assembly of the first europium nanowheel containing europium ions in two different coordination environments. Moreover the self-assembly of bis(terpyridinecarboxylate) europium species to form a hexameric wheel capable of strongly binding LnIII cations is controlled by the ligand/cation ratio. 相似文献
72.
The possibility to design new composites associating biopolymers with mineral phases relies on the understanding and control of their mutual interactions. In this work, aqueous solutions of gelatine and sodium silicate were mixed at pH 5, 37 degrees C and left to stand at 20 degrees C for 1 day. At low gelatine and high silicate contents, precipitates were obtained, containing a fixed silicon/polymer molar ratio. Scanning electron microscopy (SEM) reveals that they are formed of large aggregates of platelets, constituted of closely-packed nanoparticles. For high gelatine contents, composite gels were formed consisting of silica particles dispersed in the biopolymer matrix. Swelling studies indicate that the addition of silica decreases the stability of the gels by inducing gelatine depletion in solution. Similar experiments conducted at pH 7 show that at this pH, silicates are more effective at precipitating gelatine. A model is proposed for the formation of the composites, based on the electrostatic interactions arising between silicates and polymer chains. These results are discussed in the context of hybrid biomaterials design and biosilicification processes. 相似文献
73.
The ground (X (3)Sigma(-)) and first excited triplet (A (3)Pi) electronic states of diazocarbene (CNN) have been investigated systematically starting from the self-consistent-field theory and proceeding to the coupled cluster with single, double, and full triple excitations (CCSDT) method with a wide range of basis sets. While the linear X (3)Sigma(-) ground state of CNN has a real degenerate bending vibrational frequency, the A (3)Pi state of CNN is subject to the Renner-Teller effect and presents two distinct real vibrational frequencies along the bending coordinate. The bending vibrational frequencies of the A (3)Pi state were evaluated via the equation-of-motion coupled cluster (EOM-CC) techniques. The significant sensitivity to level of theory in predicting the ground-state geometry, harmonic vibrational frequencies, and associated infrared intensities has been attributed to the fact that the reference wave function is strongly perturbed by the excitations of 1pi-->3pi followed by a spin flip. At the highest level of theory with the largest basis set, correlation-consistent polarized valence quadruple zeta (cc-pVQZ) CCSDT, the classical X-A splitting (T(e) value) was predicted to be 68.5 kcal/mol (2.97 eV, 24 000 cm(-1)) and the quantum mechanical splitting (T(0) value) to be 69.7 kcal/mol (3.02 eV, 24 400 cm(-1)), which are in excellent agreement with the experimental T(0) values, 67.5-68.2 kcal/mol (2.93-2.96 eV, 23 600-23 900 cm(-1)). With the EOM-CCSD method the Renner parameter (epsilon) and averaged bending vibrational frequency (omega(2)) for the A (3)Pi state were evaluated to be epsilon=-0.118 and omega(2)=615 cm(-1), respectively. They are in fair agreement with the experimental values of epsilon=-0.07 and nu(2)=525 cm(-1). 相似文献
74.
The problem of defining N(E), the density of states, for molecular systems is discussed. It is shown that a numeric evaluation of N(E) is often only approximate, even for continuous data, and is not well defined for quantized systems. The application of the concept of density of states is discussed, particularly with regard to the RRKM theory of unimolecular reactions. The sum of states, W(E), and density of states curves are evaluated for several harmonic and anharmonic model systems and the results discussed in order to illustrate the foregoing considerations. 相似文献
75.
Hamelin O Pécaut J Fontecave M 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(10):2548-2554
Recently, we observed that the enantiopure Lambda form of the tributylammonium salt of the chiral anion tris[tetrachlorobenzene-1,2-bis(olato)]phosphate, also named Trisphat, was able to induce an efficient resolution of a Delta,Lambda racemic mixture of cis-[Ru(dmp)2(NCCH3)2](PF6)2 (dmp=2,9-dimethyl-1,10-phenanthroline) due to the spontaneous and selective precipitation of the heterochiral pair [Delta-Ru(dmp)2(CH3CN)2][Lambda-Trisphat]2. We report here that the combination of such a stereoselective precipitation process and irradiation results in the quantitative conversion of the initial [Ru(dmp)2(NCCH3)2]2+ racemate into only one of the two enantiomers. This is the first example in inorganic chemistry of an asymmetric transformation that leads to a chiral complex with no chiral ligand. Finally, three new racemic ruthenium bis(diimine) complexes, namely [Ru(dmp)2(NCCH3)Py](PF6)2 (Py=pyridine), [Ru(dmp)2(1,3-diaminopropane)](PF6)2, and [Ru(dmp)2(ethylenediamine)](PF6)2 were synthesized. For all of them, crystallization-induced asymmetric transformation proved to be an efficient way of obtaining the corresponding optically active chiral-at-metal complexes in high yields and with excellent stereoselectivities. 相似文献
76.
Two new enantioselective syntheses of the naphthopyranquinone antibiotic frenolicin B ( 1 ), of its enantiomer 2 , and of its diastereoisomers 3 and 4 were accomplished using two different routes from optically active β-Hydroxy esters (R)- and (S)- 11 and 18. β-Hydroxy esters (R)- and (S)- 11 were prepared stereoselectively from optically active sulfenylacetates (S)- and (R)- 10 , respectively (Scheme 2, Method A). Alternatively, compound 18 was obtained in excellent yield by enantioselective hydrogenation of the corresponding β-keto ester 17 , using a chiral ruthenium-complex catalyst (Scheme 3, Method B). Subsequently, compounds (S)- 11 and 18 were transformed into frenolicin B (1). In analogy, Stereoisomers 2–4 were prepared from (S)- and (R)- 11 in good yields. 相似文献
77.
环境水中甲基对硫磷、对硫磷和辛硫磷农药残留的SPE-HPLC分析 总被引:29,自引:0,他引:29
采用离线固相萃取 (SPE)富集 -高效液相色谱(HPLC)分离和紫外分光光度法检测 ,对环境水中甲基对硫磷、对硫磷和辛硫磷3种有机磷农药进行分析;固相萃取用C18 萃取柱 ,用甲醇洗脱 ,高效液相色谱分离以Shim_PackCLCODS柱(150mm×4.6mmid,5μm)为分离柱 ,流动相为甲醇 -水(体积比70∶30) ,紫外检测波长为280nm;该法稳定可靠 ,回收率高 相似文献
78.
Iványi T Vander Heyden Y Visky D Baten P De Beer J Lázár I Massart DL Roets E Hoogmartens J 《Journal of chromatography. A》2002,954(1-2):99-114
This paper focuses on the classification or differentiation of RP-HPLC columns based on measured chromatographic properties. A chemometric study has been conducted on a published data set consisting of 85 RP-HPLC columns and on a data set consisting of 47 self-tested columns. Principal component analysis enables determination of the number of parameters necessary for a rational differentiation. The results show that reducing the number of parameters for such differentiation still allows classification of the columns just as a higher number did. It is shown that three test parameters produce a classification similar to that obtained with five parameters. 相似文献
79.
The objectives of this work was to obtain a total nitrogen concentration in milk with the Dumas method for industrial and research applications. This method was faster than the Kjheldal method (5 min against 2 h or 3 h) but less precise. A three factor experimental design was performed to optimize the instrument, a FP-2000 supplied by LECO. The first interpretation of the experimental design was disappointing and no conclusion could be done. It was not a failure of experimental design but a lack of thinking on the physical and chemical aspect of the problem. Selection and construction of composite responses based on chemical and physical consideration were the keys to optimize the Dumas method. This method is now as precise as the Kjheldal method, but considerably faster. 相似文献
80.
Dielectric spectroscopy is a powerful method that allows the study of the dynamics of polymers in a wide frequency range. The different regimes of the dielectric spectra can be observed and the dynamics of the primary and secondary relaxations can be found.In this work, the systems investigated included industrial and purified poly(lactic acid), PLA. This is an aliphatic polyester, one of the most important biocompatible and biodegradable material that has received increasing attention in the last 10 years.Thermal analyses indicated that the glass transition temperature of the polymer was about 320 K.The β relaxation was observed between −150 °C and −30 °C, depending on the measurement frequency (1 Hz-100 kHz), and was assigned to the secondary relaxation in the glassy state. We studied the changes that are connected with the water penetration in the polymer, and directly affect that relaxation process. Water molecules confined by polymer chains and in the polymer networks play an important role in the degradation of the matrix, and then we can observe the evolution of that degradation during some weeks, in a controlled humidity environment. It is accepted that water preferentially enters in the amorphous zones, but also affects the crystalline regions. It is observed a clear evolution of the relaxation activation energy during the degradation of the polymer.The dielectric relaxation results are complemented with molar mass measurements during the degradation process with time. 相似文献