X-ray single crystal diffraction demonstrates that in {[Pb2(HNTP)2(NTP)(CHZ)(H2O)2] · 2.5H2O}n (polymer, NTP = nitroterephthalate, CHZ = carbohydrazide), there are two kinds of Pb centers. By means of the bridging ligands–two
water, two CHZ and two NTP molecules, four Pb centers (two Pb1 and two Pb2) are joined together to form the rectangular grid,
and by the intense static electric interactions among the two O atoms of nitro groups in NTP, the extending two-dimensional
grids are linked together to form the three-dimensional frameworks. Thermal analyses DSC and TG-DTG have been performed on
the polymer to study its thermal decomposition mechanism and thermal kinetic properties.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
The aim of this paper is to study the static problem about a general elastic multi-structure composed of an arbitrary number of elastic bodies, plates and rods. The mathematical model is derived by the variational principle and the principle of virtual work in a vector way. The unique solvability of the resulting problem is proved by the Lax-Milgram lemma after the presentation of a generalized Korn's inequality on general elastic multi-structures. The equilibrium equations are obtained rigorously by only assuming some reasonable regularity of the solution. An important identity is also given which is essential in the finite element analysis for the problem. 相似文献
SHR110008 is a representative 9-β-dihydro-9,10-O-acetal taxane with greater anticancer activity and less toxicity than docetaxel. To support a preclinical study of its pharmacokinetics and to predict the effect of 9-β-dihydro-9,10-O-acetal modification on its pharmacokinetic properties, we have developed a sensitive and rapid liquid chromatographic–tandem mass spectrometric method for quantitative analysis of SHR110008 in rat and dog plasma. Plasma was extracted with ethyl acetate. The analytes were separated on a 150 × 4.6 mm i.d., 5 μm particle, reversed-phase C18 column with 90:10 (v/v) methanol–0.1% formic acid as mobile phase at a flow rate of 0.3 mL min−1. Detection was performed by triple-quadrupole tandem mass spectrometry in selected reaction monitoring (SRM) mode with an electrospray ionization source. The precursor-to-product ion transition m/z 933 → 142 was used. The method was validated for accuracy and precision, and linearity in the two matrices was good. Lower limits of quantification (LLOQ) in rat and dog plasma were 5 and 2 ng mL−1, respectively. There were no stability-related problems in the procedure for analysis of SHR110008. The method was successfully used in a preclinical study of the pharmacokinetics of SHR110008 in rats and beagle dogs. The pharmacokinetics of SHR110008 were non-linear in rats and dogs. The elimination half-life ranged from 5.18 to 7.32 h for the rats and from 6.42 to 8.42 h for the dogs.