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151.
苯乙烯-丁二烯-苯乙烯/聚乙烯基甲基醚共混体系相容性的FT-IR及DSC研究 总被引:2,自引:0,他引:2
嵌段高聚物、均聚物共混体系相容性是近年来研究的热点。本工作以光学显微镜、DSC、FT-IR为手段,研究了三嵌段高聚物苯乙烯-丁二烯-苯乙烯(SBS);SBS-48、SBS-30,SBS-28与聚乙烯基甲基醚共混体系的相容性。DSC结果表明,随SBS中PS含量的升高,体系相容性变好,PS段分子量增大,也有助于体系相容。FT-IR结果表明PVME中COCH_3在1100cm~(-1)附近呈现的双峰的相对强度对体系的相容性十分敏感,而由于苯环C—H振动产生的698cm~(-1)峰位却不象PS/PVME体系那样随相容性的改变而有显著的改变。总而言之,嵌段高聚物SBS/均聚物PVME共混体系中,体系的相容性依赖于嵌段高聚物在体系中的组份含量及嵌段高聚物中PS的重量百分含量,PS段分子量的大小对体系相容性也有影响。 相似文献
152.
The bis(dibutylstannylene) derivative of 1,2-cyclohexylidene-myo-inositol reacted with (S)-O-acetylmandeloyl chloride and diphosphate tetraesters to give 3,6-dimandelate and 3-phosphate, respectively. Using the stannylene methodology for the optical resolution and regioselective phosphorylation of the ketal, a concise synthesis of phosphatidylinositol with the natural configuration was accomplished. 相似文献
153.
M. Drozdowski K. apsa P. Ziobrowski Z. B aszczak E. Andrzejewska M. Andrzejewski 《Journal of Molecular Structure》1998,450(1-3):129-134
In this paper we report a temperature study of Brillouin scattering and optical Kerr effect in the ethane-1,2-diol dimethacrylate, pentane-1,5-diol dimethacrylate and hexane-1,6-diol dimethacrylate belonging to the series of dimethacrylate homologues. Using these methods we have studied the temperature behaviour of the hypersonic velocity, adiabatic compressibility and optical Kerr constant in the temperature range from 283 to 323 K.
The obtained results are compared to those obtained earlier from Brillouin scattering and optical Kerr effect experiments for butane-1,4-diol dimethacrylate and 2,2′-thiodiethyl dimethacrylate (a sulfur-containing monomer). The results are also discussed in terms of changes in the intermolecular interactions and arrangement in the liquid compounds under study. 相似文献
154.
The effects of intermolecular interactions on the second-order susceptibilities ((2)) of molecular crystals are studied by using a semiempirical quantum–chemical method. These effects are discussed on the basis of the super-molecular approach. The influence of the electrostatic interactions between adjacent unit cells on the tensor components of (2) was modeled by using the technique of cumulative atomic multipole moments (CAMMs). 相似文献
155.
The chiral separation of trimetoquinol hydrochloride, which is a bronchodilator (Inolin), and three related compounds by micellar electrokinetic chromatography was investigated using a bile salt as a chiral surfactant. Enantiomers of these compounds, except laudanosoline, were successfully separated within 12 min using a separation tube of effective length 500 mm × 0.05 rum i.d. and a 0.05 M sodium taurodeoxycholate solution of pH 7.0. The observed theoretical plate numbers of the peaks were ca. 150000. Chiral recognition was affected by the structure of bile salts, the pH of the buffer solutions used and the structure of the solutes. Of four kinds of bile salts, successful chiral separation was achieved only using sodium taurodeoxycholate solution under neutral conditions. The method was applied to the optical purity determination of trimetoquinol hydrochloride. The effects of surfactant concentrations and some additives to the micellar solution are briefly described. 相似文献
156.
Optical fiber (OF) sensors are often limited by the immobilization technique used to associate a specific sensing ligand with the OF surface. This is particularly true when the ligand is biologically active as, for example, in the case of immobilized haptens or antibodies. The dynamic modification protocol is a regenerable and experimentally simple way to immobilize a variety of sensing molecules on an OF surface. Furthermore, the protocol is immune to hydrolysis and not limited by diffusion through a membrane or sol–gel. In this publication the approach is extended by immobilizing the hydrophobic hapten (octadecyl 6-(2,4 dinitrophenyl)aminohexanoic acid) as a means to prepare an OF sensor for antibodies specific for 2,4 dinitrophenyl (DNP). The LOD for anti-DNP is 0.5 nanomolar and the Kapparent is 1.0±0.2×106. Nonspecific antibody adsorption is problematic in this sensing approach and was found to limit the quantitative capabilities of the sensor. However, time discrimination can be used to allow the nonspecific antibody to desorb prior to measurement thus minimizing the influence of nonspecific binding on sensor performance. 相似文献
157.
Novel HPLC methods were developed for the analytical and semipreparative resolution of new antidepressant drug mirtazapine enantiomers. At analytical scale, the separation of the mirtazapine enantiomers was investigated using both cellulose and amylose tris(3,5-dimethylphenylcarbamate) (CDMPC and ADMPC) chiral stationary phases under normal-phases and polar organic modes. Good baseline enantioseparation was achieved using cellulose tris(3,5-dimethylphenylcarbamate) chiral stationary phases under both normal-phases and polar organic modes. Furthermore, the elution order of mirtazapine enantiomic pairs was found reversed by changing the stationary phase from the amylose-based ADMPC–CSPs to its cellulose-based counterpart, CDMPC–CSPs. The validation of the analytical methods including linearity, limit of detection (LOD), limit of quantification (LOQ), recovery and precision, together with the semipreparative resolution of mirtazapine racemate were carried out using cellulose tris(3,5-dimethylphenylcarbamate) chiral stationary phases and methanol as mobile phase without any basic additives under polar organic mode. At analytical scale, the elution times of both enantiomers were less than 6 min at normal temperature and 1.0 ml/min, with the separation factor () 1.99 and the resolution factor (Rs) 3.56. Then, the analytical methods were scaled up to semipreparative loading to obtain small quantities of both mirtazapine enantiomers. At semipreparative scale, about 16 mg/h enantiomers could be isolated and elution times of both enantiomers were less than 10 min at 2.0 ml/min. To increase the throughput, the technique of boxcar injections was used. One enantiomer ((−)-(R)-mirtazapine) was isolated with purity of >99.9% e.e. and >98.0% yield and another ((+)-(S)-mirtazapine) was isolated with purity of >97.0% e.e. and >99.0% yield. In addition, optical rotation and circular dichroism (CD) spectroscopy of both mirtazapine enantiomers isolated were also investigated. 相似文献
158.
光纤松耦合型传感器特性研究 总被引:1,自引:1,他引:0
本文介绍一种实用的光纤传感器,它由二根光纤或多根光纤紧靠一起,并在同一位置除去局部包层,成为松耦合状态,在这种状态下,研究了它的特性和应用。 当耦合间隙中充满某种液体介质时,耦合效率明显增大,因此可以方便地判别该介质是否存在。并且实验证明了一种光纤只能有一种相近于光纤芯子折射率的介质具有最大的灵敏度。当间隙内的介质不变时,耦合功率的大小决定于耦合距离d和耦合长度l,l一旦决定以后,d的调节精度为0.1mm量级,易于在机械结构上实现线性检测。 相似文献
159.
Peter Kremminger Walter Weissensteiner 《Monatshefte für Chemie / Chemical Monthly》1991,122(6-7):571-576
Summary The optically active sexidentate Schiff bases [H3
L
5] and [H3
L
6] were prepared from tris[(S)-2-aminopropyl]amine and 5-chlor- and 5-isopropylsalicylaldehyde, respectively. Reaction of rhodium trichloride with [H3
L
6] gave an enantiomerically pure [RhL
6] complex with an absolute configuration of for the octahedral arrangement. The chiroptical properties are given.
Synthese, stereochemische Charakterisierung und Absolutkonfiguration enantiomerenreiner Komplexe sechszähniger Liganden (Kurze Mitt.)
Zusammenfassung Ausgehend von Tris[(S)-2-aminopropyl]amin und 5-Chlor- beziehungsweise 5-Isopropylsalicylaldehyd wurden die optisch aktiven sechszähnigen Schiffschen Basen [H3 L 5] und [H3 L 6] hergestellt. Die Umsetzung von Rhodiumtrichlorid mit [H3 L 6] ergab einen enantiomerenreinen Komplex [RhL 6] mit einer Absolutkonfiguration von für die oktaedrische Anordnung des Liganden. Die chiroptischen Eigenschaften werden angegeben.相似文献
160.
W. Ryba-Romanowski S. Go
b G. Dominiak-Dzik W. A. Pisarski D. Podsiada Z. Czapla 《Journal of Molecular Structure》1998,450(1-3):219-222
Chromium doped (CH3)2NH2Al(SO4)2·6H2O (DMAAlS) and (CH3)2NH2Ga(SO4)2·6H2O (DMAGaS) single crystals were grown and investigated using the methods of optical spectroscopy. It was found that the Cr3+ ions in the two crystals are situated in a strong crystal field in which the 2E state is the lowest. The single narrow R-line associated with the 2E–4A2 phosphorescence of Cr3+ in DMAAlS in a ferroelectric phase indicates an undistorted octahedral site, whereas important distortion of Oh symmetry and structural disorder was inferred from spectral data obtained with DMAGaS:Cr3+ in a low temperature phase. Results of optical investigation are discussed taking into account the structural data. 相似文献