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41.
A sequential polydepsipeptide containing a tripeptide sequence L-alanyl-Lalanyl-ethyl L-glutamyl and an-hydroxy acid L-lactic acid, poly(Ala-Ala-Glu(OEt)-Lac), was synthesized to prepare the microspherical particles by the solvent evaporation process. In this case, the solvents play the most important role for the preparation of polydepsipeptide microspheres and, as an example, when 200 mg of the polydepsipeptide dissolved in 10 ml of 98/2% chloroform/dichloroacetic acid mixture was stirred at 400 rpm and 30 C, the microspherical particles with mean diameter of 58m were formed after pouring into 200 ml of 1% (w/v) poly(vinyl alcohol) solution. 17-Estradiol was incorporated into the particles, and the resulting particles were found to contain 5 mg of drug per 25 mg of the particle. The in vivo release of drug from the microspherical formulation was evaluated by measuring the pharmacological influence on rat prostate. It was found that the sufficient amount of drug, keeping the effective pharmacological influence, is supplied during the first 12-week period, followed by an incomplete supplying of drug intil the implant is perfectly degraded in vivo in the 25th week from the start of implantation.  相似文献   
42.
A polyphosphide of the type (NaP)X 1 was obtained from red phosphorus and sodium in presence of small amounts of naphthalene in 1,2-dimethoxyethane as solvent. 1 reacts with alkyl halides in dependence on the kind of alkyl group with formation of different alkylcyclophosphanes. As definite compounds Me5P5 2 , Et5P5 3 (with not definite constitution), i-Pr4P4 4 and t-Bu4P4 5 could be isolated. 1 was identified by X-ray diffraction, 2 – 5 by means of their 1H, 13C, 31P n.m.r. and mass spectra. The molecular structure of 4 was identified by electron diffraction.  相似文献   
43.
太阳红外光谱中蕴含着丰富的物理信息,其中CO 4.6μm波段是具有代表性的分子谱带,其形成于温度极小区附近,对研究太阳物理具有极其重要的意义。为获得CO 4.6μm波段太阳单色像,本文建立了一套全反射太阳红外成像观测系统。该系统采用定天镜跟踪引光,通过成像反射镜将太阳成像于3~5μm波段红外相机的焦平面上,该相机采用的是国产HgCdTe焦平面阵列器件。同时,为提高信噪比,提出了一种有效计算平场提取观测目标的方法,并利用该方法获得了CO 4.6μm波段的太阳单色像。  相似文献   
44.
The values of the second dissociation constant, pK 2, for the dissociation of the NH+ charge center of the zwitterionic buffer compounds 4-(N-morpholino)butanesulfonic acid (MOBS), and N-(2-hydroxyethyl)piperazine-N-4-butanesulfonic acid (HEPBS) have been determined from 5 to 55°C, including, 37°C at intervals of 5°C. The electromotive-force (emf) measurements have been made utilizing hydrogen electrodes and silver–silver chloride electrodes. The value of pK 2 for MOBS was found to be 7.702 ± 0.0005, and 8.284 ± 0.0004 for HEPBS, at 25°C, respectively. The related thermodynamic quantities, G o, H o, S o, and C p o for the dissociation processes of MOBS and HEPBS have been derived from the temperature coefficients of pK 2. Both the MOBS and HEPBS buffer materials are useful as primary pH standards for the control of pH 7.3 to 8.6 in the region close to that of physiological fluids.  相似文献   
45.
Composite membranes were prepared by (a) infiltrating NAFION with SiO2-P2O5-ZrO2 sol, and (b) recasting a film using NAFION solution containing SiO2-P2O5-ZrO2 sol. The membranes were characterized by Differential Thermal Analysis and ac-impedance spectroscopy as a function of relative humidity. The influences of the heat treatment (80°C–150°C) and cleaning on the electrical properties were investigated. The incorporation of SiO2-P2O5-ZrO2 gels into NAFION lead to improvements in its thermal stability and proton conductivity.  相似文献   
46.
    
Under the influence of perpendicularly applied positive electro-static field less than 103V/cm to silk fibron textiles, at the high frequency side of the C2–O bending reflection band (450350 cm–1), effect of step creation and step annihilation of the C2–O pseudo dending bands was induced in three stages at 600450 cm–1 region IR spectroscopically relating to the stepnized statistical transfer of the unbonded 2P2, electrons in carbon which present with density of 4.0×1014/cm2 in the surface mono-layer of silk fibroin from the states formed in (–C1–C2–N–)m spiral chains upto the pseudo-bending states formed in C2–O bondings. Fine 90 steps measured overlapping on these four types of C2–O reflection bands were analysed as to consist four step series and they were shown as,y = A·Jm + B cm–1 with A=20, B=521, m=0.55 and J=1, 2...18 for the B-series.And with A=39, B=283, m=0.63 and J=1, 2 ...17 for the C-series.y J = A·J + B cm–1 with A=11.42, B=201 and J=1, 2...13, for the D-series. And, stepnized C2–O bending bands including that of permanent oscillators and pseudo-bending oscillators induced by the effect of transfer of the unbonded 2P2 electrons in carbon atoms were shown as, EN=A·N2+B·N+C (eV) with A=–1.50×10–3, B=1.65×10–2 and C=2.4×10–2.  相似文献   
47.
ab initio Calculation of the Cl2C=CHOMe molecule has been carried out with geometrical optimization in the split valence basis set in the RHF/6-31G*//RHF/6-31G* approximation. An analysis of the populations of the p-orbitals of the Cl atoms implies the absence of p,-conjugation between the unshared electron pairs of these atoms and the -bond. The asymmetry parameters of the electric field gradient at the35Cl nuclei, calculated from the 3p-orbital populations of the Cl atoms, practically coincide with the experimental values.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2369–2372, December, 1995.The authors are grateful to G. S. Beloglazov for assistance in accomplishingab initio calculations.  相似文献   
48.
The vapor phase catalytic reaction between aromatic carboxylic acid and acetic acid was investigated. Many metal oxides catalyzed the reaction between 2methylbenzoic acid (OTA) and acetic acid (AA) to produce 2methylacetophenone (OMA), and weakly acidic oxides such as Th, U, Ce, and La oxide exhibited higher yield of OMA. The OMA yield depended on the catalyst support. SiO2, Al2O3, TiO2, and ZrO2 with a surface area of less than 200 m2 g–1 appeared to be suitable as industrial catalyst supports. CeO2 on Al2O3was chosen as an industrial catalyst for the synthesis of OMA because of higher productivity, longer catalyst life, and lifting of legal restrictions on catalyst handling. This catalyst system can also be applied to the syntheses of acetophenone, nitroacetophenone, and chloroacetophenone.  相似文献   
49.
The i.r., u. v.,1H n.m.r.,13C n.m.r., and11B n.m.r. spectra of several substituted diphenylboron chelates derived from salicylaldehyde azomethines were compared with respect to the influence of the amine substituentR. O–B–N-6-ring constitution of the chelates29–32 [R=OH, NH2, NHC6H5, N(CH3)2] can be deduced from the spectra.
Als 3. Mitt. gilt:F. Umland undE. Hohaus mit Beiträgen vonW. Riepe, K. Brodte, C. Schleyerbach undD. Szonn. Untersuchungen über borhaltige Ringsysteme vom Chelattyp. Forschungsbericht des Landes Nordrhein-Westfalen Nr. 2538. Opladen: Westdeutscher Verlag. 1976.  相似文献   
50.
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