共查询到20条相似文献,搜索用时 265 毫秒
1.
本实验合成了2,6-0-二丁基-3-0-三氟乙酰基-γ-环糊精,2,6-0二戊基-3-0三氟乙酰基基-β-环糊精,全戊基-β-CD。分离了一些氨基酸酯,羟基酸酯,卤代酸酯,卤代烃,醇等对映体。比较了OV-7和OV-1701作混合固定相稀释液对离析性能的影响。 相似文献
2.
3.
合成了全戊基化(Ⅰ)和部分戊基化三氟乙酰化(Ⅱ)的两种“环糊精手性固定相。将它们分别与OV-7混合制备出柱效大于4100塔片/m,热稳定性可达210℃的手性石英毛细管住。对映体拆分结果表明,固定相Ⅰ对醇、二醇、胺、γ-内酯等对映体比Ⅰ有更高的选择性。 相似文献
4.
两种β-环糊精衍生物手性石英毛细管柱拆分对映体 总被引:2,自引:0,他引:2
合成了全戊基化(Ⅰ)和部分戊基化三氟乙酰化(Ⅱ)的两种“环糊精手性固定相。将它们分别与OV-7混合制备出柱效大于4100塔片/m,热稳定性可达210℃的手性石英毛细管住。对映体拆分结果表明,固定相Ⅰ对醇、二醇、胺、γ-内酯等对映体比Ⅰ有更高的选择性。 相似文献
5.
盐酸美西律对映体的毛细管电泳分离 总被引:4,自引:0,他引:4
以β-环糊精的两种生物做为毛细管电泳手性分离添加剂,对盐酸美西律的对映体进行了拆分研究。其中,2,6-O-二甲基β-环糊精可将对映体部分拆分,而2,3,6-O-三甲基β-环糊精时,可基线分离对映体。研究了两种甲基化β-环糊精的浓度及工作电压对分离的影响。 相似文献
6.
合成了一种新的手性固定相2,6-O-二庚基-3-O三甲基硅烷基-β环糊精,以甲基苯硅油为稀释剂,采用快速超动态法,成功地制备了高效手性毛细管柱,考察了手性柱的色谱性能,分离了醇、酮、烯烃类等一些对映体。 相似文献
7.
8.
9.
10.
11.
12.
The spectral-polarization characteristics of absorption and phosphorescence of molecules of the initial form of nitro-substituted
indolinospirobenzothiopyran were studied in oriented polyethylene films and in solutions with different polarity. An oscillator
model of the electron transitions responsible for the formation of absorption and luminescence spectra was suggested. It was
established that the principal differences in the spectral and photophysical properties of the compound studied and its oxygen-containing
analog are associated with the fact that the electronegativity of the S atom is lower than that of the O atom.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1143–1146, June, 1997. 相似文献
13.
Two vanilloids, (5E)-8-(4-hydroxy-3-methoxyphenyl)oct-5-en-4-one (1) and 4-[3-hydroxydecyl]-2-methoxyphenol (2), isolated from the dried seeds of Grains of Paradise (Aframomum melegueta), were synthesized; the latter compound was made as the S-enantiomer and the material derived from the seeds was found to be a 1:1.7 mixture of the R and S isomers. The synthetic route used should allow the preparation of analogs having extended alkyl chains and consequently different lipophilicity, and 3, a homolog of 2, was also prepared. 相似文献
14.
Cotton cellulose was swollen in a sodium hydroxide solution and carboxymethylated by a two-bath method for different periods of time for each process. The kinetics of acid hydrolysis and the crystallinity of the swollen and carboxymethylated samples were measured. The proportion of broken bonds, rate constants for hydrolysis, and permeability of cellulose to hydrolyzing agents were calculated. The susceptibility of glycosidic linkages to acid hydrolysis was improved by carboxymethylation more than by swelling in alkali. The increased accessibility of carboxymethylcellulose to acid was regarded as a consequence of increased intra-and intercrystalline swelling and of the glycosidic bonds' weakness caused by the electron-attracting carboxymethyl group on the C-6 position. 相似文献
15.
Stepkowska E. T. Perez-Rodriguez J. L. Jimenez de Haro M. C. Sayagues M. J. 《Journal of Thermal Analysis and Calorimetry》2002,69(1):187-204
Main hydration products of two cement pastes, i.e. CSH-gel, portlandite (P) (and specific surface S) were studied by static heating, and by SEM, TEM and XRD, as a function of cement strength (C-33 and C-43) hydration time (th) and subsequent hydration in water vapour.Total change in mass on hydration and air drying, Mo, increased with strength of cement paste and with hydration time. Content of water escaping at 110 to 220°C, defined as water bound with low energy, mainly interlayer and hydrate water, was independent on cement strength but its content increased with (th). Content of chemically bound (zeolitic) water in CSH-gel, escaping at 220-400°C, was slightly dependent on strength and increased with (th). It was possibly derived from the dehydroxylation of CSH-gel and AFm phase. Portlandite water, escaping at 400-500°C, was independent on cement strength and was higher on longer hydration. Large P crystals were formed in the weaker cement paste C-33. Smaller crystals were formed in C-43 but they increased with (th). Carbonate formated on contact with air (calcite, vaterite and aragonite), decomposed in cement at 600-700oC. It was high in pastes C-33(1 month) and C-43(1 month), i.e. 5.7 and 3.3%, respectively; it was less than 1% after 6 hydration months (low sensitivity to carbonation) in agreement with the XRD study showing carbonates in the air dry paste (1month), and its absence on prolonged hydration (6 months) and on acetone treatment. Water vapour treatment of (6 months) pastes or wetting-drying increased this sensitivity.Nanosized P-crystals, detected by TEM, could contribute to the cement strength; carbonate was observed on the rims of gel clusters.This revised version was published online in November 2005 with corrections to the Cover Date. 相似文献
16.
The aim of the presented work was the investigation of thermal oxidation of ilmenite in static air atmosphere. The investigations
were carried out by use of a derivatograph (MOM, Hungary). The changes of crystallographic structure of investigated samples
were identified by X-ray diffractometry on Philips PW-1710 diffractometer. In temperature above 500°C appears structure of
hematite Fe2O3. On the basis of the thermogravimetric measurements, the contracting area and contracting volume models were found as the
best fitting experimental data.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
17.
Cyclopropyl derivative of 2,6-di-tert-butylphenol is synthesized as a probe to investigate the mechanism of base-catalyzed autooxidation of phenol derivatives. Our study indicates that one electron reduction of molecular oxygen from phenolate gives phenoxyl radical 3, a key intermediate of autooxidation. The coupling of phenoxyl radical and superoxide radical gives peroxylate anion 4 and produces the final epoxy alcohol adduct 6. 相似文献
18.
19.