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101.
The oxidative polycondensation of 4-[(pyridin-3-ylimino)methyl]phenol (4-PIMP) with O2, H2O2, and NaOCl was studied in an aqueous alkaline medium between 50°C and 90°C. Oligo-4-[(pyridin-3-ylimino)methyl]phenol (O-4-PIMP)
prepared was characterized by 1H-NMR, 13C-NMR, FT-IR, UV-VIS, size-exclusion chromatography, and elemental and thermal analyses techniques. At the optimum reaction
conditions, the yield of O-4-PIMP was 18.9%, 39.4%, and 46.8% using H2O2, O2, and NaOCl oxidant, respectively. According to the TG analysis, the initial degradation temperature of O-4-PIMP was 218°C,
which was by 50°C higher than that of 4-PIMP. Thermal analyses of 4-PIMP and O-4-PIMP were carried out in N2 atmosphere at 15–1000°C. The highest occupied molecular orbital, the lowest unoccupied molecular orbital, and electrochemical
energy gaps of 4-PIMP and O-4-PIMP were determined from the onset potentials for n-doping and p-doping, respectively. Also, optical band gaps of 4-PIMP and O-4-PIMP were determined according to UV-VIS measurements. 相似文献
102.
A sensitive and selective method is described for the determination of neodymium in mixed rare earths using fourth-derivative spectrophotometry. The method is based on the absorption spectra of 4f electron transitions of the complex of neodymium with methyl thymol blue and cetylpyridinium chloride. The influence of various instrumental parameters and reaction conditions for maximum colour development are investigated. The calibration curve is linear over the range 0–3.5 g ml–1 neodymium. The relative standard deviation for determination of 1.4 g ml–1 neodymium (n = 7) is 1.6%. The detection limit (signal-to-noise ratio = 3) is 0.2 g ml–1. 相似文献
103.
Cerebrosterol (2 4S hydroxycholesterol,1)formedinsmallamountsinhumanandanimalbrain1fromcholes terolisimportantforcholesterolhomeostasisinthisorgan .Theexcesscholesterolisconvertedinto 2 4S hydroxy cholesterolbyauniquebrain specific 2 4S hydroxylase ,whichcouldber… 相似文献
104.
105.
Dan Donescu Sever Serban Kristiana Gosa Cristian Petcu 《Central European Journal of Chemistry》2005,3(1):10-27
The possibility to prepare hybrids made by poly(vinyl acetate) (PVAc), poly(methyl methacrylate) (PMMA) and/or poly(ethyl
acrylate) (PEtA) with TiO2 was studied. The processes of polymer formation-radical polymerization and sol-gel process for inorganic network —were achieved
simultaneously. Due to a high reactivity of titanium isopropoxide (TIP) in the sol-gel process, a complexant comonomer, allyl
acetoacetate (AlAcAc), was used. Covalent bonds between polymer and inorganic chains were obtained by addition of trialkoxysilane
derivates with vinyl (VTES) or methacryloyl (MPTS) groups. The presence of TIP inhibits the radical polymerization of vinyl
acetate (VAc). The PVAc-TiO2 hybrids were produced by the sol-gel process of TIP in the presence of pre-obtained PVAc. Except for VTES and MPTS, trialkoxysilane
derivates with methyl (MeTES), octyl (OTES) and phenyl (PTES) groups were used. The thermal stability of hybrids is strongly
affected by TiO2 presence and by the type of trialkoxysilane derivates. The thermal stability of PVAc hybrids decreases in the presence of
TiO2 inorganic network. The glass transition temperature of polymers increases in the presence of the inorganic network. 相似文献
106.
通过氧化偶联聚合方法成功地合成出电活性聚芳醚酮. 该反应条件温和, 操作简单, 室温下即可进行. 用红外光谱、核磁共振谱、高效凝胶渗透色谱、循环伏安、热失重、X射线衍射等技术对所合成的聚合物进行了表征, 并探讨了聚合物的性能. 相似文献
107.
V. Slavinska Dz. Sile G. Rozenthal G. Maurops J. Popelis M. Katkevich V. Stonkus E. Lukevics 《Chemistry of Heterocyclic Compounds》2006,42(5):570-573
The hydrogenation of ethyl 4-R-2,4-dioxobutyrates (R = phenyl, 2-furyl) at 5% Pt/Al2O3 catalyst, modified with cinchonidine, and at palladium black was investigated. The former had low activity under the conditions
we tested. The main products during the hydrogenation of these compounds at palladium black are ethyl 4-R-2-hydroxy-4-oxobutyrates.
The yield of the phenyl derivative amounts to 68.5%, while the yield of the corresponding 2-furyl derivative amounts to 97%.
In the last case ethyl 2-hydroxy-4-oxo-4-(2-tetrahydrofuryl)butyrate was detected as impurity. The optimum conditions for
the formation of ethyl 2-hydroxy-4-phenylbutyrate (yield 88.2%) were determined.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 655–659, May, 2006. 相似文献
108.
The heat of formation (H
f) of unsymmetrical ketone phenylhydrazones and their enehydrazine tautomers was calculated by the semi-empirical quantum-chemical AM1 method. It is concluded that from H
f values it is possible to judge the regioselectivity of indolization of unsymmetrical ketone phenylhydrazones.Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 1, pp. 220–221, January, 1993. 相似文献
109.
N. Ya. Grigorieva 《Russian Chemical Bulletin》2005,54(4):1046-1047
High (Z)-stereoselectivity of olefination of methyl α-phenylthioalkyl and methyl α-phenylthioalkenyl ketones with methyl trimethylsilylacetate
decreases in the case of ketones containing a higher alkyl-substituent in place of the methyl group.
Dedicated to Corresponding Member of the Russian Academy of Sciences E. P. Serebryakov on the occasion of his 70th birthday.
__________
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 1020–1021, April, 2005. 相似文献
110.
G. Glöckner 《Chromatographia》1987,23(7):517-524
Summary Prerequisite of quantitative evaluation in chromatography is equivalence of sample composition and detector signal. This includes
complete retention and proper elution of all sample constituents. In polymer HPLC, complete retention requires a poor starting
eluent, a sufficiently active column, and a low ratio of injection volume to column volume. On small pore columns, insufficient
retention caused the polymer to elute either in the interstitial volume (sample exclusion), together with the sample solvent,
or immediately after the solvent plug.Stat-copoly(styrene/ethyl methacrylate) samples are more difficultly retained thanstat-copoly(styrene/acrylonitrile) specimes. With the former copolymer it could be shown that incomplete retention did not cause
sample demixing. In order to gain complete retention, non-exclusion HPLC of polymers should be performed with columns whose
solvent volume is at least 50 times as large as the injection volume. This consequence is of practical importance in chromatographic
cross-fractionation where rather large volumes of SEC eluate are injected into the apparatus for gradient HPLC. 相似文献