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1.
V. V. Potekhin 《Russian Chemical Bulletin》2007,56(5):875-882
The oxidation of lower aliphatic alcohols C1–C4 with dioxygen to form the corresponding carbonyl compounds in the presence of the PdII tetraaqua complexes and FeII-FeIII aqua ions in an aqueous medium was studied at 40–80 °C. The introduction of an aromatic compound (acetophenone, benzonitrile,
phenylacetonitrile, o-cyanotoluene, nitrobenzene) and FeII aqua ion instead of the FeIII aqua ion into the reaction system increases substantially the catalytic activity and the yield of the carbonyl compound.
The key role of the Pd species in the intermediate oxidation state stabilized by the aromatic additive in the catalytic cycle
of alcohol oxidation with dioxygen to the carbonyl compound was shown. An increase in the kinetic isotope effect with an increase
in the temperature of methanol oxidation indicates a change in the rate-determining step of alcohol oxidation with dioxygen
in the presence of PdII-FeII-FeIII and the aromatic compound. At temperatures below 60 °C, the catalytically active palladium species are mainly formed upon
the reduction of the PdII tetraaqua complex with the FeII aqua ion, whereas at higher temperatures the reaction between the alcohol and PdII predominates. The mechanism and kinetic equation of the process were proposed.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 842–848, May, 2007. 相似文献
2.
Kinetics of hydrogen peroxide decomposition in the presence of the tetraaquapalladium(II) complex in an aqueous solution at
40–70 °C was studied. The reaction rate is the first order with respect to the concentration of both PdII and H2O2 and the negative first order with respect to perchloric acid. Using free radicals traps, the reaction mechanism was found
to differ from the traditional free-radical mechanism known for d-metal aqua ions and proceeds without generation of hydroxyl
radicals. The kinetic data obtained suggest a mechanism involving the formation of an intermediate palladium complex with
oxygen.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1077–1082, May, 2005. 相似文献
3.
Mushroom tyrosinase was immobilized on modified polystyrene—polyaminostyrene (PSNH) and polymethylchloridestyrene (PSCL)—to
produce l-DOPA from l-tyrosine. Glutaraldehyde was used as an activating agent for the PSNH to immobilize the tyrosinase and 10% (w/v) glutaraldehyde
was optimal in conferring the highest specific activity (11.96 U/g) to the PSNH. Methylchloride on the PSCL was directly linked
with the tyrosinase, and 1.5 mmol of Cl/g was optimal in attaining the specific activity of 17.0 U/g. The temperature and
optimal acidity were, respectively, 60°C and pH 5.5 for the PSNH, and 70°C and pH 3.0 for the PSCL. In a 50-mL batch reactor
working over 36 h, the l-DOPA production rate at 30°C was 1.44 mg/(L·h) for the PSNH and 2.33 mg/(L·h) for the PSCL. The production rate over 36 h
was 3.86 mg/(L·h) for the PSNH at 60°C and 5.54 mg/(L·h) for the PSCL at 70°C. Both of the immobilized enzymes showed a remarkable
stability with almost no change in activity after being stored wet. The operational stability study indicated a 22.4% reduction
in l-DOPA production for the PSNH and an 8.63% reduction for the PSCL over seven runs (each run was for 144h at 30°C) when the
immobilized enzymes were used under turnover conditions. The immobilized tyrosinase was more stable on the PSCL than on the
PSNH. 相似文献
4.
An enzymatic method for determining L-malic acid in wine based on an L-malate sensing layer with nicotinamide adenine dinucleotide (NAD+), L-malate dehydrogenase (L-MDH) and diaphorase (DI), immobilized by sol-gel technology, was constructed and evaluated. The sol-gel glass was prepared
with tetramethoxysilane (TMOS), water and HCl. L-MDH catalyzes the reaction between L-malate and NAD+, producing NADH, whose fluorescence (λ
exc = 340 nm, λ
em = 430 nm) could be directly related to the amount of L-malate. NADH is converted to NAD+ by applying hexacyanoferrate(III) as oxidant in the presence of DI. Some parameters affecting sol-gel encapsulation and the
pH of the enzymatic reaction were studied. The sensing layer has a dynamic range of 0.1–1.0 g/L of L-malate and a long-term storage stability of 25 days. It exhibits acceptable reproducibility [s
r(%)≈10] and allows six regenerations. The content of L-malic acid was determined for different types of wine, and polyvinylpolypyrrolidone (PVPP) was used as a bleaching agent
with red wine. The results obtained for the wine samples using the sensing layer are comparable to those obtained from a reference
method based on UV-vis molecular absorption spectrometry, if the matrix effect is corrected for. 相似文献
5.
S Yashonath P K Basu A Srinivasan M S Hedge C N R Rao 《Journal of Chemical Sciences》1982,91(2):101-128
Ultraviolet and x-ray photoelectron spectroscopy have been employed to investigate the adsorption of methanol, ethanol, diethylether,
acetaldehyde, acetone, methyl acetate and methylamine on surfaces of Fe, Ni and Cu. All these molecules adsorb molecularly
at low temperatures (≤100 K). Lone pair orbitals of these molecules are stabilized on these metal surfaces (by 0·4–1·0eV)
due to molecular chemisorption. The molecules generally undergo transformations as the temperature is raised to 120 K or above.
The new species produced seems to depend on the metal surface. Some of the product species identified are methoxy species,
formaldehyde and carbon monoxide in the case of methanol and methyl acetate, ethoxy species in the case of ethanol and 2-propanol
in the case of acetone.
Contribution No. 166 from the Solid State and Structural Chemistry Unit. 相似文献
6.
Zahradnícková H Husek P Simek P Hartvich P Marsálek B Holoubek I 《Analytical and bioanalytical chemistry》2007,388(8):1815-1822
A rapid and simple method was developed for the determination of free amino acids (AAs) released from cyanobacteria. The procedure
involves trapping of AAs from the centrifuged cyanobacterial culture fluid on a cation-exchange resin, their release together
with the resin by direct treatment with the reaction medium, followed by immediate derivatization with a corresponding chloroformate.
The extractive alkylation transfers the analytes into an organic phase, an aliquot of which is subjected to GC analysis. Identification
and quantification of AAs was performed by GC/MS and GC/FID, respectively, using propyl chloroformate (PCF) as the derivatization
reagent. For chiral analysis, the cyanobacteria extracts were treated with 2,2,3,3,3-pentafluoropropyl chloroformate (PFPCF)
to create more volatile analytes. Separation of the AA enantiomers was accomplished on a Chirasil-Val capillary column and
the D/L enantiomeric ratios were determined. AAs of cyanobacteria are considered to be important for the assessment of energy flow
in an aquatic food web, nutrition value of cyanobacteria in a food web and for cell–cell communication within cyanobacteria.
The highest levels of AAs were found in the summer period at the beginning of the season (July). In the September and October
samples, the amount of AAs was lower, the number of D-AAs decreased and the D/L ratio was higher than in the July sample. Based on the obtained results it can be assumed that young populations excrete
AAs in higher concentrations and a different composition compared to actively growing populations.
Figure PFPCF derivatization scheme 相似文献
7.
T. N. Kropacheva V. I. Kornev D. A. Loginov V. I. Meshcheryakov E. V. Mutseneck D. V. Muratov D. S. Perekalin L. S. Shul’pina A. R. Kudinov 《Russian Chemical Bulletin》2005,54(10):2354-2358
New dinuclear ruthenium manganese complexes of general composition (bpy)2Ru(L)MnClx(H2O)2 (L is 1,10-phenanthroline-5,6-dione, 3,3′-dicarboxy-2,2′-bipyridyl, or bis(pyrazolyl); x = 2 or 4) were synthesized by the reaction of (bpy)2Ru(L) with MnCl2 · 4H2O. These compounds and the starting mononuclear ruthenium complexes were studied by spectrophotometric and electrochemical
methods in MeCN. The position of the charge-transfer band RuII → L in the spectra depends on the donor-acceptor characteristics of the ligand L. For the dinuclear complex under study,
the formal potentials of reversible one-electron oxidation of RuII are in the range of 0.9–1.2 V (vs. the standard hydrogen electrode), whereas oxidation of MnII occurs at more positive (by 0.1–0.2 V) potentials.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2281–2285, October, 2005. 相似文献
8.
J. Csapó J. Schmidt Zs. Csapó-Kiss É. Varga-Visi G. Pohn É. Csokona 《Chromatographia》2002,56(1):S169-S171
Summary In recent decades several methods have been developed for determination of the proportion of nitrogen-containing substances
passed from the rumen into the abomasum, or small intestine, which are of microbial origin. Recently, when examining thed-amino acid content of foodstuffs, particularly milk and milk products, it was observed that, in addition tod-alanine (d-Ala,d-glutamic acid (d-Glu) andd-aspartic acid (d-Asp) can also be detected in similar quantities, primarily in products which have links with bacterial activity. This gave
rise to the idea of examining the diaminopimelic acid (DAPA),d-Glu, andd-Asp content of bacteria extracted from the rumen of cattle, and that of chyme from the same cattle, to establish whetherd-Asp andd-Glu can be used to estimate protein of bacterial origin.
The investigations performed have provided evidence that bothd-Asp andd-Glu might be appropriate for determination of protein of bacterial origin. The results obtained using these two bacterial
markers (d-Asp andd-Glu) proved to the approximately 10% lower than those obtained using DAPA; this was not because of to error attributable
to the new markers but rather to the unreliability of determination using DAPA Analyses performed on samples of known bacterial
protein content indicate thatd-Asp andd-Glu gave almost identical results for bacterial protein content which were very close to the theoretical (calculated) values.
Presented at Balaton Symposium '01 on High-Performance Separation Methods, Siófok, Hungary, September 2–4, 2001. 相似文献
9.
To express high-active soluble d-amino acid oxidase (DAAO), a constitutive plasmid that is regulated by a native hydantoinase promoter (PHase), was constructed. A d-amino acid oxidase gene (dao) was ligated with the PHase and cloned into pGEMKT to constitutively express protein of DAAO without the use of any inducer such as isopropyl β-d-1-thiogalactopyranoside which is poisonous to the cells and environment. The ribosome binding site region, host strain, and
fermentation conditions were optimized to increase the expression level. When cultivated in a 5-m3 fermenter, the enzyme activity of JM105/pGEMKT-R-DAAO grown at 37 °C was found to be 32 U/mL and increase 16-fold over cells
of BL21(DE3)/pET-DAAO grown at 28 °C. These results indicate the success of our approaches to overproducing DAAO in soluble
form in Escherichia coli. 相似文献
10.
Mishra A 《Applied biochemistry and biotechnology》2006,135(1):33-42
This article reports the production of high levels of l-asparaginase from a new isolate of Aspergillus niger in solid state fermentation (SSF) using agrowastes from three leguminous crops (bran of Cajanus cajan, Phaseolus mungo, and Glycine max). When used as the sole source for growth in SSF, bran of G. max showed maximum enzyme production followed by that of P. mungo and C. cajan. A 96-h fermentation time under aerobic condition with moisture content of 70%, 30 min of cooking time and 1205–1405 μ range
of particle size in SSF appeared optimal for enzyme production. Enzyme yield was maximum (40.9±3.35 U/g of dry substrate)
at pH 6.5 and temperature 30±2°C. The optimum temperature and pH for enzyme activity were 40°C and 6.5, respectively. The
study suggests that choosing an appropriate substrate when coupled with process level optimization improves enzyme production
markedly. Developing an asparaginase production process based on bran of G. max as a substrate in SSF is economically attractive as it is a cheap and readily available raw material in agriculture-based
countries. 相似文献