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81.
Kaname SasakiHideyuki Nagai Shuichi MatsumuraKazunobu Toshima 《Tetrahedron letters》2003,44(30):5605-5608
The glycosidations of glucopyranosyl diethyl phosphite and alcohols using an ionic liquid, 1-n-hexyl-3-methylimidazolium trifluoromethanesulfonimidide (C6mim[NTf2]) containing a protic acid, trifluoromethanesulfonimide (HNTf2), as a novel solvent-catalyst system, effectively proceeded under mild conditions to give the corresponding glycosides in good to high yields. Furthermore, this acid-ionic liquid combination could be reused many times for the glycosidations without any loss in efficiency. 相似文献
82.
Brian H. Davison Nhuan P. Nghiem Gerald L. Richardson 《Applied biochemistry and biotechnology》2004,114(1-3):653-669
More than 25 sorbents were tested for uptake of succinic acid from aqueous solutions. The best resins were then tested for
successive loading and regeneration using hotwater. The key desired properties for an ideal sorbent are high capacity, complete
stable regenerability, and specificity for the product. The best resins have a stable capacity of about 0.06 g of succinic
acid/g of resin at moderate concentrations (1–5 g/L) of succinic acid. Several sorbents were tested more exhaustively for
uptake of succinic acid and for successive loading and regeneration using hot water. One resin, XUS 40285, has a good stable
isotherm capacity, prefers succinate over glucose, and has good capacities at both acidic and neutral pH. Succinic acid was
removed from simulated media containing salts, succinic acid, acetic acid, and sugar using a packed column of sorbent resin,
XUS 40285. The fermentation byproduct, acetate, was completely separated from succinate. A simple hot water regeneration successfully
concentrated succinate from 10 g/L (inlet) to 40–110 g/L in the effluent. If successful, this would lower separation costs
by reducing the need for chemicals for the initial purification step. Despie promising initial results of good capacity (0.06
g of succinic/g of sorbent), 70% recovery using hot water, and a recovered concentration of >100 g/L, this regeneration was
not stable over 10 cycles in the column. Alternative regeneration schemes using acid and base were examined. Two (XUS 40285
and XFS-40422) showed both good stable capacities for succinic acid over 10 cycles and >95% recovery in a batch operation
using a modified extraction procedure combining acid and hot water washes. These resins showed comparable results with actual
broth. 相似文献
83.
84.
Huseyin Bekir Yildiz Jaime Castillo Dmitrii A. Guschin Levent Toppare Wolfgang Schuhmann 《Mikrochimica acta》2007,159(1-2):27-34
An amperometric biosensor for the detection of phenolic compounds was developed based on the immobilization of tyrosinase
within an Os-complex functionalized electrodeposition polymer. Integration of tyrosinase within the redox polymer assures
efficient catechol recycling between the enzyme and the polymer bound redox sites. The non-manual immobilization procedure
improves the reproducibility of fabrication process, greatly reduces the desorption of the enzyme from the immobilization
layer, and, most importantly prevents fast inactivation of the enzyme by its substrate due to fast redox cycling.
A two-layer sensor architecture was developed involving ascorbic acid oxidase entrapped within an electrodeposition polymer
in a second layer on top of the redox polymer/tyrosinase layer. Using this sensor architecture it was possible to eliminate
the current interference arising from direct ascorbate oxidation up to a concentration of 630 μM ascorbic acid. The effects
of the polymer thickness, the enzyme/polymer ratio, and the applied potential were evaluated with respect to optimal sensor
properties. The sensitivity of the optimized sensors for catechol was 6.1 nA μM−1 with a detection limit of 10 nM, and for phenol 0.15 nA μM−1 with a detection limit of 100 nM. 相似文献
85.
Peng Ping Wenshou Wang Xuesi Chen Xiabin Jing 《Journal of Polymer Science.Polymer Physics》2007,45(5):557-570
Poly(ε‐caprolactone)‐based segmented polyurethanes (PCLUs) were prepared from poly(ε‐caprolactone) diol, diisocyanates (DI), and 1,4‐butanediol. The DIs used were 4,4′‐diphenylmethane diisocyanate (MDI), 2,4‐toluenediisocyanate (TDI), isophorone diisocyanate (IPDI), and hexamethylene diisocyanate (HDI). Differential scanning calorimetry, small‐angle X‐ray scattering, and dynamic mechanical analysis were employed to characterize the two‐phase structures of all PCLUs. It was found that HDI‐ and MDI‐based PCLUs had higher degree of microphase separation than did IPDI‐ and TDI‐based PCLUs, which was primarily due to the crystallization of HDI‐ and MDI‐based hard‐segments. As a result, the HDI‐based PCLU exhibited the highest recovery force up to 6 MPa and slowest stress relaxation with increasing temperature. Besides, it was found that the partial damage in hard‐segment domains during the sample deformation was responsible for the incomplete shape‐recovery of PCLUs after the first deformation, but the damage did not develop during the subsequent deformation. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 557–570, 2007 相似文献
86.
A liquid chromatography-mass spectrometry method for the determination of the coccidiostats metronidazole, ronidazole, dimetridazole,
secnidazole, tinidazole and ipronidazole in feedstuff was developed. The 5-nitroimidazoles were extracted from animal feed
with a pH 2 phosphate buffer solution followed by a solid phase extraction procedure based on HLB cartridges. The liquid chromatographic
separation of the extracts was performed on a C18 bonded silica column applying a gradient of elution with pH 4.3 ammonium acetate buffer solution and acetonitrile. Quantification
for each 5-nitroimidazole was carried out monitoring its molecular ion [M + H]+ obtained by positive electrospray ionisation mode. A pool of feedstuffs was used to optimise and validate the method. Linearity,
quantification limit, intra-day and inter-day reproducibility and accuracy were estimated using this pool of feedstuffs spiked
with the drugs. For the confirmatory assay, several fragment ions from each 5-nitroimidazole were obtained and monitored.
The method was applied successfully to determine 5-nitroimidazoles in feedstuff at level of 0.05 mg kg−1. 相似文献
87.
Efficient synthesis of ferrocenylenones using a Friedel-Crafts acylation reaction is described. Acryloyl, methacryloyl, crotonoyl, cinnamoyl, and β-methylcrotonoyl chlorides react with ferrocene in the presence of a Lewis acid (EtAlCl2 or EtAlCl2-Me3Al) to give the corresponding ferrocenylenones (acryloyl, methacryloyl, crotonoyl, cinnamoyl, and methylcrotonoylferrocenes) in good isolated yields. Besides ferrocenylenones, chloroactylferrocene is also synthesised by this method. 相似文献
88.
Diethoxyphosphinyl acetic acid hydrazide is a unique reagent that provides a convenient and efficient process to prepare fused [5,5]-, [5,6]-, and [5,7]-3-[(E)-2-(arylvinyl)]-1,2,4-triazoles from aldehydes and alkoxyimines. The process involves three steps without isolation of any intermediates to afford 1,2,4-triazoles in modest to excellent overall yield. 相似文献
89.
K. Popov-Pergal L. Cuckovic M. Rancic M. Pergal D. Djokovic 《Chemistry of Heterocyclic Compounds》2003,39(8):1090-1093
A series of methyl 2-(arylidene-2,4-dioxotetrahydrothiazol-3-yl)propionates were prepared. A study of the 3D structure was performed. The log P values are given for all the synthesized compounds. 相似文献
90.