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51.
The synthesis of a new series of 5‐oxy‐pyrido[2,3‐b]quinoxaline‐9‐carboxamides 4a‐i and N1,N2‐Bis(5‐oxy‐pyrido[2,3‐b]quinoxaline‐9‐benzoyl)ethylenediamine ( 5 ) is reported starting from 2‐chloro‐3‐nitropyri‐dine. Fundamental steps of the synthetic pathway are i) preparation of 2‐(3‐nitro‐pyridin‐2‐ylamino)benzoic acid ( 1 ) via copper‐catalyzed condensation of 2‐chloro‐3‐nitropyridine with o‐anthranilic acid, ii) intramolecular cyclization of the acid 1 to 5‐oxy‐pyrido[2,3‐b]quinoxaline‐9‐carboxylic acid ( 2b ) upon treatment with concentrated sulfuric acid and oleum and iii) conversion of the acid 2 to the desired amides 4a‐i and 5 . Compounds 4a‐i and 5 are oxygenated azaanalogs of phenazines, a wellknown series of intercalators with cytotoxic activity. 相似文献
52.
Georgia Ch. Lainioti John Kapolos Lambros Farmakis Athanasia Koliadima George Karaiskakis 《Chromatographia》2010,72(11-12):1149-1156
Reversed flow gas chromatography (RFGC) was applied for the kinetic study of the alcoholic fermentation processes conducted with cells of the alcohol-resistant and psychrophilic Saccharomyces cerevisiae AXAZ-1 yeast strain, either free or immobilized on wheat, barley and corn grains as well as on potato pieces. Repeated alcoholic fermentations with must of varying initial glucose concentrations were performed in order to estimate the catalytic efficiency of the biocatalysts used in the present study. With the RFGC method, the distinction of the duration of alcoholic fermentation phases was achieved, which may be correlated to the phases of AXAZ-1 cells growth cycle. The rate constants of ethanol production for each phase of the alcoholic fermentations, conducted with free and immobilized cells, were also determined with the aid of RFGC, confirming the predominance of the immobilized against free cells in the fermentation process. Comparing the supports used for immobilization, wheat and barley grains seemed to be more efficient than corn grains and potato pieces, as they provided a higher number of immobilized cells and rate constant values. 相似文献
53.
Aristeidis E. Niotis Christos Mastichiadis Panagiota S. Petrou Ion Christofidis Sotirios E. Kakabakos Athanasia Siafaka-Kapadai Konstantinos Misiakos 《Analytical and bioanalytical chemistry》2010,396(3):1187-1196
The early diagnosis of acute myocardial infarction requires the determination of several markers in serum shortly after its
incidence. The markers most widely employed are the isoenzyme MB of creatine kinase (CK-MB) and the cardiac troponin I (cTnI).
In the present work, a capillary waveguide fluoroimmunosensor for fast and highly sensitive simultaneous determination of
these markers in serum samples is demonstrated. The dual-analyte immunosensor was realized using glass capillaries internally
modified with an ultrathin poly(dimethylsiloxane) film by creating discrete bands of analyte-specific antibodies. The capillary
was then filled with a mixture of sample and biotinylated detection antibodies followed by reaction with streptavidin–horseradish
peroxidase and incubation with a fluorescently labeled tyramide derivative to accumulate fluorescent labels onto immunoreaction
bands. Upon scanning the capillary with a laser beam, part of the emitted fluorescence is trapped and waveguided through the
capillary wall to a photomultiplier placed on one of its ends. The employment of tyramide signal amplification provided detection
limits of 0.2 and 0.5 ng/mL for cTnI and CK-MB, respectively, in a total assay time of 30 min compared to 0.8 and 0.6 ng/mL
obtained for the corresponding assays when the conventional fluorescent label R-phycoerythrin was used in a 65-min assay.
In addition, the proposed immunosensor provided accurate and repeatable measurements (intra-assay and interassay coefficients
of variation lower than 10%), and the values determined in serum samples were in good agreement with those obtained with commercially
available enzyme immunoassays. Thus, the proposed capillary waveguide fluoroimmunosensor has all the required characteristics
for fast and reliable diagnosis of acute myocardial infarction.
相似文献
54.
Dervisi A Koursarou D Ooi LL Horton PN Hursthouse MB 《Dalton transactions (Cambridge, England : 2003)》2006,(48):5717-5724
The synthesis of the benzyl phosphinothioether derivatives Ph(2)PCH(2)CH(Et)SR and their corresponding palladium complexes are reported, where R = CH(2)Ph, R = CH(2)-3,5-Me-C(6)H(3) and R = 1-CH(2)C(10)H(7)(5). Crystallographic data obtained for the complexes Pd(3)Cl(2) and Pd(4)Cl(2) show intra- and inter-molecular pi-pi interactions between the aromatic rings on the P and S substituents, and NOE experiments for Pd(4)Cl(2) show that these interactions persist in solution. The performance of the phosphinothioether palladium complexes in aryl-aryl cross-coupling reactions is compared with that of the corresponding complex of the parent phosphinothiolato ligand Ph(2)PCH(2)CH(Et)S(-)(1). High turnover numbers up to 2000000 are reported for the coupling of bromobenzene, using the palladium dimer [Pd(1)I](2) as the catalyst precursor. Kinetic studies show a linear dependence of the reaction on catalyst loading. The effect of other variables on the cross-coupling reaction, such as temperature, solvent and base, is also reported. 相似文献
55.
van der Waals forces are one of several forces that control the adhesion between two materials. These forces are important to quantify in adhesion studies because they are always present and are always attractive. The major problem in calculating the van der Waals interaction between colloidal particles is that of evaluating the Hamaker constant. Hence, an accurately determined Hamaker constant for a given material is needed when interfacial phenomena such as adhesion are discussed in terms of the total potential energy between a particle and a substrate. In this paper, a new simple and accurate methodology for the estimation of the Hamaker constant is introduced. The results are in good agreement with those values found in literature. 相似文献
56.
Reaction of [(Me3Si)2CH]2Al? CH2? Al [CH(SiMe3)2]2 with Neopentyllithium: Formation of {[(Me3Si)2CH]2Al? CH2? Al [CH(SiMe3)2]2CH2CMe3} ? [Li(TMEDA)2]⊕ The recently synthesized methylene bridged dialuminium compound [(Me3Si)2CH]2Al? CH2? Al [CH(SiMe3)2]2 reacts with neopentyl lithium in the presence of TMEDA to give the stable {[(Me3Si)2CH]2Al? CH2? Al [CH(SiMe3)2]2CH2 · CMe3}? [Li(TMEDA)2]⊕ decomposing at 115°C. The aluminium atoms therein are not additionally bridged, but the new substituent is occupying a terminal position as detected by crystal structure determination. A compound is formed containing a saturated, fourfold coordinated neighbouring a formally unsaturated, threefold coordinated aluminium atom. Due to high sterical restrictions the Al? C bonds are lengthened up to 209.0(3) pm at the alanate site and the Al? C? Al angle in the methylene bridge is extraordinarily enlarged to 144.4(2)°. 相似文献
57.
58.
The total conversion coefficient of the lowest excited state in73Ge has been measured to be αtot=1310±60, which is close to the theoretically predicted value 1080 of Hager and Seltzer for a pureE2 transition. The energy of the γ-line is (13.34±0.04) keV. A calculation, based on the experimental data, shows that the Mössbauer effect on this level is measurable. 相似文献
59.
Andersen NK Døssing H Jensen F Vester B Nielsen P 《The Journal of organic chemistry》2011,76(15):6177-6187
5-(1-Phenyl-1,2,3-triazol-4-yl)-2'-deoxycytidine was synthesized from a modified CuAAC protocol and incorporated into mixed pyrimidine oligonucleotide sequences together with the corresponding 5-(1-phenyl-1,2,3-triazol-4-yl)-2'-deoxyuridine. With consecutive incorporations of the two modified nucleosides, improved duplex formation with a complementary RNA and improved triplex formation with a complementary DNA duplex were observed. The improvement is due to π-π stacking of the phenyl-triazole moieties in the major groove. The strongest stacking and most pronounced positive influence on thermal stability was found in between the uridine analogues or with the cytidine analogue placed in the 3' direction to the uridine analogue. Modeling indicated a different orientation of the phenyl-triazole moieties in the major groove to account for the difference between the two nucleotides. The modified oligonucleotides were all found to be significantly stabilized toward nucleolytic degration. 相似文献
60.
Elisa Biasin Tim B. van Driel Gianluca Levi Mads G. Laursen Asmus O. Dohn Asbjørn Moltke Peter Vester Frederik B. K. Hansen Kasper S. Kjaer Tobias Harlang Robert Hartsock Morten Christensen Kelly J. Gaffney Niels E. Henriksen Klaus B. Møller Kristoffer Haldrup Martin M. Nielsen 《Journal of synchrotron radiation》2018,25(2):306-315
Time‐resolved X‐ray scattering patterns from photoexcited molecules in solution are in many cases anisotropic at the ultrafast time scales accessible at X‐ray free‐electron lasers (XFELs). This anisotropy arises from the interaction of a linearly polarized UV–Vis pump laser pulse with the sample, which induces anisotropic structural changes that can be captured by femtosecond X‐ray pulses. In this work, a method for quantitative analysis of the anisotropic scattering signal arising from an ensemble of molecules is described, and it is demonstrated how its use can enhance the structural sensitivity of the time‐resolved X‐ray scattering experiment. This method is applied on time‐resolved X‐ray scattering patterns measured upon photoexcitation of a solvated di‐platinum complex at an XFEL, and the key parameters involved are explored. It is shown that a combined analysis of the anisotropic and isotropic difference scattering signals in this experiment allows a more precise determination of the main photoinduced structural change in the solute, i.e. the change in Pt—Pt bond length, and yields more information on the excitation channels than the analysis of the isotropic scattering only. Finally, it is discussed how the anisotropic transient response of the solvent can enable the determination of key experimental parameters such as the instrument response function. 相似文献