If (, M)is a factorization system on a category C, we define new classes of maps as follows: a map f:AB is in if each of its pullbacks lies in (that is, if it is stably in ), and is in M* if some pullback of it along an effective descent map lies in M(that is, if it is locally in M). We find necessary and sufficient conditions for (, M*) to be another factorization system, and show that a number of interesting factorization systems arise in this way. We further make the connexion with Galois theory, where M*is the class of coverings; and include self-contained modern accounts of factorization systems, descent theory, and Galois theory. 相似文献
Ozonation of adamantane adsorbed on silica gel produces visible chemiluminescence in the wavelength range of 400–650 nm. When the supply of O3 stops, chemiluminescence decays in a first order reaction with the effective rate constant k. Its dependence on the initial amount of adamantane and temperature has been studied. 相似文献
The repetitive discoloration kinetics of the azo-dye Methyl Orange (taken as a model organic compound) was followed under solar simulated radiation (90 mW/cm2) to assess the performance of the TiO2/Tedlar® composite photocatalyst. The influence of solution parameters on the photo-discoloration process: pH, dye concentration, applied light intensity and concentration of H2O2 were systematically investigated. During the photocatalysis a modification occurs in the TiO2/Tedlar® composite due to the TiO2 interaction with the Tedlar® film. Physical insight is given for the stabilization mechanism of the TiO2 particles in the Tedlar matrix based on the data obtained by X-ray photoelectron spectroscopy (XPS). The F 1s peak of the Tedlar film indicates that the TiO2 is loaded on the Tedlar fluoro-groups. The loading of TiO2 on the 75 μm thick Tedlar® film was 0.9% (w/w) as determined by atomic absorption spectrophotometry (AAS). Attenuated total reflection infrared spectroscopy (ATRIR) shows no formation of additional bands within the photodiscoloration reaction. This shows that an efficient catalysis taking place on the TiO2/Tedlar® surface. The rugosity (mean square roughness, rms) of the TiO2/Tedlar® film was determined by atomic force microscopy (AFM) to be 19.7 nm. This value remained constant during long-term operation. Transmission electron microscopy (TEM) reports the thickness and coverage of TiO2 Degussa P-25 on the Tedlar® surface before and after photocatalysis. 相似文献
Three new derivatives of 2,6-diacyldiaminopyridine are reported. NMR shift titrations were performed in CDCl3 with barbiturates. The diamide1 affords a greater complexation energy (–13.00 kJ mol–1) with bemegride than the dithioamide2 (–9.15 kJ mol–1). This result, unexpected on the basis of the proton acidities, is explained by the great torsion energy induced in2 by the bulky sulfur atom. Compounds3 and4 present unusual four and five H-bond features with barbital and relatively weak complexation energies (–9.53 and –16.34 kJ mol–1, respectively). Molecular mechanics indicates that ligand4 displays a helical secondary structure which is disrupted by complexation. Calculations of the H-bond energies (Ecalc.) of the intermolecular assemblies with barbital or phenobarbital and other host-guest complexes given in the literature give a good correlation (r=0.98) with experimental values: Ecalc.=1.07 Ga–42.0. Limitations of this relation are discussed. 相似文献
The title compounds are prepared via Gabriel-synthesis following known or improved procedures. Novel methods using 31P{1H}-NMR controlled titrations of aminomethylphosphine oxides lead to dissociation constants (given as basicity or acidity constants resp.) and to stability constants. Dynamically averaged and ion specific chemical shifts δP were derived. 相似文献
The synthesis of the new host molecule1b is described. Its complexation properties towards 1,8-ANS as a guest are reported. Compared to the monomacrocyclic host molecules2c and2e, the complex stabilities of1b with ANS as a guest are particularly higher, suggesting that the macrobicyclic host forms a better fitting niche to allow the nestling of guest molecules in solution. 相似文献
The concept of virtual potential (employed here in modelling operations), a unique experimental setup designed and built in our laboratories, and new regression equations derived for nonlinear fitting of quasi‐reversible direct‐current polarograms were combined with the existing rigorous treatment and refinement of polarographic data to establish reliable metal/ligand models and accurate stability constants for the lead(II)/glycine/OH? and lead(II)/sarcosine/OH? systems (sarcosine = N‐methylglycine). In the case of glycine, the complexes [M(HL)], [ML], [ML2], and [ML3] were identified, and their stability constants (as log β) were established to be 10.51 ± 0.06, 4.58 ± 0.02, 7.19 ± 0.10, and 9.27 ± 0.02, respectively, the complex [ML3] being reported here for the first time (Table 2). The system with sarcosine involving [M(HL)], [ML], [ML2], [ML3], and [ML2(OH)2], with the stability constants (as log β) 11.01 ± 0.04, 4.18 ± 0.03, 7.23 ± 0.03, 9.1 ± 0.3, and 15.97 ± 0.07, respectively, is reported for the first time (Table 3). The log K1 value for PbII with sarcosine is a fraction of a log unit smaller when compared with the PbII complex with glycine, in agreement with the literature data for CuII, NiII, and ZnII showing the same trend for these two ligands. The proposed nonlinear curve‐fitting operations expand the applicability of polarography to study reliably and conveniently quasi‐reversible, on the polarographic time scale, metal/ligand systems (systems with involved heterogeneous kinetics). 相似文献
The influence of [(2-hydroxy-1,1-bis(hydroxymethyl)ethyl)amino]-1-propanesulfonic acid (TAPS) on solutions containing lead(II) was studied by direct current polarography (DCP) and glass electrode potentiometry (GEP). The readings were taken at fixed total TAPS to total lead(II) concentration ratios and various pH values, at 25.0 ± 0.1 °C and ionic strength 0.1 M KNO3.Due to the basic pKa of the ligand, which occurs in the pH range where large amount of lead polynuclear species are formed, and the occurrence of ligand adsorption, that disabled the use of high concentrations of TAPS on DCP experiments, GEP and DCP experimental conditions were put to the limit in order to provide the correct Pb-TAPS-OH model and reliable stability constants.The proposed final model is: PbL, PbL2, PbL2(OH) and PbL2(OH)2 with overall stability constants values, as log β, 3.27 ± 0.06, 6.5 ± 0.1, 12.7 ± 0.1 and 17.27 ± 0.06, respectively.A comparative analysis of the strength of complexation of TAPS and a structural related buffer, 2-hydroxy-3-[tris(hydroxymethyl)methylamino]-1-propanesulfonic acid (TAPSO), with lead is also discussed. 相似文献
Thermogravimetric analyses of diclofenac sodium, its Ca2+ and Fe3+ complexes manifested a decreasing trend of the onset decomposition temperatures at which these compounds dissociated. The drop in the temperature was metal ion dependent; the sodium salt showed thermal stability up to 245 °C, whereas the complexes started their degradation processes at temperatures starting from 90 °C. While G* for the cleavage of the acetate moiety in the sodium salt was 63.76 kJmol−1, it was 82.06 and 140.57 kJmol−1 in the cases of Ca2+ and Fe3+, respectively. However, their complete fusion took place at 187.65, 150.34 and 98.77 °C, respectively, displaying a reversed trend which is probably indicative of some catalytic part on the binding metals.
Using the Gaussian 98W package of programs, ab initio molecular orbital treatments were applied to diclofenac and its Ca2+ and Fe3+ metal complexes to study their electronic structure at the atomic level. The thermochemistry of diclofenac sodium was followed through the TG fragmentation peak temperatures using the density functional theory calculations at the 6-31G(d) basis set level. The FT-IR data were in good agreement with the theoretically calculated values.
Single point calculations at the B3LYP/ 6-311G(d) level of theory, were used to compare the geometric features, energies and dipole moments of these compounds to detect the effect of the binding metal ions on the thermal dissociation of their diclofenac complexes. 相似文献