Inclusion of Polyphenol Oxidase Substrates in β-Cyclodextrin: A 1 H-NMR Study

A ¹H-NMR study of the interactionsbetween -cyclodextrin (-CD) and included phenolic molecules (chloragenic acid and caffeic acid ) in aqueous medium is reported. The results confirm that inclusion occurs. Data analysis by the continuous variation method shows that all the complexes have 1 : 1 stoichiometries. Values for the apparent association constants of the inclusion compounds are estimated and compared with previously reported values.     

Structural defects cause TiO2-based photocatalysts to be active in visible light

Oxidation of TiO or Ti2O3 led to the formation of TiO2 with activity in visible light much higher than when TiN was used as a precursor, pointing out the importance of oxygen defects/vacancies for extension of activity of TiO2 into the visible region.     

Mass spectrometric study of aliphatic alpha-carbonyl azides

A series of derivatives of 2-azidoacetic acid and 2-azidoacetone were synthesized and their behaviour under electron ionization conditions was investigated. This paper reports the electron ionization fragmentation mechanisms for five aliphatic alpha-carbonyl azides, which were clarified by accurate mass measurements and B/E linked scans. The substituent influences the abundance and the nature of the ions resulting from the molecular ion fragmentation.     

Selective recovery of solutes from ionic liquids by pervaporation--a novel approach for purification and green processing

Non-porous membranes with the selective layer consisting of hydrophilic or hydrophobic polymers have been applied for the quantitative and selective recovery of solutes with different physico-chemical properties from a room-temperature ionic liquid, ([bmim][PF6]).     

Automated molecule editing in molecular design

The ability to modify chemical structures in an automated and controlled manner is useful in molecular design. This Perspective introduces the MUDO molecule editor and shows how automated molecule editing can be used to standardize structures, enumerate tautomeric and ionization states, identify matched molecular pairs. Unlike its predecessor Leatherface, MUDO can also process 3D structures and this capability can be used to link non-covalently docked ligands to proteins.     

A contribution to the global formulation of the higher-order Poincaré-Cartan form

The global formulation of the higher-order Poincaré-Cartan form for Lagrangian field theories in the calculus of variations is re-examined in terms of the theory of lifts of tensor fields on a manifold to its higher-order prolongated jet bundles.Partially supported by CNPq, Brazil, Proc. MA 30.1115/79.     

Reaction of 3-methylindole and 2,3-dimethylindole with dimethyl acetylenedicarboxylate using boron trifluoride-diethyl ether catalysis

Reactions of dimethyl acetylenedicarboxylate with 3-methylindole and 2,3-dimethylindole under boron trifluoride-diethyl ether catalysis were carried out at low temperature (0–25°). Thermally unstable cyclobutenes were isolated, mainly in apolar solvents, which isomerized to benzazepines. The other compounds isolated were Michael adducts and dihydro-2-oxocarbazoles.     

Decay rates for Bresse system with arbitrary nonlinear localized damping

In this paper we consider a vibrating system of Bresse type, in a one-dimensional bounded domain with nonlinear localized damping mechanisms acting in all the three wave equations. We obtain some rates of decay for its solutions with no restrictions around the coefficients as well as the condition of equal-speed wave propagation. A new result concerning an internal observability for the conservative system was also proved in order to reach the asymptotics above.     

Thermal decomposition of the [Pt(NH3)4]2+ complex in NaX zeolite

The effect of the calcination procedure on the decomposition of the [Pt(NH₃)₄]²⁺ complex in a cesium-containing NaX zeolite was studied by thermal decomposition accompanied by mass spectrometry and diffuse reflectance spectroscopy, as well as electron paramagnetic resonance and infrared spectroscopy. The decomposition of the complex took place in two steps. Under oxygen, the [Pt(NH₃)₄]²⁺ complex was first converted into the [Pt(NH₃)₂]²⁺ complex in the first step, with predominant nitrogen release. In the second step, corresponding to the decomposition of the remaining two amine ligands, NO was also formed and adsorbed. Oxygen paramagnetic species were also observed. Under He, the decomposition also occurred in two steps with H₂ release.