ABSTRACT
Efficient enantiodiscrimination of some alanine-containing di- and tri-peptides by using chiral protonated bis(diamido)-bridged basket resorcin[4]arenes depends on several factors, including the basicity of the amino acid residues at the C- and N-termini of the peptide.
Subject(s)
Alanine/chemical synthesis , Calixarenes/chemistry , Diamide/chemistry , Peptides/chemical synthesis , Phenylalanine/analogs & derivatives , Alanine/chemistry , Kinetics , Molecular Conformation , Peptides/chemistry , Phenylalanine/chemistry , Protons , Quantum Theory , StereoisomerismABSTRACT
Infrared multiple-photon dissociation spectroscopy has been used to record vibrational spectra of charged copper-resveratrol complexes in the 3500-3700 cm(-1) and 1100-1900 cm(-1) regions. Minimum energy structures have been determined by density functional theory calculations using plane waves and pseudopotentials. In particular, the copper(I)-resveratrol complex presents a tetra-coordinated metal bound with two carbon atoms of the alkenyl moiety and two closest carbons of the adjoining resorcinol ring. For these geometries vibrational spectra have been calculated by using linear response theory. The good agreement between experimental and calculated IR spectra for the selected species confirms the overall reliability of the proposed geometries.
Subject(s)
Copper/chemistry , Quantum Theory , Stilbenes/chemistry , Models, Molecular , Molecular Conformation , Resveratrol , Spectrophotometry, InfraredABSTRACT
The protonation of cyclopropane by gaseous Brønsted acids of varying strength in radiolytic experiments at atmospheric pressure leads to two distinct C3H7- isomers that have been sampled by their reaction with benzene. The neutral end products, nC3H7-C6H5 and iC3H7-C6H5, arise from the electrophilic aromatic substitution reaction with the cC3H7+ and iC3H7+ ions, respectively. Their relative abundance was studied as a function of pressure, temperature, and the presence of additives in the gaseous systems; the results indicate a large extent of isomerization to the thermodynamically favored iC3H7+ from the protonation by strong acids. The presence of a kinetic barrier prevents any thermal isomerization from taking place in the time frame of 10(-8) s. In the peculiar case in which protonated benzene is the Brønsted acid, C3H7+ ions are formed in the presence of neutral benzene within the same ion - molecule complex. The ensuing reaction shows that cC3H7+ ions are formed exclusively and react in the 10(-10) s(-1) estimated lifetime of the complex. Still, such cC3H7+ ions undergo complete randomization of their hydrogen atoms; this points to a low kinetic barrier for the process. Agreement is found between the reported experimental results and updated computations of the relevant species in the C3H7+ potential energy surface.
ABSTRACT
The paper describes the analysis of nine sulfonamides, chosen as the most widely used representatives of an important class of antibacterial drugs. Atomic emission detection has been found to allow simultaneous quantification and identification of the N1-methylated derivatives, which are resolved efficiently by conventional capillary gas chromatography. Results are given concerning the linearity of the response and the characterization of the individual compounds by the elemental ratio of their carbon, nitrogen and sulfur content. The method looks promising for the quantitative analysis and confirmation of sulfonamide residues in complex mixtures.
