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Bistren cryptands can be easily synthesised through the Schiff base condensation of two molecules of tren and three molecules of a dialdehyde, followed by hydrogenation of the six C=N double bonds to give octamine cages, whose ellipsoidal cavity can be varied at will, by choosing the appropriate dialdehyde, in order to include substrates of varying sizes and shapes. Bistrens can operate as effective anion receptors in two ways: (i) in their protonated form, providing six secondary ammonium groups capable of establishing hydrogen bonding interactions with the anion; (ii) as dicopper(II) cryptates, in which the two coordinatively unsaturated metal centres can be bridged by an ambidentate anion. Representative examples of the two approaches, as well as the design of an anion molecular dispenser, in which a dicopper(II) bistren cryptate acts as a bottle will be illustrated.

This paper proposes a new type of molecular device that is able to act as an inverse proton sponge to slowly decrease the pH inside a reaction vessel. This makes the automatic monitoring of the concentration of pH-sensitive systems possible. The device is a composite formed of an alkyl chloride, which kinetically produces acidity, and a buffer that thermodynamically modulates the variation in pH value. Profiles of pH versus time (pH-t plots) have been generated under various experimental conditions by computer simulation, and the device has been tested by carrying out automatic spectrophotometric titrations, without using an autoburette. To underline the wide variety of possible applications, this new system has been used to realize and monitor HCl uptake by a di-copper(II) bistren complex in a single run, in a completely automatic experiment., (© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The combined activity of the 1.1.1-cryptand and of a dicopper(II) bistren cryptate complex including chloride makes the Cl(-) ion be continuously and slowly delivered to the solution, without any external intervention. The 1.1.1-cryptand slowly releases OH(-) ions, according to a defined kinetics, and each OH(-) ion displaces a Cl(-) ion from the cryptate. Chloride displacement induces a sharp colour change from bright yellow to aquamarine and can be conveniently monitored spectrophotometrically, even in diluted solutions. The 1.1.1-cryptand is the motor of a molecular dispenser (the dicopper(II) cryptate) delivering chloride ion automatically, from the inside of the solution., (Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Variable-parameter kinetic experiments were carried out using HPLC as analytical instrument. The hydrolysis of aspirin was followed both at variable-temperature and at variable-pH conditions. The peak areas relative to salicylic acid were processed by direct fit to a mathematical model and/or by differential method obtaining, by single experiments, the values of the apparent rate constant in the whole range of temperature and pH studied. The results, although the discontinuity of this kind of analysis, are in agreement with those obtained by constant-parameter kinetics but saving experimental time.

The dependence of the pseudo-first-order rate constant on the ionic strength for the alkaline hydrolysis of indomethacin has been obtained, for the first time, in a single kinetic experiment carried out by varying with time the salt concentration inside the reaction vessel. The kinetic profile obtained was processed using as a mathematical model the variable-parameter kinetic equation containing the Bronsted-Bjerrum equation as the dependence function. The results are in good agreement with those obtained by the traditional method but the experimental time is reduced to about one-tenth., (Copyright 2003 Wiley-Liss, Inc.)

In this paper a new non isothermic method for the determination of the release drug rate constant (k) from a transdermal delivery system is proposed. The new method was applied to transdermal patches Trans-Ver-Sal. The results obtained prove to be able to release salicylic acid of transdermal system and the effectiveness of the new method propose.

The pseudo-first order rate constant for the hydrolysis of rolitetracycline as a function of temperature was obtained by performing variable-temperature kinetic experiments. The results are in agreement with those obtained at constant-parameter kinetics but saving experimental time and chemicals.

The racemization of (-)-adrenaline was followed by polarimetric variable-temperature kinetic experiments obtaining activation parameters and k(obs)(T) profile in one tenth of the time usually spent for traditional kinetic runs. A polarimeter connected to a computer for the acquisition and processing of the analytical data was used. The kinetic profiles were processed by both an integral method and a differential method. The results are in good agreement with each other and with those obtained by constant-temperature kinetics.

The complete pH-rate profile of the hydrolysis reaction of aspirin, requiring many experiments in the past, was obtained by a single variable-parameter kinetic experiment carried out by varying the hydrogen ion concentration. The experiment was carried out spectrophotometrically, reading automatically absorbance, pH, and temperature inside the reaction vessel. The results obtained by the fast processing of the kinetic profile are identical to those obtained under the same conditions but using traditional constant-pH kinetic runs. This method provides the possibility of reducing the amount of time and chemicals usually spent in collecting kinetic data in such mechanistic studies by nearly two orders of magnitude.

Complexes of the type cis-[PtL(2)Me(2)] (1-14) (L = an extended series of phosphines of widely different steric and electronic properties) were synthesized, characterized, and used as precursors for the formation of cis-monoalkylplatinum(II) solvento species in methanol. The cleavage of the first platinum-alkyl bond by protonolysis is a fast process, but the subsequent cis to trans isomerization of the cationic solvento species [PtL(2)(Me)(MeOH)](+) is relatively slow and it can be( )()monitored using (31)P NMR or conventional spectrophotometry. A large collection of (1)H and (31)P NMR data for cis-[PtL(2)Me(2)], cis-[PtL(2)Me(MeOH)](+), and trans-[PtL(2)Me(MeOH)](+) complexes showed interesting dependencies upon the size, the sigma-donor capacity, and the mutual position of the phosphines in the coordination sphere of the metal. The rate constants for isomerization of cis-[PtL(2)Me(MeOH)](+) were resolved quantitatively into steric and electronic contributions of the phosphine ligands, by means of correlations with parameters which reflect their sigma-donor ability (chi values) and steric requirements (Tolman's cone angles, theta). The electronic and steric profiles obtained for these reactions are discussed within the framework of a mechanism which involves dissociative loss of the solvent molecule and interconversion of two geometrically distinct 3-coordinate T-shaped 14-electron intermediates. The factors controlling the stability of these coordinatively unsaturated species are discussed. The electronic and steric influences of phosphines as "spectator" ligands in a dissociative process are compared with those shown by these ligands when used as nucleophiles in associative substitution processes. The activation parameters DeltaH() and DeltaS() were measured using both conventional isothermal and non-isothermal spectrophotometric kinetics.

Pseudo-first-order rate constants for the hydrolysis of acetylsalicylic acid as a function of temperature have been obtained by variable-temperature kinetic experiments. A method, based on a generalization of non-isothermal analysis, has been used that takes advantage of the capabilities of modern data collection and processing systems. Both spectrophotometric and, for the first time under non-isothermal conditions, fluorometric measurements have been carried out. The results obtained are identical to those obtained under the same conditions but using traditional constant-temperature kinetic runs. This provides the possibility of reducing the amounts of time and chemicals usually spent in collecting kinetic data in mechanistic studies in solution by an order of magnitude.