Bistren cryptands and cryptates: versatile receptors for anion inclusion and recognition in water.

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.

Kinetic buffers.

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.

An automatic molecular dispenser of chloride.

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.