The condensation of aromatic dialdehydes with chiral diamines, such as 1, 2-trans-
diaminocyclohexane, leads to various enantiopure or meso-type macrocyclic Schiff bases …

Macrocyclic nitrogen-containing compounds are versatile molecules. Supramolecular,
noncovalent interactions of these macrocycles with guest molecules enables them to act as …

Here we introduce for the first time a metal-free trianglamine-based supramolecular organic
framework, T-SOF-1, with permanent intrinsic porosity and high affinity to CO2. The …

A chiral pillar [3] trianglimine (C60H72N6O6) with a deep cavity has been developed as a
chiral selector and bonded to thiolated silica by thiol‐ene click reaction to fabricate a novel …

A unique combination of structural flexibility, shape persistency and functionality, makes
macrocycles and molecular cages as essential molecular entities that have displayed …

A novel highly fluorinated dialdehyde was prepared by a two-stage synthesis. This reactive
building block for dynamic imine chemistry was used in a condensation reaction to generate …

2, 2′-Bipyridyl (bpy) is widely used as a chelating unit for metal complexation but is not
usually considered as a hydrogen-bonding unit. This is because the metal-free bpy units are …

Chiral isotrianglimines were synthesized by the [3+ 3] cyclocondensation of (R, R)-1, 2-
diaminocyclohexane with C5-substituted isophthalaldehyde derivatives. The substituent's …

The chiral, triangular‐shape hexaimine macrocycles (trianglimines), bearing bulky alkynyl or
aryl substituents were synthesized and studied by means of experimental and theoretical …

The introduction of urea or thiourea functionality to the macrocycle skeleton represents an
alternative way to control conformational dynamics of chiral, polyamines of a figure-shaped …