A series of chiral synthetic compounds is reported that shows intricate but specific
hierarchical assembly because of varying positions of coordination and hydrogen bonds …

Twists and turns in the hierarchical self-assembly pathways of a non-amphiphilic chiral
supramolecular material - Chemical Communications (RSC Publishing) DOI:10.1039/C2CC30789H …

The review summarizes published data on the methods for preparation of meso-
arylporphyrins with higher alkyl substituents. The methods for creation of self-organized …

The solvent driven aggregation of porphyrin derivatives, covalently linked to a L-or D-
prolinate enantiomer, results in the stereospecific formation of species featuring remarkable …

Two chiral porphyrin based ligands bearing, at their opposite meso positions, two appended
pyridyl or ethynylpyridyl units and chiral groups have been designed. For each ligand, both …

Supramolecular chirality is one of the most important issues in different branches of science
and technology, as stereoselective molecular recognition, catalysis, and sensors. In this …

The solvent‐driven aggregation of metalloporphyrin derivatives, bearing an L‐or D‐prolinate
appendage, results in the stereospecific formation of chiral species that are strictly …

Dichroic optical spectroscopies and theoretical modelling have been used to describe the
structure of aggregates of porphyrins in their gels in terms of:(i) the formation of helicoidal …

A chiral ZnII porphyrin derivative 1 and its achiral analogue 2 were studied in the solid state.
Considering the rich molecular recognition of designed metalloporphyrins 1 and 2 and their …

The supramolecular chirogenesis in porphyrin self-assembled architectures is a field of high
importance, with wide application in technology, material chemistry and medicine. In this …