Chirality is a special phenomenon exhibited by two compounds with non-superimposing
mirror images of each other. Chiral enantiomers have the same composition and similar …

Chiral substances occur naturally in abiotic and living systems. The recognition and
detection of chiral substances in the natural environment or their analysis and detection in …

The interaction of an equilibrium mixture of monomeric and aggregated cationic trans-5, 15-
bis (N-methylpyridinium-4-yl)-10, 15-bis-diphenylporphine (t-H2Pagg) chloride salt with …

A rationalization for the chirality transfer mechanism in the supramolecular host–guest
assemblies of an achiral Zn (II) porphyrin dimer (host) and a series of chiral diamines and …

Conjugating the porphyrin ring with an amino acid via amide linkage represents a
straightforward way for conferring both amphiphilicity and chirality to the macrocycle. Proline …

The development of nanotools for chemical sensing and macromolecular modifications is a
new challenge in the biomedical field, with emphasis on artificial peptidases designed to …

In recent years, supramolecular chirality has been greatly developed in asymmetric
synthesis, chiral sensing and other research fields, but its application in molecular chiral …

Heliphyrin, a new porphyrinoid with a helicene-type structure, can be produced in two steps
from commercially available reagents. Three macrocycle–like structures were produced via …

A highly flexible pyrrole-bridged Zn (II) porphyrin dimer has been successfully utilized as an
efficient host which enables an accurate determination of the absolute configuration directly …

An efficient strategy for high‐performance chiral materials is to design and synthesize host
molecules with left‐and right‐(M‐and P‐) twisted conformations and to control their twisted …