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 residue is a good choice in this context since its conformational rigidity allows for porphyrin assembling where molecular chirality is efficiently transferred and amplified using properly honed aqueous environments. Herein, we describe the evolution of the studies carried out by our group to achieve chiral systems from some porphyrin-proline derivatives, both in solution and in the solid state. The discussion focuses on some fundamental aspects reflecting on the final molecular architectures obtained, which are related to the nature of the appended group (stereochem...
An overview of the solvent-driven aggregation of a series of chiral porphyrin derivatives studied by...
An easy and fast method to achieve chiral porphyrin films on glass is herein reported. The on-surfac...
An easy and fast method to achieve chiral porphyrin films on glass is herein reported. The on-surfac...
Conjugating the porphyrin ring with an amino acid via amide linkage represents a straightforward way...
The solvent driven aggregation of porphyrin derivatives, covalently linked to a L- or D-prolinate e...
Supramolecular chirality is one of the most important issues in different branches of science and te...
A porphyrin derivative functionalized with the L-enantiomer of proline amino acid was characterized ...
A porphyrin derivative functionalized with the L-enantiomer of proline amino acid was characterized ...
An overview of the solvent-driven aggregation of a series of chiral porphyrin derivatives studied by...
An easy and fast method to achieve chiral porphyrin films on glass is herein reported. The on-surfac...
An easy and fast method to achieve chiral porphyrin films on glass is herein reported. The on-surfac...
Conjugating the porphyrin ring with an amino acid via amide linkage represents a straightforward way...
The solvent driven aggregation of porphyrin derivatives, covalently linked to a L- or D-prolinate e...
Supramolecular chirality is one of the most important issues in different branches of science and te...
A porphyrin derivative functionalized with the L-enantiomer of proline amino acid was characterized ...
A porphyrin derivative functionalized with the L-enantiomer of proline amino acid was characterized ...
An overview of the solvent-driven aggregation of a series of chiral porphyrin derivatives studied by...
An easy and fast method to achieve chiral porphyrin films on glass is herein reported. The on-surfac...
An easy and fast method to achieve chiral porphyrin films on glass is herein reported. The on-surfac...