Confusion is a novel concept of isomerism in porphyrin chemistry, delivering a steady
stream of new chemistry since the discovery of N-confused porphyrin, a porphyrin mutant, in …

1. INTRODUCTION Porphyrins (Ps) 1, 2 and their best known synthetic analogues, the
phthalocyanines (Pcs; 2− 10 Chart 1) represent one of the most widely studied macrocyclic …

Two-dimensionally extended, polycyclic heteroaromatic molecules (heterocyclic
nanographenes) are a highly versatile class of organic materials, applicable as functional …

This review underscores the conformational flexibility of porphyrinoids, a unique class of
functional molecules, starting from the smallest triphyrins (1.1. 1) via [18] porphyrins (1.1 …

The aromatic character of porphyrins, which has significant chemical and biological
consequences, can be substantially altered by judicious modifications of the parent ring …

The use of cyclic polyene perimeter-model approaches, such as Gouterman's four-orbital
model and Michl's perimeter model, to analyze trends in the electronic structures and optical …

This article introduces an overview of progressively developing chemistry of N-confused
porphyrin and related macrocycles. Study on confusion results in discovery of fusion and …

N-confused porphyrin (NCP) is a porphyrin isomer that is different largely from the parent
porphyrin, particularly in the physical, chemical, structural, and coordination properties …

Core alteration, affording heteroporphyrinoids and carbaporphyrinoids, allows for the
exploration of porphyrin-like or porphyrin-unlike coordination chemistry. Such a strategy has …

Four free-base corroles with electron-donating or electron-withdrawing groups on the para
or 2 through 6-positons of the meso phenyl rings were prepared via either Paolesse or …