Related Experiment Video
Updated: May 28, 2025

Synthesis of pH Dependent Pyrazole, Imidazole, and Isoindolone Dipyrrinone Fluorophores using a Claisen-Schmidt Condensation Approach
Published on: June 10, 2021
Panchromatic PAH-Porphyrin Hybrids with a Step-Wise Increasing π-System
Christoph Oleszak1, Christian L Ritterhoff2, Bernd Meyer2
1Department of Chemistry and Pharmacyhsch &, Interdisciplinary Center for Molecular Materials (ICMM), Chair of Organic Chemistry II, Friedrich-Alexander-University Erlangen-Nürnberg, Nikolaus-Fiebiger-Str. 10, 91058, Erlangen, Germany.
Abstract:
The rational synthesis of three β-meso-fused porphyrins with a step-wise increasing π-system size is presented. The synthetic route, which introduces a five-membered ring between the macrocycle and an aromatic fragment, is modular in its nature and proceeds straightforwardly. The well-soluble conjugates have intriguing optical properties, namely bathochromically shifted and flattened absorption curves. Density functional theory (DFT) calculations provide insights into the electronic structure and transitions, unveiling small HOMO-LUMO gaps.
Related Concept Videos
¹H NMR: Pople Notation
A proton...
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Five-Membered Heterocyclic Aromatic Compounds: Overview
The Antenna Complex
UV–Vis Spectroscopy: Woodward–Fieser Rules

![[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59739.jpg&w=3840&q=50)