Related Experiment Video
Updated: Jun 10, 2026

Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology
Published on: March 12, 2015
Unexpected fluorescence properties in an axially sigma-bonded ferrocenyl-containing porphyrin
Pavlo V Solntsev1, Jared R Sabin, Samantha J Dammer
1Department of Chemistry & Biochemistry, 1039 University Drive, University of Minnesota Duluth, Duluth, MN 55812, USA.
Abstract:
Molecular structure, redox, and unexpected fluorescence properties of a tetraphenylporphyrin tin(iv) complex axially sigma-bonded with two ferrocene substituents were investigated using UV-vis, MCD, electro- and spectroelectrochemical methods as well as DFT calculations and X-ray crystallography.
Related Concept Videos
Variables Affecting Phosphorescence and Fluorescence
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group with both...
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous overlap of p...
Frost Circles for Different Conjugated Systems
Valence Bond Theory
π Electron Effects on Chemical Shift: Overview

