Related Experiment Video
Updated: Jun 22, 2026

Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology
Published on: March 12, 2015
A click-generated triazole tethered ferrocene-pyrene dyad for dual-mode recognition of the pyrophosphate anion
Tomás Romero1, Antonio Caballero, Alberto Tárraga
1Departamento de Química Orgánica, Facultad de Química, Universidad de Murcia, Campus de Espinardo, E-30100, Spain.
Abstract:
The ferrocene-pyrene dyad 3 is able to selectively sense the pyrophosphate anion. The anion recognition was evaluated using electrochemistry, (1)H NMR, as well as fluorescence spectroscopy. The binding event can be inferred from either the redox-shift (DeltaE(1/2) = -100 mV) or the emission intensity ratio of the pyrene monomer to the excimer emission bands in both the neutral and oxidized forms of the receptor upon complexation.
More Related Videos
14:11Synthesis of pH Dependent Pyrazole, Imidazole, and Isoindolone Dipyrrinone Fluorophores using a Claisen-Schmidt Condensation Approach
Published on: June 10, 2021
07:14Experimental Approaches for the Synthesis of Low-Valent Metal-Organic Frameworks from Multitopic Phosphine Linkers
Published on: May 12, 2023
Related Concept Videos
Thermal and Photochemical Electrocyclic Reactions: Overview
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group with both...
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.