Related Experiment Video
Updated: Dec 9, 2025

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Production and Characterization of Molecular Dications: Experimental and Theoretical Efforts
Stefano Falcinelli1, Marzio Rosi1,2
1Department of Civil and Environmental Engineering, University of Perugia, Via G. Duranti 93, 06125 Perugia, Italy.
Abstract:
Molecular dications are doubly charged cations of importance in flames, plasma chemistry and physics and in the chemistry of the upper atmosphere of Planets. Furthermore, they are exotic species able to store a considerable amount of energy at a molecular level. This high energy content of several eV can be easily released as translational energy of the two fragment monocations generated by their Coulomb explosion. For such a reason, they were proposed as a new kind of alternative propellant. The present topic review paper reports on an overview of the main contributions made by the authors' research groups in the generation and characterization of simple molecular dications during the last 40 years of coupling experimental and theoretical efforts.
More Related Videos
09:45Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
Published on: March 20, 2017
10:17Creating Highly Specific Chemically Induced Protein Dimerization Systems by Stepwise Phage Selection of a Combinatorial Single-Domain Antibody Library
Published on: January 14, 2020
Related Concept Videos
Cationic Chain-Growth Polymerization: Mechanism
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Cycloaddition Reactions: Overview
Diels–Alder Reaction: Characteristics of Dienes
Characteristics of the diene
Conformation
The simplest example of a diene is 1,3-butadiene, an acyclic conjugated π system. At room temperature, the molecule exists as a mixture of s-cis and s-trans conformers by virtue of rotation around the carbon–carbon single bond. Although the s-trans isomer is more stable,...
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry
Intramolecular Claisen Condensation of Dicarboxylic Esters: Dieckmann Cyclization