An effective trigger for energy release of vinylheptafulvene-based solar heat batteries
Martina Cacciarini1, Alexandru Vlasceanu, Martyn Jevric
1Department of Chemistry 'Ugo Schiff', Università di Firenze, Via della Lastruccia, 3-13, I-50019 Sesto Fiorentino, Italy. martina.cacciarini@unifi.it.
Abstract:
Stoichiometric copper(i) tetrakis(acetonitrile) is found to activate the thermal ring-closure reaction of a series of high-energy vinylheptafulvene isomers to the corresponding low-energy and photoactive dihydroazulenes, allowing the release of energy upon request.
More Related Videos
11:26Integrating a Triplet-triplet Annihilation Up-conversion System to Enhance Dye-sensitized Solar Cell Response to Sub-bandgap Light
Published on: September 12, 2014
10:15Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
Published on: November 7, 2025
Related Concept Videos
Batteries and Fuel Cells
Thermal and Photochemical Electrocyclic Reactions: Overview
Voltaic/Galvanic Cells
Spontaneous redox reactions occur abundantly in nature. The chemical reaction occurring in a disposable AA battery powering our remote controls is one such example of a spontaneous redox reaction. Another example is the immersion of coiled copper wire into an aqueous silver nitrate solution. The reaction shows a gradual, visually impressive color change from colorless to bright blue and the formation of a grey precipitate on the copper wire. In this experiment,...
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
P-N junction
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.
