Organic electrochemistry is concerned with the reduction and oxidation of organic molecules
at electrodes. Although it is now more than 200 years ago that the so-called Volta pile was …

A novel approach of electrolysis using alternating current was applied in the sulfur–sulfur
bond metathesis of symmetrical disulfides towards unsymmetrical disulfides. As initially …

A dimeric ZnII carbene complex featuring bridging and chelating benzene‐1, 2‐dithiolate
ligands is highly stable towards air and water. The donor‐Zn‐acceptor structure leads to …

Organosulfides (R–Sn–R) exhibit a high theoretical capacity and low cost, but suffer from
sluggish kinetics and poor reversibility. Here, we demonstrate an effective and universal …

We disclose a mild, scalable, electricity-promoted cross coupling protocol between allylic
iodides and disulfides/diselenides for the formation of C–S/Se bonds in the absence of …

The direct synthesis of alkylthioimidazoles was initially accomplished via a one‐pot three‐
component cross‐coupling mediated by a paired electrolysis strategy using non‐activated …

Addressing control over molecular machines resulting in variable output modulation by
mimicking nature mechanisms is a current hot topic. The exploitation of reversibility in …

Recently, Professor David MacMillan introduced an original light-mediated catalytic process
where simple aldehyde substrates undergo coupling with a variety of olefin partners to …

We show that a new terpyridine ligand comprising a directly-connected methyldisulfide
group (tpySSMe) can be used to prepare a modular series of metal bis (terpyidine) …

In this work, a new simple molecule, 4‐nitrobenzyl phenyl thioether (1), is prepared and
used for controlling and tuning CO2 reactivity in function of the electrode potential. The first …