Designing long and highly conducting molecular wires has been a great challenge for decades. It has now been shown that an oxidized 2.6-nm-long oligophenylene-bridged bis(triarylamine) can show a single-molecule junction conductance over 0.1G0.

We report in situ continuous anthraquinone electrosyntheses from lower-cost anthracene feedstock in a flow cell reactor to lower mass production cost of anthraquinone-based electrolytes, and in situ electro-resyntheses of active molecules from decomposed species to extend lifetime of aqueous anthraquinone redox flow batteries.

The asymmetric hydrogenation of oximes to chiral hydroxylamines is a long-standing problem due to the labile N-O bond and inert C=N bond. It has now been enabled by a chiral nickel catalyst with excellent results in which the weak interactions between catalyst and substrate play crucial roles.

In phytochrome Agp2 ultrafast proton-transfer occurs from the chromophore to a hydrogen-bonded water network in the protein prior to photoisomerization. The altered hydrogen bonds persist after photoisomerization and trigger together with the new chromophore geometry the activated protein conformation.

Porphyrin ligand modification by acceptor-acceptor iodonium ylides is not necessarily a dead-end catalyst deactivation pathway, but can actually have a useful protective function by slowing-down deactivation pathways of the metalloradical cobalt(II)-tetraphenylporphyrin catalyst.

We have developed a general methodology for heterogeneous iron-catalysed deuteration reactions. The catalytic system is effective for selective deuteration of anilines, indoles, phenols, and other heterocyclic compounds including late-stage labelling of natural products as well as bioactive molecules and can be readily used for the preparation of deuterated compounds on kg-scale.