We report an achiral bisphosphine rhodium complex equipped with a binding site for the recognition of chiral anion guests. Upon binding small chiral guests--cofactors--the rhodium complex becomes chiral and can thus be used for asymmetric catalysis. Screening of a library of cofactors revealed that the best cofactors lead to hydrogenation catalysts that form the products with high enantioselectivity (ee's up to 99%). Interestingly, a competition experiment shows that even in a mixture of 12 cofactors high ee is obtained, indicating that the complex based on the best cofactor dominates the catalysis.
Iridium(III) and ruthenium(II) polypyridyl based photocatalysts have been prepared and their structure determined using 1H NMR, HR‐MS and single crystal XRD. Their spectroscopic and electrochemical properties have been studied by UV‐vis absorption, emission spectroscopy and cyclic voltammetry. These complexes have been used as photoredox homogeneous catalysts in an intramolecular cyclization model reaction in which they show high activity. They have been covalently anchored on graphene oxide (GO) via an esterification reaction and non‐covalently fixed on reduced graphene oxide (rGO) via pyrene moieties. Heterogenized complexes exhibit good photocatalytic activities and, interestingly, the use of a pyrene‐derivatized Ir(III) terpyridine‐based complex highlights an unexpected “on/off” effect of the photocatalytic activity triggered by the presence or absence of rGO.
DNA-based nanomaterials are the subject of numerous researches. A series of modified nucleobases were synthesized either to construct a double helix where the natural Hbonded bases are replaced by metal-coordinated liganosides or to introduce a punctual modification inside a natural DNA structure. Thanks to their photophysical and photochemical properties, iridium(III) complexes are of increasing interest in
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