Correction: On the mercuration, palladation, transmetalation and direct auration of a C

Correction for 'On the mercuration, palladation, transmetalation and direct auration of a C^N^C pincer ligand' by Alice Jane McEllin et al., Dalton Trans., 2023, 52, 872-876, https://doi.org/10.1039/d2dt04114f.

Gold(III), Mercury(II), and Palladium(II) Complexes of a Series of Isomeric Bis(mono- and dialkoxyphenyl)pyridines: Introduction of Gold through Transmetalation and Catalysis.

A series of isomeric bis-2,6-(monoalkoxyphenyl)pyridine and bis-2,6-(dialkoxyphenyl)pyridine ligands were synthesized and characterized. In order to prepare their chlorogold(III) complexes, intermediate chloromercury(II) complexes were first prepared, but unlike observations from previous studies where they were obtained impure and at best in moderate yield, here pure complexes were synthesized, many in rather high yields. Depending on the substitution pattern of the alkoxy chains on the ligands, mono- and/or dimercurated complexes were obtained, characterized by 1H, 13C{1H}, and 199Hg NMR spectroscopy as well as, in several cases, by X-ray crystallography. Factors that may explain this unusual reactivity are discussed. In most cases, transmetalation to the related chlorogold(III) complex proceeded smoothly, although lower yields were obtained when starting from doubly mercurated precursors. Prompted by the propensity of these ligands to mercurate, attempts were made to effect direct auration, but none was successful. However, dimeric, orthometalated complexes of palladium(II) could be prepared and were also amenable to transmetalation to the chlorogold(III) complex, providing for a mercury-free synthesis.

On the mercuration, palladation, transmetalation and direct auration of a C

The C^N^C ligand 2,6-bis(2,3-dialkoxyphenyl)pyridine forms dimercury and orthopalladated complexes, both of which may be transmetallated to gold(III) complexes; the gold complexes may also be formed directly in a Rh(III)-catalysed process, hence it is possible to circumvent the use of organomercury intermediates in the synthesis of this important class of compound.

Enhancing the Air Stability of Dimolybdenum Paddlewheel Complexes: Redox Tuning through Fluorine Substituents.

The optical and electrochemical properties of quadruply bonded dimolybdenum paddlewheel complexes (Mo2PWCs) make them ideal candidates for incorporation into functional materials or devices, but one of the greatest bottlenecks for this is their poor stability toward atmospheric oxygen. By tuning the potential at which the Mo2 core is oxidized, it was possible to increase the tolerance of Mo2PWCs to air. A series of homoleptic Mo2PWCs bearing fluorinated formamidinate ligands have been synthesized and their electrochemical properties studied. The oxidation potential of the complexes was tuned in a predictable fashion by controlling the positions of the fluorine substituents on the ligands, as guided by a Hammett relationship. Studies into the air stability of the resulting complexes by multinuclear NMR spectroscopy show an increased tolerance to atmospheric oxygen with increasingly electron-withdrawing ligands. The heteroleptic complex Mo2(DFArF)3(OAc) [where DFArF = 3,5-(difluorophenyl)formamidinate] shows remarkable tolerance to oxygen in the solid state and in chloroform solutions. Through the employment of easily accessible ligands, the stability of the Mo2 core toward oxygen has been enhanced, thereby making Mo2PWCs with electron-withdrawing ligands more attractive candidates for the development of functional materials.

Hydrogen/Halogen Exchange of Phosphines for the Rapid Formation of Cyclopolyphosphines.

The hydrogen/halogen exchange of phosphines has been exploited to establish a truly useable substrate scope and straightforward methodology for the formation of cyclopolyphosphines. Starting from a single dichlorophosphine, a sacrificial proton "donor phosphine" makes the rapid, mild synthesis of cyclopolyphosphines possible: reactions are complete within 10 min at room temperature. Novel (aryl)cyclopentaphosphines (ArP)5 have been formed in good conversion, with the crystal structures presented. The use of catalytic quantities of iron(III) acetylacetonate provides significant improvements in conversion in the context of diphosphine (Ar2P)2 and alkyl-substituted cyclotetra- or cyclopentaphosphine ((AlkylP)n, where n = 4 or 5) formation. Both iron-free and iron-mediated reactions show high levels of selectivity for one specific ring size. Finally, investigations into the reactivity of Fe(acac)3 suggest that the iron species is acting as a sink for the hydrochloric acid byproduct of the reaction.