Mechanochemical Synthesis of a Sodium Anion Complex [Na(2,2,2-cryptand)Na] and Studies of Its Reactivity: Two-Electron and One-Electron Reductions.

Group 1 metal molecular chemistry is dominated by a +1 oxidation state, while a 0 oxidation state is widespread in the metals. A more exotic, yet still available, oxidation state of group 1 metal is -1, i.e.

Synthesis, structure and stereodynamics of atropisomeric -chloroamides.

Atropisomeric -chloroamides were efficiently accessed by electrophilic halogenation of -substituted secondary anilides. The stereodynamics of atropisomerism in these novel scaffolds was interrogated by detailed experimental and computational studies, revealing that racemization is correlated with amide isomerization. The stereoelectronic nature of the amide was shown to significantly influence racemization rates, with potentially important implications for other C-N atropisomeric scaffolds.

Stereochemical Control of Secondary Benzamide-based BODIPY Emitters.

Aromatic amides can be used to construct light-harvesting materials with valuable optical properties. The amide bond is formed using well-known coupling agents in near quantitative yield, as illustrated here through the synthesis of two boron dipyrromethene derivatives bearing an amide linkage. The primary concern with acyl amides is rotation around the C-N bond, leading to cis and trans isomers.

Impact of a rigid backbone on the structure of an agostically-stabilised dialkylstannylene: isolation of an unusual bridged stannyl-stannylene.

The reaction between the phosphine-borane-stabilised dicarbanion complex [1,2-C6H4{CHP(BH3)Cy2}2][Li(THF)n]2 and Cp2Sn gives the unusual stannyl-stannylene [[1,2-C6H4{CHP(BH3)Cy2}2]Sn]2·1½PhMe, in which one dicarbanion ligand chelates a tin centre, while the other bridges a tin-tin bond. The stannylene centre is stabilised by an agostic-type B-H···Sn interaction.