Feb 012011

Presented by:  Dr. Andrew D. Schwarz & Liban M. A. Saleh
Research Leader:  Prof. Philip Mountford & Prof. Simon Aldridge
Published:  Journal of the American Chemical Society

Transition-metal boryl compounds (L)M(BX2)x, containing 2‑center, 2‑electron σ‑bonds have been a topic of outstanding interest due to pivotal roles in a variety of catalytic and stoichiometric transformations, e.g. hydroboration and diboration of C–C π-bonds, and functionalization of alkane and arene C‑H bonds. To date, virtually all boryl complexes have been prepared either by B‑X (X = H or halogen) or B‑B oxidative addition to a low oxidation state (L)M species, or by nucleophilic attack of a [(L)M]‑ anion on a XBR2 or related source of the boryl moiety. However, utilisation of the nucleophilic Li{B(NArCH)2}(THF)2 (Ar = 2,6‑C6H3iPr2), allows access to rare earth metal boryl compounds.  Data were collected on a small colourless crystal (0.05 × 0.05 × 0.05 mm) using the new Oxford Diffraction (Agilent) SuperNova diffractometers and copper radiation.

Structure of the Month - February 2011

Structure of the Month – February 2011