Abstract

Using the pentadentate tetrapyrazolylpyridyl diborate (B2Pz4Py) ligand allowed for the isolation of overall seven group 13 complexes, which have been fully characterised and whose solid-state structures were obtained by single-crystal X-ray diffraction analysis. The aluminium chloride (1) and bromide (2) complexes as well as the gallium chloride (3) and iodide (4) complexes are accessible by deprotonation of the ligand precursors [B2Pz4LiPyH]2 with lithium hexamethyldisilazide and subsequent reaction with aluminium and gallium trihalides. Using indium(I) chloride instead gives rise to the indium(III) bis(trimethylsily)amide complex 5. Chloride abstraction from the aluminium(III) complex 1 using a combination of TlBArF24 and TlPF6 affords the related aluminium(III) fluoride complex 6 while using the gallium(III) complex 3 yields the dinuclear cationic PF2O2-bridged gallium(III) complex 7.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call