Reaction of several N-heterocyclic carbenes, a carbodiphosphorane and bis(diphenylphosphino)ethane (DPPE) with [BeX2(OEt2)2] (X = Br or I) have yielded a variety of beryllium dihalide adduct complexes, all of which were crystallographically characterised. Attempts to reduce the compounds to low oxidation state beryllium complexes using a variety of reducing agents have been carried out, but were of limited success. However, reaction of [(IPr)BeBr2] (IPr = :C{(DipNCH)2}; Dip = 2,6-diisopropylphenyl) with the aluminium(i) heterocycle, [:Al(DipNacnac)] (DipNacnac = [HC(MeCNDip)2]−) afforded the adduct complex, [{(IPr)(Br)Be(μ-H)}2], while reduction of [(IPr)BeBr2] with potassium naphthalenide gave the beryllium naphthalenediyl complex, [(IPr)Be(C10H8)]. Furthermore, reaction of [{(DPPE)BeI2}∞], with [:Al(DipNacnac)] led to insertion of the Al centre of the heterocycle into a Be-I bond and formation of a rare example of an Al-Be bonded complex, [(DPPE)(i)Be-Al(i)(DipNacnac)]. © The Royal Society of Chemistry 2021.