Abstract:Three Lewis acid–base adducts t‐Bu3Ga–EPh3 (E = P 1, As 2, Sb 3) were synthesized by reactions of Ph3E and t‐Bu3Ga and characterized by heteronuclear NMR (1H, 13C (31P)) and IR spectroscopy, elemental analysis and single crystal X‐ray diffraction. Their structural parameters are discussed and compared to similar t‐Bu3Ga adducts. The strength of the donor‐acceptor interactions within 1–3 was investigated in solution by temperature‐dependent 1H NMR spectroscopy and by quantum chemical calculations.
The zerovalent carbodiphosphorane, (Ph3P)2C, reacts with Me3Al and Me3Ga to afford the adducts, [(Ph3P)2C]MMe3 (M = Al, Ga), whereas Me2Zn and Me2Mg react to afford mononuclear and dinuclear cyclometalated derivatives.
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