Abstract

Reaction of Ph2P(8-CH2C9H6N)NBut (1) with 2 equiv of AlMe3 in toluene under reflux conditions afforded aluminum iminophosphorano(2-methyl-8-quinolyl)methandiide complex (2). The reaction proceeded via the intermediates of a coordination complex, [(AlMe3){Ph2P(8-CH2C9H6N)NBut}] (3), and then an addition complex (4) of AlMe3 to the carbon−nitrogen double bond of the quinolyl ring of the neutral ligand. The coordination complex was converted to the singly deprotonated complex [(AlMe2){CH(8-C9H6N)(Ph2PNBut)}] (5) at 60 °C, which further reacted with AlMe3 in toluene under reflux conditions to yield aluminum iminophosphorano(8-quinolyl)methandiide (6). The structures of complexes 2, 4, and 6 were proved by single-crystal X-ray diffraction techniques, and the five-coordinate complexes 3 and 5 were characterized by 27Al NMR spectroscopy.

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