Rc. Crittendon et al., SYNTHESES, STRUCTURE, AND REACTIVITY OF 2,6-DIMESITYLPHENYL-BASED STERICALLY DEMANDING GALLIUM ARYLS, Organometallics, 16(11), 1997, pp. 2443-2447
Reaction of gallium chloride with (2,6-dimesitylphenyl)lithium, (Mes(2
)C(6)H(3))Li (Mes = 2,4,6-Me3C6H2), gives bis[(dimesitylphenyl)gallium
dichloride], [(Mes(2)C(6)H(3))GaCl2](2), I. Treatment of I with {2-[(
dimethylamino)methyl]phenyl}lithium [2-(Me2NCH2)C6H4]Li, affords (dime
sitylphenyl)-2-((dimethylamino)methyl) chloride, (Mes(2)C(6)H(3))[2-(M
e2NCH2)C6H4]GaCl, II. Reaction of (Mes(2)C(6)H(3))Li with gallium brom
ide affords bis(dimesitylphenyl)gallium bromide, (Mes(2)C(6)H(3))(2)Ga
Br, III, while reaction of I with (Mes)Li yields (dimesitylphenyl)dime
sitylgallium, (Mes(2)C(6)H(3))(Mes)(2)Ga, IV. GalIium aryls I-IV have
been characterized by elemental analyses, H-1 and C-13 NMR and IR spec
troscopies, and single-crystal X-ray diffraction. I assumes a mu(2)-ch
loro-bridged dimeric structure, while the coordination of gallium in I
I is completed by one Mes(2)C(6)H(3) Ligand and one chloride ligand an
d is intramolecularly stabilized by the nitrogen atom of [2-(Me2NCH2)C
6H4]. III assumes a rare T-shaped coordination about the gallium cente
r (C-Ga-C 153.5(2)degrees), while TV represents, arguably, the most st
erically crowded trigonal planar gallium aryl reported with the aromat
ic rings about the GaC3 plane approaching 90 degrees.