The Salen(Bu-t) ligands, Salen(Bu-t), N'-ethylenebis(3,5-di-tert-butyl
salicylideneimine) and Salpen(Bu-t), '-propylenebis(3,5-di-tert-butyls
alicylideneimine) can be combined with GaEt3 to prepare the 'open' mon
ometallic compounds, Salen(Bu-t)H(GaEt2) (1) and Salpen(Bu-t)(GaEt2) (
2). These, in turn, can be converted to the bimetallic derivatives, Sa
len(t)Bu(GaEt2)(2) (3) and Salpen(Bu-t)(GaEt2)(2) (4) by addition of G
aEt3. Alternatively, 3 and 4 can be made by the addition of two moles
of GaEt3 to the appropriate ligand. This was the method used to prepar
e Salben(Bu-t)(GaEt2)(2) (5) (Salben(Bu-t) = N'-butylenebis(3,5-di-ter
t-butylsalicylideneimine) and Salhen(Bu-t)(GaEt2)(0) (6) [Salhen(Bu-t)
= '-hexylenebis(3,5-di-tert-butylsalicylideneimine]. Compounds 1 and
2 can be utilized to form the unique mixed-metal derivatives L(GaEt2)
(MR2) (where L = Salen(Bu-t), M : R = Al, Me (7); Al, Et (9); and L =
Salpen(Bu-t), M: R = Al, Me (8); Al, Et (10). At ambient temperatures
in non-polar solvents, 7-12 do not undergo exchange of either the alky
l or MR2 groups. All of the compounds were characterized by Mp, analys
es, H-1 NMR, IR and, in the case of 1 and 3-6, by X-ray crystallograph
y. (C) 1998 Elsevier Science Ltd. All rights reserved.