Wj. Zheng et al., An unusual monomeric alkenyl-substituted pyrazolato aluminum dichloride and its derivatives with both terminal and eta(2)-pyrazolato ligands, ORGANOMETAL, 20(15), 2001, pp. 3299-3303
The facile formation of the unusual monomeric alkenyl-substituted pyrazolat
o aluminum dichloride [(3,5-Bu-t(2)-N-CH=C(SiMe3)-pz)AlCl2] (2; 3,5-(t)Bu(2
)pz = 3,5-di-tert-butylpyrazolato) was achieved in high yield by reacting d
imeric pyrazolato aluminum dichloride [eta (1)-eta (1)-3,5-(t)Bu(2)pz(mu -A
l)Cl-2](2) (1) with 2 equiv of trimethylsilylethine. The addition of 1 and
2 equiv of K[3,5-(t)Bu(2)pz] to 2, respectively, resulted in the formation
of two novel complexes, [(3,5-Bu-t(2)-N-CH=C(SiMe3)-pz)AlCl(3,5-(t)Bu(2)pz)
] (3) and [(3,5-Bu-t(2)-N-CH=C(SiMe3)-pz)Al(eta (1)-3,5-(t)Bu(2)pz)(eta (2)
-3,5-(t)Bu(2)pz)] (4), for which crystallographic data are presented. The c
oordination of the pyrazolato ligand in 3 represents an extreme example of
a "slipped" eta (2)-coordination.