CHEMICAL REACTIVITIVES OF [ME(2)AL (MU-NIPR2)(2)MGME](4) AND [ME(2)AL(MU-NIPR2)(2)MGCL](2) - CRYSTAL-STRUCTURES OF [ME(2)AL(MU-PZ)(2)ALME(2)], [ME(2)AL(MU-PZ)(2)MG(MU-PZ)(2)ALME(2)], AND E(2)AL(MU-NIPR2)(MU-ME)MG(MU-NIPR2)(MU-ME)ALME(2)]
Cc. Chang et al., CHEMICAL REACTIVITIVES OF [ME(2)AL (MU-NIPR2)(2)MGME](4) AND [ME(2)AL(MU-NIPR2)(2)MGCL](2) - CRYSTAL-STRUCTURES OF [ME(2)AL(MU-PZ)(2)ALME(2)], [ME(2)AL(MU-PZ)(2)MG(MU-PZ)(2)ALME(2)], AND E(2)AL(MU-NIPR2)(MU-ME)MG(MU-NIPR2)(MU-ME)ALME(2)], Journal of the Chinese Chemical Society, 41(6), 1994, pp. 783-789
[Me(2)Al(mu-NiPr2)(2)MgMe]( )4 (A) reacted with chloroform to give the
starting material [Me(2)Al(mu-NiPr2)(2)MgCI](2) (4) in high yield. Co
mpound 4 underwent metathesis with LiR (R = t-C4H9, C6H5) to give [Me(
2)Al(mu NiPr2)(2)MgR](n) (n = 1, 2). Compound A reacted with pyrazole
(Pz) in a molar ratio I:I to produce [Me(2)Al(mu-NiPr2)(2)Mg(Pz)](2) (
1), and in a molar ratio 1:3 to produce degradation products [Me2Al(mu
-Pz)(2)AlM e(2)](4) (2) and [Me(2)Al(mu-Pz)(2)Mg(mu-Pz)2AlMe(2)] (3).
Compound A reacted with AlMe(3) to give [Me(2)Al(mu-NiPr2)(2)Mg(mu-Me)
(2)AlMe(2)] (8). Compound 8 isomerized to [Me(2)Al(mu-NiPr2)(mu-Me)Mg(
mu NiPr2)(mu-Me)AlMe(2)] (7) upon heating. Compound 7 was also obtaine
d from reaction of AlMe(3) with Mg(NiPr2)(2) in a molar ratio 3:1. The
crystal structures of compounds 2, 3, and 8 were determined by xray d
iffraction analysis.