Abstract
The reaction [Co(dpt)Cl3]+ dien in
propan-2-ol [dpt=di(3-aminopropyl)amine,
dien = diethylene-triamine]
gives mer-[Co(dpt)2]3+ and the three geometric
isomers of [Co(dien)2]3+,
almost quantitatively. The reaction [Co(dien)Cl3]
+ dpt in propan-2-ol, catalysed by water, yields the three
isomers of [Co(dien)(dpt)]3+
as the main products, in the approximate ratio u-fac : mer : s-fac 4 : 2 : 1. Preparation of mixed amine complexes by
substitution therefore requires that the amine (dien)
forming the more stable complexes be incorporated in the reactant complex. The
geometric structures of the isolated [Co(dien)(dpt)] (ClO4)3 isomers are assigned by
13C n.m.r. spectra. They each hydrolyse in
water or base, the mer
isomer rapidly, and no isomerization has been detected. X-ray crystallographic
analysis of mer-[Co(dien)(dpt)]2 (S2O6)3,H2O,EtOH
(from the isolated perchlorate by metathesis)
confirms the assigned mer
geometry. The two independent complex molecules in the asymmetric unit have
different conformational geometries. The crystals are monoclinic, space group
P21/c, with a 15.548(4), b 9.178(3), c 31.664(8) �,β 89,04(2)�. The
structure was refined by blocked-matrix least-squares techniques to an R-factor
(on 2752 F) of 0.058.
Cited by
17 articles.
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