M. Yashiro, T. Murata, Mitsunobu Sato
1994
Citations
0
Influential Citations
4
Citations
Journal
Journal of The Chemical Society-dalton Transactions
Abstract
The chiral diamine (2R), (4R)-pentane-2,4-diamine (2R,4R-ptn) has been found efficiently to regulate the stereochemistry of the cobalt(III) complex [Co(edda)(2R,4R-ptn)]+(edda = ethylenediamine-N,N′-diacetate). The product ratio Λ-sym-cis:Δ-sym-cis is 3:97. The stereoselectivity is surprisingly high in comparison with that for the analogous complex involving (1R),(2R)-cyclohexane-1,2-diamine (R,R-chxn), Λ-sym-cis:Δ-sym-cis= 60:40. It is discussed on the basis of crystal structure determinations carried out for both diastereoisomers of sym-cis-[Co(edda)(2R,4R-ptn)]+. A notable difference was observed in the six-membered chelate ring of 2R,4R-ptn which adopts the chair conformation in Λ-sym-cis-[Co(edda)(2R,4R-ptn)]ClO4·H2O 1a but the λ skew-boat conformation in Δ-sym-cis-[Co(edda)(2R,4R-ptn)]ClO41b. The chair conformation in 1a is due to steric repulsions between the chelates, which is the important factor for the preferential formation of 1b over 1a. Such steric repulsions between the chelates are remarkably efficient for the chiral six-membered chelate compared with those for the five-membered one. N-Alkyl substitutions on the edda ligand caused preferential formation of the Λ-sym-cis form, as is the case for the [Co(R2edda)(R,R-chxn)]+ system.