8-(Dimethylamino)naphthylcopper(I), a novel stable organocopper compound with unusual structural features. A study concerning its synthesis, structure (X-ray) and reactivity. Its synthesis, crystal structure (X-ray) and reactivity

Publication date

1987

Authors

Koten, G. van
Wehman, E.
Knotter, M.
Spelten, H.
Heijdenrijk, D.
Mak, A.N.S.
Stam, C.H.

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Abstract

The synthesis and isolation of a hydrocarbon- and ether-insoluble organocopper compound containing the rigid 8-(dimethylamino)naphthyl group is described. An X-ray determination of its structure revealed a tetranuclear copper aggregate, in which the Cu atoms are arranged in a parallelogram (Cu...Cu 2.407(2) and 2.430(2) @9) and are three-center, two-electron bridged by C(ipso) (Cu-C 2.025(6) @9 mean) of the naphthyl group. The amine ligands coordinate pairwise to opposite copper atoms. The copper aggregate thus contains two distinct types of Cu atoms, involving two nucleophilic two-coordinate and two electrophilic four-coordinate sites, pointing to a strong cuprate character. Reaction of the organocopper compound with several copper(I) salts resulted either in the formation of binaphthyl and dimethylaminonaphthalene or a stable mixed copper cluster, depending on the anion in the copper salt. With dimethyl acetylenedicarboxylate the copper compound, without added lithium or magnesium salts, gave the (syn) addition product 8-Me{2}NnaphthylC(CO{2}Me)=C(CO{2}Me)Cu. These reactions are discussed in relation to the structural features of the tetranuclear organocopper compound.

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