Issue 14, 1974

The stabilities of Meisenheimer complexes. Part VIII. Equilibrium and kinetic data for spiro-complex formation in water

Abstract

Equilibrium and rate constants for the formation in water of spiro-complexes from four ring-activated aromatic glycol ethers are reported. Values of the rate constants K–1 for opening of the dioxolan ring of these complexes are much higher than those for the expulsion of base from non-cyclic analogues. This may indicate ring strain in the spiro-complexes.

In moderately concentrated (>0·1M) sodium hydroxide solutions complexes are formed by addition of hydroxide ions at unsubstituted ring positions in the spiro-complexes. Addition of hydroxide ions at two ring positions to the spiro-complex from the glycol ether of 2,4,6-trinitrobenzene gives an adduct (XIII) which may be regarded as a 1 : 3 σ-complex.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1974, 1681-1686

The stabilities of Meisenheimer complexes. Part VIII. Equilibrium and kinetic data for spiro-complex formation in water

M. R. Crampton and M. J. Willison, J. Chem. Soc., Perkin Trans. 2, 1974, 1681 DOI: 10.1039/P29740001681

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