Crystallographic characterisation of arenesulfonyl azides. Structural and kinetic effects induced by ortho- and para-substituents

The molecular structures of six arenesulfonyl azides, ArSO2N3 (Ar=4-nitroph enyl, 4-acetylphenyl, 4-methoxyphenyl, 2-nitrophenyl, 2,4,6-triisopropylphe nyl or ferrocenyl group), have been characterised by X-ray diffraction stud ies. The N-N bond lengths are influenced only to a negligible extent by the nature of para-substituents. In contrast, the C-S and S-N distances are se nsitive to the electron-withdrawing power of para-substituents and undergo opposing changes. These bond lengths as well as the nu(as)(N-3) frequencies of the 4-substituted azides show linear dependencies as a function of Hamm ett's sigma constants, which agree well with earlier results on the relativ e reactivities of arenesulfonyl azides toward [Pd2Cl2(dppm)(2)]. The unusua l structural properties of o-nitrobenzenesulfonyl azide are attributed to d ipole-dipole interactions of the nitro group with the sulfonyl and the azid e moieties. Although electronic effects due to para-substituents govern the magnitude of the second-order rate constants, the reactivity of o-nitroben zenesulfonyl azide seems to be determined by steric interactions.