The Basicity of Unsaturated Hydrocarbons As Probed by Hydrogen-bond-acceptor Ability: Bifurcated N-H+ ...pi Hydrogen Bonding

The competitive substitution of the anion (A(-)) in contact ion pairs of the type [Oct3NH+]B(C6F5)4 (-) by unsaturated hydrocarbons (L) in accordance with the equilibrium Oct3NH+...A(-) + nL right arrow over left arrow [Oct3NH+...Ln]A(-) has been studied in CCl4. On the basis of equilibrium constants, K, and shifts of nuNH to low frequency, it has been established that complexed Oct3NH...+Ln cations with n=1 and 2 are formed and have unidentate and bifurcated N--H+...pi hydrogen bonds, respectively. Bifurcated hydrogen bonds to unsaturated hydrocarbons have not been observed previously. The unsaturated hydrocarbons studied include benzene and methylbenzenes, fused-ring aromatics, alkenes, conjugated dienes, and alkynes. From the magnitude of the redshifts in the N--H stretching frequencies, Delta nuNH, a new scale for ranking the pi basicity of unsaturated hydrocarbons is proposed: fused-ring aromatics<or=benzene<toluene<xylene<mesitylene<durene<conjugated dienes approximately 1-alkynes<pentamethylbenzene<hexamethylbenzene<internal alkynes approximately cycloalkenes<1-methylcycloalkenes. This scale is relevant to the discussion of pi complexes for incipient protonation reactions and to understanding N--H+...pi hydrogen bonding in proteins and molecular crystals.