David W. Allen, Jacqueline Hawkrigg, Harry Adams, Brian F. Taylor, David E. Hibbs and Michael B. Hursthouse
The synthesis is described of three series of 2-(phosphonioaryl)(benz)imidazolide betaines, viz (i) the 2-(2- or 3- or 4-tributylphosphoniophenyl)benzimidazolides, (ii) the 2-(2- and 4-triorganophosphoniophenyl)-1H-phenanthro[9,10-d]imidazolides, and (iii) the 2-(2- and 4-triorganophosphoniophenyl)-4,5-diphenylimidazolides. A detailed 1H, 13C and 31P NMR study of the 2-(tributylphosphoniophenyl)benzimidazolides reveals significant differences in the spectroscopic parameters of the betaines compared with those of the phosphonium salts from which they are derived. Full X-ray structural studies are reported for 2-(4-triphenylphosphoniophenyl)-1H-phenanthro[9,10-d]imidazol-1-ide and 2-(4-triphenylphosphoniophenyl)-4,5-diphenylimidazol-1-ide, and comparisons made with related pyridiniumimidazolide systems. The phosphonioimidazolide betaines exhibit negative solvatochromism.