O tautomerismo de cinco 2,2'-bis-benzimidazóis, simetricamente substituídos, [5(6),5'(6')-tetrametil- (1); 5(6),5'(6')-dimetil-(2); 5(6),5'(6')-dicloro- (3); 5(6),5'(6')-dimetoxi- (4) e 4(7),4'(7')-dimetil-2,2'-bis-benzimidazol (5)], foi estudado por espectroscopia de ¹H RMN, a várias temperaturas, e a influência dos substituintes nas barreiras energéticas de interconversão tautomérica, interpretada através de cálculos teóricos.
The tautomerism of five symmetrically substituted 2,2'-bis-benzimidazoles [5(6),5'(6')-tetramethyl- (1); 5(6),5'(6')-dimethyl-(2); 5(6),5'(6')-dichloro- (3); 5(6),5'(6')-dimethoxy- (4) and 4(7),4'(7')-dimethyl-2,2'-bis-benzimidazole (5)], was studied by means of ¹H NMR spectroscopy at variable temperatures, and the influence of the substituents on the energy barriers for tautomeric interconversion was interpreted with the aid of theoretical calculations.