| Abstract: | The photopolymerization of acrylamide (AA) initiated by the metallic complex tris(2,2′‐bipyridine)ruthenium(II) Ru(bpy)3+2] in the presence of aliphatic and aromatic amines as co‐initiators was investigated in aqueous solution. Aromatic amines, which are good quenchers of the emission of the metal‐to‐ligand‐charge‐transfer excited state of the complex, are more effective co‐initiators than those that do not quench the luminescence of Ru(bpy)3+2, such as aliphatic amines and aniline. Laser‐flash photolysis experiments show the presence of the reduced form of the complex, Ru(bpy)3+1, for all the amines investigated. For aliphatic amines, the yield of Ru(bpy)3+1 increases with temperature, and on the basis of these experiments, a metal‐centered excited state is proposed as the reactive intermediate in the reaction with these amines. The decay of the transient Ru(bpy)3+1 is faster in the presence of AA. This may be understood by an electron‐transfer process from Ru(bpy)3+1 to AA, regenerating Ru(bpy)3+2 and producing the radical anion of AA. It is proposed that this radical anion protonates in a fast process to give the neutral AA radical, initiating in this way the polymerization chain. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 4265–4273, 2001 |
