Journal of the American Chemical Society, Vol.128, No.1, 250-256, 2006
Intramolecularly sensitized precipitons: A model system for application to metal sequestration
We have investigated light-triggered or catalytically activated precipitation agents and have proposed the name "precipiton" for such molecules or molecular fragments. A phase separation is induced when the precipiton isomerizes to a low-solubility form. In this paper we describe the first intramolecularly activated precipitons. The isomerization process is induced by intramolecular triplet energy transfer from a covalently attached metal complex. As expected, intramolecular sensitization leads to a more rapid isomerization than can be achieved by intermolecular sensitization at accessible concentrations. Two isomeric bichromophoric precipiton species, each containing [Ru(bpy)(3)](2+) and 1,2-bis(biphenyl)ethene units covalently linked together by an ether tether, have been synthesized and characterized, and their photochemical properties have been investigated. The rates of photoisomerization of these complexes, [((Z)-1,2-bis(biphenyl)ethene-bpy)Ru(bpy)(2)](PF6)(2) (2Z) and [((E)-1,2-bis(biphenyl)ethene-bpy)Ru(bpy)(2)](PF6)(2) (2E), were compared to those of their untethered analogues, (Z)-1,2-bis(biphenyl)ethene-OTBS (1Z) and (E)-1,2-bis(biphenyl)ethene-OTBS (1 E), where ruthenium sensitization occurred through an intermolecular pathway. Upon irradiation with visible light (lambda >= 400 nm) in degassed solution, 2Z/E and 1 Z/E obeyed reversible first-order rate kinetics. The intramolecularly sensitized precipiton 2Z isomerized 250 times faster (k(2Z -> 2E) = 1.0 x 10(-3) s(-1) with a 51% neutral density filter) than the intermolecular case 1Z (k(1Z -> 1E) = 0.80 x 10(-5) s(-1)). For 1E and 2E, the isomerization rates were k(1E -> 1Z) = 11.0 x 10(-5) s-1 and k(2E -> 2Z) = 1.6 x 10(-3) s-1, respectively. The average Z/E mole ratio at the photostationary state was 62/38 for 2Z/E and 93/7 for 1 Z/E The impetus for this study was our desire to evaluate the possibility of using metal-binding precipitons that would precipitate only upon metal-to-precipiton binding and would be inert to visible light in the absence of metals.