Reduction of CoIII centre in CoIII(pn)2(Cl)(L)2+ with reference to solvent medium and structure of the
complex via ion pair charge transfer (IPCT) paves way for the novel reaction mechanism route. In this
work, we prepared, characterized and photoinduced the complexes CoIII(pn)2(Cl)(L)2+ (where L =
RC6H4NH2, R = m-OMe, p-F and H) in the presence of iodide ion. Quantum yield for 254 nm excitation
of CoIII(pn)2(Cl)(L)2+(where L = RC6H4NH2, R = m-OMe, p-F and H) in water-1,4-dioxane mixtures
(Diox = 0, 5, 10, 15, 20, 25, and 30% (v/v)) were also derived for all the complexes in presence of
added iodide ion, in which CoIII was reduced via [CoIII(pn)2(Cl)(L)2+….. I-] ion-pair formation. The
photoinduced state is ion-pair charge transfer transition state and the quantum efficiency is solvent
reliant and they are non-reactive. That is, change in ΦCo(II) is dependable with observed increase in xDiox
of the mixed solvent medium. Correlation analysis using empirical parameters εr, Y, ET
N and DNN
provides a model to understand the solvent medium participation and interaction. This work gains an
insight into the role of aqueous-organic solvent medium in CoIII(pn)2(Cl)(L)2+ photoreduction, which
may be of great significance in developing novel approaches in the field of high performance catalysis
Very strong Rydberg atom scattering in K(12p)–CH3NO2collisions: Role of transient ion pair formation