ABSTRACT
Optical and thermodynamic measurements on fac-Re(CO)(3)(dpknph)Cl in polar non aqueous solvents revealed the existence of two interlocked conformational forms for fac-Re(CO)(3)(dpknph)Cl. The equilibrium distribution of the low (alpha-) and high (beta-) energy conformations is solvent dependent, controlled by the dipole moment of the solvent molecules and their orientation around the total dipole of fac-Re(CO)(3)(dpknph)Cl. The interplay between the alpha- and beta-conformations of fac-Re(CO)(3)(dpknph)Cl, allowed calculations of their extinction coefficients, by forcing the equilibrium to shift to one conformation, using chemical stimuli. In DMSO and DMF extinction coefficients of 87 000+/-2000 and 35 000+/-2000 M(-1) cm(-1) were calculated for the beta- and alpha-conformations of fac-Re(CO)(3)(dpknph)Cl at lambda(max.), respectively. Thermo-optical measurements on fac-Re(CO)(3)(dpknph)Cl, allowed calculations of the activation parameters for the interconversion between the alpha- and beta-conformations of fac-Re(CO)(3)(dpknph)Cl. In DMSO and DMF changes in enthalpy (DeltaH(ø)) of -11.2+/-1.3 and 10.9+/-0.5 kJmol(-1), entropy (DeltaS(ø)) of -12.7+/-4.3 and 29.4+/-1.7 JK(-1) mol(-1), and free energy (DeltaG(ø)) of -7.5+/-0.2 and+2.2+/-0.2 kJmol(-1) and hence equilibrium constants of 20.9+/-1.7 and 0.4+/-0.1 were calculated for fac-Re(CO)(3)(dpknph) at 295 K. The high values for the extinction coefficients and low values for the activation parameters for the interconversion between the alpha- and beta-conformations of fac-Re(CO)(3)(dpknph)Cl, in polar non aqueous solvents allowed the use of these systems as molecular sensors to probe their structural relaxation and interactions with their surroundings. These systems (fac-Re(CO)(3)(dpknph)Cl and surrounding solvent molecules) optically sense chemical and physical stimuli and their sensing power depends on the intensity and nature of these stimuli, i.e. the systems exhibit a high degree of sensitivity and selectivity.
