Time-resolved resonance heterodyne optical Kerr-effect spectroscopy is
employed to measure the solvation dynamics of rhodamine 800 in water
and D2O. Unlike other large dye molecules, rhodamine 800 solvation dyn
amics in water exhibits a long-time component which we attribute to hy
drogen-bond formation (breaking). We also find a rather unusual large
isotope effect which does not exist in other dyes. An important part o
f the experimental data is a bimodal solvation correlation function wi
th an ultrafast femtosecond component < 100 fs.