摘要
A new fluorescent resonance energy transfer (FRET) based fluorescent probe (compound 1) containing a dansyl unit as a donor and rhodamine 101 as an acceptor was developed to detect Fe3+ from other transition metal ions through ratiometric sensing in organic-aqueous solutions. Fe3+ induced a ring-opening reaction of the spirolactam rhodamine moiety of 1 resulting in the formation of a fluorescent derivative that can serve as the FRET acceptor. Ratiometric sensing of Fe3+ was accomplished by plotting the fluorescence intensity ratio at 605 nm and 515 nm versus ferric ion concentration. The probe displayed a linear response to Fe3+ in the range of 5.5-25 mu M with a detection limit of 0.64 mu M. A 1:1 stoichiometry for the 1-Fe3+ complex was formed with an association constant of 1.74 x 10(4) M-1. The probe also exhibited a large Stokes shift (225 nm) which can eliminate backscattering effects of excitation light.