Computational insights into the underlying mechanism of zinc ion-specificity of the fluorescent probe, BDA-1.

With the addition of Zn2+ or Cd2+ ions, photoinduced electron transfer preferentially occurs upon photo-excitation for the forming [M:BDA-1 -H+ ]+ (M = Zn, Cd) complexes. Different from the completely suppressed radiation in the excited [Cd:BDA-1 -H+ ]+ system, fluorescence emission of the excited [Zn:BDA-1 -H+ ]+ still exhibits a considerable oscillator strength. This difference validates the zinc ion-specific fluorescence enhancement effect of BDA-1. [Display omitted] • Internal conversion suppresses the fluorescence of BDA-1 rather than photoinduced electron transfer. • Adding Zn or Cd ions causes photoinduced electron transfer in [M:BDA-1 -H+ ]+ (M = Zn, Cd) complexes upon photoexcitation. • Compared to the suppressed radiation from [Cd:BDA-1 -H+ ]+ in the S1 state, [Zn:BDA-1 -H+ ]+ has considerable oscillator strength. Ion specificity is crucial for developing fluorescence probes. Using a recently reported optical sensor (BDA-1) of Zn2+ as a representative, we carried out extensive quantum chemical calculations on its photophysical properties using density function theory. According to the calculated optimized geometries, excitation energies and transition oscillator strengths, the weak fluorescence of BDA-1 observed in experiments is attributed to the suppression of fluorescence emission by efficient internal conversion, rather than the previously proposed photoinduced electron transfer (PET) mechanism. With the addition of Zn2+ or Cd2+ ions, the tetradentate chelates [M:BDA-1 -H+ ]+ (M=Zn, Cd) are produced. According to frontier molecular orbital and interfragment charge transfer analyses of these complexes, PET is preferentially confirmed to occur upon photo-excitation. Notably, as one coordination bond in the excited [Cd:BDA-1 -H+ ]+ complex is significantly weakened in comparison to that of [Zn:BDA-1 -H+ ]+, their molecular orbital compositions in the S 1 state are completely different. As a result, absorption and radiation transitions of [Zn:BDA-1 -H+ ]+ both have considerable oscillator strength, while fluorescence radiation from the excited [Cd:BDA-1 -H+ ]+ is doubly suppressed. This difference causes that the fluorescence intensity of BDA-1 is sensitive to the addition of metal ions, and exhibits the zinc ion-specificity. [ABSTRACT FROM AUTHOR]