Optical properties of two fluorene derived BODIPY molecular rotors as fluorescent ratiometric viscosity probesElectronic supplementary information (ESI) available: NMR characterization and experimental procedures. See DOI: 10.1039/c5nj03339j

BODIPY-derived molecular fluorescent rotors are one of the most useful families of fluorescent probes for the quantitative measurement of microviscosity. Here, we report the photophysical properties of two molecular rotors as ratiometric viscosity sensors, meso -(4-(9 H -fluoren-2-yl)ethynyl)phenyl-4,4-difluoro-4-bora-3 a ,4 a -diaza- s -indacene ( 1 ) and meso -(5-(9 H -fluoren-2-yl)ethynyl)thiophen-2-yl-4,4-difluoro-4-bora-3 a ,4 a -diaza- s -indacene ( 2 ) having two independent chromophores; one (fluorene) is not influenced by viscosity and is used to determine concentration properties, and the other chromophore (BODIPY) acts as a molecular rotor. The fluorescence ratiometric calibration against microviscosity for the most sensitive probe ( 1 ), was obtained in a wide linear dynamic range. The sensitivity of the spectroscopic observables for 1 and 2 towards solvent viscosity and the typical analytical interfering solvent polarity and polarizability parameters were investigated by means of two different solvent scales, namely Lippert-Mataga and Catalán, finding consistent results. Quantum chemical calculations were conducted to analyze the probe mechanism in terms of Natural Transition Orbitals (NTOs) and the spatial extent of charge transfer excitations. Two fluorescent ratiometric fluorene derived BODIPY probes present a sensitive response to microviscosity changes.