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Fluorophores molecular rotors

Fig. 6.7. Viscosity sensitive fluorophores molecular rotors. DCVJ = 9-(dicyanovinyl)-julolidine, CCVJ = 9-(carboxy-2-cyano)vinyl julolidine, CMAM = 2-cyano-3-(p-dimethyl-aminophenyl)acrylic acid, methyl ester. Fig. 6.7. Viscosity sensitive fluorophores molecular rotors. DCVJ = 9-(dicyanovinyl)-julolidine, CCVJ = 9-(carboxy-2-cyano)vinyl julolidine, CMAM = 2-cyano-3-(p-dimethyl-aminophenyl)acrylic acid, methyl ester.
One of the most popular applications of molecular rotors is the quantitative determination of solvent viscosity (for some examples, see references [18, 23-27] and Sect. 5). Viscosity refers to a bulk property, but molecular rotors change their behavior under the influence of the solvent on the molecular scale. Most commonly, the diffusivity of a fluorophore is related to bulk viscosity through the Debye-Stokes-Einstein relationship where the diffusion constant D is inversely proportional to bulk viscosity rj. Established techniques such as fluorescent recovery after photobleaching (FRAP) and fluorescence anisotropy build on the diffusivity of a fluorophore. However, the relationship between diffusivity on a molecular scale and bulk viscosity is always an approximation, because it does not consider molecular-scale effects such as size differences between fluorophore and solvent, electrostatic interactions, hydrogen bond formation, or a possible anisotropy of the environment. Nonetheless, approaches exist to resolve this conflict between bulk viscosity and apparent microviscosity at the molecular scale. Forster and Hoffmann examined some triphenylamine dyes with TICT characteristics. These dyes are characterized by radiationless relaxation from the TICT state. Forster and Hoffmann found a power-law relationship between quantum yield and solvent viscosity both analytically and experimentally [28]. For a quantitative derivation of the power-law relationship, Forster and Hoffmann define the solvent s microfriction k by applying the Debye-Stokes-Einstein diffusion model (2)... [Pg.274]

In (8), the solvent-independent constants kr, kQnr, and Ax can be combined into a common dye-dependent constant C, which leads directly to (5). The radiative decay rate xr can be determined when rotational reorientation is almost completely inhibited, that is, by embedding the molecular rotor molecules in a glass-like polymer and performing time-resolved spectroscopy measurements at 77 K. In one study [33], the radiative decay rate was found to be kr = 2.78 x 108 s-1, which leads to the natural lifetime t0 = 3.6 ns. Two related studies where similar fluorophores were examined yielded values of t0 = 3.3 ns [25] and t0 = 3.6 ns [29]. It is likely that values between 3 and 4 ns for t0 are typical for molecular rotors. [Pg.276]

Molecular rotors are useful as reporters of their microenvironment, because their fluorescence emission allows to probe TICT formation and solvent interaction. Measurements are possible through steady-state spectroscopy and time-resolved spectroscopy. Three primary effects were identified in Sect. 2, namely, the solvent-dependent reorientation rate, the solvent-dependent quantum yield (which directly links to the reorientation rate), and the solvatochromic shift. Most commonly, molecular rotors exhibit a change in quantum yield as a consequence of nonradia-tive relaxation. Therefore, the fluorophore s quantum yield needs to be determined as accurately as possible. In steady-state spectroscopy, emission intensity can be calibrated with quantum yield standards. Alternatively, relative changes in emission intensity can be used, because the ratio of two intensities is identical to the ratio of the corresponding quantum yields if the fluid optical properties remain constant. For molecular rotors with nonradiative relaxation, the calibrated measurement of the quantum yield allows to approximately compute the rotational relaxation rate kor from the measured quantum yield [Pg.284]

The examples in the previous section give a comprehensive overview of application areas where molecular rotors have become important fluorescent reporters. Current work on the further development of molecular rotors can broadly be divided into three areas photophysical description, structural modification, and application development. Although a number of theories exist that describe the interaction between a TICT fluorophore and its environment, the detailed mechanism of interaction that includes effects such as polarity, hydrogen bonding, or size and geometry of a hydrophobic pocket are not fully understood. Molecular simulations have recently added considerable knowledge, particularly with... [Pg.299]

Molecular rotors are fluorophores characteristic for having a fluorescent quantum yield that strongly depends on the viscosity of the solvent [50], This property relies on the ability to resume a twisted conformation in the excited state (twisted intramolecular charge transfer or TICT state) that has a lower energy than the planar conformation. The de-excitation from the twisted conformation happens via a non-radiative pathway. Since the formation of the TICT state is favored in viscous solvents or at low temperature, the probability of fluorescence emission is reduced under those conditions [51]. Molecular rotors have been used as viscosity and flow sensors for biological applications [52], Modifications on their structure have introduced new reactivity that might increase the diversity of their use in the future [53] (see Fig. 6.7). [Pg.249]

Many fluorophores are sensitive to changes in the hydropho-bicity of the immediate environment. Therefore, bringing these fluorophores into a different environment may also produce a change in FRET, when a second fluorophore is affected by the emission change of the first. Fluorophores like Nile Red with changes of up to 100 nm when transferred from water to an aprotic organic solvent are principally suitable for such an approach [71], Molecular rotors have the characteristic of having a quantum yield that depends on the viscosity. Such dyes are formed by an electron donor unit and an electron acceptor unit that can rotate relative to each other upon photoexcitation with a behavior that depends on the viscosity of the environment. These dyes have been included in FRET probes for viscosity studies [53],... [Pg.265]

Steady-state fluorescence anisotropy In low-viscosity solvents the rotational depolarization of low molecular weight compounds occurs on the picosecond timescale [124]. Since in this case the rotation is much faster than the fluorescence, the steady-state emission is unpolarised. If the rotational motion of the fluorophore is on the same timescale as the fluorescence, a steady state polarisation is observed. In the simplest case for a spherical rotor and a single-exponential fluorescence intensity decay (r), the measured anisotropy is given by... [Pg.149]


See other pages where Fluorophores molecular rotors is mentioned: [Pg.267]    [Pg.268]    [Pg.269]    [Pg.278]    [Pg.286]    [Pg.288]    [Pg.293]    [Pg.295]    [Pg.297]    [Pg.298]    [Pg.264]    [Pg.423]   
See also in sourсe #XX -- [ Pg.238 ]




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Fluorophores

Molecular rotors

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