Solvatochromic constants

The dyes prepared in this way show a positive solvatochromism as the dielectric constant of the solvent increases, indicating that they possess a predominantly nonpolar structure. Substituents on the phenyl group in the 4-position of the selenazole ring have little influence on the absorption spectra. 

The dyestuffs show positive solvatochromism on transition to solvents of greater dielectric constant. From this, it is deduced that the compounds are of predominantly nonpolar character. 

The merocyanine dye mentioned above shows solvatochromism, which means that the absorption band maximum of the quinoid form (D form) is sensitive to solvent polarity [40,41]. In Fig. 3, the absorption maximum of the solvatochromic band for M-Mc (a low molecular weight merocyanine analog) is plotted against the dielectric constant of 1,4-dioxane/water mixtures [42]. With the relationship... 

Note Solvent classification into groups based on solvent polarity selectivity parameters proton acceptor, proton donor, x dipole interactors) and solvent strength on alumina nd on silica gel 0. Physical constants viscosity (t)), surface tension (y), dielectric constant (8). Solvatochromic polarity parameters 7, j.(30) and Ej. ... 

The dielectric constant and refractive index parameters and different functions of them that describe the reactive field of solvent [45] are insufficient to characterize the solute-solvent interactions. For this reason, some empirical scales of solvent polarity based on either kinetic or spectroscopic measurements have been introduced [46,47]. The solvatochromic classification of solvents is based on spectroscopic measurements. The solvatochromic parameters refer to the properties of a molecule when its nearest neighbors are identical with itself, and they are average values for a number of select solutes and somewhat independent of solute identity. 

Casassas, E. Fonrodona, G. de Juan, A., Solvatochromic parameters for binary mixtures and a correlation with equilibrium constants. 1. Dioxane-water mixtures, J. Solut. Chem. 

In addition to the described above methods, there are computational QM-MM (quantum mechanics-classic mechanics) methods in progress of development. They allow prediction and understanding of solvatochromism and fluorescence characteristics of dyes that are situated in various molecular structures changing electrical properties on nanoscale. Their electronic transitions and according microscopic structures are calculated using QM coupled to the point charges with Coulombic potentials. It is very important that in typical QM-MM simulations, no dielectric constant is involved Orientational dielectric effects come naturally from reorientation and translation of the elements of the system on the pathway of attaining the equilibrium. Dynamics of such complex systems as proteins embedded in natural environment may be revealed with femtosecond time resolution. In more detail, this topic is analyzed in this volume [76]. 

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]

Hawker, D. W. (1990a) Vapor pressures and Henry s law constants of polychlorinated biphenyls. Environ. Sci. Technol. 23, 1250-1253. Hawker, D. W. (1990b) Description of fish bioconcentration factors in terms of solvatochromic parameters. Chemosphere 20, 267-477. Hawker, D. W., Connell, D. W. (1988) Octanol-water partition coefficients of polychlorinated biphenyl congeners. Environ. Sci. Technol. 22, 382-387. 

The marked changes in the carbonyl IR bands accompanying the solvent variation from tetrahydrofuran to MeCN coincide with the pronounced differences in colour of the solutions. For example, the charge-transfer salt Q+ Co(CO)F is coloured intensely violet in tetrahydrofuran but imperceptibly orange in MeCN at the same concentration. The quantitative effects of such a solvatochromism are indicated by (a) the shifts in the absorption maxima and (b) the diminution in the absorbances at ACT. The concomitant bathochromic shift and hyperchromic increase in the charge-transfer bands follow the sizeable decrease in solvent polarity from acetonitrile to tetrahydrofuran as evaluated by the dielectric constants D = 37.5 and 7.6, respectively (Reichardt, 1988). The same but even more pronounced trend is apparent in passing from butyronitrile, dichloromethane to diethyl ether with D = 26, 9.1 and 4.3, respectively. The marked variation in ACT with solvent polarity parallels the behaviour of the carbonyl IR bands vide supra), and the solvatochromism is thus readily ascribed to the same displacement of the CIP equilibrium (13) and its associated charge-transfer band. As such, the reversible equilibrium between CIP and SSIP is described by (14), where the dissociation constant Kcip applies to a... 

Hydrogen bond formation between dissimilar molecules is an example of adduct formation, since the hydrogen atom that is bonded to an electronegative atom, such as oxygen or nitrogen, is a typical acceptor atom. The ability of molecules to donate a hydrogen bond is measured by their Taft-Kamlet solvatochromic parameter, a, (or a . for the monomer of self-associating solutes) (see Table 2.3). This is also a measure of their acidity (in the Lewis sense, see later, or the Brpnsted sense, if pro tic). Acetic acid, for instance, has a = 1.12, compared with 0.61 for phenol. However, this parameter is not necessarily correlated with the acid dissociation constant in aqueous solutions. 

However, it was noted that the discrepancy between the micellar rate constant and the rate constant in the model compound solution was largest for 4, which was known to be more sensitive toward hydrophobic interactions than 5. In addition, the solvatochromic Ex30 probe indicated a much more hydrophobic environment and other authors similarly found systems for which a model solution only mimicking the surfactant headgroups was insufficient to reproduce properties of the micellar pseudophase. The Hammett p-value for hydrolysis of substituted 1-benzoyl-1,2,4-triazoles 6a-f could similarly not be reproduced using a model solution mimicking ionic interactions only. " ... 

Separation of Electronic and Nuclear Motions. The polarizabilities of the ground state and the excited state can follow an electronic transition, and the same is true of the induced dipole moments in the solvent since these involve the motions of electrons only. However, the solvent dipoles cannot reorganize during such a transition and the electric field which acts on the solute remains unchanged. It is therefore necessary to separate the solvent polarity functions into an orientation polarization and an induction polarization. The total polarization depends on the static dielectric constant Z), the induction polarization depends on the square of the refractive index n2, and the orientation polarization depends on the difference between the relevant functions of D and of n2 this separation between electronic and nuclear motions will appear in the equations of solvation energies and solvatochromic shifts. 

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