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Dipolarity/Polarizability of Reaction MediaThe solvatochromisms of Michler's Ketone (1) and the iron (11) complex Fe(phen)z(CN)z (2) has been investigated in 73 solvents of different polarity. The solvent-induced UV/Vis-absorption shifts of 1 and 2 are mainly attributed to both the hydrogen-bond donor acidity and dipolarity/polarizability of the solvent as verified by a Kamlet-Taft correlation analysis and comparison with common solvent-polarity scales such as a Common Indicator of the Acidity and Reichardt's ET(30) values and the acceptor scale of Gutmann. Michler's Ketone exhibits the largest positive solvatochromism known so far. The specific role of phenolic solvents has been discussed with regard to a charge-transfer complexation between the positively polarized ring of 1, caused by the hydrogen-bond formation at the carbonyl oxygen, and the aromatic ring of the phenol. . Ahnliches gilt fur Michlers Keton, wobei nach selektiver Monoprotonierung am Carbonylsauerstoff, was in CF3S03H/Dichlormethan unter Inertbedingungen moglich ist['', die n-x*-Absorption nach 19800 cm-' bathochrom verschoben wird. In konzentrierter Schwefelsaure, in der auDer dem Carbonylsauerstoff auch noch eine der Dimethylaminogruppen von 1 protoniert wird, kommt es dagegen wieder zu einer starken hypsochromen Verschie-

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In order to improve the experimental database about the additional nonrotational broadening of vibrational line shapes observable when a simple fluid approaches its gas–liquid critical point, we improved the pioneering measurements of Clouter and Kiefte [for their own review see Phys. Rev. A 33, 2749 (1986)] on the critical behavior of the polarized Raman line of fluid nitrogen by using the isotopic mixture (14N2).975−(14N15N).025, giving special attention to the fact that the isotropic line shape of liquid N2 (ν̃≈2327 cm−1) is affected by intermolecular vibrational resonance couplings. Using a highest-resolution double monochromator and modern CCD detection techniques, we were able to follow the temperature dependencies of the line shape parameters (i.e., shift, width, and asymmetry) of the coupled N142 and, depending on the S/N ratio available, of the uncoupled N1415N in the range 45 K≲T≲300 K with up to mK resolution (1) in the β-solid phase, (2) in the coexisting liquid and gas phases, and (3) along the critical isochore. Comparing the line shifts of both isotopic species, clear evidence was found that vibrational resonance couplings are present in all dense phases studied, the line position ν̃0 being more density than temperature dependent. Additionally, the existence of (negative) cross correlations between resonant and nonresonant dephasing mechanisms has been confirmed by the change in sign observed for the small but non-negligible difference in the linewidths between coupled N142 and uncoupled N1415N around 90 K. The λ-shaped dependencies of the width parameters, observed when moving along the coexistence line through the critical point, Tcrit=126.192 K, and along the critical isochore, is much more evident in the line asymmetry than in the usually considered linewidth. Clear proof was found that, in accordance with theoretical predictions, the linewidth converges to a constant maximum value regardless if the critical point is reached along the coexistence line or along the critical isochore, i.e., it does not diverge approaching the critical temperature up to our closest value |T/Tcrit−1|≈10−5.