PtII-Catalyzed Hydroxylation of Terminal Aliphatic C(sp3)−H Bonds with Molecular Oxygen

The practical application of Shilov-type Pt catalysis to the selective hydroxylation of terminal aliphatic C−H bonds remains a formidable challenge, due to difficulties in replacing Pt^IV with a more economically viable oxidant, particularly O₂. We report the potential of employing FeCl₂ as a suitable redox mediator to overcome the kinetic hurdles related to the direct use of O₂ in the Pt reoxidation. For the selective conversion of butyric acid to γ-hydroxybutyric acid (GHB), a significantly enhanced catalyst activity and stability (turnover numbers (TON)>30) were achieved under 20 bar O₂ in comparison to current state-of-the-art systems (TON<10). In this regard, essential reaction parameters affecting the overall activity were identified, along with specific additives to attain catalyst stability at longer reaction times. Notably, deactivation by reduction to Pt⁰ was prevented by the addition of monodentate pyridine derivatives, such as 2-fluoropyridine, but also by introducing varying partial pressures of N₂ in the gaseous atmosphere. Finally, stability tests revealed the involvement of Pt^II and FeCl₂ in catalyzing the non-selective overoxidation of GHB. Accordingly, in situ esterification with boric acid proved to be a suitable strategy to maintain enhanced selectivities at much higher conversions (TON>60). Altogether, a useful catalytic system for the selective hydroxylation of primary aliphatic C−H bonds with O₂ is presented.     

Combined supercritical-fluid chromatography/mass spectrometry in the analysis of diuron in plasma using on-line phase-system switching

On-line sample pretreatment by means of the phase-system switching approach is an interesting technique for the analysis of aqueous samples, e.g., plasma, by means of supercritical-fluid chromatography. In order to analyse plasma samples the following analytical procedure is used. The plasma sample is injected on to a short precolumn, which is washed with water and subsequently dried with nitrogen. Next, the solutes are desorbed with the supercritical mobile phase, analysed with packed-column supercritical-fluid chromatography and detected with either a UV detector or a mass spectrometer, equipped with a moving-belt interface. The herbicide diuron is selected as a test compound to study the feasibility of this approach. Using a selective detector the procedure is sufficiently sensitive to detect diuron in plasma, but not appropriate to detect the diuron metabolites in a post-mortem plasma sample. These have been identified with liquid chromatography/mass spectrometry. The detection limit of diuron in plasma using the procedure described is about 30 ng/mL.     

The synthesis of 6-trifluoroethyl-l-lysine: a method to introduce functionality at C-6 of l-lysine

Described is a method of introducing trifluoroalkyl groups at C-6 of lysine. This chemistry has the potential to introduce a variety of functionality at C-6 of lysine.     

Dark cure studies of cationic photopolymerizations of epoxides: Characterization of kinetic rate constants at high conversions

The effective propagation rate constant (k_p; averaged over all the propagating active centers) was characterized for solvent‐free cationic photopolymerizations of phenyl glycidyl ether over the entire range of conversions, including the high conversion regime in which mass transfer limitations become important. The profile for the k_p as a function of conversion was found to exhibit a constant plateau value at low to intermediate conversions, followed by a monotonic increase above a threshold value of conversion. To explain this trend, it is proposed that at high conversion the diffusional mobility of the photoinitiator counterion is reduced whereas the mobility of the cationic active center remains high because of reactive diffusion. Therefore, with increasing conversion, the average distance between the active centers and counterions may increase, resulting in an increase in the propagation rate constant. The profiles for the k_p values were investigated as a function of the temperature, photoinitiator anion, and photoinitiator concentration. As the photoinitiator concentration was increased, the plateau value of the effective propagation rate constant decreased whereas the threshold conversion increased. All of the experimental trends are consistent with the proposed increase in ion separation at high conversions. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4409–4416, 2004     

Annoyance caused by simultaneous impulse, road-traffic, and aircraft sounds: a quantitative model.

In this study, total annoyance caused by different simultaneous environmental sounds is investigated. In spite of a number of puzzling data in the literature, it is fairly well established that in combinations in which the annoyance of one source is considerably higher than that of another source, total annoyance is equal to the maximum annoyance of the separate sources. For combinations in which both sounds are about equally annoying, total annoyance seems to be higher than the maximum source-specific annoyance. The available data, however, are too rough to model total annoyance in these conditions. The present laboratory studies were therefore designed to explore further possible procedures to quantify total annoyance. Subjects rated the (total) annoyance caused by various combinations of impulse, road-traffic, and aircraft sounds. The results support a simple model which predicts the overall or total rating sound level L(t) for combinations of several types of sounds. Here, L(t) is numerically equal to the A-weighted equivalent sound level L(eq) of road-traffic sound with the same annoyance as caused by the combination of sounds. In the model, the sound exposure caused by the impulse and/or aircraft sounds is first expressed in the L(eq) of equally annoying road-traffic sound. With the help of source-specific dose-effect relationships, this is achieved by adding level-dependent penalties to the L(eq) of the respective sources. Weighted summation of the corrected L(eq)'s of the various sources then results in L(t). An optimal overall fit of the data from two separate experiments was obtained when the weighted summation of the corrected L(eq)'s was performed with the parameter k in k log(sigma 10(corrected L(eq) of source j)/k) set to 15. The standard deviation of the differences between the experimental results and the model predictions with k = 15 was equivalent to the small change in annoyance produced by a 1.5-dB shift in the L(eq) of road-traffic sound. Adoption of k = 15 implies that after correction, two equal L(eq)'s yield a total rating sound level which is 4.5 dB higher than each single-source corrected L(eq).