Das Schwingungsspektrum von Barium-Divanadat

The infrared and laser-Raman spectra of crystalline Ba₂V₂O₇ are reported and discussed by means of a Site Symmetry analysis.

28. Mitt. der Reihe Orthovanadate und verwandte Verbindungen. 27. Mitt.:E. J. Baran undM. E. Escobar, J. Phys. Chem. Solids, im Druck; 26. Mitt.:E. J. Baran, I. L. Botto, J. F. Ramos undP. J. Aymonino, Mh. Chem.109, 1139 (1978); 25. Mitt.:E. J. Baran, J. Mol. Struct.48, 441 (1978); 24. Mitt.:E. J. Baran undI. L. Botto, J. inorg. nucl. Chem.40, 1603, (1978); 23. Mitt.:M. E. Escobar undE. J. Baran, Z. Anorg. allg. Chem.,441, 273 (1978).     

The molecular structure of norbornene as determined by electron diffraction and microwave spectroscopy

The molecular structure of norbornene has been investigated in the gas phase by combining electron diffraction data with microwave spectroscopic rotational constants. The interatomic distances (r_g) and bond angles were obtained by applying a least squares program to the refined experimental molecular diffraction intensities. The CC bond length was found to be 1.336 ± 0.002 Å while the

) bond length was 1. 529 ± 0.007 Å. Other bond lengths and angles included (IUPAC numbering system was used for norbornene): C₁-C₆ = 1.550 ± 0.020 Å, C₁-C₇ = 1.566± 0.005 Å, C₅-C₆ = 1.556 ± 0.005 Å, C-H_ave. = 1.103 ± 0.003 Å, ∠C₁C₂C₄ = 95.3°. The dihedral angle between planes C₁C₂C₃C₄ and C₁C₆C₅C₄ is 110.8 ± 1.5° while that between C₁C₂C₃C₄ and C₁C₇C₄ is 122.3°. The moments of inertia calculated from ED structure are in good agreement with microwave spectroscopic values.     

Low temperature spectroscopic observation of oxygen-protonated troponeiron tricarbonyl complexes

Troponeiron tricarbonyl and 7-methyltroponeiron tricarbonyl undergo kinetically controlled oxygen protonation at low temperatures to give the corresponding hydroxytropyliumiron tricarbonyl cations, observable by ¹C and ¹H NMR spectroscopy. At higher temperatures, the oxygen-protonated species isomerize to yield the thermodynamically more stable carbon-protonated pentadienyliron tricarbonyl cations.     

Reactions of ketenes with ethoxyalkynes: Synthesis of 2,2,4-trialkylcyclobutane-1,3-diones

Treatment of dimethyl ketene with ethoxyacetylene 1a, 1-ethoxyoct-1-yne 1b, and 1-ethoxytetrade-1-yne 1c afforded the 3-ethoxycyclobutenones 2a–c. Hydrolysis of 2a–c with dilute hydrochloric acid gave the cyclobutane-1,3-diones 3a–c. The ¹H NMR spectra of these compounds indicate that in CDCl₃ solution 2,2-dimethylcyclobutane-1,3-dione 3a exists as the diketone, whereas the 2,2,4-trialkylcyclobutane-1,3-diones 3b and 3c exist as the monoenols.     

Infrared and Raman matrix isolation studies of methylamine

Infrared (4000-50 cm^?1) and Raman spectra are reported of methylamine, methylamine-d₁ and methylamine-d₂ trapped in argon and nitrogen matrices at 4–20 K. An anomalous intensity variation was found for the NH₂ wagging mode of methylamine isolated in nitrogen matrices, while in argon matrices the NH₂ wagging absorption exhibited a complex structure due to matrix site effects. A normal coordinate analysis was carried out using a new assignment of the NHD twisting frequency. Barriers to internal rotation in argon and nitrogen matrices, calculated from the observed torsional frequencies, are compared with the gas phase value.     

An improved cyclization protocol for the synthesis of diazabicyclo[4.3.0]alkanes

We have recently described the synthesis of diazabicyclo[4.X.0]alkanes and their use as ligands for the prostate specific membrane antigene (PSMA). The key step of our synthetic route toward these diazabicycloalkanes is an oxidative cleavage of a bicyclic diol moiety followed by the attack of a nitrogen nucleophile to the resulting intermediate bisaldehyde. We herein describe the mechanism of this ring closure and its stereochemical consequences. In addition, we report a convenient method for trapping intermediate bisaldehydes by Wittig reagents. This trapping allows the synthesis of 3,5-disubstituted proline derivatives, which are shown to be versatile precursors for functionalized diazabicycloalkane dipeptide mimetics.     

Experimental study of the concentration dependence of the soret coefficient by thermal field-flow fractionation: the case of polystyrene in decalin

Summary Thermal field-flow fractionation separates polymers with high selectivity according to their Soret coefficient,S _τ, hence, according to their molar mass, and therefore consitutes an efficeint physicochemical tool for the determination of the Soret coefficient of a given polymer in the carrier liquid from its retention time. However, the polymer concentration in the sample influences the retention time and, hence, the value ofS _τ derived from it. An experimental study of the influence of sample concentration on retention,S _τ, and peak shape was performed for the polystyrene-decalin system over a relatively large temperature domain and for various molar masses. It is found that the retention time and the value ofS _τ increase with increasing sample concentration, the more so as the cold wall temperature is lower. This appears to be in contradiction with the general non-equilibrium thermodynamic expression derived for polymer-solvent systems with positive second virial coefficients, such as the present system over the temperature range investigated. There seems to be a temperature for which the dependence ofS _τ on sample concentration vanishes. This temperature is about 375 K for the polystyrene-decalin system. As the sample concentration increases, the peak barycentre and the standard deviation increases. As the peaks are fronting, the skewness is negative and becomes more negative as the sample concentration increases. The peak skewness appears to be a good indicator of the onset of sample concentration effects. The threshold concentration, for which these effects begin to become significant, decreases with increasing molar mass.     

Sensitive determination of diquat by a kinetic method using the stopped-flow mixing technique

A simple, sensitive, selective, fast and inexpensive assay for the determination of diquat is proposed. The method is based on the reduction of the herbicide to a strongly fluorescent monocation radical with sodium dithionite. The initial rate of this reaction is directly proportional to the diquat concentration. The stopped-flow mixing technique was used because the kinetic data can be obtained in only 7 s, meaning that the method can be automated. The calibration graph is linear over the range 5-500 ng ml-1 and the precision (RSD) is close to 1.2%. The applicability of the method was demonstrated by determining the herbicide in different kinds of samples.     

Solid state radioluminescent lighting

We have demonstrated novel types of tritium-powered, solid-phase radioluminescent (RL) light sources. These lights include: (1) all-organic formulations comprised of polystyrene and fluorescent organic dyes; (2) polydimethylsiloxane-based systems incorporating inorganic phosphors; and (3) inorganic aerogel-based systems doped with phosphors. Three principal design consideration for these new RL lights are described. These include: (1) incorporation of tritium into the solid matrix; (2) molecular engineering to maximize light-output efficiency; and (3) strategies for increasing longevity. The advanced RL lights, which are of interest due to potential advantages in efficiency, brightness and safety, are being developed for emergency lighting uses and for battery and lighting applications in remote locations.     

Reaction of the carbonate radical with substituted anilines

Rate constants for the reaction of carbonate radical with aniline and some parasubstituted anilines have been determined by the flash photolysis technique. Using σ⁺ para values the rate constants at pH 8.5 correlate very well with the Hammett equation yielding ρ= − 1. The carbonate radical oxidises aniline giving the anilino radical. The products so formed have been identified through studies under conditions of continuous irradiation.