Inclusive K+-meson production in proton-nucleus interactions

The production of K⁺-mesons in pA (A = D, C, Cu, Ag, Au) collisions has been investigated at the COoler SYnchrotron COSY-Jülich for beam energies T_p = 1.0-2.3 GeV. Double differential inclusive pC cross-sections at forward angles _{K^+} < 12^° as well as the target mass dependence of the K⁺ momentum spectra have been measured with the ANKE spectrometer. Far below the free NN threshold at T_NN = 1.58 GeV the spectra reveal a high degree of collectivity in the target nucleus. From the target mass dependence of the cross-sections at higher energies, the repulsive in-medium potential of the K⁺-mesons can be deduced. Using pN cross-section parameterisations from the literature and our measured pD data we derive a cross-section ratio (pnK⁺X)/(ppK⁺X) (3-4).     

a+0 (980)-resonance production in pp-->dK+K-0 reactions close to threshold

The reaction pp-->dK+K(-)0 has been investigated at an excess energy of Q=46 MeV above the K+K(-)0 threshold with ANKE at the cooler synchrotron COSY-Jülich. From the detected coincident dK(+) pairs, about 1000 events with a missing K(-)0 were identified, corresponding to a total cross section of sigma(pp-->dK+K(-)0)=[38+/-2(stat)+/-14(syst)] nb. Invariant-mass and angular distributions have been jointly analyzed and reveal s-wave dominance between the two kaons, accompanied by a p wave between the deuteron and the kaon system. This is interpreted in terms of a(+)0 (980)-resonance production.     

Detailed 1H and 13C NMR structural assignment and relative stereochemistry determination for three closely related sesquiterpene lactones

A complete analysis of (1)H and (13)C NMR spectra of the trypanocidal sesquiterpene lactone eremantholide C and two of its analogues is described. These structurally similar sesquiterpene lactones were submitted to (1)H NMR, (13)C {(1)H} NMR, gCOSY, gHSQC, gHMBC, J-resolved and DPFGSE-NOE NMR techniques. The detailed analysis of those results, correlated to some computational calculations (molecular mechanics), led to the total and unequivocal assignment of all (1)H and (13)C NMR data. The determination of all (1)H/(1)H coupling constants and all signal multiplicities, together with the elimination of previous ambiguities were also achieved.     

Ueber die Methode der calorimetrischen Bestimmung mittelst Verbrennung in Sauerstoff bei hohem Druck

Ohne Zusammenfassung     

Kinetic and thermodynamic studies of aquation reactions in [RuL2(mac)]q+ complexes: [mac = 1,4,8,11-tetraazacyclotetradecane (cyclam) or 1,4,7,10-tetraazacyclododecane (cyclen); and L = Cl−, OH−, OH2]

Transition Metal Chemistry - We report here the synthesis, characterization and kinetic studies of [RuL2(mac)]n+ complexes [mac?=?1,4,8,11-tetraazacyclotetradecane (cyclam) or...     

Synthesis of non-aggregating chlorins and isobacteriochlorins from meso-tetrakis(pentafluorophenyl)porphyrin: a study using 1,3-dipolar cycloadditions under mild conditions

The 1,3-dipolar cycloaddition of meso-tetrakis(pentafluorophenyl)porphyrin and its nickel complex, with the bulky azomethine ylide dipole was studied under mild conditions, and yielded chlorin and isobacteriochlorin derivatives self-prevented from aggregation. The reactions were performed at room temperature or 0 °C, and we were able to establish a set of reaction conditions to obtain only the chlorin or the isobacteriochlorin. These compounds were evaluated in solution, and no aggregation was observed at less than 25 mM (∼30 mg mL⁻¹) using ¹H NMR experiments.     

Aromaticity and Homoaromaticity in Methano[10]annulenes

Aromaticity and neutral homoaromaticity have been evaluated in methano[10]annulenes systems, 1,4-methano[10]annulene (1), 1,5-methano[10]annulene (2), and 1,6-methano[10]annulene (3). C-C bond lengths indicate that 1 presents higher bond alternation than 2 and 3. The relative energies were determined at the B3LYP/6-311+G(d,p) level, and they pointed out that 3 is the most stable isomer. Strain energies, evaluated employing homodesmotic reactions, show the same order as the relative energies. Through a decomposition of strain energies, it could be concluded that the rings absorb more tension than the bridges. The changes in aromaticity were evaluated by magnetic susceptibilities, chiM, HOMA, NICS, and resonance energies, RE. HOMA, RE, and chiM indicate that 2 and 3 are strongly, and 1 is fairly, aromatic. NICS does not provide reliable results, due to interference of ring and bridge atoms. NBO analysis presents some interactions that suggest the existence of neutral homoaromaticity. GPA indices (evaluated at the B3LYP/6-31G* level) point out that homoaromaticity plays a relevant role only in 3. Moreover, this work is the first in the current literature that studies 1,4-methano[10]annulene (1).