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).     

Eine einfache Bestimmung des Formaldehyds

Ohne Zusammenfassung     

Zur Untersuchung der ?therischen Oele

Ohne Zusammenfassung     

Environmentally Safe Photodynamic Control of Aedes aegypti Using Sunlight-Activated Synthetic Curcumin: Photodegradation,Aquatic Ecotoxicity,and Field Trial

This study reports curcumin as an efficient photolarvicide against Aedes aegypti larvae under natural light illumination. Larval mortality and pupal formation were monitored daily for 21 days under simulated field conditions. In a sucrose-containing formulation, a lethal time 50 (LT50) of 3 days was found using curcumin at 4.6 mg L⁻¹. This formulation promoted no larval toxicity in the absence of illumination, and sucrose alone did not induce larval phototoxicity. The photodegradation byproducts (intermediates) of curcumin were determined and the photodegradation mechanisms proposed. Intermediates with m/z 194, 278, and 370 were found and characterized using LC-MS. The ecotoxicity of the byproducts on non-target organisms (Daphnia, fish, and green algae) indicates that the intermediates do not exhibit any destructive potential for aquatic organisms. The results of photodegradation and ecotoxicity suggest that curcumin is environmentally safe for non-target organisms and, therefore, can be considered for population control of Ae. aegypti.     

Quasifree photoproduction of eta mesons off the neutron

Quasifree photoproduction of eta mesons off nucleons bound in the deuteron has been measured with the CBELSA/TAPS detector for incident photon energies up to 2.5 GeV at the Bonn ELSA accelerator. The eta mesons have been detected in coincidence with recoil protons and recoil neutrons, which allows a detailed comparison of the quasifree n(gamma,eta)n and p(gamma,eta)p reactions. The excitation function for eta production off the neutron shows a pronounced bumplike structure at W=1.68 GeV (E{gamma} approximately 1 GeV), which is absent for the proton.     

Bremsstrahlung in heavy-ion reactions

We investigate bremsstrahlung processes induced by heavy ions: nuclear dipole and quadrupole radiation, radiation from bound target electrons into the continuum and secondary electron bremsstrahlung (SEB), which contribute to the background of the X-ray spectra. A comparison with experiment is presented.     

Absorptionsspektren natürlicher Granate im Bereich von 200 bis 1500 nm und ihre Bedeutung

The absorption spectra of 36 natural garnets formed under different conditions have been investigated. The results show that the [CrO₆] complex has the symmetry m3m only if the minerals crystallized under extreme conditions, expecially at high pressures and high Cr₂O₃ concentrations. Mostly the microsymmetry 4 mmm has been observed for the octahedral complexes. Corresponding to theoretical calculations based on the crystal field theory it is revealed by comparison of intensities that [CrO₆] is essentially more stable than [FeO₆] complexes. Garnet reacts under energy supply to pyroxene (bronzite) and to complex oxidie phases as shown by further studies.