Resonant electron capture by polycyclic aromatic hydrocarbon molecules: Effects of aza-substitution.

Resonant electron capture by aza and diaza derivatives of phenanthrene (7,8-benzoquinoline and 1,10-phenanthroline) and anthracene (acridine and phenazine) at incident free electron energies (Ee) in the range of 0-15 eV was studied. All compounds except 7,8-benzoquinoline form long-lived molecular ions (M-) at thermal electron energies (Ee ∼ 0 eV). Acridine and phenazine also form such ions at epithermal electron energies up to Ee = 1.

Resonant electron capture by 5-Br-2'-deoxyuridine.

The results of the study of resonant electron capture by molecules of 5-Br-2'-deoxyuridine (BrdUrd) over the range of electron energies from near zero to 14 eV are described. In the thermal energy range, long-lived molecular negative ions, unstable with respect to autoneutralization and dehalogenation, have been registered. Examination of the kinetics of these decay processes led us to the conclusion that the most probable structure for molecular negative ions is that with an extended C-Br bond, which was predicted earlier using quantum-chemical calculations.

Photoinduced Reversible Modulation of Fluorescence of CdSe/ZnS Quantum Dots in Solutions with Diarylethenes.

Steady-state absorption and fluorescence spectra, fluorescence decay kinetics of CdSe/ZnS quantum dots (QD) with photochromic diarylethenes (DAE) in toluene have been studied. Two kinds of QDs emitting at 525 and 600 nm were investigated and DAE were selected to ensure good overlap of their photoinduced absorption band with QDs emission spectra. It has been found that photochromic molecules form complexes with QD which results in partial fluorescence quenching.

Fragmentation and slow autoneutralization of isolated negative molecular ions of phthalocyanine and tetraphenylporphyrin.

Macrocyclic tetrapyrrolic compounds, such as naturally occurring or artificial porphyrins and phthalocyanines, have unique and highly attractive properties for applications in medicine and technology. The interaction of free-base phthalocyanine (HPc) and tetraphenylporphyrin (HTPP) molecules with low-energy (0-15 eV) electrons was studied in vacuo by means of negative ion resonant electron capture mass spectrometry. Close similarities in formation and decay of negative ions of these compounds were revealed.

4-Bromobiphenyl: Long-lived molecular anion formation and competition between electron detachment and dissociation.

Electron attachment to the 4-bromobiphenyl molecule and the decay channels of its molecular anion were investigated by means of Dissociative Electron Attachment (DEA) spectroscopy with two different spectrometers. The first apparatus is equipped with a static magnet mass analyzer (Ufa group) and the second one with a quadrupole mass filter (Prague group). The dominant DEA channel at low electron energy leads to formation of Br negative fragments.