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Phenanthrylene-ethynylidene macrocycles combining electron donor and electron acceptor subunits in their shape-persistent fully conjugated core were synthesized. The donor subunits consisted of two 9,10-dialkoxyphenanthrenes linked either with 1,2-ethynylidene or 2,5-thienylene bridge. The acceptors were 9,10-phenanthroquinone and dibenzoquinoxaline and dibenzophenazines derived from it. Solvatochromic photoluminescence from intramolecular-charge-transfer (ICT) excited state was observed mainly in non-polar solvents. In more polar solvents, the excited states favor non-radiative relaxation. DFT calculated HOMO/LUMO energies of the macrocycles correlate well with spectroscopic and electrochemical data. In the series of substituted dibenzophenazine acceptors a good correlation with Hammett substituent constants σp– was found. 相似文献
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The experimentally motivated question of the acetylene bromoboration mechanism was addressed in order to suggest possible radical isomerization pathways for the syn-adduct. Addition–elimination mechanisms starting with a bromine radical attack at the “bromine end” or the “boron end” of the C=C bond were considered. Dispersion-corrected DFT and MP2 methods with the SMD solvation model were employed using three all-electron bases as well as the ECP28MWB ansatz. The rate-determining, elimination step had a higher activation energy (12 kcal mol−1) in case of the “bromine end” attack due to intermediate stabilization at both the MP2 and DFT levels. In case of the “boron end” attack, two modes of C–C bond rotation were followed and striking differences in MP2 vs. DFT potential energy surfaces were observed. Employing MP2, addition was followed by either a 180° rotation through an eclipsed conformation of vicinal bromine atoms or by an opposite rotation avoiding that conformation, with 5 kcal mol−1 of elimination activation energy. Within B3LYP, the addition and rotation proceeded simultaneously, with a 9 (7) kcal mol−1 barrier for rotation involving (avoiding) eclipsed conformation of vicinal bromines. For weakly bound complexes, ZPE corrections with MP2 revealed significant artifacts when diffuse bases were included, which must be considered in the Gibbs free energy profile interpretation. 相似文献
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E. Skladnik-Sadowska J. Baranowski K. Kolacek A. Kishinets A. A. Rupasov M. Ripa P. Ctibor M. J. Sadowski B. Sartowska A. Szydlowski 《Radiation measurements》2003,36(1-6):321-325
The paper describes experimental studies of the corpuscular emission from fast Z-pinch discharges, which were performed within the CAPEX capillary pinch facility in Prague, Czech Republic. Time-integrated measurements were carried out with an ion pinhole camera equipped with CR-39 nuclear track detectors. Irradiated detectors were etched at the standard conditions, and developed tracks were analysed with an optical microscope coupled with a CCD camera. It was found that the fast capillary discharges emit strong corpuscular streams. On the basis of the optical analysis of the etched detectors it was estimated that the time-integrated particle flux, at the distance of 20 cm from the collimator outlet, was about 3.5×107 particles/cm2/pulse. Particular attention was paid to analysis of ion-track photos, which were obtained by means of an electron microscope. Details of the ion micro-craters have been observed in the photos of fractures of the CR-39 detectors after their 7 h etching. 相似文献
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