The photophysical and photochemical properties of p-substitued 2-styryl-ethylbenzothiazolium iodides, possessing different electron-withdrawing or electron-donating groups are described. The dyes were prepared by the condensation of 3-ethyl-2-methylbenzothiazole salts with p-substituted benzaldehydes. The synthesis of suitable substrates is presented as well. We describe here the absorption, emission spectra and the luminescence quantum yield of hemicyanine dyes (SH) measured in 11 different organic solvents of varying polarity. Molecular structure of the synthesized dyes was established by (1)H NMR, electronic absorption and fluorescence spectrometry. The spectral data confirmed that all the compounds exist in E-configuration of their styryl residues. The planar molecular conformation is typical for the compounds with five-membered side aromatic moieties (for example benzothiazole). The compounds possessing N-alkyl substituent in phenyl ring, in contrast to the compounds with other substituents, exhibit low fluorescence quantum yield in THF solution. This indicates that for N-alkyl derivatives the non-radiative processes are much more effective than the radiative ones. The electronic absorption and fluorescence emission spectra of tested dyes demonstrate high sensitivity to the nature of substituent introduced into the aromatic ring. 相似文献
A global forcing set in a simple connected graph G with a perfect matching is any subset S of E(G) such that the restriction of the characteristic function of perfect matchings of G on S is an injection. The number of edges in a global forcing set of the smallest cardinality is called the global forcing number
of G. In this paper we prove several results concerning global forcing sets and numbers of benzenoid graphs. In particular, we
prove that all catacondensed benzenoids and catafused coronoids with n hexagons have the global forcing number equal to n, and that for pericondensed benzenoids the global forcing number is always strictly smaller than the number of hexagons. 相似文献
The reactions of dialkylaluminium acetylacetonates, R2Al(acac),(where R = CH3, C2H5 and i-C4H9; I–III) with Lewis bases Et2O, THF, Py, 2,6-dimethylpyridine (DMP), DSMO and HMPT, have been studied. The reaction was found to proceed according to the equation: With strong bases (B) the reaction is shifted completely to the right, with bases of moderate strength an equilibrium is established and with weak bases the reaction is shifted completely to the left. The reaction rate constant k1 depends on R and increases in the order i-C4H9 < C2H5 < CH3. The reaction starts from the formation of the complex R2Al(acac)-B (consisting of a five-coordinated aluminium atom) and its further dissociation. The reaction mechanism is discussed. 相似文献
Low molecular weight tri-podal biphenyl- and benzoate-type mesogens [C6H5C6H4O(CH2)5SiMe2CH2CH2SiMe2]3CH (4), [C11H23O(C6H4)2O(CH2)5SiMe2]3CH (5) and [MeOC6H4OC(O)C6H4O(CH2)5SiMe2]3CH (6) (C6H4 = 1,4-phenylene) were obtained, from branched silyl substituted methane precursors [CH2CH(Me)2Si]3CH (1) and (HMe2Si)3CH (2). The biphenyl-containing ones (4) and (5) were converted into terminal alkenes, which were subsequently hydrosilylated with poly(methylsiloxanes). The polymer derived from (5) exhibited mesomorphic properties. Such systems have the potential to significantly increase the density of liquid crystal rod-like structures in side chains of linear polymers (or dendritic liquid crystal polymers). 相似文献
Summary The synthesis and spectroscopic characterization of seven new tetraphenyl-porphyrins (1–7) derivatized with 12-crown-4, 14-crown-4, 15-crown-5, or 18-crown-6 ether units inortho orpara position of one of the phenyl rings is described.
In einem Phenylring mit Kronenethern monosubstituierte Tetraphenylporphyrine. Synthese und Charakterisierung
Zusammenfassung Die Synthese und die spektroskopische Charakterisierung sieben neuer Tetraphenylporphyrine (1–7), die mit 12-Krone-4, 14-Krone-4, 15-Krone-5 oder 18-Krone-6 in derortho-oderpara-Position eines Phenylrings substituiert sind, werden beschrieben.
Tritium exchange at C-8 of xanthosine, theobromine, 1-, 3- and 7-methylxanthine in water has been studied. The rates of detritiation of these compounds have been determined over a pH range at constant temperature. Several mechanisms of exchange involving various ionic forms of substrate operating at different pH have been suggested. 相似文献
The refined theory of the electroviscous lift forces is presented for the case when the separation distance between the particle and the wall is larger than the double-layer thickness. The theory is based on the lubrication approximation for motion of a long cylinder near a solid wall in creeping flow. The approximate analytical formula for the lift force valid for Pe=1 is derived and compared with the results of numerical calculations performed for an arbitrary Peclet number. The resulting electrokinetic lift force exceeds by several orders of magnitude one predicted by the previously developed theories of the lift force. The results for the electroviscous drag force indicate that when the double layer is thin compared with the particle size, the electroviscous drag is only a small correction (at most 10%) to the hydrodynamic drag force acting on a neutral particle moving near the wall. Copyright 2000 Academic Press. 相似文献
The silica-based Fe(III)-protoporphyrin and Zn-tetraphenylporphyrin stationary phases were examined for the HPLC separation of anions. The retention of nine common inorganic anions as well as benzoate anion (BA) and its hydroxy analogues (HBA) was examined using tartrate, acetate, and succinate eluents. The retention factors of inorganic anions on the FeProP stationary phase were in the order Cl- < NO3- < ClO4- < I- < SCN- and for organic anions benzoate < p-hydroxybenzoate < m-hydoxybenzoate < o-hydroxybenzoate. The retention factors of organic anions examined for a ZnTPP column were in the order p-HBA < m-HBA < BA < o-HBA. 相似文献
The significant role of the proton exchange and homoconjugation (formation of AHA– and A1HA
1–
complexes) equilibria in protonic hetero systems (HA+A
1–
) has been shown from analysis of published data and from my own simple experiments. It is concluded that there is a need to reconsider some basic hydrogen bond problems. One of these problems-the existence of heteroconjugates in polar solvents — has been verified and illustrated with suitable experimental evidence (IR and UV-VIS spectra). The most accepted experimental evidence for the double minimum potential in the hydrogen bridge has been questioned as being in disagreement with the equilibrium law. A simple relation between the heteroconjugation constant, the parent homoconjugation constants and the proton exchange constant is also postulated. This relation fulfills important theoretical requirements, however, it is not applicable in extreme cases.To the memory of Bogdan Przybyszewski. 相似文献