Reactivity of sites on Al2O3 surface modified by Ni

It has been established that CO oxidation with excess O₂ on Ni/Al₂O₃ forms an inhomogeneous NiO contact surface that smoothes critical effects in the sharp reactivity change.     

Spectroscopic factors of9Be,10B and13C from (d,t) reactions

The differential cross sections of tritons from the (d, t) reaction on⁹Be,¹⁰B and¹³C targets have been measured in the angular range of 5° _LAB110° with relatively small errors, 5%. The experimental data were analysed in terms of the standard DWBA using both zero-range and exact finite-range approaches.     

Macroheterocyclic Compounds with 2,3-Pyridino(pyrazino)pyrrole and 1,3,4-Thiadiazole Residues

Novel symmetrical macroheterocyclic compounds were prepared by the reactions of 2,3-dicyanopyridine and 2,3-dicyanopyraine with 2,5-diamino-1,3,4-thiadiazole in butanol in the presence of sodium butylate. Physicochemical properties and biological activity of the products were studied.     

Composition of the coats and kernels of the seeds ofNepeta pannonica andLavandula vera

The lipid compositions of the coats and kernels of the seeds ofNepeta pannonica andLavandula vera have been studied. It has been established that the lipids of the seed coats of the two species of plants differ substantially in their composition. The lipids of the kernels ofNepeta have been found to contain free fatty acids with chain lengths of from C₂₀ to C₃₅. Ursolic acid and its acetate have been isolated from extracts of the seed coats ofLavandula, and dimethyladipic acid from the seed oil of this species. Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 614–620, September–October, 1980.     

Evidence for Kinetic Nucleation in Helical Nanofiber Formation Directed by Chiral Solvent for a Perylene Bisimide Organogelator

The self‐assembly behavior of an achiral perylene bisimide (PBI) organogelator that bears two 3,4,5‐tridodecyloxybenzoylaminoethyl substituents at the imide positions has been investigated in chiral solvents (R)‐ and (S)‐limonene in great detail by circular dichroism (CD) spectroscopy and atomic force microscopy (AFM). CD spectroscopic studies on dilute solutions revealed a preferential population of one‐handed helical assemblies in chiral solvent with an enantiomeric excess close to 100 %, whereas AFM images of more than 100 nanofibers of the organogel obtained from more concentrated solutions were found to consist of both handed helices with an enantiomeric excess of only 20 %. This discrepancy is attributed to the fast gelation process at high dye concentration that evidently proceeds through non‐equilibrated nuclei in a kinetic rather than thermodynamic self‐assembly process. Under these conditions the chiral induction from the homochiral solvent may not be adequate in effectively populating only one‐handed helices.     

Self-Sorting Supramolecular Polymerization: Helical and Lamellar Aggregates of Tetra-Bay-Acyloxy Perylene Bisimide

A new perylene bisimide (PBI), with a fluorescence quantum yield up to unity, self-assembles into two polymorphic supramolecular polymers. This PBI bears four solubilizing acyloxy substituents at the bay positions and is unsubstituted at the imide position, thereby allowing hydrogen-bond-directed self-assembly in nonpolar solvents. The formation of the polymorphs is controlled by the cooling rate of hot monomer solutions. They show distinctive absorption profiles and morphologies and can be isolated in different polymorphic liquid-crystalline states. The interchromophoric arrangement causing the spectral features was elucidated, revealing the formation of columnar and lamellar phases, which are formed by either homo- or heterochiral self-assembly, respectively, of the atropoenantiomeric PBIs. Kinetic studies reveal a narcissistic self-sorting process upon fast cooling, and that the transformation into the heterochiral (racemic) sheetlike self-assemblies proceeds by dissociation via the monomeric state.     

Quantum interference between multi photon absorption pathways in organic solid

We demonstrate spatial interference fringe pattern by simultaneous one- and three-photon absorption of UV and near-IR femtosecond pulses in thin film organic solid at room temperature. We use organic dendrimers that are specially designed to have strong fluorescence and very large three-photon absorption cross-section. High fringe visibility allows the quantum interference to be observed by eye.     

Proof of conformal invariance in the critical regime for models of Gross-Neveu type

It is shown that for all multiplicatively renormalizable fermionic models without derivativs in the interaction, in particular, for the Gross—Neveu model, conformal invariance of the Green's functions of the fields in the critical regime (massless model at fixed renormalization-group point) automatically follows from the scale invariance for arbitrary space dimension.St Petersburg State University. Translated from Teoreticheskaya i Matematicheskaya Fizika, Vol. 92, No. 3, pp. 486–497, September, 1992.     

Combined Resonance of the Interlayer Conductivity in Quasi-Two-Dimensional Conductors

JETP Letters - Analytical expressions have been obtained for the resonance component of the interlayer conductivity of quasi-two-dimensional conductors in an inclined magnetic field in the presence...     

Persistent Room Temperature Phosphorescence from Triarylboranes: A Combined Experimental and Theoretical Study

Achieving highly efficient phosphorescence in purely organic luminophors at room temperature remains a major challenge due to slow intersystem crossing (ISC) rates in combination with effective non‐radiative processes in those systems. Most room temperature phosphorescent (RTP) organic materials have O‐ or N‐lone pairs leading to low lying (n, π*) and (π, π*) excited states which accelerate k_isc through El‐Sayed's rule. Herein, we report the first persistent RTP with lifetimes up to 0.5 s from simple triarylboranes which have no lone pairs. RTP is only observed in the crystalline state and in highly doped PMMA films which are indicative of aggregation induced emission (AIE). Detailed crystal structure analysis suggested that intermolecular interactions are important for efficient RTP. Furthermore, photophysical studies of the isolated molecules in a frozen glass, in combination with DFT/MRCI calculations, show that (σ, B p)→(π, B p) transitions accelerate the ISC process. This work provides a new approach for the design of RTP materials without (n, π*) transitions.