Decomposition mechanism of triethylindium (TEI) on a GaP(0 0 1)-(2×1) surface studied by LEED, AES, TPD and HREELS

Adsorption and decomposition of triethylindium (TEI: (C₂H₅)₃In) on a GaP(0 0 1)-(2×1) surface have been studied by low-energy electron diffraction (LEED), Auger electron spectroscopy (AES), temperature-programmed desorption (TPD) and high-resolution electron energy loss spectroscopy (HREELS). It is found from the TPD result that ethyl radical and ethylene are evolved at about 300–400 and 450–550 K, respectively, as decomposition products of TEI on the surface. This result is quite different from that on the GaP(0 0 1)-(2×4) surface. The activation energy of desorption of ethyl radical is estimated to be about 93 kJ/mol. It is suggested that TEI is adsorbed molecularly on the surface at 100 K and that some of TEI molecules are dissociated into C₂H₅ to form P–C₂H₅ bonds at 300 K. The vibration modes related to ethyl group are decreased in intensity at about 300–400 and 450–550 K, which is consistent with the TPD result. The TEI molecules (including mono- and di-ethylindium) are not evolved from the surface. Based on the TPD and HREELS results, the decomposition mechanism of TEI on the GaP(0 0 1)-(2×1) surface is discussed and compared with that on the (2×4) surface.     

Recursive Fermion System in Cuntz Algebra. I

Embeddings of the CAR (canonical anticommutation relations) algebra of fermions into the Cuntz algebra ?₂ (or ?_{2 d} more generally) are presented by using recursive constructions. As a typical example, an embedding of CAR onto the U(1)-invariant subalgebra of ?₂ is constructed explicitly. Generalizing this construction to the case of ?_{2 p} , an embedding of CAR onto the U(1)-invariant subalgebra of ?_{2 p} is obtained. Restricting a permutation representation of the Cuntz algebra, we obtain the Fock representation of CAR. We apply the results to embed the algebra of parafermions of order p into ?_{2 p} according to Green's ansatz. Received: 3 September 2001 / Accepted: 19 January 2002     

Improvement of Dispersion and Release Properties of Nifedipine in Suppositories by Complexation with 2-Hydroxypropyl-β-cyclodextrin

Geometries, electronic properties and NMR-shielding of cucurbit[5]uril, decamethylcucurbit[5]uril, cucurbit[6]uril, cucurbit[7]uril, and cucurbit[8]uril are investigated with DFT calculations. All molecules are highly symmetrical with a distinct geometric flexibility. In addition with a characteristic partial charge distribution these findings account for their chemical complex building ability.     

HeII(304Å) photoelectron spectrum of N2O4

The 304 Å HeII photoelectron (PE) spectrum of a mixture of NO₂ and N₂O₄ in the gaseous phase has been measured in the region up to 29 eV. By subtracting the HeII spectrum of NO₂ from the mixed spectrum, the HeII spectrum due to N₂O₄ has been deduced, indicating that there are three new PE bands in the region 20—29 eV. Relative band intensities have also been obtained from the HeII of N₂O₄ below 16 eV, corrected for electron collecting efficiency.     

Regioselective 2 A -2 D -Disulfonylations of Cyclodextrins for Practical Bifunctionalization on the Secondary Hydroxyl Face

A useful technique to bifunctionalize the secondary hydroxyl faces of cyclodextrins is described. Regioselective2^A,2^D-disulfonylations ofcyclodextrins were achieved by reacting cyclodextrins with a combinationof a novel disulfonyl imidazole reagent and molecular sieves inN,N-dimethylformamide. The resulting disulfonates were convertedto 2^A,3^A,2^D,3^D-dimannoepoxy-cyclodextrins and3^A,3^D-diamino-3^A,3^D-dideoxy-(2^AS,3^AS),(2^DS,3^DS)-cyclodextrins, which contain twofunctional groups on the periphery of the molecules.     

Construction of nitrogen-heterocyclic compounds through zirconium mediated intramolecular alkene-carbonyl coupling reaction of N-(o-alkenylaryl)carbamate derivatives

Intramolecular alkene-carbonyl coupling reaction of N-benzyl-N-(o-alkenylaryl)carbamate derivative derived from o-aminostyrene, o-(aminomethyl)styrene and o-aminoallylbenzene smoothly proceeded by treating with zirconocene-butene complex to give the corresponding lactam derivative.     

Simultaneous determination of radionuclides separable into natural decay series by use of time-interval analysis

A delayed coincidence method, time-interval analysis (TIA), has been applied to successive – decay events on the millisecond time-scale. Such decay events are part of the ²²⁰Rn²¹⁶Po (T_1/2 145 ms) (Th-series) and ²¹⁹Rn²¹⁵Po (T_1/2 1.78 ms) (Ac-series). By using TIA in addition to measurement of ²²⁶Ra (U-series) from -spectrometry by liquid scintillation counting (LSC), two natural decay series could be identified and separated. The TIA detection efficiency was improved by using the pulse-shape discrimination technique (PSD) to reject -pulses, by solvent extraction of Ra combined with simple chemical separation, and by purging the scintillation solution with dry N₂ gas. The U- and Th-series together with the Ac-series were determined, respectively, from alpha spectra and TIA carried out immediately after Ra-extraction. Using the ²²¹Fr²¹⁷At (T_1/2 32.3 ms) decay process as a tracer, overall yields were estimated from application of TIA to the ²²⁵Ra (Np-decay series) at the time of maximum growth. The present method has proven useful for simultaneous determination of three radioactive decay series in environmental samples.     

Magnetic structure of graphite ribbon

Anoble mechanism of spin polarization is proposed for finite graphite sheet with edge. For graphite ribbon with zigzag edge, there appear peculiar ‘edge states’. These localized states comprise nearly flat band at the Fermi level, which easily causes magnetic instability. Magnetic structure is suggested from Hartree-Fock analysis of the Hubbard model, where huge magnetic moments are induced at around both of edges by weak HubbardU and are coupled antiferromagnetically with each other.