Reductive coupling of N-methoxycarbonyl lactams with benzophenone and 9-fluorenone by low-valent titanium

The reductive coupling of N-methoxycarbonyl lactams with benzophenone by Zn-TiCl₄ in THF gave cross-coupled products as cyclic α-diphenylidene-N-methoxycarbonylamines and ring-opening α,α-diphenyl-α-hydroxy-ω-(N-methoxycarbonyl)amino ketones selectively depending on the reduction conditions. The reductive coupling of N-methoxycarbonyl lactams with 9-fluorenone by Zn-TiCl₄ gave cyclic α-(9H-fluoren-9-ylidene)-N-methoxycarbonylamines preferentially irrespective to the conditions.     

Ultrasonic irradiation effect in the quenched benzene

On slow cooling, a precursor phenomenon in supercooled benzene was probed by longitudinal absorption. On quenching, in-situ observation of ultrasonic measurements was carried out at the fixed temperature. Sequence of the transmitted waves was multiple scattered in quenched benzene. The dynamic ultrasound scattering is sensitive to the local strain and dynamic inhomogeneous fluctuations. The quenched benzene shows the maximum value of longitudinal absorption at incubation time, t_inc. Crystal domain growth/coarsening is promoted by the ultrasonic irradiation at t_inc < t. In addition, t_inc depends on the quenching temperature. Ultrasonic irradiation and quenching effects dominate the extraordinal nucleation and growth process of benzene in spite of simple and non-polar molecular liquid.     

Hyperfine structure of the electron spin resonance of phosphorus-doped Si nanocrystals

Electronic states of P donors in Si nanocrystals (nc-Si) embedded in insulating glass matrices have been studied by electron spin resonance. Doping of P donors into nc-Si was demonstrated by the observation of optical absorption in the infrared region due to intraconduction band transitions. P hyperfine structure (hfs) was successfully observed at low temperatures. The observed splitting of the hfs was found to be much larger than that of the bulk Si:P and depended strongly on the size of nc-Si. The observed strong size dependence indicates that the enhancement of the hyperfine splitting is caused by the quantum confinement of P donors in nc-Si.     

Origin of the stability of Ge(105) on si: a new structure model and surface strain relaxation

The structure of Ge(105)-(1 x 2) grown on Si(105) is examined by scanning tunneling microscopy (STM) and first-principles calculations. The morphology evolution with an increasing amount of Ge deposited documents the existence of a tensile surface strain in Si(105) and its relaxation with increasing coverage of Ge. A detailed analysis of high-resolution STM images and first-principles calculations produce a new stable model for the Ge(105)-(1 x 2) structure formed on the Si(105) surface that includes the existence of surface strain. It corrects the model developed from early observations of the facets of "hut" clusters grown on Si(001).     

Synthesis, complexation, and fluorescence behavior of armed crown ethers carrying naphthyl group

Armed crown ethers (1-4) bonding through an amine, amide, ether, or ester linkage to naphthyl group were found to display unique photophysical properties in the presence of guest salts. Complexation of PET fluoroionophores (1a and 1b) with Zn(2+) increased the fluorescence intensities of the host by a factor of 2.4 and 2.7, respectively. (1)H and (13)C NMR analyses of this complexation behavior of 1a revealed that Zn(2+) strongly coordinates with the armed crown nitrogen to cause a dramatic decrease in an intramolecular charge-transfer character. The armed crowns (2 and 3), bonding through an ether or ester linkage to a naphthalene, gave fluorescence quenching with guest thiocyanates. While the amide derivative (4) exhibited high Ba(2+) fluorescence selectivity and in the presence of this cation the host fluorescence intensity was by a factor of 3.69.