Infrared spectra of 1-phosphapropyne,CH3CP,and its perdeuteride,CD3CP

The infrared spectra of 1-phosphapropyne, CH₃CP, and its perdeuteride, CD₃CP, have been measured in the gaseous and solid states. The Q_K branches of perpendicular bands have been analyzed in terms of the usual quadratic expression in K. Fermi resonances were identified for the ν₁, ν₂ + ν₃, 2ν₃, 2ν₆⁰; and ν₅, 2ν₃ + ν₈ band systems of CH₃CP and the ν₁, 2ν₃, 2ν₆⁰; ν₆, ν₇ + ν₈; and ν₇, 3ν₈¹ band systems of CD₃CP. The xy Coriolis interaction was also identified between the ν₃ and ν₆ bands of the two species. All the fundamentals were assigned and the normal coordinate treatment was carried out along with the Coriolis constants, ζ^z.     

Cationic (carbene) organopalladium(II) complexes coordinated with cyclic diolefin or organic nitrile

The chloro-bridged (carbene)organopalladium(II) complex, di-μ-chlorobis(1,3-diphenyl-2-imidazolidinylidenato-2-C,2′-C)dipalladium(II) underwent chlorine abstraction with silver perchlorate in the presence of a cyclic diolefin or an organic nitrile, to give new cationic (carbene)organopalladium(II) complexes coordinated with the respective substrates. These new complexes were characterized by means of elemental analysis, molar conductivities, and IR and ¹H NMR spectroscopy.     

Time-resolved optical transmission during pulsed-laser annealing of ion-implanted amorphous silicon-on-sapphire

Time-resolved optical transmission of annealing dye laser pulse (wavelength : 590 nm and pulse width : 250 nsec) itself has been measured in thin layers of Si⁺-implanted amorphized silicon-on-sapphire (SOS) with several energy densities in the range of 0.02 to 2.64 J/cm². At the energy densities where the amorphized SOS is recrystallized, the transmission exhibits a sudden drop and subsequently remains at a detectable level. This laser-induced absorption is inconsistent with the presence of ordinary molten silicon but suggests an electronic structural-change from amorphous to crystalline state.     

DNA DAMAGE and ITS REPAIR IN Dictyostelium discoideum IRRADIATED BY HEALTH LAMP LIGHT (UV- B)

Irradiation by health lamp (HL) light (280–320 nm) more efficiently induced cell killing and mutation in a radiation sensitive mutant (TW8) of Dictyostelium discoideum as compared with the parental wild-type strain (NC4). This light as well as a germicidal lamp-light (254 nm) produced pyrimidine dimers. The dimers were removed from DNA molecules by excision repair in NC4, but more slowly in TW8. It is suggested that pyrimidine dimers are the main DNA damage caused by HL light in D. discoideum , and that this results in cell killing and induced mutation.     

Single-electron-capture cross sections for 0.4–5.0 keV He+ ions incident on alkali-vapor targets

Total cross sections for single-electron capture by He⁺ ions in vapor targets of Cs, Rb, K and Na have been determined in the energy range 0.4–5.0 keV. The energy dependence of the cross-section curves is very similar for all the targets. The cross sections for all the targets are maximum at about the same energy, 1.5 keV. Comparison is made with other reported experimental and theoretical results.     

4-Diazomethylcoumarins and related stable heteroaryldiazomethanes. Thermal conversion into condensed pyrazoles

4-Diazomethyl-substituted coumarins, 1-methyl-2(1H)-quinolinones, 1 -thiocoumarin and their tricyclic analogs were found to be easily cyclized into the corresponding pyrazole isomers condensed with heteroaromatics. Thermodependent feature of these conversions and the remarkably accelerating effect of the alkyl substituent peri to the diazomethyl group were realized. Some other diazomethyl compounds connected with 2-pyridinone, 3-pyrazolone, chromone and 1-thiochromone were prepared, and their stability and thermal properties were compared.     

The regioselective alkylation of 4,6-dimethyl-1-phenyl-2(1H)-pyrimidinone

4,6-Dimethyl-1-phenyl-2(1H)-pyrimidinone (I) was treated with alkyl halides in the presence of sodium hydride at low temperature to afford only C-6 alkylated products III and IV in good yields. Further, the mono-, IIIa-d, and di-alkylated 2(1H)-pyrimidinones IVa-d were selectively obtained by changing the amount of alkyl halides.