Elongation of carbonyl compounds by utilizing electroreduction as a key step

The transformation of aldehydes, ketones and esters to the next higher homologous aldehydes was accomplished by utilizing electroreductive 1,2-elimination as a key step.     

Molecular structure and puckering potential of gas-phase 1-pyrroline as determined by microwave and infrared spectroscopy

The microwave spectrum of 1-pyrroline has been measured from 8 to 48 GHz. The transitions have been assigned to those of the ground state and the four lowest excited states of the ring-puckering vibration of monomer, which is a five-membered ring molecule with one CN double bond. The trimer, which exists in the liquid phase, has not been detected in the gas phase. The geometrical structure of the monomer has been estimated by an ab initio calculation and the trimer by a molecular mechanics calculation. The former is consistent with the experimental rotational constants. A gas-phase infrared spectrum has also been measured, and the ring-puckering potential has been determined by an analysis of the combination bands of the ring-puckering mode and the ring-stretching modes. The potential is described using a puckering coordinate, z, as V(z) = az² + bz⁴, where $\text{a = ?3.358(16) × 10}{}^4\text{cm}{}^{\mathrm{?1}}\text{A}\text{?}{}^{\mathrm{?2}}$ and $\text{b = 1.345(9) × 10}{}^6\text{cm}{}^{\mathrm{?1}}\text{A}\text{?}{}^{\mathrm{?4}}$; these values are intermediate of the corresponding values for cyclopentene and 1-pyrazoline. The nuclear quadrupole coupling constants, χ_aa = ?4.39(10), χ_bb = 1.04(10), and χ_cc = 3.35(10) MHz, have been determined by an analysis of well-resolved hyperfine splittings. These constants have been reproduced by an ab initio calculation with a 4-31G(N¹) basis set.     

NMR study of the self-induced vortex in (Ce1−xGdx)Ru2

NMR measurement of ¹⁵⁷Gd has been performed in zero external field in (Ce_1?xGd_x)Ru₂ for x = 0.100and 0.119 at low temperature down to 25 mK. Zero field NMR is observed with large enhancements both of H₁ and the intensity of the signal that are characteristic in ferromagnet. T₁T increases rapidly with decreasing temperature, which is attributed to the appearance of the superconducting energy gap whose magnitude is estimated to be 0.066kT_Cforx = 0.100. The NMR intensity in the superconducting state decreases not so drastically as expected in the perfect Meissner state. These results are qualitatively the same as reported previously for x ≥ 0.105 and T ≥ 60 mK. The results suggest that the system is in the state of self-induced vortices predicted theoretically.     

Anisotropic optical properties of pure and doped polyacetylene

Optical absorption and reflection measurements have been carried out on pure and doped polyacetylene films. The absorption data are consistent with a model of (CH)_X as a direct gap quasi-l d semiconductor; doping with AsF₅ or iodine introduces absorption within the gap, but appears to leave the interband transition intact. The anisotropic reflectance from partially aligned films and the increased optical anisotropy upon doping provide evidence of quasi-l d behavior of the semiconducting pure polymer and the metallic doped polymer.     

The light acceptance angle of a graded index fibre

The acceptance angle of a graded index fibre, which corresponds to the numerical aperture, is presented. A geometrical technique is used to obtain the exact ray trajectory of the beam propagating along the fibre. The acceptance angle in a conventional multimode fibre is not influenced by the position in the fibre cross-sectional area, especially for the meridional rays. However in a graded index fibre, it is a function of position on the cross section of the fibre and of the incident angle of the beam. As the position moves into the fibre periphery, the acceptance angle decreases monotonically and approaches zero.     

Copolymerization of propylene with acrylate by a Ziegler-Natta type catalyst

Propylene was polymerized by using a Ziegler-Natta type catalyst in the presence of ethylchloroaluminum acrylate, which was formed by the reaction of diethylaluminum chloride with acrylic acid. The polymer obtained contained acrylic units which were proved to be copolymerized with propylene units by solvent extraction, infrared spectrum, and NMR spectrum. The copolymer showed much improved properties compared with the polypropylene homopolymer.