Holography in partially coherent light

A Michelson interferometer has been used to obtain good holographic carrierfringes of the order of 200 to 300 fringes/ mm over an area of 1 cm × 1.5 cm with a Hg-are source and extended aperture with and without filter. The fringes have been used to record holograms. The image reconstruction has been done with light from the Hg-arc without the use of any filter. Experimental results for a continuous-tone object have been presented. The advantages and disadvantages and some of the potential applications of this technique have been mentioned.     

Phenyl-6 phospha-5 phenanthrene

The title compound has been prepared by a three-step method including a ring enlargement of benzyl-5 dibenzophosphole by reaction with benzoyl chloride.     

Transcutaneous Blood Flow Measurements Using Pseudorandom Noise Doppler System

In order to obviate the limitations of the conventional coherent ultrasonic Doppler flowmeters we have developed a new device. In this apparatus the continuous wave is replaced by a pseudorandom signal. We show, both theoretically (Waag et al. [12]) and experimentally, that the pseudorandom system offers advantages. The most important result concerns the improvement of the signal-to-noise ratio which can be as large as 20 dB. Furthermore, it is possible to decrease the frequency and the distance ambiguity by a factor of two. Compared to the "random noise flowmeter" (Newhouse et al. [7], Jethwa et al. [5]) our system measures flow near the wall of vessels or in ultrasonic field in which there are important fixed echoes. To illustrate the feasibility of this new device, we show some results obtained by the transcutaneous method.     

Etude sur les composés organométalliques. XVIII. Synthèse et caractérisation du μ-oxo-bis (dicyclopentadiènylméthyltitane IV)

Studies of Organometallic Compounds. XVII: Synthesis and Caracterisation of μ-oxo-bis(dicyclopentadienylmethyltitane IV) (Cp₂TiCH₃)₂O is obtained by reacting (Cp₂TiCl)₂O with methyllithium. IR., NMR. and MS. spectrum are reported. Autocatalytic decomposition of the product is inferred from differential thermal analytic measurements.     

Electro-optical studies on synthetic polyelectrolytes—III: Electric birefringence of poly-n-alkyl-4-vinylpyridinium bromides in various solvents

The field strength dependences of the electric birefrigence of poly-N-butyl-4-vinylpyridinium (4-PVP · BuBr) samples have been measured in water and in various organic polar solvents. The observed change of sign of the birefringence, negative in water and positive in nitromethane, is explained by considering the respective influences of the intrinsic and form optical anisotropies. The lower degree of extension of the polyelectrolyte in some organic solvents is attributed to a lower degree of dissociation of the ionic sites. The influence of the dielectric constant and of the functional character of the solvent on the dissociation and solvation processes of the ionic sites is taken into account. Relaxation measurements in dimethylsulphoxide as a function of the molecular weight allow quantitative expression of the degrees of extension and of rigidity of the polyelectrolyte; the presence of aggregates has also been detected in DMSO solutions. A long alkyl chain, such as octyl, attached to the quaternary pyridinium groups strongly modifies the conformation of the polyelectrolyte and a polyelectrolyte-polysoap transition has been observed as a function of the solvent composition in water-ethanol mixtures.     

The equation of state of solids

An equation of state for solids, in reduced variables, is obtained within the context of a system-independent formulation of the thermodynamics of high pressures. This formulation is valid for materials obeying a linear relationship between shock and particle velocities. An adequate set of scaling factors for pressure, compression, specific energy, and temperature, is first introduced. A modified Mie-Grüneisen equation, as well as many other thermodynamic relationships and coefficients, are then expressed in terms of reduced variables. Explicit expressions for the temperature along the Hugoniot, and for the equation of state, are obtained. It is also shown that when given in their reduced form, each of the two thermodynamic coefficients appearing in the equation of state can be considered as having the same constant value for many different materials. The possibility and convenience of using a “standard material” is discussed. Numerical results obtained using this reduced variables formalism are in good agreement with those computed or measured, by different authors, for various materials over a wide range of pressures. This is a good indication of the “universality” of the reduced equations obtained, and of the usefulness of the formalism.     

Optically active alternating copolymers of maleic anhydride and alkylvinylethers

Maleic anhydride (MAn) was copolymerized in benzene solution at 60° using AIBN with some optically active alkylvinylethers (RVE) having an asymmetric carbon atom at the α, β, γ or δ position with respect to the oxygen atom [R = (S)-1-methylpropyl, (R)-1-methylbutyl, (S)-2-methylbutyl, (S)-3-methylpentyl, (S)-4-methylhexyl, (S)-1-methylheptyl and (S)-3,7-dimethyloctyl]. Chemical compositions and solubilities of the polymeric products as well as optical rotation properties and spectroscopic measurements (i.r. and NMR) confirmed the formation of copolymers with a predominantly alternating structure. Two Cotton effects of low but definite intensity attributable to $\text{n → π}{}^1$ electronic transitions of carbonyl groups of anhydride moieties were observed between 200 and 250 nm. Failure to achieve complete cleavage of chiral side chains does not enable us to attribute the induced optical activity of anhydride moieties either to the asymmetric carbon atom present in the side chain or to the tertiary chiral centres present in the main chain or both.     

A chiral cyclohexanone linked to polystyrene for solid-phase synthesis of chiral alpha-carbonyls

Two chiral cyclohexanones were linked to polystyrene resin. The polymer-bound auxiliaries were subjected to a sequence of four reactions, the last of which cleaves the desired alpha-chiral carbonyl compound off the resin, concurrently regenerating the resin-bound auxiliary in its original form. The resin can then be reused.