Optical clock distribution for multichip module

We propose an optical H-tree structure to distribute a clock signal onto 16 electronic chips at 1 Gb/s for a clock skew and timing jitter of less than 100 ps. Fabrication steps and performance results are presented.     

Template synthesis and spectroscopic studies of highly conjugated tetraiminetetraamide macrocyclic complexes from 1,2-diphenylethane-1,2-dione dihydrazone

A new class of tetraiminetetraamide macrocyclic (Ph4[20]tetraene, N8O4, and Ph6[20]tetraene, N8O4) complexes have been prepared through the metal ion controlled reaction of 1,2-diphenylethane-1,2-dione dihydrazone (DPEDDH) with succinic acid [ML1X2] or phthalic acid [ML2X2] [M=Mn, Co, Ni, Cu or Zn; X=Cl or NO3]. The structures of the complexes have been elucidated on the basis of i.r, 1H-n.m.r, e.p.r. and electronic spectral data and conductance, as well as magnetic, properties. An octahedral geometry is assigned for all the complexes, involving coordination of the all-imine nitrogens.     

Evaluation of gel permeation chromatography to Fourier transform infrared spectrometric detection using a modified thermospray for analysis of polystyrene samples

A heated gas flow modified thermospray was used to couple gel permeation chromatography (GPC) to Fourier transform infrared spectrometry (FTIR) for the analysis of the standard polystyrene samples. Effluents from the GPC column were evaporated and the solutes were deposited as a series of spots on the surface of a moving stainless steel belt (0.025 mm thickness × 13 mm width). The belt continuously transferred the spots into the diffuse reflectance (DRIFT) accessory of the FTIR spectrometer, enabling identification of the deposited solutes by measurement of the diffuse reflectance IR spectrum. The IR spectra of the separated components showed excellent agreement of the spectral features to those of standard FTIR spectra and no thermal degradation was observed. Received: 20 May 1996 / Revised: 17 October 1996 / Accepted: 28 November 1996     

Pion-proton elastic scattering at 200 GeV/c

Recent measurements of differential and elastic cross-sections, slope parameters and ratios of the real and imaginary parts of the forward scattering amplitudes for pion-proton elastic scattering at 200 GeV/c have been fitted by using a simple Regge pole model with phenomenological residue functions. The computed results for total cross-sections have also been compared with the experimental data.     

Principle of massive support in the opposed anvil high pressure apparatus

The Bridgman anvil technique offers a simple and versatile means of generating very high pressures required in solid state studies. The opposed anvil technique is based on the principle of massive support. The practical case of a gasketted anvil is considered, and an expression for the maximum pressure generated under massive support is derived in terms of the geometric parameters, the strength of the anvil material and the gasket properties. In particular, for a given maximum pressure, it is possible to calculate the taper angle, the taper height and the gasket thickness from this expression. The anvil is assumed to be in the elastic region under load. Good agreement is obtained between the calculated and the experimental values for the massive support factor (msf) for various taper angles. By choosing the proper geometry, it is possible to achieve a pressure as high as 130 kbar in an alloy steel anvil. It has been clearly found that the straight portion, where the taper ends, does not really take any part in changing the stress pattern. Thus the minimum straight portion can serve the purpose, and will result in material saving. Anvils exhibit yielding at very high pressure. It is also pointed out that a further strengthening of the anvil can extend the ultimate pressure. Several methods of further strengthening the anvils are discussed.     

Infra-red behaviour in non-abelian gauge theories

The leading infra-red divergent corrections to massive quark scattering in quantum chromodynamics are very simple to fourth order. A simple dependence on the effective coupling constant is conjectured to hold to all orders.     

Antitumor metallothiosemicarbazonates: structure and antitumor activity of palladium complex of phenanthrenequinone thiosemicarbazone

The crystal structure of the potential antitumor metal compound, viz. chloro, mono(phenanthrenequinone thiosemicarbazonato) palladium(II) dimethyl formamide solvate, is reported. The central palladium(II) atom is in a square planar environment provided by the tridentate, monoanionic thiosemicarbazone ligand and the ancillary chloride ion. The compound exhibited remarkable activity against drug-sensitive and drug-resistant breast cancer cell lines and was relatively nontoxic toward the normal mammary epithelial cells. The drug-induced killing effect against breast cancer cell lines was predominantly mediated via apoptosis, a physiologic form of cell death.