Bis[N,N′‐bis(2‐nitrocinnamaldehyde)phenylenediimine]copper(I) Perchlorate

The complex [Cu(nitroca₂ph)₂]ClO₄, where nitroca₂ph is N,N′‐bis(2‐nitrocinnamaldehyde)phenylenediimine, crystallizes in the triclinic space group with a = 13.167(1), b = 13.209(1), c = 14.465(1) Å, α = 83.209(9)°, β = 68.438(2)°, γ = 70.803(2)°, V = 2209.4(3) ų, Z = 2, D_calc = 1.527 mg/m³. The coordination polyhedron about the Cu(I) atom is best described as a distorted tetrahedron. 2‐nitroca₂en acts as a bidentate ligand coordinating via two N atoms to the copper. The four Cu–N distances are 2.04 (2), 2.038(2), 2.046(2), and 2.062(2) Å.     

Coordination chemistry of a terpyridine-tris(pyrazolyl) ditopic ligand

A new ditopic ligand, 4'-(4-(2,2,2-tris(1H-pyrazol-1-ido)ethoxymethyl)phenyl)-2,2':6',2'-terpyridine (pzt), has been prepared and its coordination chemistry studied. Metal ions with a preference for octahedral geometry form ML(2) complexes that are readily isolated and characterised, with the metal ion being bound to the terpyridine sites of both ligands. Other metal ions bind to the terpyridine site of just one ligand. In the case of silver(i), a dinuclear M(2)L(2) complex has been isolated in which each silver ion is coordinated to the terpyridine site of one ligand and to a single pyrazolyl donor group from the second ligand. Evidence for binding of metal ions to the tris(pyrazolyl) binding site was obtained by electrospray mass spectrometry and NMR techniques. The free ligand and three metal complexes, including the disilver complex, have been characterised by X-ray crystallographic techniques.     

Enhanced photoreduction of water catalyzed by a cucurbit[8]uril-secured platinum dimer

A cucurbit[8]uril (CB[8])-secured platinum terpyridyl chloride dimer was used as a photosensitizer and hydrogen-evolving catalyst for the photoreduction of water. Volumes of produced hydrogen were up to 25 and 6 times larger than those obtained with the corresponding free and cucurbit[7]uril-bound platinum monomer, respectively, at equal Pt concentration. The thermodynamics of the proton-coupled electron transfer from the Pt(ii)–Pt(ii) dimer to the corresponding Pt(ii)–Pt(iii)–H hydride key intermediate, as quantified by density functional theory, suggest that CB[8] secures the Pt(ii)–Pt(ii) dimer in a particularly reactive conformation that promotes hydrogen formation.

The cucurbit[8]uril macrocycle can secure a platinum terpyridyl complex into a particularly reactive dimer that catalyzes the photoreduction of water.     

Reversible strain-induced order in the amorphous phase of a low-density ethylene/butene copolymer

This article deals with the characterization of the structural changes induced by uniaxial extension in the amorphous phase of an ethylene/butene copolymer. Volume change measurements indicate a reversible densification relevant to a strain-induced organization in the amorphous phase. The dynamic mechanical behavior shows an improvement of the β relaxation that reveals an important immobilization of the amorphous chains. The vibrational behavior investigated by means of Raman spectroscopy suggests that the strained amorphous chains are structurally analogous to the mesomorphic interfacial component. A discussion is made about the mechanism of the transformation of the amorphous phase into a mesomorphic structure compared to the more common strain-induced crystallization phenomenon. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2151–2159, 1997     

Conjugated 1,10-Phenanthrolines as Tunable Fluorophores

Multiple emission colors can be generated with the same compound from a novel family of highly emissive and visibly fluorescent 1,10-phenanthrolines 1 . The emission wavelength of any derivative is dictated by the nature of its substituent and can be further modulated by exogenous additives such as protons or metal ions. R=H, Me, OMe, NMe₂.     

Analysis of ethanol and methanol in human body fluids by headspace solid phase microextraction coupled with capillary gas chromatography.

A new method for extraction and analysis of ethanol and methanol in human whole blood, urine and saliva samples based on headspace solid phase microextraction (SPME) using silver sulfide (Ag(2)S) and polyvinyl chloride (PVC) coated on silver wire is described. Unlike commercial fibers, which are coated on fused silica, the proposed fiber has a metallic base to which the coating adheres very strongly. Due to metallic base, this fiber is very durable and is thermally stable up to 250 degrees C. After optimization of coating composition and microextraction conditions, the fiber was used for sampling of methanol and ethanol from human body fluids prior to capillary gas chromatographic analysis. The high recovery (>94%), low detection limits (5.6 mg/L for ethanol and 12.8 mg/L for methanol) and excellent linearity (>0.9900) of calibration graphs made the proposed method suitable for this purpose.     

Foliations transverse to fibers of Seifert manifolds

In this paper we prove the conjecture of Jankins and Neumann [JN2] about rotation numbers of products of circle homeomorphisms, which together with other results of [EHN] and [JN2] (mentioned below) implies that a Seifert manifold admits foliations tranverse to its fibers only if it admits such foliations with a projective transverse structure. 1991Mathematics Subject Classification: Primary 55R05, 57R30, Secondary 47A35, 57M99, 58F11. Partially supported by a Sloan Doctoral Dissertation Fellowship, and by the Technion-Israel Institute of Technology.     

Vibration analysis and design optimization of viscoelastic sandwich cylindrical shell

Damping properties of viscoelastic sandwich structure can be improved by changing some parameters such as thickness of the layers, distribution of partial treatments, slippage between layers at the interfaces, cutting and its distribution at the top and core layers. Since the optimization problem may result in a thick core layer, for achieving more accuracy a new higher-order Taylor's expansion of transverse and in-plane displacement fields is developed for the core layer of sandwich cylindrical shell in which the displacement fields at the core layer are compatibly described in terms of the displacement fields at the elastic faces. The presented model includes fewer parameters than the previously developed models and therefore decreases the number of degree of freedom in the finite element modeling. The transverse normal stress in the core layer is also considered. The formulations are developed to consider the slippage between layers at the interfaces. Finally, by combining the finite element method and the optimization algorithms based on the genetic algorithm and sequential quadratic programming technique, a design optimization methodology has been formulated to maximize the damping characteristics using the optimal number and location of cuts and partial treatments with optimal thicknesses of top and core layers.