Copper and iron interactions with angiotensin-converting enzyme inhibitors. A study by fast-atom bombardment tandem mass spectrometry

Fast atom bombardment, combined with high-energy collision-induced tandem mass spectrometry, has been used to investigate gas-phase metal-ion interactions with captopril, enalaprilat and lisinopril, all angiotensin-converting enzyme inhibitors.Suggestions for the location of metal-binding sites are presented. For captopril, metal binding occurs most likely at both the sulphur and the nitrogen atom. For enalaprilat and lisinopril, binding preferably occurs at the amine nitrogen. Copyright 1999 John Wiley & Sons, Ltd.     

Effects of strontium and calcium simultaneous substitution on electrical and structural properties of Pb1?x?yCaxSryTiO3 thin films

Ferroelectric Pb_1−x−y Ca _x Sr _y TiO₃ thin films (denoted by PCST90, PCST70, and PCST30) were deposited on the Pt/Ti/SiO₂/Si substrates by a chemical solution deposition method. Their properties were investigated from the viewpoint of crystal structure, microstructure, dielectric, and ferroelectric properties. X-ray diffraction patterns revealed the formation of PCST90, PCST70, and PCST30 thin films without any secondary phases. Infrared and Raman spectroscopy results show that a gradual phase transition from tetragonal to pseudocubic or cubic perovskite structure may occur in PCST thin films with the simultaneous increase of Ca²⁺ and Sr²⁺ contents. Both substitution of isovalent Ca²⁺ and Sr²⁺ at Pb²⁺-site enhanced the dielectric constant and reduced the remnant polarization. In addition, ferroelectric test analyses show that the PCST thin films undergo a ferroelectric-to-paraelectric phase transformation with an amount of Pb²⁺, Ca²⁺, and Sr²⁺ at 30%, 35%, and 35% mol, respectively. Hence, the absence of ferroelectric property may be attributed to a decreasing of the octahedron distortion in the perovskite structure accompanied by a weakening of long-range ferroelectric order.     

Temperature dependence of electron properties of Sn doped nanobelts

This paper reports on the measurements of transport properties of high crystalline quality Sn doped In₂O₃ nanobelts. The samples presented metallic conduction in a large range of temperatures; however, at low temperatures, the resistivity showed a slight increase and the current–voltage curves showed a tendency to saturate even in the low-voltage range. From these observations, we discuss some arguments on the possibility of low dimensional conducting channels as the main responsible for the conduction at low temperatures. Additionally, we present an alternative technique for production of low resistance ohmic contacts, which can be further used in devices’ construction.     

Temperature dependence of the electron distribution in a GaAs matrix with embedded InAs quantum dots

We report on the effect of the Debye averaging process on the CV characteristics of a sample containing four coupled planes of InAs self-assembled quantum dots. The observed electron distribution presented a dynamical dependence of the temperature during the C–V measurements which was explained in terms of the screening length dependence on the temperature. In addition, using the C–V data, we calculated the electron density at the planes containing the InAs dots and we have observed a high-temperature stability: the electron density at the quantum dots remained constant over a large range of temperature.     

Influence of a co-substituted A-site on structural characteristics and ferroelectricity of (Pb,Ba, Ca)TiO3 complex perovskites: analysis of local-, medium- and long-range order

Thin films of A-site co-substituted, PbTiO₃ (PTO) by Ba²⁺ and Ca²⁺, i.e., PBCT70, PBCT60, PBCT50 and PBCT40 were fabricated on Pt/Ti/SiO₂/Si substrates by chemical solution deposition. Structures of the samples were investigated from the viewpoint of local-, medium- and long-range order by X-ray absorption near structure (XANES), micro-Raman and infrared spectroscopies and by X-ray diffraction (XRD). The films thickness were determined by using field-emission scanning electron microscope. The experimental results demonstrate that BaO₁₂ clusters are the critical dominant ferroelectricity cause in PBCT thin films rather than CaO₁₂ clusters. XRD analysis which was applied to investigate the crystal symmetry indicates the absence of long-range structural distortion for samples at higher concentrations of Ba²⁺ and Ca²⁺. However, an analysis of structural medium- and local-range order such as infrared, micro-Raman and XANES spectroscopies revealed that symmetry changes are much more prominent; i.e., local structural distortions remain. Temperature-dependent dielectric permittivity measurements confirmed a decreasing ferroelectric-to-paraelectric phase transition temperature and showed a broad phase transition with an increase in BaO₁₂ and CaO₁₂ clusters. In addition, the lack of long-range polar ordering for the ferroelectric dipole caused by symmetry changes decreases the remanent polarization.