Complexes of vitamin B6. Part XI. Ternary complexes of some bivalent metal ions with ethylenediamine and pyridoxamine

Summary The stability constants of ternary Co^II, Ni^II, Cu^II, Zn^II and Cd^II complexes containing pyridoxamine as a first and ethylenediamine as a second ligand were determined by pH titration at I =0.50M NaNO₃ and 30 °C. Most of the complexes are protonated, probably on the pyridoxamine moiety. The formation of the ternary complex species is discussed in terms of binary species formation. Spectral characteristics of some of the ternary complex systems are discussed.Part X. Binary, Ternary and Quaternary Complexes Involved in Systems of Pyridoxamine-Glycine or Glycylglycine-Imidazole with Some Bivalent Metal Ions,21st Internat. Conf. on Coord. Chem., Toulouse, France (1980);     

Self-assembled monolayers of benzylmercaptan and p-cyanobenzylmercaptan on Au(111) surfaces: structural and spectroscopic characterization

The formation of self-assembled monolayers of benzylmercaptan (BM) and p-cyanobenzylmercaptan (pCBM) on Au(111) surfaces is investigated by a combination of X-ray photoelectron spectroscopy (XPS), near-edge X-ray absorption fine structure (NEXAFS), and scanning tunneling microscopy (STM). The NEXAFS results of pCBM are supported by ab initio calculations. It is found that BM as well as pCBM form well-ordered monolayers with the molecules oriented almost perpendicular to the surface. BM forms a ( radical 3 x radical 3)R30 degrees structure whereas pCBM forms a slightly different c(7 x 7) hexagonal structure. No phase separation is detected for the adsorption of a 1:1 mixture of the two molecules. The implications of the results for the covalent attachment of transition-metal complexes to thiol-functionalized surfaces are discussed.     

Experimental performance analysis of two different passive cooling techniques for solar photovoltaic installations

Journal of Thermal Analysis and Calorimetry - At higher ambient temperatures during summer months, the cell temperature of a photovoltaic (PV) module increases to 50–60 °C and sometimes...     

Nonexistence results for higher order pseudo‐parabolic equations in the Heisenberg group

Sufficient conditions are obtained for the nonexistence of solutions to the nonlinear higher order pseudo‐parabolic equation where is the Kohn‐Laplace operator on the (2N + 1)‐dimensional Heisenberg group , m≥1,p > 1. Then, this result is extended to the case of a 2 × 2‐system of the same type. Our technique of proof is based on judicious choices of the test functions in the weak formulation of the sought solutions. Copyright © 2016 John Wiley & Sons, Ltd.     

Surface topography of ultrashort laser-irradiated CaF2

A single-crystal CaF₂ (111) was irradiated with single and multiple laser (Ti:sapphire, 800 nm, 25 fs) shots at fluences ranging from 0.25 to 1.5 J cm^?2. In this fluence regime, a single laser pulse usually leads to typical bump-like features ranging from 200 nm to 1.5 μm in diameter and 10–50 nm in height. These bumps are related to compressive stresses due to a pressure build-up induced by fast laser heating and their subsequent relaxation. When CaF₂ is irradiated with successive (in our case 20) shots at a laser fluence of 1.5 J cm^?2, nanocavities at the top of the microbumps are observed. The formation of these nanocavities is regarded as an explosion and is attributed to the explosive expansion generated by shock waves due to laser-induced plasma after the nonlinear absorption of the laser energy by the material. Such kinds of surface structures at the nanometre scale could be attractive for nanolithography.     

The ligational behavior of a phenolic quinolyl hydrazone towards copper(II)- ions

Background  

The heterocyclic hydrazones constitute an important class of biologically active drug molecules. The hydrazones have also been used as herbicides, insecticides, nematocides, redenticides, and plant growth regulators as well as plasticizers and stabilizers for polymers. The importance of the phenolic quinolyl hydrazones arises from incorporating the quinoline ring with the phenolic compound; 2,4-dihydroxy benzaldehyde. Quinoline ring has therapeutic and biological activities whereas, phenols have antiseptic and disinfectants activities and are used in the preparation of dyes, bakelite and drugs. The present study is planned to check the effect of the counter anions on the type and geometry of the isolated copper(II)- complexes as well as the ligational behavior of the phenolic hydrazone; 4-[(2-(4,8-dimethylquinolin-2-yl)hydrazono)methyl] benzene-1,3-diol; (H₂L).     

Influence of ambient gas and its pressure on the laser-induced breakdown spectroscopy and the surface morphology of laser-ablated Cd

The ablation of Cd has been performed by employing Q-switched Nd: YAG 10 ns laser pulses with a central wavelength of 1064 nm for a pulsed energy of 200 mJ under various ambient environments of argon, air and helium. The optical emission spectroscopy of Cd plasma has been studied under different filling pressures of shield gases ranging from 5 torr to 760 torr using LIBS spectrometer system. The effect of different gases and their pressures on the intensity of spectral emission, electron temperature and density of the laser-produced plasma has been investigated. SEM analysis has been performed to investigate the dependence of surface morphological changes of an irradiated target on the nature and pressure of an ambient gas. A strong correlation has revealed the vital role of electron temperature and density of laser-induced plasma for the surface modification of Cd. These results strongly indicate that the nature and pressure of the ambient atmosphere is one of the controlling factors of the plasma characteristics, as well as the factors related to the laser energy absorption for surface modification.     

Collective Perspective on Advances in Dyson-Schwinger Equation QCD

We survey contemporary studies of hadrons and strongly interacting quarks using QCD's Dyson-Schwinger equations, addressing the following aspects: confinement and dynamical chiral symmetry breaking; the hadron spectrum; hadron elastic and transition form factors, from small- to large-Q²; parton distribution functions; the physics of hadrons containing one or more heavy quarks; and properties of the quark gluon plasma.     

Tunable intramolecular multicenter H-bonding interactions in first-row metal complexes bearing bidentate redox-active ligands

Abstract

In this research article, we report the synthesis and structural characterization of a family of first-row metal complexes bearing redox-active ligands with tunable H-bonding donors. We observed that these coordination complexes can adopt three different geometries and that they are stabilized by intramolecular multicenter H-bonding interactions, which are systematically modified by changing the metal ion (Co, Ni, Cu, Zn), the ligand scaffold (variations in the diamine and ureanyl substituents used) and the solvent of crystallization.