WATER MOVEMENT CAUSED BY SPREADING SURFACTANTS IN UNSATURATED SYSTEMS OF PARTICLES OF NONUNIFORM SIZE

The movement of water originated by the spreading of two surfactants was analyzed in glass beads as well as on soil systems, both of particles of nonuniform size

The higher difference of surface tension produced in the system by 1 -hexadecanol compared to that of 1-tetradecanol led therefore to a higher amount of water moved. Decreased proportion of the smaller sized particles in glass beads system produced a decrease in the total water moved by both surfactants.

Organic matter acted in soil as a second surfactant in glass beads. This effect was compared in glass beads systems once 1-hexadecanol was evenly distributed among the particles as continuous film, which played a role alike that of organic matter in soil and then a second surfactant 1-tetradecanol was added. These additional surfactant effect diminished the difference between initial and final surface tension (surface tension depression) of the system and so the total water moved.

The soil organic matter (1.7%) modified the water movement curve in the presence of low (0.2g) content of 1-hexadecanol, whereas for high content of either alcohol (0.4g) or low content of 1-tetradecanol content (0.2g) the water movement curves were the same     

Synthesis and Biological Evaluation of Novobiocin Core Analogues as Hsp90 Inhibitors

Development of heat shock protein 90 (Hsp90) C‐terminal inhibitors has emerged as an exciting strategy for the treatment of cancer. Previous efforts have focused on modifications to the natural products novobiocin and coumermycin. Moreover, variations in both the sugar and amide moieties have been extensively studied, whereas replacements for the coumarin core have received less attention. Herein, 24 cores were synthesized with varying distances and angles between the sugar and amide moieties. Compounds that exhibited good anti‐proliferative activity against multiple cancer cell lines and Hsp90 inhibitory activity, were those that placed the sugar and amide moieties between 7.7 and 12.1 Å apart along with angles of 180°.     

Alkyne Difunctionalization by Dual Gold/Photoredox Catalysis

Highly selective tandem nucleophilic addition/cross‐coupling reactions of alkynes have been developed using visible‐light‐promoted dual gold/photoredox catalysis. The simultaneous oxidation of Au^I and coordination of the coupling partner by photo‐generated aryl radicals, and the use of catalytically inactive gold precatalysts allows for high levels of selectivity for the cross‐coupled products without competing hydrofunctionalization or homocoupling. As demonstrated in representative arylative Meyer–Schuster and hydration reactions, this work expands the scope of dual gold/photoredox catalysis to the largest class of substrates for gold catalysts and benefits from the mild and environmentally attractive nature of visible‐light activation.     

Hypernuclear physics at \overline{\mbox{P}} anda

Samples obtained as a result of the valleriite synthesis process under different conditions (temperature and proportion Cu:Fe:Mg in the initial mixture) were investigated by ⁵⁷Fe M?ssbauer spectroscopy with attraction data of X-ray diffraction. Parameters of hyperfine interactions for valleriite were determined and crystal chemical identification of ⁵⁷Fe subspectra was carried out. It was found that valleriite was formed in samples synthesized at 150°C and 180°C and not formed in samples synthesized at 250°C.     

[HFe(CO)4 – A Versatile Reagent toward Dichlorophosphines,Phosphenium Salts,Phospha-alkenes and Diphosphenes

Abstract

A new entry to non classical phosphorus complexes is reported.     

Hydroxyalkylation of α-Phosphonylated α-Silylated Allylic Carbanions. An Unexpected Cyclization Reaction

Abstract

When reacted with aldehydes, in situ generated title carbanions 2 can give phosphonodienes (4 or 6), phosphonolactones (5 or 8) or phosphonoalcohols 7, depending on structure of reagents and on reaction conditions.     

“Integrative sol–gel chemistry”: a nanofoundry for materials science

Integrative sol–gel chemistry based strategies allow, through the strong coupling between materials chemistry and advanced processing, the fabrication of functional inorganic and hybrid materials. The following article will highlight some of the main accomplishments performed during the last years in the design of nano- and multi-scale structured materials shaped as thin films, powders and monoliths with additional functionalities and outstanding properties in several fields of application such as optics, catalysis and nanomedicine. In particular we discuss the key role played by the adapted liquid processing of sol–gel based solution. We will describe some technologies (including dip coating, spray drying, droplet-microfluidics, ink-jet and foaming) in which a high degree of control in term of liquid shaping/evaporation/manipulation is required in order to achieve specific functionalities.     

A variational approach for a generalized emden-fowler equation

Existence of positive solutions of singular boundary value problems related to Emden-Fowler equation is proved. A general minimization theorem in Sobolev spaces is applied.     

Organic‐acid mediated bulk polymerization of ε‐caprolactam and its copolymerization with ε‐caprolactone

Polyamides (PA) constitute one of the most important classes of polymeric materials and have gained strong position in different areas, such as textiles, fibers, and construction materials. Whereas most PA are synthesized by step‐growth polycondensation, PA 6 is synthesized by ring opening polymerization (ROP) of ε‐caprolactam (ε‐CLa). The most popular ROP methods involve the use of alkaline metal catalyst difficult to handle at large scale. In this article, we propose the use of organic acids for the ROP of ε‐CLa in bulk at 180 °C (below the polymer's melting point). Among evaluated organic acids, sulfonic acids were found to be the most effective for the polymerization of ε‐CLa , being the Brønsted acid ionic liquid: 1‐(4‐sulfobutyl)?3‐methylimidazolium hydrogen sulfate the most suitable due to its higher thermal stability. End‐group analysis by ¹H nuclear magnetic resonance and model reactions provided mechanistic insights and suggested that the catalytic activity of sulfonic acids was a function of not only the acid strength, but of the nucleophilic character of conjugate base as well. Finally, the ability of sulfonic acid to promote the copolymerization of ε‐CLa and ε‐caprolactone is demonstrated. As a result, poly(ε‐caprolactam‐co‐ε‐caprolactone) copolymers with considerably randomness are obtained. This benign route allows the synthesis of poly(ester amide)s with different thermal and mechanical properties. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 2394–2402