Design of organophosphorus materials for organic electronics and bio-applications

π-Extended molecules are key components for the development of materials science. In fact, polyaromatic structures are fundamental for the scientific and technological progress of fields such as organic electronics and bio-applications. Beneficial properties of π-extended structures are absorption in the visible region, often luminescence, high electron mobilities and stability. Common approaches to adjust the properties of polyaromatic structures to functional setups involve changes in shape and size at the molecular level. Recently, incorporating hetero-elements emerged as successful approach. In this regard, organophosphorus conjugated molecules are new materials holding great promise for potential applications. In this review, we comprehensively discuss the design/development of polyaromatic phosphorus materials and their applicability. We establish structure/property/applicability relationships to provide key guidelines for the engineering of newer, future applications. This article thus provides a source of information for the further development of this rapidly evolving field of research.     

Gradient structure of polypropylene composites filled with carbon black

Russian Chemical Bulletin - Gradient polymer composites were prepared by melt-mixing of carbon black and polypropylene in a compounder and subsequent hot pressing of pellets. The thermally treated...     

Quenching of Axial-Vector Weak Interaction Constant in Halo Nuclei

Physics of Particles and Nuclei Letters - Resonance structure of the beta decay strength function Sβ(E) for GT β–-decay of halo nuclei 6He and 11Li is analyzed. Compare experimental...     

Conformal Mappings of Riemannian Spaces onto Ricci Symmetric Spaces

Mathematical Notes -     

Efficient Tosylation of Dihydroxybenzenes in a Two-Phase Water–Dichloromethane System

Theoretical and Experimental Chemistry - The effect of the structure of the catalyst and the type of base on the reaction rate and product yield of the tosylation of dihydroxybenzenes in a...     

Transfer and Trapping of Resonance Radiation in a Two-Level System

Optics and Spectroscopy - The population kinetics of a two-level system has been theoretically investigated taking into account the transfer of spontaneous radiation under continuous optical...     

Boiling Water Reactor with a Combined Moderator for Utilization of Reactor Grade Plutonium

Physics of Atomic Nuclei - The article presents the concept of a channel-type reactor with a combined cooled moderator. The moderator consists of ceramic beryllium oxide and a liquid...     

Aryl Boronic Acid Catalysed Dehydrative Substitution of Benzylic Alcohols for C−O Bond Formation

A combination of pentafluorophenylboronic acid and oxalic acid catalyses the dehydrative substitution of benzylic alcohols with a second alcohol to form new C−O bonds. This method has been applied to the intermolecular substitution of benzylic alcohols to form symmetrical ethers, intramolecular cyclisations of diols to form aryl-substituted tetrahydrofuran and tetrahydropyran derivatives, and intermolecular crossed-etherification reactions between two different alcohols. Mechanistic control experiments have identified a potential catalytic intermediate formed between the aryl boronic acid and oxalic acid.