Relativistic Contributions to Deuteron Photodisintegration in the Bethe-Salpeter Formalism

In plane wave one-body approximation the reaction of deuteron photodisintegration is considered in the framework of the Bethe-Salpeter formalism for two-nucleon system. Results are obtained for deuteron vertex function, which is the solution of the homogeneous Bethe-Salpeter equation with a multi-rank separable interaction kernel, with a given analytical form. A comparison is presented with predictions of non-relativistic, quasipotential approaches and the equal time approximation. It is shown that important contributions come from the boost in the arguments of the initial state vertex function and the boost on the relative energy in the one-particle propagator due to recoil.Comment: 29 pages, 6 figure

Diagnostic utility of zinc protoporphyrin to detect iron deficiency in Kenyan pregnant women

Iron-deficient erythropoiesis results in excess formation of zinc protoporphyrin (ZPP), which can be measured instantly and at low assay cost using portable haematofluorometers. ZPP is used as a screening marker of iron deficiency in individual pregnant women and children, but also to assess population iron status in combination with haemoglobin concentration. We examined associations between ZPP and disorders that are common in Africa. In addition, we assessed the diagnostic utility of ZPP (measured in whole blood and erythrocytes), alone or in combination with haemoglobin concentration, in detecting iron deficiency (plasma ferritin concentratio

Self-assembled monolayers of 1-alkenes on oxidized platinum surfaces as platforms for immobilized enzymes for biosensing

Alkene-based self-assembled monolayers grafted on oxidized Pt surfaces were used as a scaffold to covalently immobilize oxidase enzymes, with the aim to develop an amperometric biosensor platform. NH2-terminated organic layers were functionalized with either aldehyde (CHO) or N-hydroxysuccinimide (NHS) ester-derived groups, to provide anchoring points for enzyme immobilization. The functionalized Pt surfaces were characterized by X-ray photoelectron spectroscopy (XPS), static water contact angle (CA), infrared reflection absorption spectroscopy (IRRAS) and atomic force microscopy (AFM). Glucose oxidase (GOX) was covalently attached to the functionalized Pt electrodes, either with or without additional glutaraldehyde crosslinking. The responses of the acquired sensors to glucose concentrations ranging from 0.5 to 100 mM were monitored by chronoamperometry. Furthermore, lactate oxidase (LOX) and human hydroxyacid oxidase (HAOX) were successfully immobilized onto the PtOx surface platform. The performance of the resulting lactate sensors was investigated for lactate concentrations ranging from 0.05 to 20 mM. The successful attachment of active enzymes (GOX, LOX and HAOX) on Pt electrodes demonstrates that covalently functionalized PtOx surfaces provide a universal platform for the development of oxidase enzyme-based sensors. (C) 2016 Elsevier B.V. All rights reserved

Covalent Attachment of 1-Alkenes to Oxidized Platinum Surfaces

We report the formation of covalently bound alkyl layers onto oxidized Pt (PtOx) substrates by reaction with 1-alkenes as a novel way to bind organic molecules to metal surfaces. The organic layers were characterized by static contact angle, infrared reflection absorption spectroscopy (IRRAS), X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM). The grafted alkyl layers display a hydrolytic stability that is comparable to that of alkyl thiols on Au. PtOx-alkene attachment is compatible with terminal ester moieties enabling further anchoring of functional groups, such as redox-active ferrocene, and thus has great potential to extend monolayer chemistry on noble metals

Stable Protein-Repellent Zwitterionic Polymer Brushes Grafted from Silicon Nitride

Zwitterionic poly(sulfobetaine acrylamide) (SBMAA) brushes were grafted from silicon-rich silicon nitride (SixN4, x > 3) surfaces by atom transfer radical polymerization (ATRP) and studied in protein adsorption experiments. To this aim ATRP initiators were immobilized onto SixN4 through stable Si−C linkages via three consecutive reactions. A UV-induced reaction of 1,2-epoxy-9-decene with hydrogen-terminated SixN4 surfaces was followed by conversion of the epoxide with 1,2-ethylenediamine resulting in primary and secondary amine-terminated surfaces. A reaction with 2-bromoisobutyryl bromide led to ATRP initiator-covered surfaces. Zwitterionic polymer brushes of SBMAA were grown from these initiator-coated surfaces (thickness ∼30 nm), and the polymer-coated surfaces were characterized in detail by static water contact angle measurements, X-ray photoelectron spectroscopy (XPS), and an atomic force microscope (AFM). The adsorption of proteins onto zwitterionic polymer coated surfaces was evaluated by in situ reflectometry, using a fibrinogen (FIB) solution of 0.1 g·L−1, and compared to hexadecyl-coated SixN4 surfaces (C16−SixN4), uncoated air-based plasma oxidized SixN4 surfaces (SiOy−SixN4), and hexa(ethylene oxide)-coated SixN4 surfaces (EO6−SixN4). Excellent protein repellence (>99%) was observed for these zwitterionic polymer-coated SixN4 surfaces during exposure to FIB solution as compared to C16−SixN4 surfaces. Furthermore, the stability of these zwitterionic polymer-coated SixN4 surfaces was surveyed by exposing the surfaces for 1 week to phosphate buffered saline (PBS) solution at room temperature. The zwitterionic polymer-coated SixN4 surfaces before and after exposure to PBS solution were characterized by XPS, AFM, and water contact angle measurements, and their protein-repelling properties were evaluated by reflectometry. After exposure to PBS solution, the zwitterionic polymer coating remained intact, and its thickness was unchanged within experimental error. No hydrolysis was observed for the zwitterionic polymer after 1 week exposure to PBS solution, and the surfaces still repelled 98% FIB as compared to C16−SixN4 surfaces, demonstrating the long-term efficiency of these easily prepared surface coatings

Long-Lived Mobile Charge Carriers Formed on Photoexcitation of UV-Polymerized, Spin-Coated Films of Arylimido-Spacer-Diacetylene Derivatives

The photopolymerization of spin-coated films of diacetylene derivatives containing phthalimido or naphthaldiimido moieties has been studied by monitoring the increase in the optical absorption in the visible region on irradiation at 308 nm. The phthalimido derivatives form blue polymers with absorption maxima at ca. 630 nm, corresponding to a highly conjugated, close to planar polydiacetylene (PDA) backbone configuration. The naphthaldiimido derivative yields a red polymer with an absorption maximum at 535 nm, indicating a backbone structure with a substantially reduced degree of -bond conjugation. The initial, "low-dose" quantum yields for monomer conversion, based on the total number of photons absorbed at 308 nm, range from 2 to 20. Monomer conversions up to ca. 50re found. The polymerized films are found to be photoconductive using the time-resolved microwave conductivity technique (TRMC). Mobile charge carriers are suggested to be formed via the triplet state of the arylimido moieties which undergoes long-distance charge transfer to polydiacetylene chains to form the arylimido radical anion and the mobile PDA radical cation or "hole". A maximum value of 1.4 x 10-2 cm2/(V s) for the product of the quantum yield for charge carrier formation and the hole mobility is found. The photoconductivity of the "blue" polymer is approximately an order of magnitude larger than for the "red" variety. This is attributed to a higher mobility of PDA holes in the former compound, resulting from the higher degree of backbone conjugation. The lifetime of the mobile carriers extends well into the microsecond region, which is considerably longer than previously found on direct ionization of PDA chains

Microwave-Assisted Formation of Organic Monolayers from 1-Alkenes on Silicon Carbide

The rate of formation of covalently linked organic monolayers on HF-etched silicon carbide (SiC) is greatly increased by microwave irradiation. Upon microwave treatment for 60 min at 100 °C (60 W), 1-alkenes yield densely packed, covalently attached monolayers on flat SiC surfaces, a process that typically takes 16 h at 130 °C under thermal conditions. This approach was extended to SiC microparticles. The monolayers were characterized by X-ray photoelectron spectroscopy and static water contact angle measurements. The microwave-assisted reaction is compatible with terminal functionalities such as alkenes that enable subsequent versatile “click” chemistry reactions, further broadening the range and applicability of chemically modified SiC surfaces

Fluorinated alkyne-derived monolayers on oxide-free silicon nanowires via one-step hydrosilylation

Passivation of oxide-free silicon nanowires (Si NWs) by the formation of high-quality fluorinated 1-hexadecyne-derived monolayers with varying fluorine content has been investigated. Alkyl chain monolayers (C16H30−xFx) with a varying number of fluorine substituents (x = 0, 1, 3, 9, 17) were attached onto hydrogen-terminated silicon (Si[sbnd]H) surfaces with an effective one-step hydrosilylation. This surface chemistry gives well-defined monolayers on nanowires that have a cylindrical core–shell structure, as characterized by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR) and static contact angle (SCA) analysis. The monolayers were stable under acidic and basic conditions, as well as under extreme conditions (such as UV exposure), and provide excellent surface passivation, which opens up applications in the fields of field effect transistors, optoelectronics and especially for disease diagnosis.</p

Preparation and gas sensing properties of nanocomposite polymers on micro-Interdigitated electrodes for detection of volatile organic compounds at room temperature

A room-temperature chemocapacitive gas sensor based on polymeric nanocomposites (NCs) consisting of amine-terminated silicon nanoparticles (Si NPs-NH2) and poly (4-vinylphenol) was fabricated on a micro-gap interdigitated electrode (M-IDE), and used for the detection of acetone. Several polymers were explored to capture acetone, of which poly (4-vinylphenol) showed best results. The response of the sensor was significantly improved by the addition of silicon nanoparticles to the polymer layer. The response characteristics of the NC film towards volatile organic compounds (VOCs) were determined and compared with the pristine polymeric layer in this study. It was shown that the polymeric NC layer can detect acetone at room temperature within one minute. The sensing response towards acetone at room temperature proved that the turn–on and −off exposure to this analyte was reversible with good reproducibility (5% decay) after multiple cycles of gas exposure. The proof-of-concept results are promising for the development of novel gas detectors that are applicable in many fields such as industrial and laboratorial security.</p