Water vapor sorption kinetics of wood modified with glutaraldehyde

The modifying effects of Scots pine (Pinus sylvestris L.) wood with the crosslinking agent glutaraldehyde (GA) on the water vapor sorption kinetics were studied by curve fitting the experimental isotherm sorption data obtained using a Dynamic Vapor Sorption apparatus using the parallel exponential kinetics model (PEK model) and the Hailwood–Horrobin model (H–H model) for the isotherm. Both the H–H model and the PEK model provided good fits to the experimental data. Modification of wood with GA reduced both the time to equilibrium and the equilibrium moisture content (EMC). According to the PEK and H–H models, the reduction in EMC was mainly due to the decrease of moisture content (MC) associated with the slow sorption processes and polylayer water. The fast sorption processes and monolayer water were little affected by GA modification. Compared to the untreated control, the estimated total water absorbed by wood treated to a WPG of 20.9% at 100% RH decreased by 52.2%, by extrapolating the fitted curves derived from the H–H model. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Iron and Copper Salts in the Synthesis of Benzo[b]furans

Intramolecular C O bond forming reactions of aryl 2‐bromobenzyl ketones lead to benzo[b]furans. The cyclizations can be catalyzed by 10 mol% of iron trichloride (of 98% or of 99.995% purity) or sub‐mol% quantities of copper(II) chloride (of 99.995% purity).     

Radiofluorinated Pyrimidine‐2,4,6‐triones as Molecular Probes for Noninvasive MMP‐Targeted Imaging

Matrix metalloproteinases (MMPs) are zinc‐ and calcium‐dependent endopeptidases. Representing a subfamily of the metzincin superfamily, MMPs are involved in the proteolytic degradation of components of the extracellular matrix. Unregulated MMP expression, MMP dysregulation and locally increased MMP activity are common features of various diseases, such as cancer, atherosclerosis, stroke, arthritis, and others. Therefore, activated MMPs are suitable biological targets for the specific visualization of such pathologies, in particular by using radiolabeled MMP inhibitors (MMPIs). The aim of this work was to develop a radiofluorinated molecular probe for noninvasive in vivo imaging for the detection of up‐regulated levels of activated MMPs in the living organism. Fluorinated MMPIs ( 26 , 31 and 38 ) based on the pyrimidine‐2,4,6‐trione lead structure RO 28‐2653 ( 1 ) were synthesized, and their MMP inhibition potency was evaluated in vitro. The radiosynthesis and the in vivo biodistribution of the first ¹⁸F‐labeled prototype, MMP‐targeted tracer [¹⁸F] 26 , suitable for molecular imaging by means of positron emission tomography (PET) were realized.     

Inhibition of Eimeria tenella CDK‐Related Kinase 2: From Target Identification to Lead Compounds

Apicomplexan parasites encompass several human‐ and animal‐pathogenic protozoans such as Plasmodium falciparum, Toxoplasma gondii, and Eimeria tenella. E. tenella causes coccidiosis, a disease that afflicts chickens, leading to tremendous economic losses to the global poultry industry. The considerable increase in drug resistance makes it necessary to develop new therapeutic strategies against this parasite. Cyclin‐dependent kinases (CDKs) are key molecules in cell‐cycle regulation and are therefore prominent target proteins in parasitic diseases. Bioinformatics analysis revealed four potential CDK‐like proteins, of which one—E. tenella CDK‐related kinase 2 (EtCRK2)—has already been characterized by gene cloning and expression. 1 By using the CDK‐specific inhibitor flavopiridol in EtCRK2 enzyme assays and schizont maturation assays (SMA), we could chemically validate CDK‐like proteins as potential drug targets. An X‐ray crystal structure of human CDK2 (HsCDK2) served as a template to build protein models of EtCRK2 by comparative homology modeling. Structural differences in the ATP binding site between EtCRK2 and HsCDK2, as well as chicken CDK3, were addressed for the optimization of selective ATP‐competitive inhibitors. Virtual screening and “wet‐bench” high‐throughput screening campaigns on large compound libraries resulted in an initial set of hit compounds. These compounds were further analyzed and characterized, leading to a set of four promising lead compounds for development as EtCRK2 inhibitors.     

Incineration of diesel particulate matter using induction heating technique

Incineration of diesel particulate matter for the regeneration of a mesh-type particulate-filter is achieved using induction heating technique. Heating of the diesel particulates deposited on the mesh-type particulate-filter at around 600 °C is investigated. In the case of the particulate filter, stainless-steel mesh-type filters are considered and the influence on filtering efficiency, the engine performance due to back-pressure generation is studied. Theoretical estimation shows that induction heating approach for the regeneration via exhaust gas heating requires high power (>3 kW). On the other hand, regeneration of mesh-type particulate-filter using induction heating technique requires a low input power of around 0.5 kW in the off-line condition. The proposed mesh-type particulate-filter allowed a filtration efficiency of around 30–40% at lower engine speeds and part loads. Particulate combustion through induction heating at static condition is studied and power required for mesh-type filter and sintered metal filter regeneration during engine operation is estimated theoretically.     

Prospects for fast Rydberg gates on an atom chip

Atom chips are a promising candidate for a scalable architecture for quantum information processing provided a universal set of gates can be implemented with high fidelity. The difficult part in achieving universality is the entangling two-qubit gate. We consider a Rydberg phase gate for two atoms trapped on a chip and employ optimal control theory to find the shortest gate that still yields a reasonable gate error. Our parameters correspond to a situation where the Rydberg blockade regime is not yet reached. We discuss the role of spontaneous emission and the effect of noise from the chip surface on the atoms in the Rydberg state.     

Least-squares estimation of anisotropic similarity transformations from corresponding 2D point sets

Pose estimation is a problem that occurs in many applications. In machine vision, the pose is often a 2D affine pose. In several applications, a restricted class of 2D affine poses with five degrees of freedom consisting of an anisotropic scaling, a rotation, and a translation must be determined from corresponding 2D points. A closed-form least-squares solution for this problem is described. The algorithm can be extended easily to robustly deal with outliers.     

When prevention promotes creativity: The role of mood, regulatory focus, and regulatory closure.

Promotion-focused states generally boost creativity because they associate with enhanced activation and cognitive flexibility. With regard to prevention-focused states, research evidence is less consistent, with some findings suggesting prevention-focused states promote creativity and other findings pointing to no or even negative effects. We proposed and tested the hypothesis that whether prevention-focused states boost creativity depends on regulatory closure (whether a goal is fulfilled or not). We predicted that prevention-focused states that activate the individual (unfulfilled prevention goals, fear) would lead to similar levels of creativity as promotion-focused states but that prevention-focused states that deactivate (closed prevention goals, relief) would lead to lower levels of creativity. Moreover, we predicted that this effect would be mediated by feelings of activation. Predictions were tested in 3 studies on creative insights and 1 on original ideation. Results supported predictions. Implications for self-regulation, motivation, mood, and creativity are discussed. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

The Chemical Biology of Phosphoinositide 3‐Kinases

Since its discovery in the late 1980s, phosphoinositide 3‐kinase (PI3K), and its isoforms have arguably reached the forefront of signal transduction research. Regulation of this lipid kinase, its functions, its effectors, in short its entire signaling network, has been extensively studied. PI3K inhibitors are frequently used in biochemistry and cell biology. In addition, many pharmaceutical companies have launched drug‐discovery programs to identify modulators of PI3Ks. Despite these efforts and a fairly good knowledge of the PI3K signaling network, we still have only a rudimentary picture of the signaling dynamics of PI3K and its lipid products in space and time. It is therefore essential to create and use novel biological and chemical tools to manipulate the phosphoinositide signaling network with spatial and temporal resolution. In this review, we discuss the current and potential future tools that are available and necessary to unravel the various functions of PI3K and its isoforms.