Employing

Distribution by Scientific Domains
Distribution within Chemistry


Selected Abstracts


Comparison of continuous subcutaneous insulin infusion (CSII) and multiple daily injections (MDI) in paediatric Type 1 diabetes: a multicentre matched-pair cohort analysis over 3 years

DIABETIC MEDICINE, Issue 1 2008
B. I. Jakisch
Abstract Aims To conduct a multicentre, matched-pair cohort analysis comparing glycaemic control and adverse events of continuous subcutaneous insulin infusion (CSII) with multiple daily injections (MDI) in paediatric patients. Methods Using standardized computer-based prospective documentation, HbA1c, insulin dose, body mass index,standard deviation score (BMI,SDS), rate of hypoglycaemia, rate of diabetic ketoacidosis (DKA) and intensity of care were analysed in 434 matched pairs during a follow-up period of 3 years after initiation of MDI or CSII. Results HbA1c was significantly lower in the CSII group during the first year of new regimen (CSII 7.5 ± 0.05 vs. MDI 7.7 ± 0.06; P < 0.05), but rose to the same level as in the MDI group during year 3. Insulin requirement remained significantly lower in the CSII group. The BMI,SDS increased in both study groups, with no significant difference. The rate of severe hypoglycaemia decreased significantly after the change of regimen (CSII 17.87 ± 2.85 vs. MDI 25.14 ± 3.79; P < 0.05) and during year 3 of the regimen, particularly when compared with baseline (,21% vs. ,16%). The rate of DKA was lower at baseline in the CSII group and remained significantly lower over all 3 years. Intensity of care was the same in both subsets. Conclusions Employing a large cohort, this matched-pair analysis has demonstrated over a 3-year study period that CSII is a safe form of intensive insulin therapy with similar glycaemic effects, but with significantly reduced rates of hypoglycaemia and DKA and a lower insulin requirement when compared with MDI. [source]


A simple procedure to approximate slip displacement of freestanding rigid body subjected to earthquake motions

EARTHQUAKE ENGINEERING AND STRUCTURAL DYNAMICS, Issue 4 2007
Tomoyo Taniguchi
Abstract A simple calculation procedure for estimating absolute maximum slip displacement of a freestanding rigid body placed on the ground or floor of linear/nonlinear multi-storey building during an earthquake is developed. The proposed procedure uses the displacement induced by the horizontal sinusoidal acceleration to approximate the absolute maximum slip displacement, i.e. the basic slip displacement. The amplitude of this horizontal sinusoidal acceleration is identical to either the peak horizontal ground acceleration or peak horizontal floor response acceleration. Its period meets the predominant period of the horizontal acceleration employed. The effects of vertical acceleration are considered to reduce the friction force monotonously. The root mean square value of the vertical acceleration at the peak horizontal acceleration is used. A mathematical solution of the basic slip displacement is presented. Employing over one hundred accelerograms, the absolute maximum slip displacements are computed and compared with the corresponding basic slip displacements. Their discrepancies are modelled by the logarithmic normal distribution regardless of the analytical conditions. The modification factor to the basic slip displacement is quantified based on the probability of the non-exceedence of a certain threshold. Therefore, the product of the modification factor and the basic slip displacement gives the design slip displacement of the body as the maximum expected value. Since the place of the body and linear/nonlinear state of building make the modification factor slightly vary, ensuring it to suit the problem is essential to secure prediction accuracy. Copyright © 2006 John Wiley & Sons, Ltd. [source]


Stereoselective Synthesis of (2E,4Z)-Dienamides Employing (Triphenylphosphoranylidene)ketene

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 17 2009
Steffen Pachali
Abstract The three-component reaction between ylide Ph3PCCO, amines and aldehydes is known to afford selectively (E)-,,,-unsaturated amides. We applied a variant of this methodology to the preparation of (2E,4Z)-dienamides 11 utilizing the phosphonium salt formation from ethyl 5-aminopentanoate hydrochloride and Ph3PCCO followed by deprotonation with DBU and a Wittig olefination of the corresponding ylide with various (Z)-,,,-unsaturated aldehydes 10. The (2E,4Z)-dienamides 11 were isolated in yields of up to 80,%. The (Z)-configuration of the starting aldehydes 10 remained untouched during the reaction.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source]


Synthesis of the Carbon Framework of the Stephaoxocanes Employing a Sequential RCM/Pomeranz,Fritsch Approach

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 31 2007
Andrea B. J. Bracca
Abstract The syntheses of two cyclodeca[ij]isoquinoline derivatives, which embody the carbon framework of stephaoxocanidine, excentricine and the recently isolated stephalonganines A, B and C, are reported. The target tricyclic compounds were prepared from isovanillin, employing a ring-closing metathesis approach towards the synthesis of a benzocyclodecane-type common intermediate; different modifications of thePomeranz,Fritsch protocol allowed the installation of the heterocyclic ring.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source]


Effect of temperature on development and growth of the raptorial cladoceran Leptodora kindtii under laboratory conditions

FRESHWATER BIOLOGY, Issue 11 2004
Jacobus Vijverberg
Summary 1. Leptodora is a key species in many temperate freshwater systems, but so far its role in the food web could not be properly evaluated because detailed information about its secondary production was lacking. As we wanted to estimate the secondary production of Leptodora, we measured its development and growth rates in the laboratory. 2. Employing improved methods to estimate growth and instar durations, we cultured Leptodora kindtii in the laboratory at four constant temperatures (15, 17.5, 20 and 25 °C). Growth in length and development times of eggs and instar stages were assessed. 3. Growth rates at 15, 17.5 and 20 °C were similar, but at 25 °C growth was distinctly faster. At 17.5 °C we observed seven juvenile instar stages before the first adult instar stage was reached. [source]


Cutting Long Syntheses Short: Access to Non-Natural Tyrosine Derivatives Employing an Engineered Tyrosine Phenol Lyase

ADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 4 2010
Birgit Seisser
Abstract The chemical synthesis of 3-substituted tyrosine derivatives requires a minimum of four steps to access optically enriched material starting from commercial precursors. Attempting to short-cut the cumbersome chemical synthesis of 3-substituted tyrosine derivatives, a single step biocatalytic approach was identified employing the tyrosine phenol lyase from Citrobacter freundii. The enzyme catalyses the hydrolysis of tyrosine to phenol, pyruvate and ammonium as well as the reverse reaction, thus the formation of tyrosine from phenol, pyruvate and ammonium. Since the wild-type enzyme possessed a very narrow substrate spectrum, structure-guided, site-directed mutagenesis was required to change the substrate specificity of this CC bond forming enzyme. The best variant M379V transformed, for example, o -cresol, o -methoxyphenol and o -chlorophenol efficiently to the corresponding tyrosine derivatives without any detectable side-product. In contrast, all three phenol compounds were non-substrates for the wild-type enzyme. Employing the mutant, various L -tyrosine derivatives (3-Me, 3-OMe, 3-F, 3-Cl) were obtained with complete conversion and excellent enantiomeric excess (>97%) in just a single ,green' step starting from pyruvate and commercially available phenol derivatives. [source]


Highly Efficient and Stereoselective Julia,Kocienski Protocol for the Synthesis of ,-Fluoro-,,,-unsaturated Esters and Weinreb Amides Employing 3,5-Bis(trifluoromethyl)phenyl (BTFP) Sulfones

ADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 11-12 2008
Diego
Abstract ,-Fluoroacetates 3 and Weinreb amide 4, bearing a ,-[3,5-bis(trifluoromethyl)phenyl]sulfonyl (BTFP-sulfonyl) group at the ,-position, are employed in the highly stereoselective synthesis of ,-fluoro-,,,-unsaturated alkenoates and Weinreb amides, respectively. Aromatic and aliphatic aldehydes are condensed under extremely mild and simple reaction conditions using potassium carbonate in dimethylformamide at room temperature under solid-liquid phase-transfer catalysis conditions in good yields and high Z -diastereoselectivities, specially in the case of the fluorinated Weinreb amides. A detailed computational mechanistic study suggests a final non-concerted elimination of sulfur dioxide and 3,5-bis(trifluoromethyl)phenoxide and explains the observed high stereoselectivities for the reaction on the basis of thermodynamic and kinetic considerations. [source]


Critical role of ADP interaction with P2Y12 receptor in the maintenance of ,IIb,3 activation: association with Rap1B activation

JOURNAL OF THROMBOSIS AND HAEMOSTASIS, Issue 6 2006
T. KAMAE
Summary.,Objective:,Platelet integrin ,IIb,3 plays a crucial role in platelet aggregation, and the affinity of ,IIb,3 for fibrinogen is dynamically regulated. Employing modified ligand-binding assays, we analyzed the mechanism by which ,IIb,3 maintains its high-affinity state. Methods and results:,Washed platelets adjusted to 50 × 103 ,L,1 were stimulated with 0.2 U mL,1 thrombin or 5 ,m U46619 under static conditions. After the completion of ,IIb,3 activation and granule secretion, different kinds of antagonists were added to the activated platelets. The activated ,IIb,3 was then detected by fluorescein isothiocyanate (FITC)-labeled PAC1. The addition of 1 ,m AR-C69931MX (a P2Y12 antagonist) or 1 mm A3P5P (a P2Y1 antagonist) disrupted the sustained ,IIb,3 activation by ,92% and ,38%, respectively, without inhibiting CD62P or CD63 expression. Dilution of the platelet preparation to 500 ,L,1 also disrupted the sustained ,IIb,3 activation, and the disruption by such dilution was abrogated by the addition of exogenous adenosine 5,-diphosphate (ADP) in a dose-dependent fashion. The amounts of ADP released from activated platelets determined by high-performance liquid chromatography were compatible with the amounts of exogenous ADP required for the restoration. We next examined the effects of antagonists on protein kinase C (PKC) and Rap1B activation induced by 0.2 U mL,1 thrombin. Thrombin induced long-lasting PKC and Rap1B activation. AR-C69931MX markedly inhibited Rap1B activation without inhibiting PKC activation. Conclusions:,Our data indicate that the continuous interaction between released ADP and P2Y12 is critical for the maintenance of ,IIb,3 activation. [source]


Enantioselective Total Synthesis of the Marine Toxin (,)-Gymnodimine Employing a Barbier-Type Macrocyclization,

ANGEWANDTE CHEMIE, Issue 40 2009
Ke Kong
Exoten des Meeres: tert -Butyllithium vermittelt bei Umgebungstemperatur eine Barbier-Makrocyclisierung in der ersten Totalsynthese von (,)-Gymnodimin (Ts: Toluol-4-sulfonyl; TBS: tert -Butyldimethylsilyl), einem marinen Toxin aus der Familie der spirocyclischen Imine. Die Synthese enthält außerdem eine vinyloge Mukaiyama-Aldolreaktion zur Kupplung der labilen Butenolidgruppe an eine makrocyclische Keton-Zwischenstufe. [source]


Oxidoreductases Working Together: Concurrent Obtaining of Valuable Derivatives by Employing the PIKAT Method

CHEMCATCHEM, Issue 8 2010
Fabricio
Flying PIKATs: The stereoselective oxidation of several sulfides linked to the enantioselective oxidation of different sec -alcohols are combined in a parallel interconnected kinetic asymmetric transformation (PIKAT) fashion. Furthermore, the cofactor concentration employed in these processes is investigated, demonstrating a high capacity of performance, even at micromolar concentrations of the mediator. [source]


ChemInform Abstract: Chromium-Catalyzed Homoaldol Equivalent Reaction Employing a Nucleophilic Propenyl Acetate.

CHEMINFORM, Issue 42 2010
Jun Yong Kang
Abstract Acetate (II) is employed as a masked homoenolate nucleophile in addition reactions to aromatic, aliphatic and ,,,-unsaturated aldehydes under mild Cr/Mn redox conditions. [source]


ChemInform Abstract: Highly Efficient and Stereoselective Julia,Kocienski Protocol for the Synthesis of ,-Fluoro-,,,-unsaturated Esters and Weinreb Amides Employing 3,5-Bis(trifluoromethyl)phenyl (BTFP) Sulfones.

CHEMINFORM, Issue 50 2008
Diego A. Alonso
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]


ChemInform Abstract: Carbonyl Propargylation from the Alcohol or Aldehyde Oxidation Level Employing 1,3-Enynes as Surrogates to Preformed Allenylmetal Reagents: A Ruthenium-Catalyzed C,C Bond-Forming Transfer Hydrogenation.

CHEMINFORM, Issue 41 2008
Ryan L. Patman
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]


ChemInform Abstract: Rapid and Efficient Entry to Vinyl Silanes from Aldehydes Employing a Novel Metalation,Peterson Sequence.

CHEMINFORM, Issue 28 2008
James McNulty
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]


Chemoenzymatic Synthesis of Enantiomerically Pure 1,2-Diols Employing Immobilized Lipase in the Ionic Liquid [bmim]PF6.

CHEMINFORM, Issue 9 2005
Ahmed Kamal
Abstract For Abstract see ChemInform Abstract in Full Text. [source]


Synthesis of Oligosaccharides as Potential Novel Food Components and Upscaled Enzymatic Reaction Employing the ,-Galactosidase from Bovine Testes.

CHEMINFORM, Issue 26 2004
Sven Schroeder
No abstract is available for this article. [source]


ChemInform Abstract: Elaboration of 1-Benzoyltetrahydroisoquinoline Derivatives Employing a Pictet,Spengler Cyclization with ,-Chloro-,-phenylthioketones.

CHEMINFORM, Issue 11 2002
Synthesis of O-Methylvelucryptine (XI).
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]


Noncovalent Functionalization, Exfoliation, and Solubilization of Graphene in Water by Employing a Fluorescent Coronene Carboxylate

CHEMISTRY - A EUROPEAN JOURNAL, Issue 9 2010
Anupama Ghosh
Single-layer graphene stabilization: An efficient methodology to make stable aqueous solutions of single-layer graphene has been demonstrated by exploiting charge-transfer interactions with a coronene tetracarboxylate acceptor molecule (see figure). Microscopic studies reveal exfoliation of few-layer graphene and selective stabilization of single-layer graphene in large quantities. [source]


A Novel Tripodal Ligand Containing Three Different N -Heterocyclic Donor Functions and Its Application in Catechol Dioxygenase Mimicking

CHEMISTRY - A EUROPEAN JOURNAL, Issue 22 2009
Marit Wagner Dipl.-Chem.
Abstract Prominent donors: A pyridyl, an imidazolyl, and a pyrazolyl donor function are part of the novel tripodal ligand depicted, which thus combines three of the most prominent donors applied in ligands for bioinorganic chemistry within one coordination unit. To exploit its behaviour and potential, first investigations have been carried out in relation to catechol dioxygenase mimicry. We describe a novel chiral ligand, L, in which three different N -donor functions are linked to a methoxymethine unit: a methylpyrazole derivative, a methylimidazole unit, and a pyridyl residue. Complexes with FeCl2, FeBr2, and FeCl3 have been synthesized and fully characterized, including with respect to their molecular structures. While in combination with FeCl3L coordinates in a tripodal fashion, with FeX2 (X=Cl, Br) it binds only through two functions and the pyridyl unit remains dangling. For potential modelling of intradiol and extradiol catechol dioxygenase reactivity, the complexes [LFeCl2], 1, and [LFeCl3], 3, have been treated with 3,5-di- tert -butylcatechol, triethylamine, and O2. Both complexes yielded similar results in such investigations, since the LFeII,catecholate complex reacts with O2 through one-electron oxidation in the first step. Employing 3 in acetonitrile solution, intradiol cleavage occurred, although the undesired quinone was formed as the main product. If reagents were added (NaBPh4, H+) or reaction conditions were chosen (CH2Cl2 instead of CH3CN as the solvent) that made the coordination sphere at the iron centre more accessible for a third substrate donor function, an alternative reaction route, presumably involving O2 binding at the metal, became more important, which led to extradiol cleavage. In the extreme case (CH2Cl2 as the solvent and with the addition of NaBPh4), mainly the extradiol cleavage products were formed; the intradiol products were only observed as side products then and quinone formation became negligible. Protonated base functions in the second coordination sphere increased the efficiency of extradiol cleavage only slightly. The obtained results are in line with current understanding of the function of intradiol/extradiol dioxygenases. [source]


Employing following eye movements to discriminate normal from glaucoma subjects

CLINICAL & EXPERIMENTAL OPHTHALMOLOGY, Issue 3 2000
Wl Severt MDPhD
ABSTRACT We recorded optokinetic nystagmus (OKN) to see if slow phase velocity, duration or other measures were affected by glaucoma. Drifting grating patterns that either weakly or strongly evoked the spatial frequency doubling illusion were employed. Analysis of 68 variables characterizing the OKN revealed that small subsets of these variables were good at discriminating normal from primary open angle glaucoma subjects. The variables were related to the regularity of following eye movements. Models including the best five variables selected in two different ways classified about 90% of subjects correctly. Impaired accuracy of eye movements suggests that glaucoma changes the signal to noise ratio available to the brain. The gross changes observed permit the use of electro-oculography or other simple methods in the clinic. [source]


Survey of Theoretical Work for the Proposed HEDgeHOB Experimental Schemes: HIHEX and LAPLAS

CONTRIBUTIONS TO PLASMA PHYSICS, Issue 4-5 2007
N. A. Tahir
Abstract This paper presents a review of the theoretical work that has resulted in a scientific proposal on studies of High-Energy-Density (HED) states in matter using intense beams of energetic heavy ions that will be available at the future Facility for Antiprotons and Ion Research (FAIR) at Darmstadt [W.F. Henning, Nucl. Inst. Meth B 24 (2003) 725-729]. The proposal is named HEDgeHOB that stands for High Energy Density Matter Generated by Heavy Ion Beams. Two experimental schemes have been worked out for the HEDgeHOB experimental proposal, namely, HIHEX and LAPLAS. The first scheme allows for studies of HED states by isochoric and uniform heating of matter by an intense heavy ion beam that is followed by isentropic expansion of the heated material. Numerical simulations have shown that using the beam parameters that will be available at the FAIR, one can access all the interesting physical states of HED matter including an expanded hot liquid state, twophase liquid-gas region, critical point parameters and strongly coupled plasmas for all the materials of interest. The second scheme involves a low-entropy compression of a test material like hydrogen that is enclosed in a cylindrical shell of a high-Z material like gold or lead. The target can be driven by a hollow or a circular beam. This compression scheme relies on multiple shock reflection between the hydrogen-gold (lead) boundary and the cylinder axis. The hydrodynamic stability of the LAPLAS target has also been analyzed that shows that the implosion is completely stable to Rayleigh-Taylor and Richtmyer-Meshkov instabilities. LAPLAS implosion using a hollow beam is suitable for studying the problem of hydrogen metallization whereas the one employing a circular focal spot leads to physical conditions that are expected to exist in the interiors of the giant planets. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


PbS crystals with clover-like structure: Preparation, characterization, optical properties and influencing factors

CRYSTAL RESEARCH AND TECHNOLOGY, Issue 3 2004
Yonghong Ni
Abstract A new and simple route to synthesize Lead sulfide (PbS) crystals with the clover-like structure was described in the current paper. PbS was prepared in a simple aqueous solution employing (CH3COO)2Pb and thiourea as the initial materials under 130 W microwave irradiation. No any surfactant or template including organic polyamines with N-chelation property was needed. The phase and composition of the product were identified by X-ray powder diffraction (XRD) and X-ray photoelectron spectra (XPS). TEM observation showed that the product with the six-petal flower-shaped structures was obtained, but SEM observation confirmed the clover-like structure of the product; and the six-petal flowers were formed via the overlap of two clovers revolved 60° around the center of the flower. Some factors affected the shape of the final product were studied and the optical properties of PbS crystals with the clover-like structure were measured. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


Changes in microbial community composition following treatment of methanogenic granules with chloroform

ENVIRONMENTAL PROGRESS & SUSTAINABLE ENERGY, Issue 1 2009
Bo Hu
Abstract Eliminating hydrogen consuming bacteria is a critical step in anaerobic fermentation for biohydrogen production. Treatment of anaerobic granular sludge with chloroform was reported as effective in transforming a methane-producing system into a hydrogen-producing system by eliminating methane production. This study, using 16S rRNA gene sequences, further assessed changes in microbial community composition as a result of chloroform treatment and during continuous cultivation of chloroform-treated granules in a continuous upflow reactor employing immobilized cells. Profiles of terminal restriction fragment length polymorphisms (T-RFLP) of 16S rRNA genes sequences cloned from samples before and after chloroform treatment showed that methanogenic hydrogen consumers and Methanosaeta harundinacea sp. were eliminated. Methanosaeta concilii, however, was not eliminated from the hydrogen-producing system, which might explain, in part, the granulation phenomena in the anaerobic hydrogen fermentation system. The results also showed that Clostridium butyricum dominated the hydrogen-production system. © 2009 American Institute of Chemical Engineers Environ Prog, 2009 [source]


Rational Design of Charge-Neutral, Near-Infrared-Emitting Osmium(II) Complexes and OLED Fabrication

ADVANCED FUNCTIONAL MATERIALS, Issue 16 2009
Tsang-Chi Lee
Abstract A new series of charge neutral Os(II) isoquinolyl triazolate complexes (1,4) with both trans and cis arrangement of phosphine donors are synthesized, and their structural, electrochemical and photophysical properties are established. In sharp contrast to the cis -arranged complexes 2,4, the trans derivative 1, which shows a planar arrangement of chromophoric N -substituted chelates, offers the most effective extended , -delocalization and hence the lowest excited state energy gap. These complexes exhibit phosphorescence with peak wavelengths ranging from 692,805,nm in degassed CH2Cl2 at room temperature. Near-infrared (NIR)-emitting electroluminescent devices employing 6,wt % of 1 (or 4) doped in Alq3 host material are successfully fabricated. The devices incorporating 1 as NIR phosphor exhibit fairly intense emission with a peak wavelength at 814,nm. Forward radiant emittance reaches as high as 65.02,µW,cm,2, and a peak EQE of ,1.5% with devices employing Alq3, TPBi and/or TAZ as electron-transporting/exciton-blocking layers. Upon switching to phosphor 4, the electroluminescence blue shifts to 718,nm, while the maximum EQE and radiance increase to 2.7% and 93.26 (,W,cm,2) respectively. Their performances are optimized upon using TAZ as the electron transporting and exciton-blocking material. The OLEDs characterized represent the only NIR-emitting devices fabricated using charge-neutral and volatile Os(II) phosphors via thermal vacuum deposition. [source]


Epitaxial Growth of Indium Arsenide Nanowires on Silicon Using Nucleation Templates Formed by Self-Assembled Organic Coatings,

ADVANCED MATERIALS, Issue 14 2007
T. Mårtensson
Indium arsenide nanowires are grown directly on silicon substrates (see figure and cover) using a method employing self-assembled organic coatings to create oxide-based growth templates. High-performance materials, such as InAs, could have great impact on future nanoelectronics if integrated with Si, but integration has so far been hard to realize with other methods. [source]


Enantioselective Organocatalytic Synthesis of Arylglycines via Friedel,Crafts Alkylation of Arenes with a Glyoxylate Imine

ADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 9 2010
Dieter Enders
Abstract The enantioselective organocatalytic synthesis of arylglycines has been developed employing 1,mol% of an enantiopure N -triflyl phosphoramide Brønsted acid as organocatalyst. Various differently substituted phenylglycine derivatives can be synthesized in good to excellent yields and enantiomeric excesses based on a Friedel,Crafts alkylation of electron-rich arenes with a glyoxylate imine. A novel protocol for the deprotection of the N - tert -butylsulfonyl (Bus) group has also been developed. [source]


Study of the design of waveguide filters with improved suppression of modal interference through the cross-shaped slot

INTERNATIONAL JOURNAL OF RF AND MICROWAVE COMPUTER-AIDED ENGINEERING, Issue 4 2003
Sungtek Kahng
Abstract In this article, a new method is suggested to improve the frequency responses of dual-mode waveguide filters employing cross-shaped slots. According to this method, regarding one cross-shaped slot between two cavities, the horizontal (vertical) mode in one cavity influences the vertical (horizontal) mode in the other cavity to a much lesser extent. It enhances the overall performances. A 4th -order dual-mode filter is used as an example and it validates the method. © 2003 Wiley Periodicals, Inc. Int J RF and Microwave CAE 13: 285,292, 2003. [source]


Formation and reactions of cluster ions from aromatic carboxylic acids together with amino acids

ISRAEL JOURNAL OF CHEMISTRY, Issue 2 2001
Anja Meffert
The cluster formation of several aromatic carboxylic acids, ferulic acid, vanillic acid, sinapinic acid, and 3,4-dihydroxybenzoic acid was investigated by means of laser desorption into a supersonic beam followed by multiphoton ionization-time-of-flight mass spectrometry. The formation of not only homogeneous clusters, but also of heterogeneous clusters with some small amino acids was studied. The different neutral clusters formed in the supersonic expansion were ionized by a multiphoton process employing either nano- or femtosecond laser pulses. Strong differences in the detection of cluster ions due to the laser pulse length employed for multiphoton ionization were observed. Only femtosecond activation led to mass spectra with intense signals of the cluster ions. In addition, in the case of femtosecond ionization, protonated amino acids were detected in the mass spectra. As direct ionization of the free amino acids is not possible under the chosen ionization conditions because they lack an adequate chromophore, these protonated amino acids are assumed to be formed via an intracluster proton transfer in the heterogeneous dimer and subsequent decay of the ionized cluster (dissociative proton transfer). Such well-known processes for heterogeneous clusters consisting of a substituted aromatic molecule and small polar solvent molecules may be involved in the matrixassisted laser desorption ionization (MALDI) process. [source]


Reverse atom transfer radical polymerization of MMA via immobilized catalysts in imidazolium ionic liquids

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007
Najun Li
Abstract Reverse atom transfer radical polymerization (RATRP) of methyl methacrylate (MMA) employing immobilized catalyst was approached at 50 and 60°C in [C8mim]PF6, and compared with the polymerization of MMA DMF as solvent. Other ionic liquids, [C6mim]BF4, [C8mim]BF4, and [C12mim]BF4, were used as solvents to perform the RATRP of MMA. By comparison, we found that the [C8mim]PF6 was the best solvent in this immobilized catalyst system and the polymerization was best controlled. In addition, the immobilized catalyst spherules can easily separate from the reaction mixture, which avoids the prevalent problem of the catalyst residual in RATRP and also gives us a possibility to recycle the catalyst system. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3915,3919, 2007 [source]


Ambivalent Sexism and Misogynistic Rap Music: Does Exposure to Eminem Increase Sexism?,

JOURNAL OF APPLIED SOCIAL PSYCHOLOGY, Issue 12 2007
Michael D. Cobb
We evaluate the oft-repeated but typically untested claim that rap music encourages sexism. We randomly assigned participants to 1 of 3 conditions: no music, misogynistic rap music, and nonmisogynistic rap music. The first study (treated as a pilot; N = 232) weakly demonstrated the differential impact of exposure on male and female participants, but our measures of sexism were unreliable. We then conducted a second study (N = 175) employing well-validated (and more subtle) measures taken from the Ambivalent Sexism Inventory (ASI). While we replicated the weak differential impact of participants' sex, we also find that sexism increased after listening to nonmisogynistic rap music, especially among males. Implications for the debate about labeling and censoring rap music are discussed. [source]