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  • Electronic Resource  (13)
  • 1995-1999  (13)
  • 1995  (13)
  • Chemistry  (12)
  • Analytical Chemistry and Spectroscopy  (3)
  • Computational Chemistry and Molecular Modeling
  • Inorganic Chemistry
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  • Electronic Resource  (13)
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  • 1995-1999  (13)
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Keywords
  • 1
    Electronic Resource
    Electronic Resource
    Metal Complexes with Macrocyclic Ligands. Part XXXVIIIPart XXXVII: [1].. Steric effects in the copper(II) and nickel(II) complexes with tetra-N-alkylated 1,4,8,11-tetraazacyclotetradecanes (1995)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 78 (1995), S. 505-513 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of tetra-N-alkylated 1,4,8,11-tetraazacyclotetradecanes have been synthesized and their complexation potential towards Ni2+ and Cu2+ studied. In the case of sterically demanding alkyl substituents, such as i-Pr, PhCH2, or 2-MeC6H4CH2, no metal complexes are formed, whereas for substituents such as Me, Et, and Pr, the metal ion is incorporated into the macrocycle. The spectroscopic properties of the Ni2+ and Cu2+ complexes in aqueous solution indicate that, depending on the sterical hindrance of the N-substituents, the complexes are either square planar or pentacoordinated. All these Ni2+ and Cu2+ complexes react with N3- to give ternary species, the stability of which have been determined by spectrophotometric titrations. The tendency to bind N3- decreases with increasing steric hindrance of the alkyl substituents. The X-ray studies of the Ni2+ complex with the macrocycle 11, substituted by two Me and two Pr groups, and that of the Cu2+ complex with the tetraethyl derivative 8 show that in the solid state, the metal ions exhibit square planar coordination with a small distortion towards tetrahedral geometry.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19950780220
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  • 2
    Electronic Resource
    Electronic Resource
    Metal Complexes with Macrocyclic Ligands. Part XL.Part XXXIX: [1]. Syntheses and silver(I) complexes of mono- and disubstituted dithiadiazamacrocycles (1995)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 78 (1995), S. 1325-1333 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of N2S2-macrocycles with ring sizes varying between 12 and 16, as well as two 12-membered N2S2-rings with a pendant carboxylic and amino group, respectively, were synthesized. Their complexation properties towards Ag+ were studied by pH titrations and by potentiometry with a silver electrode. The observation that 1:1 ([AgLH2]3+, [AgLH]2+, [AgL]+) and 1:2 species ([AgL2H2]3+, [AgL2H]2+, [AgL2]+) were formed is interpreted by postulating that Ag+ can bind either to the S-donors only, or to both the N- and S-atoms. The most stable complex [AgL]+ in the series of the nonfunctionalized macrocycles was found for the 12-membered N2S2-ring 3. The stability of it increased when an additional donor group was introduced into the side chain. The highest formation constant (logβ110 = 14.43(1)) was obtained with the 12-membered ring 12 carrying the ethanamine side chain. In view of a radiochemical application, all Ag+ complexes were tested in blood serum for their stability, but were not stable enough against transmetallation.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19950780522
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  • 3
    Electronic Resource
    Electronic Resource
    Metal Complexes with Macrocyclic Ligands. Part XXXIXPart XXXVIII:[1].. Mono- and binuclear copper(II) complexes of a bridging bis[1, 4, 7-triazacyclononane] (1995)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 78 (1995), S. 693-702 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new bis-macrocycle 1, 1′-[(1H-pyrazol-3], 5-diyl)bis(methylene)bis[1, 4, 7-triazacyclononane] (1) was synthesized and its complexation with Cu2+ studied. Potentiometric and spectrophotometric titrations indicate that, in addition to the mononuclear species [Cu(LH2)]4+, [Cu(LH)]3+, [CuL]2+, and [Cu(LH-1)]+, binuclear complexes such as [Cu2L]4+, [Cu2(LH-1)]3+, and [Cu2(LH-2)]2+ are also formed in solution. The stability constants and spectral properties of these are reported. The binuclear species [Cu2(LH-1)]3+ specifically reacts with an azide ion to give a ternary complex [Cu2(LH-1)(N3)]2+, the stability and structure of which were determined spectrophotometrically and by X-ray diffraction, respectively. The two Cu2+ ions are in a square-pyramidal coordination geometry. The axial ligand is one of the N-atoms of the 1, 4, 7-triazacyclononane ring, whereas at the base of the square pyramid, one finds the other two N-atoms of the macrocycle, one N-atom of the pyrazolide and one of the azide, both of which are bridging the two metal centres. In [Cu2(LH-1)(N3)]2+, a strong antiferromagnetic coupling is present, thus resulting in a species with a low magnetic moment of 1.36 B.M. at room temperature.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19950780316
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  • 4
    Electronic Resource
    Electronic Resource
    Thin-layer composite enzyme electrodes for glucose determinations (1995)
    Weinheim : Wiley-Blackwell
    Electroanalysis 7 (1995), S. 1035-1040 
    Details
    ISSN: 1040-0397
    Keywords: Glucose ; Biosensor ; Nafion ; Oxygen dependence ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have prepared amperometric glucose sensitive electrodes with a composite active layer consisting of Nafion, glucose oxidase, and carbon-supported platinum particles. A particularly advantageous configuration results from the use of such a film on a gas diffusion electrode. We demonstrate that the gas diffusion electrode configuration enables us to supply oxygen from the back of the electrode, thus providing the capability of operating the sensor independent of dissolved oxygen. The insensitivity to solution oxygen concentration has been demonstrated by monitoring the glucose response of the electrode after extensive deoxygenation of solution. Cast composite layers yield mechanically robust coatings with high enzyme loadings, and thus high sensitivity to glucose. The electrode responds rapidly and is stable over a long period (90% activity after more than half a year) when stored in solution. We have optimized the composition of the sensitive layer with respect to Nafion to C/Pt ratio and enzyme loading.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/elan.1140071108
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  • 5
    Electronic Resource
    Electronic Resource
    Brushes formed by self-similarly branched polymers and random manifolds (1995)
    Weinheim : Wiley-Blackwell
    Macromolecular Theory and Simulations 4 (1995), S. 111-117 
    Details
    ISSN: 1022-1344
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When randomly branched polymers are grafted to a surface, polymer brushes are the result, similarly as well known in the case of linear grafted polymer chains. These brushes behave, however, special, as severe restrictions in the conformation of individual polymers are present. These restrictions are firstly due to the high degree of branching and secondly to the natural maximum stretching ratio of the branched molecules, that is given by Hmax = aM1/D. a is the typical size of a monomeric unit, D is the spectral dimension and M the total mass of the branched polymer. Brushes cannot exceed this height, and limits on the grafting density as functions of the spectral dimension are investigated. For all thermodynamic situations the minimum area per chain scales as σmin = aM(D - 1)/D.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mats.1995.040040107
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  • 6
    Electronic Resource
    Electronic Resource
    Scattered intensity by a cross-linked polymer blend (1995)
    Weinheim : Wiley-Blackwell
    Macromolecular Theory and Simulations 4 (1995), S. 67-76 
    Details
    ISSN: 1022-1344
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cross-linked mixtures of polystyrene and poly(vinyl methyl ether) exhibit a non-vanishing zero-angle intensity in small-angle neutron scattering experiments. A possible explanation is that fluctuations in composition in the mixture may be frozen by the presence of cross-links. Assuming this, we introduce a screening length κ by the condition that the scattered intensity should not be changed by cross-linking. We find κ2 ∼ C/(χ - χi), where C is an elastic constant, χ and χi, respectively, the inverse temperature and that where cross-linking is performed. When the temperature is varied, we find three regimes. In the first one, the scattered intensity is monotonously decreasing. In the second one, it has a finite maximum. In the last one, the maximum eventually diverges.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mats.1995.040040104
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  • 7
    Electronic Resource
    Electronic Resource
    Analysis of enzymatic DNA sequencing reactions by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (1995)
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 9 (1995), S. 942-947 
    Details
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The products from base-specific, dideoxy-nucleotide chain-termination DNA sequencing reactions catalyzed by the modified T7 DNA polymerase have been analyzed by using the technique of matrix-assisted laser desorption/ionization (MALDI) time-of-flight mass spectrometry. Preliminary experiments were performed to determine detection limits for a synthetic mixture of mixed-base single-stranded DNA which contained a 14-mer, a 21-mer, and a 41-mer; acceptable spectra, showing peaks for each component, were obtainable for samples that contained as little as 5 fmol per component. Initial sequencing reactions were therefore carried out on 2-pmol amounts of a short synthetic template that was 45 nucleotides in length, employing 2 pmol of 12-mer as the primer strand. This provided readable sequence information out to the 19th base past the primer. Using a 21-mer primer, nearly the entire sequence of the template could be read.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/rcm.1290091015
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  • 8
    Electronic Resource
    Electronic Resource
    Studies on the formation of reactive intermediates from the antineoplastic agent N,N′Bis(2-chloroethyl)-N-nitrosourea (BCNU) in vitro and in Vivo. Characterization of novel glutathione adducts by ionspray tandem mass spectrometry (1995)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 30 (1995), S. 57-68 
    Details
    ISSN: 1076-5174
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In a study designed to examine the nature of short-lived, electrophilic intermediates liberated during decomposition of N,N′-bis(2-chloroethyl)-N-nitrosourea (BCNU) in vitro and also on administration of BCNU (140 μmol i.p.) to rats in vivo, both on-line and off-line LC/MS/MS techniques were employed to detect and characterize the corresponding glutathione (GSH) adducts present in incubation media and excreted into bile, respectively. In vitro, four GSH conjugates were formed and these were identified, on the basis of their product ion spectra, as products of S-and N-carbamoylation and alkylation reactions. Although the relative proportions of these in vitro adducts were found to depend on the molar ratios of GSH and BCNU, the major adduct under all conditions studied proved to be S-(2-chloroethylcarbamoyl)glutathione (SCG). Analysis of untreated bile samples by means of on-line LC/MS/MS with constant neutral loss (129 u) and precursor ion (m/z 179) scanning techniques again led to the detection of four GSH conjugates, although only one of these (SCG) was common to the group of adducts identified in vitro. All of the GSH conjugates detected in bile represented products of S-carbamoylation, indicating that the alkylating moiety released from BCNU undergoes reactions in vivo with nucleophiles other than GSH.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jms.1190300111
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  • 9
    Electronic Resource
    Electronic Resource
    Zeta potential of bone from particle electrophoresis: Solution composition and kinetic effects (1995)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 29 (1995), S. 47-57 
    Details
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The morphology of bone may be influenced by many factors, including electromechanical ones such as electric potentials, electric fields, or zeta potentials. Stress-generated potential studies in bone and particle electrophoresis studies using calcium-deficient hydroxyapatite have shown that the zeta potential depends on the composition of the steeping fluid and steeping time. To better quantify and understand these in situ potential changes in bovine cortical bone, the effects of alterations in calcium, phosphate, and fluoride concentrations in Neuman's Fluid (NF), which simulates in vivo bone extracellular fluid, were investigated using particle electrophoresis. The zeta potential increased in magnitude with increased calcium concentration in NF in as little as 17 min. Increasing phosphate concentration in NF also increased the zeta potential magnitude. These results provide support for a structural model of the bone matrix surface-bone fluid interface, which incorporates the bone surface proper (composed of collagen, mineral, and boundary regions), stationary layer (in which ions, ionic complexes, and proteins may be adsorbed), and bone extracellular fluid. These results, coupled with those of previous studies, indicate that the protein phase probably has an important role in the determination of the physiologic zeta potential; the role of the mineral phase may also be important. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jbm.820290108
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  • 10
    Electronic Resource
    Electronic Resource
    Platelet and monoclonal antibody binding to fibrinogen adsorbed on glow-discharge-deposited polymers (1995)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 29 (1995), S. 729-739 
    Details
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The state of fibrinogen adsorbed on untreated and glow-discharge-treated surfaces was examined by measuring platelet adhesion, monoclonal antibody (mAb) binding, the amount of fibrinogen adsorbed, and the amount of adsorbed fibrinogen which could be eluted with sodium dodecyl sulfate (SDS). Tetrafluoroethylene (TFE) glow-discharge-treated polymers have a lower surface free energy (in air) and retain a larger fraction of adsorbed fibrinogen than untreated surfaces after SDS elution. Platelet adhesion was lowest on the TFE-treated surfaces which retain the highest amounts of fibrinogen after SDS elution. Fibrinogen may undergo unfolding or spreading on the TFE-treated surfaces to minimize interfacial free energy (in water) and maximize protein-;surface interactions. When it is adsorbed on the TFE-treated surfaces, fibrinogen evidently assumes a state which somehow prevents its recognition and binding by platelet receptors. Monoclonal antibodies that bind to the three regions in fibrinogen thought to be involved in platelet adhesion were therefore used to detect changes in adsorbed fibrinogen. These regions and the antibodies which bind to them are: the COOH-terminal of the γ-chain, mAb M1; the RGD peptide sequence at Aα 95-98, mAb R1; the RDG sequence at Aα 572-575, mAb R2. For fibrinogen adsorbed on the untreated or TFE-treated surfaces, M1 and R2 binding was relatively high compared to background, while R1 binding was low. However, the amount of binding of each mAb to fibrinogen adsorbed on the TFE-treated surfaces was equal to or greater than fibrinogen adsorbed to the untreated surfaces. Therefore, antibody-detectable changes in the platelet binding regions of adsorbed fibrinogen that might have been caused by conformational or orientational rearrangements were not observed for the TFE-treated surfaces. The data suggest that the tight binding of fibrinogen on a surface may directly affect the ability of the fibrinogen to interact with the platelet receptors - i.e., that fibrinogen must be loosely held to facilitate maximal interaction with platelet receptors. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jbm.820290609
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