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  • 1
    ISSN: 0899-0042
    Keywords: capillary electrophoresis ; chiral separation ; cyclodextrins ; methods development ; enantiomers ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chiral separation methods development using conventional techniques such as GC or HPLC requires a lot of experience, effort, and expense, due to the wide diversity of the optically active solutes and their possible chiral selectors. Capillary electrophoresis has received increased attention as an alternative technique for chiral separation due to its inherent high efficiencies and ease of methods development. However, due to the wide variety of chiral selectors available in CE, the benefits of this technique might be diminished without an appropriate methods development scheme. In this paper detailed examples are shown for fast, efficient, and predictable chiral capillary electrophoresis separation methods development based on a new and systematic theory. Optimized separations and their parameters are presented for several enantiomeric acids and bases. All the three possible cases, such as the use of low and high pH, as well as pH = pK buffer systems are thoroughly discussed. © 1995 Wiley-Liss, Inc.
    Additional Material: 5 Ill.
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  • 2
    ISSN: 0947-6539
    Keywords: crown ethers ; layered materials ; molecular recognition ; zirconium phosphate ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The topotactic exchange reactions of γ-zirconium phosphate and γ-zirconium phosphate/methylphosphonate with phosphonic acids derived from azacrown ethers of different sizes was examined. Prior intercalation of hexylamine was necessary in most cases to attain the maximum exchange level predicted by molecular modeling. Materials with imbricated or nonimbricated layers were obtained depending on crown size and exchange level. Exchange of methylphosphonates in γ-zirconium phosphate/methylphosphonate was only observed when hexylamine had previously been intercalated. The exchange with the bisphosphonic acid derived from 1,10-diaza[18]-crown-6 gave a material with an interlayer distance compatible with pillaring of the γ-phase. The materials obtained from the exchange reactions of γ-zirconium phosphate with phosphonic acids derived from [12]crown-4 and [18]crown-6 showed thermodynamic selectivities towards Na+ and K+, respectively, that were much higher than those observed for the simple crowns in solution. This observation suggests that the inorganic molecular framework enhances molecular recognition by minimization of solvation effects.
    Additional Material: 4 Ill.
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  • 3
    ISSN: 1434-193X
    Keywords: Chirality ; Catalysis ; Amino acids ; Crown ethers ; Heterocyclic compounds ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The enantioselectivity exerted by a new series of chiral catalysts containing N,O-heterocycles of different sizes has been checked in the addition of diethylzinc to benzaldehyde, which was used as a model reaction. The catalysts were derived from natural amino acids, following a relatively simple procedure, and in several cases excellent ee values were obtained. The results were complementary since ee's ranged from 98% (R) to 94% (S) excesses of the final 1-phenylpropan-1-ol. Molecular mechanics calculations suggested that the production of the R alcohol may be explained by a mechanism similar to that described by Noyori, in which ZnEt2 interacts solely with the N-C-C-OH fragment, whereas the formation of the S enantiomer needed the direct participation of the lateral chain of the parent amino acid and the N,O-heterocycle.
    Additional Material: 3 Ill.
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  • 4
    ISSN: 1434-1948
    Keywords: Rhodium ; Phosphanes ; Ligand redistribution ; Dichloromethane activation ; Oxidative addition ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dichloromethane reacts with dinuclear rhodium complexes [{(PR3)2Rh}2(μ-Cl)2] to give the bridging-methylene complexes [{(PR3)2RhCl}2(μ-Cl)2(μ-CH2)] (PR3 = PEt3, PPh2Me). The structure of the PEt3 complex has been established by X-ray diffraction study. The early stages of the reaction of [{(C8H14)2Rh}2(μ-Cl)2] with monophosphanes have been monitored by 31P NMR, evidencing chloride bridges cleavage and phosphane redistribution processes.
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  • 5
    ISSN: 1434-193X
    Keywords: Allosterism ; Crown compounds ; Molecular receptors ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation of compounds 1-4 as simple systems to display allostery is described. Transport experiments (bulk liquid membrane) of ammonium cations in the presence or absence of ZnI2 in the receiving and donor phases evidenced strong negative or positive allosteric effects of the metal towards ammonium complexation, which depended on the relative arrangement of crowns with respect to the pyrazole nitrogens.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 18 (1972), S. 173-178 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Certain systems are characterized by a nonuniform distribution of matter in space. Examples of such systems are liquid-fluid (1 to 3) and the solid-fluid interfaces (4). It is the main purpose of this paper to extend thethermodynamics of nonuniform systems to multicomponent reactive mixtures in the presence of an external field and to apply the above formalism to physical adsorption. This amounts to an extension of Hart's original analysis (5 to 7) as well as an improved analysis of the solid-fluid interface presented recently by Metiu and Ruckensteein (8). Furthermore, various approximate solutions for the solid-fluid interface are considered, all of which reduce properly to known results.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 713-716 
    ISSN: 1434-1948
    Keywords: Chromates ; Catalytic transfer hydrogenation ; Hydrogenations ; Reductions ; α,β-Unsaturated ketones ; Asymmetric synthesis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the presence of a HCO2H/Et3N (1:1) mixture, KHCr(CO)5 is an efficient catalyst precursor for the transfer hydro-genation of ketones in THF at room temperature. KHCr(CO)5 is also a stoichiometric reagent for the selective reduction of the carbon-carbon double bond of α,β-unsaturated ketones.
    Additional Material: 1 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 50 (1850), S. 204-204 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 40 (1998), S. 324-335 
    ISSN: 0021-9304
    Keywords: titanium ; bioactive coating ; immobilization ; silanization ; covalent attachment ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The surface of implantable biomaterials is in direct contact with the host tissue and plays a critical role in determining biocompatibility. In order to improve the integration of implants, it is desirable to control interfacial reactions such that nonspecific adsorption of proteins is minimized and tissue-healing phenomena can be controlled. In this regard, our goal has been to develop a method to functionalize oxidized titanium surfaces by the covalent immobilization of bioactive organic molecules. Titanium first was chemically treated with a mixture of sulfuric acid and hydrogen peroxide to eliminate surface contaminants and to produce a consistent and reproducible titanium oxide surface layer. An intermediary aminoalkylsilane spacer molecule was then covalently linked to the oxide layer, followed by the covalent binding of either alkaline phosphatase or albumin to the free terminal NH2 groups using glutaraldehyde as a coupling agent. Surface analyses following coating procedures consisted of X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and atomic force microscopy (AFM). Enzymatic activity of coupled alkaline phosphatase was assayed colorimetrically, and surface coverage by bound albumin was evaluated by SEM visualization of colloidal gold immunolabeling. Our results indicate that the linkage of the aminoalkylsilane to the oxidized surface is stable and that bound proteins such alkaline phosphatase and albumin retain their enzymatic activity and antigenicity, respectively. The density of immunolabeling for albumin suggests that the binding and surface coverage obtained is in excess of what would be expected for inducing biological activity. In conclusion, this method offers the possibility of covalently linking selected molecules with known biological activity to oxidized titanium surfaces in order to guide and promote the tissue healing that occurs during implant integration in bone and soft tissues. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res, 40, 324-335, 1998
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 20 (1986), S. 1347-1357 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Ultra low temperature isotropic (ULTI) carbon-coated polyester suture material was evaluated histologically and mechanically in dogs. These results were compared to those obtainedfor uncoated polyester and polybutylate coated polyester. The suture materials were used in therepair of the surgically incised medical collateral ligament and subcutaneous tissues to evaluate the potential of the carbon-coated system for ligamentous repairs. Following surgery, the dogs were sacrificed at periods of 1-48 weeks postoperatively for evaluation of tissue biocompatibility and mechanical strength of the materials. The polybutylate-coated polyester suture broke at lower force levels than did comparable sizes of uncoated or carbon-coated polyester. All three types showed a high retention (〉98%) of mechanical strength at 48weeks, often exhibiting an increase in tensile strength due to tissue ingrowth. The histologic response to carbon-coated polyester was equal to or better than the response to either the uncoated polyester or polybutylate-coated polyester. A greater degree of tissue growth into the carbon-coated material was evident at most time periods following an initial acute inflammatory response which was also present in the other materials.
    Additional Material: 11 Ill.
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