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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 4 (1969), S. 78-83 
    ISSN: 1432-0827
    Keywords: Bone ; Calcification ; Osteomalacia ; Phosphorus ; Vitamin D
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Description / Table of Contents: Résumé Les effects d'une dose de 1 mg de vitamine D3 (40 000 Unités,) administrée par voie intra-veineuse, ont été étudiés sur l'histologie osseuse et le métabolisme du phosphore chez 19 sujets contrôles dont l'histologie était normale et 28 malades présentant les caractères histologiques de l'ostéomalacie par carence vitaminique D. L'administration de la vitamine D n'a entraîné aucune modification histologique ou biologique significative chez les sujets contrôles. Mais chez les ostéomalaciques, il est apparu en moins de sept jours une augmentation très significative du front de calcification à l'interface tissue-ostéoïde-tissue-calcifié. Cette modification s'accompagnait d'une ascension progressive de la phosphatémie et de la réabsorption tubulaire du phosphore atteignant dans le même délai des valeurs normales.
    Abstract: Zusammenfassung Bei 19 Patienten mit normaler Knochenhistologie und bei 28 Patienten mit histologisch gesicherter Osteomalacie wurde die Wirkung von 1 mg Vitamin D3 (40000 Iv) i.v. auf die Knochenhistologie und den Phosphatmetabolismus untersucht. Bei den Kontrollpatienten konnten keine signifikanten Änderungen nach Vitamin D festgestellt werden, wogegen die Osteomalacie-patienten innerhalb von 7 Tagen eine deutliche Zunahme der Verkalkungszone an der Grenze zwischen Osteoid- und Knochengewebe zeigten. Diese Änderung war von einer fortschreitenden Zunahme des Serum-Phosphates, verbunden mit einer gesteigerten renalen tubulären Rückabsorption des Phosphates begleitet; beide kehrten anschließend gleichzeitig wieder zur Norm zurück.
    Notes: Abstract The effect of a 1 mg dose of intravenous Vitamin D3 (40,000 i.u.) on bone histology and phosphate metabolism was investigated in 19 patients with normal bone histology and 28 patients with histological evidence of osteomalacia. No significant changes occurred in the control patients after Vitamin D but the patients with osteomalacia showed a marked increase, within seven days, in the proportion of osteoid having a calcification front. This was accompanied by a progressive rise in the serum phosphate, which was associated with an increase in the renal tubular reabsorption of phosphate to normal.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 8 (1969), S. 660-671 
    ISSN: 0570-0833
    Keywords: Phosphorus ; History of chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Exactly 300 years ago in the city of Hamburg, a certain Hennig Brand, self-styled doctor medicinae, and chymist, discovered a strange substance in human urine, which was later called phosphorus (light bearer), a name then common to various luminous substances, and which created much excitement in the latter years of the 17th century on account of its properties. However, it was not Brand who profited from the discovery but others: Johann Daniel Krafft, Johann Kunckel, and Gottfried Wilhelm Leibniz, men who knew only too well how to exploit the weaknesses of the discoverer. “Cold fire”, Brand's own name for the new substance, was originally regarded as elemental light or fire, and it was not until the conception of the antiphlogistic theory by Antoine Laurent Lavoisier that the proper position of phosphorus among the chemical elements was recognized. In fact, the element played a decisive role in the overthrow of the phlogiston doctrine, a little over one hundred years after its discovery and almost two hundred years ago.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0570-0833
    Keywords: Aluminum ; Silicon ; Boron nitride ; Phosphorus ; Polymers ; Silicic acid ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The differences between compounds of carbon and of silicon are discussed, and the role of silicon as a fundamental structural component in inanimate nature is described. Starting with silicic acid and silicates, the structure and properties of the silicones and of compounds having Si—C—Si skeletons are described. The possibilities for the formation of high molecular-weight compounds between elements of Groups 3 and 5 of the periodic system are considered, with particular reference to boron nitride and to aluminum-phosphorus compounds.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0570-0833
    Keywords: Electrophilic reactions ; Substitution ; Phosphorus ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions belonging to the formal category of electrophilic substitutions at phosphorus are classified according to mechanism and the coordination number of the phosphorus atom.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 5 (1966), S. 53-57 
    ISSN: 0570-0833
    Keywords: Aluminum ; Phosphorus ; Silicon ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The formation and properties of silicon-phosphorus and aluminum-phosphorus compounds are described. Silylphosphines are decomposed solvolytically by H2O, C2H5OH, NH3, hydrogen halides, C2H5I, and boron halides at the Si—P bond; decomposition may be preceded by formation of an addition compound. Extensive side reactions during the reaction of halogenosilanes with LiPEt2The following abbreviations are used in this paper: Et = C2H5; Me = CH3; M = alkali metal (formation of Et2P—PEt2, HPEt2, Si-rich residues) are due to an excess of LiPEt2 in the reaction mixture. The reaction of LiPEt2 with AlCl3, AlHCl2, and AlH2Cl leads to definite aluminum-phosphorus compounds if only one PEt2 group is present per Al atom, e.g. in (Cl2Al-PEt2)3, or if salts such as Li[Al(PEt2)4] and Li[AlH2(PEt2)2] can be formed with an excess of LiPEt2.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 1023-1038 
    ISSN: 0570-0833
    Keywords: Heterocycles ; Phosphorus ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation of heterocycles containing phosphorus is described. The chemical behavior of ring systems containing trivalent phosphorus is mainly determined by their phosphine character; heterocyclic behavior in the ordinary sense is shown by rings containing functional groups. Syntheses and reactions of cyclic compounds of pentavalent and hexavalent phosphorus are particularly interesting.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 1007-1013 
    ISSN: 0570-0833
    Keywords: Sulfur ; Selenium ; Tellurium ; Phosphorus ; Organometallic compounds ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bond fission of molecular sulfur, selenium, and tellurium by lithiotriphenylmetal compounds (of Ge, Sn, Pb) is summarized. The products are suitable as starting materials for synthesis of new “ether analogues”. Transphenylation with tetraphenylstannane is interpreted as a high-temperature variant of the usual fission of chalcogen molecules by nucleophilic reagents. In principle, transphenylation can be applied also to other elements, as is illustrated for phosphorus. In the syntheses achieved, many of the tin-phosphorus compounds arising as intermediates can be isolated.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 457-471 
    ISSN: 0570-0833
    Keywords: Color ; Azo compounds ; Azobisphosphoric acid ; Phosphorus ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Attempts to explain the surprising violet color of the new azobisphosphonic acid derivatives Y2OP—N=N—POY2 have led to the preparation and spectroscopic characterization of more than 60 azo compounds. The long-wavelength n → π* transitions on which the color depends exhibit regularities which justify the assumption of substitutent-specific absorption increments. The complex relation between color and constitution of azo compounds can be qualitatively explained with the aid of orbital models. Infrared and ultraviolet spectral data show that conjugation is inhibited by tetra-coordinated phosphorus (V). the π-system of these compounds therfore comprises only for atoms, P·N·N·P. The unexpected violet color of the phosphorus azo compounds can be ascribed to a π*/d orbital interaction. The substituent effects described have general significance, and n→π*transitions of other chromophores are similarly affected.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0570-0833
    Keywords: Tetradentate ligands ; P ligands ; Arsenic ligands ; Phosphorus ; Arsenic ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of ligand shape on coordination numbers and geometry of coordination compounds has been studied using two tetradentate ligands containing phosphorus and arsenic. These tend to form five-coordinate complexes with trigonal bipyramidal structure [Fe(II), Co(I), Co(II), Rh(I), Ni(II), Pd(II), Pt(II)], but can also form six-coordinate complexes with octahedral structure [Fe(II), Ru(II), Os(II), Co(III), Rh(III), Pd(IV), Pt(IV)]. The magnetic properties and the stereochemistry of the complexes are explained by ligand field theory which predicts that, for metal ions with d6-electronic configuration, a low overall field strength should favor the formation of five-coordinate paramagnetic complexes while a high overall field strength should favor the formation of six-coordinate diamagnetic complexes. - This work provides further indication that the tendency of polydentate ligands to use all the potential donor atoms is not as pronounced as is generally believed. This is shown by the isolation of chromium(III) complexes in which the tetradentate ligands are, in fact, acting as tridentate, and by the isolation of mercury(II) complexes where only two of the four donor atoms of the polydentate ligand are actually bonded to the central metal atom.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 523-530 
    ISSN: 0570-0833
    Keywords: Semimetals ; Metallic structure ; Nonmetallic structure ; Antimony ; Arsenic ; Bismuth ; Phosphorus ; Tellurium ; Tin ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Measurements on semimetals have been continued. Studies of the dependence on temperature of various properties have provided details regarding the transition from the nonmetallic to the more metallic structure. A second-order transition has been found for tin at 170 °C, in which the c-axis remains unchanged, while the a-axis undergoes a small, discontinuous elongation.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 11
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 646-654 
    ISSN: 0570-0833
    Keywords: Polyphosphanes ; Phosphanes ; Phosphorus ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: While silicon and sulfur, which are situated to the left and to the right of phosphorus in the periodic table, from numerous chain and cyclic Si-Si and S-S-compounds with varying numbers of members, until recently the polyphosphance chemistry has been limited to the two-membered compounds diphosphane P2H4 and its derivatives. A number of results obtained in studies on polyphosphanes carried out in recent years will therefore be discussed, which, together with some more recent work by other authors, have led to an expansion of our knowledge of the prepration and properties of straight and branched-chain as well as of cyclic and polycylic -P-P-systems.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 1 (1962), S. 617-621 
    ISSN: 0570-0833
    Keywords: Isocyanates ; Phosphorus ; Silicon ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several aminoaryl esters of phosphoric and thiophosphoric acids were prepared by the reaction of phosphorus pentahalides with nitrophenols, followed by catalytic hydrogenation, or by treating aminophenols with phosphorus trihalides and oxidation to pentavalent phosphorus. These amino esters were then converted into isocyanato esters by the action of phosgene. Isocyanates of phosphonates have been synthetized on the same principle, as well as via the Arbusov reaction of halogen-substituted isocyanates with trialkyl phosphites. The reaction of silicon halides or alkylhalogenosilanes with aminophenols yielded aminoaryl esters of silicic acid or its derivatives, which could also be treated with phosgene to convert them into isocyanato esters.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 1 (1962), S. 652-656 
    ISSN: 0570-0833
    Keywords: β-Chloroethanephosphonic dichloride ; Phosphorus ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ethylene, phosphorus trichloride, and oxygen react together to give β-chloroethylphosphonic dichloride in good yields. Being a bifunctional acid chloride, this compound undergoes polycondensation reactions with other, at least bifunctional, compounds affording polyesters, polyamides, epoxy resins, etc. β-Chloroethylphosphonic dichloride also may be converted into vinylphosphonic dichloride, thus serving as a starting material for the preparation of vinylphosphonic acid and its derivatives. These undergo both homopolymerization and copolymerization with compounds containing olefinic double bonds. The products are used in the field of synthetic resins, for dressing textiles, and as protective surface coatings.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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