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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European radiology 10 (2000), S. 1085-1094 
    ISSN: 1432-1084
    Keywords: Key words: Crohn's disease – Paediatrics – Investigation – Complications
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Paediatric Crohn's disease can be a serious and complex condition which is not always easy to diagnose if it presents in an atypical manner. Although the pathological processes are the same in adults and children, the clinical presentation and disease distribution can be different in children. The impact of the disease can also be much more significant in a growing and developing child than in an adult. Numerous investigations are available to establish the diagnosis, define the complications and to demonstrate the extra-intestinal manifestations. Close co-operation is required between the clinician and radiologist when investigating a child suspected of having Crohn's disease or its symptoms to minimise the radiation dose and the psychological and physical trauma. We review the clinical and radiological aspects of Crohn's disease and discuss the imaging modalities available in diagnosing Crohn's disease and its complications and suggest an investigation pathway as used in our institution.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 218 (1968), S. 492-493 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] This complex has many ecological races well adapted to situations ranging from high altitude to desert conditions. I studied the breeding system of six genoecodemes?five from Australia and one from New Zealand?and found that only the latter was self-compatible. Furthermore, the self-compatible ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 38 (1992), S. 1391-1398 
    ISSN: 1572-8943
    Keywords: adducts ; complexes ; 8-hydroxyquinoline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Die hergestellten Addukte von [Mo(CN)8]3− und von [W(CN)8]3− mit 8-Hydroxyquinolin (Oxin) haben die allgemeine Formel K3[Mo(CN)8](C9H7ON)8·4H2O bzw. K3[W(CN)8](C9H7ON)6·3H2O. Die FTIR-Spektren beweisen die Gegenwart der (CN)- bzw. der Oxingruppen in den Adduktverbindungen durch die Peaks im Bereich 2047–2108 cm bzw. 1015–1461 cm−1. Die untere Region des FTIR-Spektrums zeigt die M=O Valenzschwingung, die obere Region (N-H) und (OH). Nichtkoordiniertes Wasser wird in diesen Addukten in einem einzigen Schritt bei 110°C abgegeben. Die Zersetzung der Adduktverbindungen beginnt bei 125°C und setzt sich in verschiedenen Schritten bis hin zu 850°C fort. Der zweite Schritt der Zersetzung wird durch die Abgabe von Oxinmolekülen beherrscht, wobei polymere Oxide der allgemeinen Formel K2OM2O5 (mitM= Mo oder W) als Pyrolyseprodukte erhalten werden.
    Notes: Abstract The adducts of [Mo(CN)8]3− and [W(CN)8]3− with 8-hydroxyquinoline (oxine) synthesized were of the type K3[Mo(CN)8]·(C9H7ON)8·4H2O and K3[W(CN)8]·(C9H7ON)6·3H2O. The FTIR spectra show the presence of the (CN) and oxine group in the adduct compounds through the peaks in the range 2047–2108 cm−1 and 1015–1461 cnf−1 respectively. The lower region of FTIR spectra show the M=O stretching while the higher range to v(N-H) and v(OH) modes. The uncoordinated water in these adducts was removed at around 110°C in a single step. The decomposition of adduct compounds starts from 125°C and continues to higher temperatures upto 850°C in different stages. The second stage of decomposition was predominant with the removal of oxine molecules with the formation of polymeric oxide of the type K2O·M2O5 (whereM=Mo or W) obtained as the pyrolysis product.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 46 (1996), S. 1763-1774 
    ISSN: 1572-8943
    Keywords: adducts ; complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The photoproduct of octacyanomolybdate(IV) and -tungstate(IV) with ethylenediamine and triethylenetetramine give complexes of the type K3[Mo(O2)(O)(OH)(C9H7ON)]·3C9H7ON I, K2[W(O2)(O) (C9H7ON)3] II and K3[Mo(CN)3(OH)4(C9H7ON)]·2C9H7ON·3H2O III with 8-quinolinol (oxine). The IR spectra of the complex III shows the presence ofv(CN) peaks in the range 2047–2108 cm−1 and oxine groupv(C-O) in the complex I, II and III in the range of 1100–1150 cm−1. The lower region of IR spectra shows the M=O stretching while the higher thev(N-H) andv(OH). Thermal studies show the removal of uncoordinated water at 131
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 58 (1999), S. 153-165 
    ISSN: 1572-8943
    Keywords: metal-8-hydroxyquinoline complexes ; photosubstitution ofpyrazine ; octacyanometallates ; thermal dissociation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The complexes formed by photosubstitution of pyrazine (Pz) in octacyanomolybdate(IV) and -tungstate(IV) with 8-hydroxyquinoline have been assigned the formulae [Mo(CN)2(OH)2(Pz)2(OX)] and [W(CN)2(OH)2(Pz)2(OX)·1.5H2O]. Coordination of Pz as an unidentate ligand by donating a lone pair of electron from nitrogen is shown by an absorption peak between 8–11 µ. Mechanism for the thermal decomposition of the complexes has been given. The formation of tungsten metal as residue in case of II has been confirmed by XRD analysis. The kinetic and thermodynamic parameters like activation energy (E a), pre-exponential factor (A) and entropy of activation (ΔS #) were calculated employing different integral methods of Doyle, Coats and Redfern and Arrhenius.ΔH for each stage of decomposition was obtained from DSC.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 42 (1991), S. 597-599 
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Mittels Kleinwinkel-Laserlichtsreuung und viskosimetrichen Messungen wurden verdünnte Lösungen von Polyurethanfraktionen untersucht. Das Polymer wurde aus Butandiol und Hexamethylendiisocyanat hergestellt. Die Grenzviskositäten wurden über die MARK-HOUWINK-SAKURADA-Gleichung zu den Molekülmassen korreliert. Die Werte der Konstanten Km und a wurden ermittelt. Trotz des niedrigen Brechungsinkrementes von Polyurethan in Benzen konnten Molekülmassen bis herab zu 4300 gemessen werden.
    Notes: Low angle laser light scattering and viscosity studies were made on dilute solution of fractions of polyurethane prepared from butandiol and hexamethylene diisocyanate. The intrinsic viscosities were correlated to molecular weights by the MARK-HOUWINK-SAKURADA equation. The values of the constants Km and a have been determined. In spite of the low refractive index increment of polyurethane in benzene, molecular weights as low as 4300 could be measured.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 379 (1970), S. 68-71 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: SiBr4, gelöst in abs. Äther, reagiert bei -60°C mit einer Lösung von KNH2 in flüssigem Ammoniak zu K2Si3(NH)7 und K2Si2(NH)5; die versuchte Darstellung von K4Si(NH)4 mit überschüssigem KNH2 gelang nicht. Unter den gleichen Bedingungen setzt sich SiJ4 nur zu 20% um; bei Raumtemperatur entsteht K2Si(NH)3. Die drei dargestellten, amorphen Imidosilicate werden durch Luftfeuchtigkeit zu Oxosilicaten zersetzt.
    Notes: SiBr4 in absolute ether reacts with KNH2 in liquid ammonia at -60°C to give K2Si3(NH)7 and K2Si2(NH)5; attempts to prepare K4Si(NH)4 by using excess KNH2 were without success. The reaction of SiI4 in absolute ether with KNH2 in liquid ammonia is incomplete at -60°C even after 48 hours, about 80% SiI4 remains unreacted. This reaction when carried out at room temperature gave K2Si(NH)3. All the three imidosilicates are amorphous and decompose in presence of traces of moisture to give corresponding oxosilicates.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 29 (1997), S. 819-824 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An investigation is presented on the kinetics of complexation of aqueous solution of octacyanomolybdate (IV) and -tungstate (IV) after photoinitiation with one of the mixed group ligands containing both N and O, diethanolamine (DEOA), [NH(CH2CH2OH)2]. Under the steady state conditions and with approximation k3 〉 k4 over a range of concentrations, the observed rate law is:\documentclass{article}\pagestyle{empty}\begin{document}$$ \cal{k}_{\rm obs.}={\cal{k}_{2}\cal{k}_{4}\rm {I}_{a}[\rm {OH}^{-}][\rm {NH}(\rm{CH}_{2}\rm{CH}_{2}\rm{OH})_{2}]\over \rm{I}+\it \cal{k}_{2}[\rm {OH}^{-}]} $$\end{document}The complexes show shift in electronic transition supporting the mechanism of association of the ligand followed by the abstraction of some small molecules and then substitution by the ligand. The presence of the specific isobestic point also contributes towards the stability of the complex. The rate constant and quantum yield values are dependent on both the concentration of the metal cyanide and the ligand predicting the mechanism to be an associative one. The complexes have strong absorption in the visible range and are assigned metal-to-ligand electron transfer transition. © 1997 John Wiley & Sons, Inc. Int J Chem Kinet 29: 819-824, 1997
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 28 (1996), S. 705-711 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dioxotetracyanomolybdate(IV) has been found to form a 1 : 2 complex with 2,2′-bipyridyl. The kinetics of the reaction has been studied over the pH range 5.3-8.7 by visible spectrophotometry under pseudo conditions. The effect of the 2,2′-bipyridyl and dioxotetracyanomolybdate(IV), temperature, ionic strength, and pH on the reaction rate was determined. The reaction follows first-order kinetics with respect to dioxotetracyanomolybdate(IV) ion and fractional-order kinetics with respect to 2,2′-bipyridyl. Values for the outer-sphere complex formation constant (Kos2) and rate constants (k2) were also calculated from the kinetic data. It was found that rate of the reaction increases with the decreasing pH. The following rate equation based on the outersphere complexation equilibrium preceding the associative interchange has been derived.\documentclass{article}\pagestyle{empty}\begin{document}$$\rm {{1}\over{{\it k}_{obs}}}={{1+K_{a2}[H^+]}\over{B_1[2,2\prime-bipyridyl]}}+B_2$$ ${\rm where}$ $\rm B_1={\it k}_1K_{os1}+{\it k}_2K_{os2}[H^+]K_{a2}$ ${\rm and}$ $\rm B_2={{K_{os1}+K_{a2}K_{os2}[H^+]}\over {{\it k}_1K_{os1}+{\it k}_2K_{os2}[H^+]K_{a2}}}.$\end{document}On the basis of the observed results probable mechanism has been proposed. © 1996 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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