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  • 1985-1989  (7)
  • 1980-1984
  • 1950-1954
  • 1925-1929
  • 1986  (7)
  • 1
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 60 (1986), S. 529-533 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Laser direct-write metallization in metallo-organic films involves complex thermal profiles and changes in optical properties that affect the spatial resolution, chemical purity, and electrical properties of the resulting features. Compositional profiles of the metal features, determined by scanning Auger electron spectroscopy, are reported and correlated with the chemistry of the laser-initiated thermal reaction and the observed feature structure. Studies of the changes in optical properties of the films by conventional thermal decomposition offer important insights into the reaction mechanisms. We also report an optimized development procedure for the laser-exposed samples.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 16 (1986), S. 265-273 
    ISSN: 1572-8838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract A preliminary experimental investigation of the electrochemical characteristics of a high and a low copper dental amalgam in contact with saline solution has been carried out. The impedance and the corrosion current (in the absence of dissolved oxygen) have been measured at each potential in the near steady state for fresh amalgam surfaces. Analysis of the electrochemical data produces charge transfer resistance, double layer capacity, ohmic resistance and Warburg coefficient curves, which are briefly discussed. The aim of the work is, ultimately, to determine thein vivo corrosion rates and heavy metal ion release from amalgams.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1440
    Keywords: Myoadenylate-(adenylate-, AMP-)deaminase deficiency ; D-ribose, metabolism ; Dribose, untoward effects ; Hyperuricemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A 55 years old patient suffering from exercise-induced muscle pain and stiffness due to primary myoadenylate deaminase deficiency has been successfully treated with D-ribose since 1984: single doses of 4 grams administered at the beginning of exercise prevented the symptoms completely; on continuation of exercise this dose had to be repeated all 10–30 min. Total doses of 50–60 g per day were tolerated without side-effects.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 31 (1986), S. 1231-1241 
    ISSN: 1572-8943
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Natur, Produkte und Enthalpie der thermischen Zersetzung von [Pd(CH3CO2)2]3 in Luft, Stickstoff und Vakuum wurden untersucht. Zur Charakterisierung des Prozesses und der Produkte wurden TG, DTA, EGA, DSC und IR-Spektroskopie herangezogen. Im Vakuum verflüchtigt sich das Trimere vollständig unterhalb 200°. Das IR-Spectrum der gasförmigen Species ist angegeben. Bei Atmosphärendruck zersetzt sich das Material, abhängig von der Aufheizgeschwindigkeit, zwischen 200 und 300° zu Pd. Die scheinbare Aktivierungsenergie für diesen Prozeß beträgt 115 ± 5 kJ · mol− 1, die Enthalpie beläuft sich auf 440 ± 20 kj · mol−1. In Gegenwart von Sauerstoff werden die gasförmigen Produkte sofort oxydiert, was ein exothermen Bruttoeffekt zur Folge hat. In Gegenwart von Sauerstoff wird Pd langsam bis zur Zersetzung des Oxids bei nahe 800° oxydiert. Es wird ein geringer Verlust einer Pd enthaltenden Species beobachtet, der vermutlich auf Sublimation oder auf Mitreißen im Gasstrom während der Zersetzung unterhalb 300° zurückzüfuhren ist. Dieser Verlust wird mit der Erhöhung der Aufheizgeschwindigkeit größer und erreicht bei einer Aufheizgeschwindigkeit von 64° · min−1 10% des Gesamt-Pd.
    Abstract: Резюме В атмосфере воздуха, а зота и в вакууме изуче н характер термическо го разложения ацетата палладия [Pd(CH3CO2)2]3, а также определе ны продукты разложения и энтальпия реакции. Процесс разл ожения и идентификац ия образующихся продук тов были проведены с помощью ТГ, ДТА, АВГ, ДСК и ИК спектроскопии. В в акууме тример ацетата палла дия полностью улетучива ется при температуре ниже 200°. Приведен ИК спектр га зообразных частиц. При атмосферн ом давлении вещество разлагается до палла дия между 200 ип 300° в зависимости от скоро сти нагрева. Кажущаяс я энергия активации процесса р азложения составляет около 155±5 кд ж · моль−1, а энтальпия −440±20 кдж · моль−1. Однако, в прис утствии кислорода газообраз ные продукты сразу же окисляются, приводя тем самым к по лностью экзотермическому пр оцессу. В присутствии кислорода палладий медленно ок исляется вплоть до температуры разложе ния окисла около 800°. Во время разложения ацетата п алладия ниже 300° происходила небольш ая потеря палладия, чт о, повидимому, обусловл ено сублимацией его и ли же уносом газом. Степе нь потери увеличивал ась при увеличении скорости нагрева и составляла 10% общего количества па лладия при скорости н агрева 64° в минуту.
    Notes: Abstract The nature, products, and enthalpy of the thermal decomposition of [Pd(CH3CO2)2]3 were determined in air, nitrogen and vacuum. Thermogravimetry, differential thermal analysis, evolved gas analysis, differential scanning calorimetry, and infrared spectroscopy were used to characterize the process and products. In vacuum the trimer volatilizes completely below 200 °C. The IR spectrum of the gas phase species is reported. At atmospheric pressure the material decomposed to Pd between 200 and 300 °C depending upon the rate of heating. The apparent activation energy for this process is about 115 ± 5 kJ mol−1 and the enthalpy is 440 ± 20 kJ mol−1. In the presence of oxygen, however, oxidation of the ligands leads to an overall exothermic process. The resulting the Pd then slowly oxidizes to PdO2 up to the decomposition temperature of the oxide near 800 °C. There is the slight loss of a Pd containing species, presumably due to sublimation or gas entrainment, during the decomposition below 300 °C. The extent of this loss increases with increasing heating rate, approaching 10% of the total Pd at heating rates of 64 °C min−1.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 21 (1986), S. 565-569 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The high-resolution mass spectra of two stable enol tautomers, 4,6-diethanoyl-1-methyl-5-phenyl-3-cyclohex-ene-1,3-diol (2) and 4-ethanoyl-5-hydroxy-2-(1-hydroxyethylidene)-5-methyl-3-phenylcyclohexanone (3), and the corresponding diketone tautomer, 2,4-diethanoyl-5-hydroxy-5-methyl-3-phenylcyclohexanone (1), are reported. Collisional activation of the molecular ions and major ionic fragments is used to assign decomposition pathways and to compare ion structures. Ionized 1 and 2 do not interconvert by a keto-enol tautomerism, but isomerize to a common intermediate. This isomerization probably involves opening of the cyclohexanone ring and transfer of the enolizable hydrogen, and is followed by elimination of water. The radical cation of 3 does not interconvert with [1]+· and [2]+· Instead, [3]+· dissociates by loss of an acetyl radical and eliminates water via a higher-energy pathway. As a result, the mass spectra of 1 and 2 are similar, whereas the mass spectrum of 3 is unique.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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