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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 102 (1981), S. 21-30 
    ISSN: 1432-1335
    Keywords: cis-Diamminedichloroplatinum(II) ; Titanocene dichloride ; Vanadocene dichloride ; Ehrlich ascites tumor ; Pulse-cytophotometry ; cis-Diammindichloroplatin(II) ; Titanocen-dichlorid ; Vanadocen-dichlorid ; Ehrlich-Aszites-Tumor ; Impulscytophotometrie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Gegenstand der Untersuchungen ist der Einfluß einer in-vivo-Behandlung mit optimal tumorhemmenden Dosen von cis-Diammindichloroplatin(II) (DDP), Titanocen-dichlorid (TDC) und Vanadocen-dichlorid (VDC) auf das impulscytophotometrisch bestimmte DNA-Verteilungsmuster und die Mitoseaktivität von EAT-Zellen. Während DDP eine sofortige und langandauernde Unterdrückung der Zellteilungen, jedoch keine Veränderung des zellkinetischen Verhaltens von EAT-Zellen bewirkt, verursacht TDC die Ausbildung eines deutlichen,: 10–12 h nach Behandlung maximalen G2-Blocks. Im Falle von DDP und TDC werden die Tumorzellen einige Tage nach Behandlung durch Zellen des wirtstiereigenen Abwehrsystems beseitig. VDC hingegen ruft die Entstehung teilsynchroner Wellen nach einer vorübergehenden Mitosehemmung und einer reversiblen Zellakkumulation in der späten S-und der G2-Phase hervor. Darüber hinaus werden 5–16% der Zellen nach VDC-Behandlung polyploid.
    Notes: Summary The influence of an in vivo treatment with optimally tumor-inhibiting doses of cis-diamminedichloroplatinum(II) (DDP), titanocene dichloride (TDC), and vanadocene dichloride (VDC) on the DNA distribution pattern, determined by pulse-cytophotometry, and on the, mitotic activity of EAT cells is investigated. Whereas DDP causes an immediate and, long-lasting decrease of mitoses but no disturbances of the EAT cell kinetics, a marked G2 block with a maximum at 10–12 h a. t. and an irreversible and extensive mitotic depression is evoked by TDC. In the case of DDP and TDC, the tumor cells are removed several days a. t. by cells belonging to the defensive system of the host animals. In contrast, VDC induces partially synchronized waves after a transient suppression of mitoses and reversible cell accumulation in the late S and in the G2 phases. Additionally, 5–16% of the cells become polyploid after VDC treatment.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 106 (1983), S. 44-52 
    ISSN: 1432-1335
    Keywords: Metallocene dichlorides ; cis-Diammine-dichloroplatinum(II) ; Ehrlich ascites tumor ; Cytokinetics in vitro
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The influence of in vitro application of the cytostatic agents titanocene dichloride (TDC), vanadocene dichloride (VDC), and cis-diamminedichloroplatinum(II) (DDP) on the cytokinetic behavior of EAT cells was investigated. All three substances induced similar cytokinetic phenomena that are characterized on the one hand, by an accumulation of cells in the late S phase and in the G2 phase during exposure periods of 8 to 20 h. On the other hand, some cells were apparently arrested at the end of the G1 phase and, after removal of the cytostatic agents, moved through the following S, G2, and M phases as synchronized cell populations. In view of this unusual cytokinetic pattern of multiple effects, it is argued that the striking similarities in cytokinetic behavior after treatment with the three different cytostatic substances indicate analogies in their molecular mechanisms of action. The different alteration patterns observed after in vivo application of the drugs are obviously due to additional processes occurring only in vivo.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 581-585 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 16 (1990), S. 331-334 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The hydrogen concentration profiles of electrochromic multilayer systems produced by evaporation have been determined by means of nuclear reaction analysis. The H content of individual oxidic materials was found to be larger than for single films, especially for SiO2. The time-dependent H uptake under various ambient conditions was investigated. Systems produced by ion plating were also profiled for hydrogen.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 65 (1993), S. 1116-1117 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 68 (1996), S. 1100-1101 
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 70 (1998), S. 1198-1199 
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 14 (1979), S. 244-253 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The very complex isomerization patterns of methoxy and carbomethoxy substituted cycloalkanes (3- to 7-membered rings) have been investigated using collisional activation, metastable ion characteristics and field ionization kinetics. The extent of isomerization depends on both the ring size and the substituent. Irrespective of the electronic properties of the substituent, ring opening involves exclusively the C-1—C-2 bond whereby linear alkene radical cations are formed. In the case of OCH3- and COOCH3 substituents the position of the resulting double bond (terminal or α,β-unsaturated) is determined more by the ring size of the precursor molecules and less by the electronic properties of the substituents. Contrary to these findings alklyl substituted cycloalkanes (3- to 5-membered rings) rearrange exclusively to terminal alkene radical cations. The barrier for double bond isomerization seems to be substantially influenced by substituents.
    Notes: Unter Benutzung mehrerer Techniken, wie Stoßaktivierung, Charakteristik metastabiler Ionen und Feldionisationskinetik, wird das äußerst komplexe Isomerisierungsverhalten von methoxy- und caarbomethoxysubstituierten Cycloalkanen (drei-bis siebengliedrege Ringe) analysiert. Das Ausmaß der Isomerisierung hängt sowohl von der Ringgröße als auch vom Substituenten ab, während die Ringöffnung unabhängig von den elektronischen Eigenschaften der Substituenten immer die C-1—C-2-Bindung betrifft. Hierbei werden ausschließlich lineare Alken-Radikalkationen erzeugt. Bei OCH3- und COOCH3-Substituenten wird die Lage der resultierenden Doppelbindung terminal oder α,β-ungesättigt hauptsächlich durch die Ringgröße des Cycloalkan-Molekülions und weniger durch den Substituenten beeinfluß. Alkylsubstituierte Cycloalkane (drei- bis fünfgliedrige Ringe) lagern sich allerdings nur zu terminalen Alken-Radikalkationen um. Die Barriere der Doppelbindungswanderung scheint vom Substituenten abhängig zsu sein.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chalcogenide Glasses with Organic Components. V. The Reactivity in the Glass-forming Systems Selenium, Arsenic, Bromine, 4,4′-Bis(selenenylbromido)azobenzene and Selenium, Arsenic, Iodine, 4,4′-Bis(diiodarsa)biphenyleneSe—As—Br glasses and 4,4′-bis(selenenylbromido)azobenzene react in the solid state. In this case arsenic is an acceptor for bromine, and azobenzene groups will be linked via poly-selenide groups with the glass matrix. The reaction is proved by DTA. At elevated temperatures, the selenium-carbon bond will be replaced by a carbon-bromine link yielding 4,4′-dibromazobenzene. Solid 4,4′-bis(diiodarsa)biphenylene shows a similar reaction with Se—As—I above TG. The pyrolysis takes place at higher temperatures.
    Notes: Gläser des Systems Se—As—Br reagieren im festen Zustand mit 4,4′-Bis-(selenenylbromido)azobenzol. Dabei wirkt Arsen als Bromakzeptor, und die Azobenzolgruppen werden über Polyselenidgruppen mit der Glasmatrix verknüpft. Die Reaktion wurde differentialthermoanalytisch verfolgt. Bei höheren Temperaturen werden die Selen-Kohlenstoff-Bindungen durch Brom-Kohlenstoff-Bindungen ersetzt. 4,4′-Dibromazobenzol kann durch Sublimation isoliert werden. Festes 4,4′-Bis(dijodarsa)biphenyl reagiert in analoger Weise mit unterkühlten Selen-Arsen-Jod-Schmelzen.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 29 (1995), S. 337-337 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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