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  • Wiley-Blackwell  (16)
  • American Physical Society (APS)  (5)
  • Springer  (4)
  • Rockefeller University Press  (2)
  • 2015-2019  (20)
  • 1930-1934  (6)
  • 1915-1919  (1)
Document type
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 86 (1931), S. 134-140 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 212 (1933), S. 145-168 
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Auf Grund der Basenreaktion des Eisenpentacarbonyls, Fe(CO)5 + 2OH- = Fe(CO)4H2 + CO3--, wird der Eisencarbonylwasserstoff dargestellt und durch fraktionierte Hochvakuumdestillation bei tiefen Temperaturen in reinem Zustand isoliert. Die thermochemischen Daten sind, wie Tensionsmessungen ergeben haben, denen des Nickel-carbonyls und Eisenpentacarbonyls sehr ähnlich; der Schmelzpunkt liegt hei -70°. Von den chemischen Eigenschaften steht die charakteristische Selbstzersetzlichkeit nach 2Fe(CO)4H2 — Fe(CO)5 + Fe(CO)3 + 2H2 im Vordergrund, deren quantitative Untersuchung zugleich die vollständige Analyse des Hydrids liefert. Die Reaktion mit Jod führt überwiegend zur Entstehung des Tetracarbonyljodids, Fe(CO)4J2. Die chemische Charakterisierung der Wasserstoffbindung im Eisencarbonylwasserstoff geschieht u. a. durch die quantitative Titration des Wasserstoffs mit Methylenblau, ferner besonders auf Grund der Feststellung, daß die Wasserstoffkerne als Additionszentren fur Pyridinstickstoff wie für Hydroxylionen fungieren können, wie die Alkalibeständigkeit des Hydrids und die präparativ auf- gefundene Bildung von stabilen Additionsverbindungen mit Pyridin oder o-Phenanthrolin beweist. Eine Rückfolgerung, daß der freie Carbonylwasserstoff „Sä:urenatur“ besitzt, erscheint indessen nicht gerechtfertigt. Vielmehr führen die chemischen wie die physikalischen Eigenschaften zu dem Schluß, daß der Eisencarbonylwasserstoff eine Verbindung von symmetrischer, abgeschlossener Elektronenkonfiguration mit 18 Elektronen darstellen muß, d. h. infolge der förmlichen oder zumindest sehr weitgehenden Einbeziehung der Wasserstoffatome in den Verband des Metallatoms bzw. des Radikals Fe(CO), liegt  -  als einzigem bisher bekannten Fall dieser Art  -  eine ähnlich tiefgehende Beeinflussung der Eigenschaften vor, wie sie entsprechend bei der Gruppe der Hydride der vor den Edelgasen stehenden Elemente bekannt ist.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 204 (1932), S. 165-173 
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Zersetzungsreaktionen des Eisencarbonylwasserstoffs, die im chemischen Verhalten alkalischer Lösungen von Eisenpentacarbonyl in Erscheinung treten, werden in ihrem Mechanismus aufgeklärt und auf die Oxydierbarkeit des Carbonylhydrids, die Disproportionierungen zwischen den Zersetzungsprodukten mit weniger als 5 Mol CO/Fe unter wechselseitigem Kohlcnoxydaustausch, sowie auf die Saurerealitionen der Carbonylverbindungen zurückgeführt. Auf Grund dieser Verhältnisse werden Darstellungsmethoden für Eisentetra- carbonyl beschrieben, die auf der direkten Dehydrierung des Car- bonylwasserstoffs im System Pentacarbonyl-4lkali unter möglichst in milden Bedingungen beruhen.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 56 (1917), S. 441-443 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 64 (1931), S. 2340-2346 
    ISSN: 0365-9631
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Publication Date: 2015-07-17
    Description: Mutations in RPGRIP1L result in severe human diseases called ciliopathies. To unravel the molecular function of RPGRIP1L, we analyzed Rpgrip1l –/– mouse embryos, which display a ciliopathy phenotype and die, at the latest, around birth. In these embryos, cilia-mediated signaling was severely disturbed. Defects in Shh signaling suggested that the Rpgrip1l deficiency causes an impairment of protein degradation and protein processing. Indeed, we detected a cilia-dependent decreased proteasomal activity in the absence of Rpgrip1l. We found different proteasomal components localized to cilia and identified Psmd2, a component of the regulatory proteasomal 19S subunit, as an interaction partner for Rpgrip1l. Quantifications of proteasomal substrates demonstrated that Rpgrip1l regulates proteasomal activity specifically at the basal body. Our study suggests that Rpgrip1l controls ciliary signaling by regulating the activity of the ciliary proteasome via Psmd2.
    Electronic ISSN: 1540-8140
    Topics: Biology
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  • 9
    Publication Date: 2015-09-04
    Description: In intestinal and pyloric epithelia leucine-rich repeat-containing G protein-coupled receptor 5 ( Lgr5 )-expressing cells represent long-lived adult stem cells which give rise to all epithelial cell types including endocrine cells. Ablation of the Apc gene in Lgr5 -expressing cells leads to intestinal and pyloric adenomas. To assess whether all epithelial tumours of the gastrointestinal tract are derived from LGR5-positive stem cells we crossed Lgr5-EGFP-IRES-creER T2 mice which express EGFP and Cre recombinase driven by the Lgr5 promoter with CEA424-SV40-TAg mice which develop pyloric neuroendocrine carcinomas of epithelial origin. In 19-day-old mice, single SV40 T antigen (TAg)-positive cells were identified preferentially at the the base of pyloric glands close to the stem cell compartment. However, contrary to previous publications describing subpopulations of LGR5-positive cells in gastrointestinal neoplasia we could not detect Lgr5- EGFP-positive tumour cells in malignant lesions. The lack of expression of the Wnt target gene Lgr5 is probably not caused by suppression of Wnt signalling by TAg since β-catenin-mediated Wnt signalling, as measured by the TOPflash assay, was not inhibited. To determine the cellular origin of CEA424-SV40-TAg tumours we performed tracing experiments using Lgr5-EGFP-IRES-creERT2:CEA424-SV40-TAg:ROSA26-tdRFP mice. Following tamoxifen induction it was possible to efficiently trace the progeny of Lgr5 -expressing cells in gastrointestinal tissue via red fluorescent protein (RFP) expression. No RFP-positive tumour cells were detected even when RFP gene activation occurred in 7-day-old mice well before the appearance of TAg-positive tumour cells. Hence we conclude that Lgr5 -expressing stem cells probably do not constitute the cells-of-origin in CEA424-SV40-TAg mice. Consequently, not all epithelial tumours in the pyloric region are initiated by transformation of LGR5-positive stem cells. Thus additional long-lived LGR5-negative stem cells or progenitor cells with low turnover rate might exist in the pyloric region which can give rise to tumours.
    Print ISSN: 0022-3417
    Electronic ISSN: 1096-9896
    Topics: Medicine
    Published by Wiley-Blackwell
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  • 10
    Publication Date: 2015-08-08
    Description: Providing enantiomerically pure products is of key importance in the fine chemicals, food, and pharmaceutical industries. A continuous preferential crystallization process is presented that allows the separation of conglomerate forming enantiomers in a stable, robust, and flexible way. This is achieved by coupling two continuous crystallizers by exchanging their clear liquid phases. Each crystallizer is connected to a suspension mill responsible for in situ seed generation through particle breakage. The dynamic and steady-state behavior of this process is extensively analyzed for racemic feed streams through process simulations, and parameter regions, which yield pure enantiomers in both crystallizers, are identified. For enriched feed streams, it is further shown when this novel flow sheet is capable of outperforming an ideal batch process in terms of solvent consumption per unit mass of desired enantiopure product produced. © 2015 American Institute of Chemical Engineers AIChE J , 61: 2810–2823, 2015
    Print ISSN: 0001-1541
    Electronic ISSN: 1547-5905
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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