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  • Polymer and Materials Science  (3)
  • Lophelia pertusa
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 176 (1975), S. 3269-3285 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The perbenzylation of polysaccharides can be achieved with benzyl chloride in DMSO under nitrogen with exclusion of moisture in the presence of methylsulfinylmethanide (1). Only one reaction step is necessary to obtain the completely substituted products of amylose, pullulan, dextran, and xylan, whereas the tribenzylethers of laminaran, glycogen, and low molecular weight mannan are received in two steps. The yields are between 60 and 90%.Under these reaction conditions pustulan and galactomannan could not be completely benzylated.High molecular weight mannan and cellulose (polyglycans which are unsoluble and don't swell in DMSO) can be benzylated in the presence of an excess of 1 (4 mol 1/mol OH-group) under similar conditions, if the corresponding monoacetylated derivatives which are soluble in DMSO are used as starting material. The fully benzylated products are obtained in two steps with yields of 30-35%.The various results obtained with the benzylation reaction are discussed in terms of solubility, degree of polymerization, and structure of the particular polysaccharide.
    Notes: Die Perbenzylierung von Polysacchariden gelingt in Gegenwart von Methylsulfinyl-methanid (1) mit Benzylchlorid in DMSO unter Stickstoff und Feuchtigkeitsausschluß. Während sich in einem Umsetzungsschritt Amylose, Pullulan, Dextran und Xylan vollständig substituieren lassen, werden Tribenzyläther von Laminaran, Glykogen und niedermolekularem Mannan erst nach der zweiten Benzylierung erhalten. Die Ausbeuten liegen zwischen 60 und 90%. Pustulan und Galaktomannan können unter diesen Reaktionsbedingungen nicht vollständig benzyliert werden.Die Benzylierung von hochmolekularem Mannan und Cellulose (in DMSO unlösliche und nicht quellbare Polyglykane) gelingt, wenn als Ausgangsmaterial die in DMSO löslichen Monoacetate verwendet und diese in Gegenwart eines Überschusses von 1 (4mol 1/mol OH-Gruppe) mit Benzylchlorid unter analogen Bedingungen umgesetzt werden. Trisubstituierte Cellulose und Mannan erhält man in zwei Umsetzungsschritten. Die Ausbeuten liegen zwischen 30 und 35%.Die unterschiedlichen Ergebnisse bei der Benzylierung werden im Zusammenhang mit Löslichkeit, Polymerisationsgrad und Struktur der einzelnen Polysaccharide diskutiert.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The 13C-NMR spectra of malto- and isomalto-oligosaccharides, amylose and dextrane were analysed. It was observed that in both series of oligosaccharides and polysaccharides the resonances of the central glucose units are independent of the chain length with the exception of the C-atoms 1 and 4 of amylose which show deviations of 0,4 and 0,5 ppm. These small effects can possibly be explained by a definite polysaccharide chain conformation in solution.
    Notes: Die 13C-NMR-Spektren von polymerhomologen Reihen der Malto- und Isomaltooligosaccharide, sowie die von Amylose und Dextran wurden aufgenommen und analysiert. Dabei wurde festgestellt, daß bei den Polymerhomologen die Resonanzen der C-Atome der mittelständigen Glucoseeinheiten unabhängig von der Kettenlänge sind. Während sich das Polysaccharid Dextran wie die Oligosaccharide verhält, zeigen im Falle der Amylose die Resonanzen der C-Atome 1 und 4 Abweichungen von 0,4 bzw. 0,5 ppm. Diese-wenn auch kleinen-Effekte geben möglicherweise einen Hinweis auf das Vorliegen einer überstruktur in Lösung.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 143 (1971), S. 275-277 
    ISSN: 0025-116X
    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
    Publication Date: 2022-05-25
    Description: © The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Quaternary Science Reviews 185 (2018): 135-152, doi:10.1016/j.quascirev.2018.02.012.
    Description: The largest coherent cold-water coral (CWC) mound province in the Atlantic Ocean exists along the Mauritanian margin, where up to 100 m high mounds extend over a distance of ∼400 km, arranged in two slope-parallel chains in 400–550 m water depth. Additionally, CWCs are present in the numerous submarine canyons with isolated coral mounds being developed on some canyon flanks. Seventy-seven Uranium-series coral ages were assessed to elucidate the timing of CWC colonisation and coral mound development along the Mauritanian margin for the last ∼120,000 years. Our results show that CWCs were present on the mounds during the Last Interglacial, though in low numbers corresponding to coral mound aggradation rates of 16 cm kyr−1. Most prolific periods for CWC growth are identified for the last glacial and deglaciation, resulting in enhanced mound aggradation (〉1000 cm kyr−1), before mound formation stagnated along the entire margin with the onset of the Holocene. Until today, the Mauritanian mounds are in a dormant state with only scarce CWC growth. In the canyons, live CWCs are abundant since the Late Holocene at least. Thus, the canyons may serve as a refuge to CWCs potentially enabling the observed modest re-colonisation pulse on the mounds along the open slope. The timing and rate of the pre-Holocene coral mound aggradation, and the cessation of mound formation varied between the individual mounds, which was likely the consequence of vertical/lateral changes in water mass structure that placed the mounds near or out of oxygen-depleted waters, respectively.
    Description: This study received funding from and contributes to the DFG-projects "Palaeo-WACOM" (HE 3412/17-1) and "Cold-water coral mound development in a tropical upwelling cell – the great wall of(f) Mauritania" (Ti 706/3-1). A. Freiwald received funding from the Hessian initiative for the development of scientific and economic excellence (LOEWE) at the Biodiversity and Climate Research Centre (BiK-F), Frankfurt, Germany.
    Keywords: Lophelia pertusa ; Coral mound ; Submarine canyon ; Uranium-series dating ; Mound aggradation rate ; Last glacial ; Dissolved oxygen concentration ; South Atlantic Central Water ; Mauritanian margin
    Repository Name: Woods Hole Open Access Server
    Type: Article
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