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  • Space Radiation  (6)
  • General Chemistry  (3)
  • Lepidoptera  (3)
  • Polymer and Materials Science  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical Systematics and Ecology 1 (1973), S. 199-201 
    ISSN: 0305-1978
    Keywords: Lepidoptera ; bile pigments ; neopterobilines ; phorcabiline I ; pterobiline ; sarpedobiline
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Comparative Biochemistry and Physiology -- Part B: Biochemistry and 44 (1973), S. 47-52 
    ISSN: 0305-0491
    Keywords: Antherea Pernyi ; Lepidoptera ; Papilio Phorcas ; Papilio sarpedon ; Pigments ; bile pigments ; neopterobilins ; pterobilin
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 16 (1990), S. 743-748 
    ISSN: 1573-1561
    Keywords: Sarpedobilin ; bile pigment ; butterfly ; Papilio graphium stresemani stresemani ; P. sarpedon ; P. weiskei ; Lepidoptera ; Papilionidae ; bioecological relationships
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The doubly cyclized bile pigment sarpedobilin (3) represents a unique case in nature. In spite of being present in trace amounts in many butterfly and moth species containing pterobilin (1) or phorcabilin (2) as the main bilin, this substance occurs as the main pigment in a restricted number of species geographically limited to Southeast Asia. We have isolated and identified sarpedobilin3 (as the dimethyl ester) as the main bile pigment fromPapilio graphium stresemani stresemani (from Ceram island, Indonesia) in the amount of ca. 0.1 mg per individual, double that found inPapilio sar-pedon orP. weiskei. We conclude thatP. sarpedon (and subspecies)P. weis-kei, andP. stresemani represent, in terms of evolution (see article), a group of closely related species. By comparison of colored wing patterns and resistance of the chromoproteins to hydrolysis by MeOH-H2SO4,P. stresemani is nearP. weiskei. The bioecological relationships of the three sarpedobilin-containing species is discussed.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1827-1830 
    ISSN: 1434-1948
    Keywords: Samarium ; Early organolanthanides ; Bis(trimethylsilyl)amido ; Cyclooctatetraenyl ; Lanthanides ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complexes [(COT)Ln{N(SiMe3)2}(THF)] (Ln = late lanthanide metal) are readily accessible but, until now, the samarium analogue has proved elusive. The latter can be formed in solution but is easily desolvated during the isolation process, leading to a highly associated complex which is only soluble in coordinating solvents or in the presence of ancillary ligands.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1434-1948
    Keywords: Samarium ; Allyl complexes ; Carbene adducts ; Organolanthanides ; trans-Polyisoprene ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New alkyl and allyl complexes 1-3 {1: [Cp′2Sm(C3H5)]n, Cp′ = Me3CC5H4; 2: [Me4C2(C5H4)2]Sm(C3H5)2Li(dme),dme = (CH3OCH2CH2OCH3); 3: Cp′2SmMe2Li(dioxane)} were synthesized from (Cp′2SmCl)2and from the magnesium derivative [Me4C2(C5H4)2]SmCl · MgCl2(THF)4 (4). The ansa anionic complex 2 exhibited good activity for the stereospecific 1,4-trans polymerization of isoprene, whereas the neutral derivative 1 was inactive. In the same way, the anionic complex [Cp′2SmMe2]Li(dioxane) (3) was found to be an ethylene polymerization catalyst of very short lifetime. The lack of reactivity of 1 is related to the associated structure of this coordinatively unsaturated complex: this fact was established by the formation of the carbene adduct Cp′2Sm(C3H5)[C(NiPr)2(CMe)2] (1′). Crystals of 1′ were isolated but this new compound undergoes a partial rearrangement into a tris-Cp′ species in solution. Similar behaviour is observed for the analogous complex Cp′2SmCl[C(NiPr)2(CMe)2] (1′′). The X-ray crystal structure revealed the formation of the adduct, as a toluene solvate, which exists in benzene solution in equilibrium with Cp′3Sm and Cp′SmCl2[C(NiPr)2(CMe)2]2. The catalytic behaviour of 2 is compared with that of other early lanthanide derivatives.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1041-1045 
    ISSN: 1434-1948
    Keywords: Organolanthanide ; Neodymium ; Samarium ; Phospholyl ; Hydrides ; Lanthanides ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of 2,3,4,5-tetramethylphospholylpotassium [C4Me4PK] with [LnCl3(THF)x] (Ln = Nd, Sm) in a 2:1 ratio gave unsolvated ate complexes of the formula [(C4Me4P)2LnCl2K]. Crystallisation of the samarium complex from ether afforded a polymeric ether solvate: {[(η5-C4Me4P)Sm(μ3-Cl)2(μ:η5,η1-C4Me4P)K(Et2O)]∞}, which was characterised by X-ray crystallography. Reaction of [(C4Me4P)2LnCl2K] with [LiCH(SiMe3)2] in toluene gave the alkyl complexes [(C4Me4P)2LnCH(SiMe3)2]; these complexes were most efficiently prepared from [LnCl3(THF)x], [KC4Me4P] and [LiCH(SiMe3)2] in a one-pot procedure. Reaction of [(C4Me4P)2LnCH(SiMe3)2] with molecular hydrogen gave [(C4Me4P)2NdH], when Ln = Nd, whereas, when Ln = Sm, reduction occurred and the already known [(C4Me4P)2Sm] was isolated instead.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 23 (1984), S. 2299-2310 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alternating poly(Arg-Leu) and copolypeptides with Arg-Leu and His-Leu sequences were prepared by condensation of the corresponding p-nitrophenyl dipeptide esters in the presence of 1-hydroxybenzotriazole. Arginine was used without any protection and histidine side chains were protected using π-benzyloxymethyl group recently introduced in peptide chemistry. The ability of these polypeptides with alternating hydrophilic and hydrophobic residues to form water-soluble β-sheets was investigated by CD.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 16 (1990), S. 336-337 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 1969-1984 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to study some aspects of radical polymerization initiated by a polymer, hexanediol sebacates in different degrees of polymerization were prepared. The endgroup was the tert-butyl perester which was used to polymerize the styrene. With such compounds, it is easy after the polymerization to take off the polyester backbone by hydrolysis. One can then study the mixture of polystyrene sequences and homopolystyrene made at the same time. It appears that if the speed of thermal decomposition of the tert-butyl perester group on the polyester is of the same order as that of the tert-butyl perbenzoate, the efficiency factor, i.e., the fraction of free radicals which effectively initiates the polymerization, is much smaller with a polymeric initiator. Moreover, the average degree of polymerization is much smaller in this case (even in the presence of a nonperoxidized polyester). It is believed that these two results can be explained by assuming each polyester backbone to act as a cage for the free radicals produced by its own perester group which aids their recombination and intramolecular transfer.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Publication Date: 2019-07-18
    Description: The ENTICE experiment is one of two instruments that make up the HNX mission. The experimental goal of ENTICE is to measure with high precision the elemental abundances of all nuclei with Z between 10 and 82. This will enable us to determine if the injection mechanism for the cosmic ray accelerator is controlled by FIP or Volatility and to study the mix of nucleosynthetic processes that contribute to the galactic cosmic ray source. The ENTICE experiment utilizes the dE/dx-C method of charge determination and consists of silicon dE/dx detectors, Cherenkov detectors with two different refractive indices, and a fiber hodoscope. We will describe the instrument and its performance based on beam tests of a prototype instrument.
    Keywords: Space Radiation
    Type: ICRC 2001 Conference; Aug 07, 2001 - Aug 15, 2001; Hamburg; Germany
    Format: text
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