ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Chemistry  (12)
  • Magnetism
  • taxonomy
  • 2000-2004  (3)
  • 1975-1979  (10)
  • 2000  (3)
  • 1975  (10)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Antonie van Leeuwenhoek 77 (2000), S. 71-81 
    ISSN: 1572-9699
    Keywords: DNA heterogeneity ; genome comparison ; Geotrichum ; taxonomy ; yeast
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The nutritional physiology and the growth rate of thirty-four strains representing species of Geotrichum without known teleomorph states were examined. From twenty-seven strains the mol% G+C were calculated from the DNA melting curves. The first derivatives of the melting curves of seven strains, including the type strain of Geotrichum clavatum, demonstrated the presence of two peaks, 12% away from each other; the remaining strains showed only a single broad peak. DNA homology values among strains of the former group were high, indicating their conspecificity. The strains of the latter group could be subdivided into six DNA homology groups, four of which could be identified with recognized species and two may represent novel taxa. A combined key of Geotrichum and its teleomorph states Galactomyces and Dipodascus is presented.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0935-6304
    Keywords: Comprehensive two-dimensional gas chromatography ; thermal desorption modulator ; temperature programming ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---In comprehensive two-dimensional gas chromatography, two individual separations are coupled by means of a rotating thermal desorption modulator interface. The injection pulse introduced via the interface onto the second column should be as short as possible. Parameters affecting the modulator operation are studied. In the set-up used in this study, the temperature of the second column can be programmed independently from that of the first column. Optimization of the second-dimension separation to minimize peak broadening and maximize resolution is discussed and an elegant approach to determine second-dimension retention times using a non-constant modulation frequency is demonstrated. The high separation power of the comprehensive system is demonstrated by the analysis of technical and biota samples containing chlorinated biphenyls and toxaphene.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 317 (1975), S. 143-152 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Tetrabenzyltitanium and its o-halogenbenzyl derivates have only a small activity for polymerizing butadien. Aluminium trialkyls accelerate the catalytic activity. A very suitable system for preparing 1,4-cis or 1,4-trans polybutadien under normal pressure is formed by tetrabenzyl titanium and aluminium chloride as a co-catalyst.
    Notes: Titantetrabenzyl sowie die erstmals näher beschriebenen Titantetra-o-halogenbenzyle weisen eine geringe Aktivität zur Polymerisation von Butadien auf. Aluminiumtriäthyl erhöht die Aktivität. Günstiger wirkt Aluminiumchlorid als Cokatalysator, wobei unter Normaldruck stereoreguläres Polybutadien mit vorwiegend 1,4-trans- bzw. 1,4-cis-Anteilen erhalten werden konnte.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 87 (1975), S. 545-546 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 48 (1975), S. 67-95 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The viscosity of solutions of polybutadiene, polymerized by n-butyllithium, with molecular weights between 22000 and 660000 in cyclohexanone, is surprisingly found dependent on the age of solutions. According to solutions in toluene and THF the dependence of concentration from ηsp/C is found in the same way for fresh solutions in cyclohexanone. With increasing age of solutions in cyclohexanone considerable decreasing of viscosity is observed. There is found at 20°C that ηsp/C is independent of concentration after 35 days and that the Staudinger index [η] does no more depend on molecular weight after 300 days. Decreasing of viscosity approaches the limiting value after about 600 days at [η] = 13 cm3/g. Viscosity and solubility in toluene of polybutadiene treated for a short period with a ketone are far extending reduced. The relationship [η] = K·Ma, investigated at solutions of polybutadiene in toluene, THF and cyclohexanone has a common point of intersection, corresponding approximately to Staudinger index and molecular weight of the ultrasonic degradation product, resp. with molecular weight of the so-called tertiary units of not degraded polymer evaluated by means of electron microscopy methods.By the aid of Einstein's relationship of viscosity and the model of pearlstring molecules, decreasing of viscosity with time may be interpreted as a consequence of alteration in the shape of macromolecules as a result of interaction with solvent environment. It can be assumed that stretched pearlstring molecules are being formed to a heap of collapsed coil containing with solvent surrounded tertiary structures. Overthat there are reasons to suppose additionally a partial degradation of solvation layer around tertiary structure.
    Notes: An Lösungen von n-BuLi-polymerisierten Polybutadienen mit Molekulargewichten zwischen 22000 und 660000 in Cyclohexanon wurde eine in der Literatur bisher nicht beschriebene Abhängigkeit der Viskosität vom Alter der Lösungen entdeckt. Während ungealterte Cyclohexanonlösungen eine mit Toluol-und THF-Lösungen übereinstimmende Konzentrationsabhängigkeit von ηspez/C aufweisen, wird mit zunehmendem Alter von Cyclohexanonlösungen ein Rückgang der Viskosität beobachtet, der  -  untersucht bei 20°C  -  nach 35 Tagen zu Konzentrationsunabhängigkeit von ηspez/C und nach 300 Tagen zu einem vom Molekulargewicht unabhängigen Staudingerindex [η] führt. Der Viskositätsrückgang endet nach ca. 600 Tagen asymptotisch bei [η] = 13 cm3/g. Kurzzeitig mit Keton behandeltes Polybutadien löst sich in Toluol nur noch extrem langsam unter gänzlich veränderten Viskositätsverhältnissen. Die für Lösungen von Polybutadien in Toluol, THF und Cyclohexanon gefundenen Beziehungen [η] = K·Ma besitzen einen gemeinsamen Schnittpunkt, dessen Koordinaten näherungsweise mit dem Staudingerindex und dem Molekulargewicht des Ultraschall-Abbauprodukts bzw. dem elektronenoptisch ermittelten Molekulargewicht der Tertiäreinheiten des unbeschallten Polymeren übereinstimmen.Auf der Grundlage von Einsteinscher Viskositätsbeziehung und Perlschnurmolekül-Modell wird der zeitabhängige Viskositätsrückgang als die Folge zweier sich überlagernder Veränderungen des solvatzustands diskutiert: Knäuelung der Perlschnurmoleküle zu einer dichten Kugelpackung der solvatisierten Tertiäreinheiten und partieller Abbau der Solvathülle der Tertiäreinheiten.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 0935-6304
    Keywords: μLC ; FID ; LC-FID ; carbohydrates ; amino acids ; alcohols ; phosphonic acids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The potential of the on-line coupling of microcolumn liquid chromatography (μLC) using aqueous eluents with a flame ionization detector (FID) was evaluated. An eluent-jet interface was modified to allow the efficient introduction of the eluent into the FID. The potential of the method is demonstrated by the μLC-FID determination of lower alcohols and bis(2-hydroxyethylthio)alkanes on porous and non-porous stationary phases, respectively. Flow injection analysis (FIA)-FID experiments with highly polar, thermolabile, semi-volatile and non-volatile compounds like amino acids, organic acids, alkylphosphonic acids, and carbohydrates showed the developed configuration to be a promising approach for the detection of a wide range of analytes. Compared with a nebulization interface, the eluent-jet interface showed 4-10 times higher peaks for citric acid. Detection limits by FIA for all compounds were in the range of 0.2-5 ng injected. With ribose as test compound, plots of peak height vs. amount injected showed good linearity (r2 〉 0.999) in the range of 75-12,000 μg/mL. The repeatability showed relative standard deviations of less than 5%.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 411 (1975), S. 192-192 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal Complexes with Anionic Ligands of Elements of the Main Group IV. VII(1) Substitution Reactions of Carbonylnitrosyl and Nitrosyltrifluorophosphine Transition Metal Complexes with TrichlorostannidL-substitution by [SnCl3]- occurs if the nitrosyl complexes Co(NO)L3 and Fe(NO)2L2 (L = CO or PF3) are reacted with [N(C2H5)4][SnCl3] thermically in tetrahydrofuran as well as photochemically induced in methylenechloride. The complexes Co(NO)L3 yield the mono-substitution products [N(C2H5)4][Co(NO)L2SnCl3], with the iron compounds Fe(NO)2L2 only the disubstituted derivative [N(C2H5)4]2[Fe(NO)2(SnCl3)2] can be isolated. On the other hand CO substitution at (π-C5H5)Mo(NO)(CO)2 by UV irradiation did not suceed both with [SnCl3]- and with PF3. From the IR-spectroscopic data a leastly with PCl3 comparable π-acceptor ability is derived for the trichlorostannido ligand.
    Notes: Die Nitrosylkomplexe Co(NO)L3 und Fe(NO)2L2 (L = CO bzw. PF3) gehen sowohl unter thermischen Bedingungen in Tetrahydrofuran wie auch photochemisch induziert in Methylenchlorid mit [N(C2H5)4][SnCl3] L/SnCl3--Substitutionsreaktionen ein. Ausgehend von Co(NO)L3 erhält man die Tetraäthylammoniumsalze der Nitrosyltrichlorstannido-metallat-Komplexe [Co(NO)L2(SnCl3)]-. Bei Fe(NO)2L2 läuft die Reaktion stets zum allein isolierbaren [N(C2H5)4]2[Fe(NO)2(SnCl3)2] durch. Hingegen geht (π-C5H5)Mo(NO)(CO)2 weder mit [SnCl3]- noch mit PF3 unter UV-Bedingungen einen CO-Austausch ein. Aus den IR-spektroskopischen Daten wird für den Trichlorstannido-Liganden ein zumindest mit dem PCl3 vergleichbares π-Akzeptorvermögen abgeleitet.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal Complexes with Anionic Ligands of Elements of the Main Group IV. VIII Pentacarbonyltrihalogenostannidometalate(O) Complexes of Chromium, Molybdenum, and Tungsten with Fluorine and Iodine Containing Trihalogenostannido LigandsIn methylenechloride [As(C6H5)4][SnF3] readily reacts with the metalhexacarbonyls forming the arsoniumsalts of the pentacarbonyltrifluorostannidometalate(O) complexes, [M(CO)5SnF3]- (M = Cr, Mo, W). Exclusively by the reaction of the intermediately formed complex Cr(CO)5THF only one pure triiodostannidometalate(O) Complex, [N(C2H5)4][Cr(CO)5SnJ3], could be isolated. The trihalogenostannidometalate(O) complexes [M(CO)5SnClX2]- (X = F: M = Cr, Mo, W; X = J: M = Cr) could be prepared by SnX2-insertion reactions of the [M(CO)5Cl]- complexes. The bonding properties of the halogenostannide ions are discussed on the bases of the IR spectra of their metalate(O) complexes.
    Notes: In Methylenchlorid setzt sich [As(C6H5)4][SnF3] glatt mit den Metallhexacarbonylen zu den Arsoniumsalzen der Pentacarbonyl-trifluorstannido-metallat(O)-Komplexe [M(CO)5SnF3]- (M = Cr, Mo, W) um. Mit [N(C2H5)4][SnJ3] konnte in THF-Lösung nur über das Zwischenprodukt Cr(CO)5 THF ein Trijodstannidochromat(O)-Komplex [N(C2H5)5][Cr(CO)5SnJ3] rein erhalten werden. Durch SnF2-bzw. SnJ2-Insertionsreaktionen an den [M(CO)5Cl]--Komplexen erhält man die Trihalogenstannidometallat(O)-Komplexe [M(CO)5SnClX2]- (X = F: M = Cr, Mo, W; X = J: M = Cr). Anhand der IR-Spektren wird das Bindungsverhalten halogenhaltiger Stannid-Ionen diskutiert.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Fluorine Exchange in Trifluorophosphine Metal Complexes. IX1. (Reactions of Tetrakis(trifluorophosphine)nickel(0) with Alkyl(trimethylsilyl)amines and Amides2)Alkylaminodifluorophosphine complexes Ni(PF3)4-n(PF2NHR)n (n = 1, 2, 3) 8-11 and Me3SiF are obtained, if alkyl(trimethylsilyl)amines NHR(SiMe3) (R=CH3 and n-C4H9) are reacted with Ni(PF3)4 (1). The mechanism of these peripheric reactions is discussed by assuming a four centered type intermediate. However reactions of 1 with the lithium amides LiNR(SiMe3) (R = CH3, C2H5, n-C4H9, and C6H5) yield LiF and the difluorotrimethylsilylaminophosphine complexes Ni(PF3)4-n[PF2NR(SiMe3)]n (n = 1, 3, 4) 12-18.
    Notes: Ni(PF3)4 (1) reagiert mit Alkyl(trimethylsilyl)aminen NHR(SiMe3) (R=CH3 und n-C4H9) unter Me3SiF-Abspaltung zu den Alkylaminodifluorphosphinkomplexen Ni(PF3)4-n(PF2NHR)n (n = 1, 2 und 3) 8-11. Der Reaktionsablauf wird anhand eines Vierzentren-Synchron-Mechanismus diskutiert. Hingegen liefern die Lithiumamide LiNR(SiMe3) (R=CH3, C2H5, n-C4H9 und C6H5) mit 1 unter LiF-Abspaltung die Organyl(trimethylsilyl)-aminodifluorphosphinkomplexe Ni(PF3)4-n[PF2NR(SiMe3)]n (n = 1, 3 und 4) 12-18.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...