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
  • 1
    ISSN: 1520-6025
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 108 (1977), S. 273-278 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract From the hydroxylaminomethylation product of 2-naphthol (3) and aliphatic resp. aromatic aldehydes resulting compounds were examined by NMR spectroscopy. In solution the products of formaldehyde, acetaldehyde and benzaldehyde show equilibria of cyclic hydroxylamine and hydroxynitrone forms2 resp.1, the state of which depends on the solvent; with the derivatives of p-nitro- and p-dimethylaminobenzaldehyde only the hydroxynitrone form1 d resp.1 e is detectable.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 109 (1978), S. 1295-1303 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The structures of the title compounds are examined by13C-NMR and ESCA spectroscopy. Every double salt shows O-protonation, the proton lying within the experimental error half-way between the carbonyl oxygen atoms of the two molecules of amides resp. vinylogous amides.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 92 (1980), S. 191-194 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolymers of acrylonitrile and vinylchloride (molar ratio ACN : VC = 44.5 : 55.5) were synthesized by continuous emulsion polymerization. Their sequence distribution was studied by 13C-NMR-spectra at 90.52 MHz. Three different methylene carbon regions were attributed to diads of the type —VC—VC—,—VC—ACN— and —ACN—ACN—. The experimentally determined diad distribution was in good agreement with the calculated diad distribution, using reactivity ratios of rACN = 3.6 and rVC = 0.05.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    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 molecular weight of butadiene-acrylonitrile copolymers containing gel and of fractions of that polymer was determined by sedimentation in the ultracentrifuge by the Archibald method and by the method of sedimentation equilibrium. Solvents were methylethylketone and the O-solvent methylethylketone-cyclohexsne (47.5 % by vol. : 52.5% by vol.). Equal molecular weights were found in both methylethylketone and &solvent, although the refractive indices and the densities of the components of the O-solvent deviate by more than 3% from each other.For determining the molecular weight distribution, three different copolymers were fractionated by solvent gradient chromatography. The limiting viscosity numbers [η], the sedimentation constants s°20, and the molecular weights Mw of the fractions were determined. In addition, the chemical composition and the sequence distribution were determined by NMR measurements. The three investigated copolymers are relatively chemical homogeneous with nearly the same sequence distribution. The molecular weight dependence of the limiting viscosity number and of the sedimentation constant is represented by the following relationships: [η]25 = 19,1 · 10-2 ml/g · M0,50w (methylethylketone-cyclohexane; 47.5 : 52.5)[η]25 = 8,1 · 10-2 ml/g · M0,64w (chloroform)[η]25 = 4,2 · 10-2 ml/g · M0,64w (benzene)s°20 = 4,2 · 10-15 sec. M0,44w (methylethylketone)s°20 = 1,14 · 10-15 sec. M0,50w (methylethylketone-cyclohexane 47.5 : 52.5)The molecular weight distribution of butadiene-acrylonitrile copolymers was determined by three methods : 1from the mass and the molecular weights of fractions obtained by solvent gradient chromatography,2from the interference patterns of sedimentation velocity experiments and the s-M-relation, as well as,3by gel chromatography.The distribution curves satisfactorily agree with one another for molecular weights M 〈 106. Unlike solvent gradient chromatography and gel chromatography, ultracentrifuge experiments allow the determination of the molecular weight distribution of the entire butadiene-acrylonitrile copolymer includingmicrogel.For methodological and principal reasons, the weight average molecular weight MAw, as determined with the ultracentrifuge by the Archibald method, is not very suitable to characterize such copolymers. For polymers with great inhomogeneity, it is more advisable to use the molecular weights Mh, M50 and M90.
    Notes: Das Molekulargewicht von gelhaltigen Butadien-Acrylnitril-Copolymeren und von Fraktionen dieses Polymeren wurde durch Sedimentation in der Ultrazentrifuge nach der Methode von Archibald und der Sedimentationsgleichgewichtsmethode in Methyläthylketon und im θ-Lösungsmittel Methyläthylketon-Cyclohexan (47,5 Vol.-% : 52,5 Vol.-%) bestimmt. Es wurden sowohl in Methyläthylketon als auch im θ-Lösungsmittel die gleichen Molekulargewichte gefunden, obgleich die Brechungsindices und die Dichten der Komponenten des θ-Lösungsmittels um mehr als 3% voneinander abweichen.Zur Ermittlung der Molekulargewichtsverteilung wurden drei verschiedene Copolymere durch Lösungsmittel-Gradienten-Chromatographie fraktioniert. Von den Fraktionen wurden die Viskositätszahlen [η], die Sedimentationskonstanten s°20 und die Molekulargewichte Mw mit Hilfe der Ultrazentrifuge bestimmt. Darüberhinaus wurde die chemische Zusammensetzung und die Sequenzverteilung durch NMR-Messungen ermittelt. Daraus geht hervor, daß die drei untersuchten Copolymerisate chemisch relativ einheitlich sind und in der Sequenzverteilung weitgehend übereinstimmen. Für die Molekulargewichtsabhängigkeit der Viskositätszahlen und der Sedimentationskonstanten gelten die Beziehungen: [η]25 = 19,1 · 10-2 ml/g · M0,50w (Methyläthylketon-Cyclohexan; 47,5 : 52,5)[η]25 = 8,1 · 10-2 ml/g · M0,64w (Chloroform)[η]25 = 4,2 · 10-2 ml/g · M0,64w (Benzol)s°20 = 4,2 · 10-15 sec M0,44w (Methyläthylketon)s°20 = 1,14 · 10-15 sec M0,50w (Methyläthylketon-Cyclohexan; 47,5 : 52,5)Die Molekulargewichtsverteilung wurde nach drei Methoden bestimmt: 1Aus dem Massenanteil und dem Molekulargewicht von Fraktionen, die durch Lösungsmittel-Gradienten-Chromatographie erhalten wurden,2aus den Interferenzaufnahmen von Sedimentationsgeschwindigkeitsversuchen und der s-M-Beziehung und3durch Gelchromatographie.Die erhaltenen Verteilungskurven stimmen für Molekulargewichte M 〈 106 befriedigend miteinander iiberein. Aus Ultrazentrifugenversuchen können im Gegensetz zur Lösungsmittel-Gradienten-Chromatographie und zur Gelchromatographie Aussagen über die Molekulargewichtsverteilung des gesamten Butadien-Acrylnitril-Copolymeren einschlielßlich des hochmolekularen Mikrogels gemacht werden.Zur Charakterisierung der Copolymeren durch ein mittleres Molekulargewicht ist das mit der Ultrazentrifuge nach der Methode von Archibald bestimmte Gewichtsmittel des Molekulargewichts MAw aus methodischen und prinzipiellen Gründen wenig geeignet. Es ist zweckmäßiger, für Polymere mit großer Uneinheitlichkeit die Molekulargewichtswerte Mh, M50 und M90 anzugeben.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 98 (1981), S. 255-263 
    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: An acrylonitrile/vinylidene chloride copolymer prepared by continuous suspension polymerization in aqueous medium was examined by carbon magnetic resonance at 90.52 MHz. The sequence distribution was evaluated from the diad and tetrad distribution of the methylene carbon regions and from the triad distributions of the other carbon atoms. The stereochemical configuration of the acrylonitrile units was determined from the peaks of the methine and the nitrile carbons which showed a low preference of the isotactic triad against the syndiotactic triad in agreement with freeradical polymerized polyacrylonitrile.
    Notes: Ein Acrylnitril/Vinylidenchlorid-Copolymerisat, hergestellt durch kontinuierliche Fällungspolymerisation in wäßrigem Medium, wurde durch 13C-Kernresonanz bei 90,52 MHz untersucht. Die Sequenzverteilung konnte übereinstimmend abgeleitet werden aus der Diaden- bzw. Tetradenverteilung des Methylenbereiches und aus den Triadenverteilungen der übrigen Kohlenstoffatome. Aus den Signalen von Methinund Nitrilkohlenstoff ließ sich die stereochemische Ordnung der Acrylnitril-Einheiten ableiten, die in Übereinstimmung mit radikalisch hergestelltem Acrylnitril-Homopolymerisat eine geringe Bevorzugung der isotaktischen Tßade gegenüber der syndiotaktischen Triade aufwies.
    Additional Material: 2 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
    Angewandte Makromolekulare Chemie 88 (1980), S. 223-225 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In comparison to smaller frequencies at 90.52 MHz the methylene region of the carbon-13 spectrum is split into signals corresponding to the configurational tetrads. Thus the carbon-13 resonance at high fields enables the tacticity determination via all the three carbon atoms of polyacrylonitrile.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 101 (1968), S. 4106-4122 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es wird über die kernresonanzspektroskopischen Parameter von zehn Tetrahydro- und vier Dihydro-cyclobut[a]inden-Derivaten sowie zwei Tetrahydro-cycloprop[a]inden-Derivaten berichtet.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 2986-2995 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Spirohexane Derivatives by Photosensitized Cycloadditions to MethylenecyclopropanePhotosensitized addition of maleic anhydride and some of its derivatives to methylenecyclopropane (1) gives spirohexanes in good yields. Dichlorovinylene carbonate and 1,3-diacetyl-4-imidazolin-2-one react with 1 in the same manner. In none of the reactions studied the formation of methylenecyclopentane derivatives was observed. A mechanism is suggested for the cycloadditions which involves as the initial step the terminal attack of the triplet excited components on the double bond of 1.
    Notes: Maleinsäureanhydrid und einige Derivate liefern bei der photosensibilisierten Addition an Methylencyclopropan (1) in guten Ausbeuten Spirohexane. Entsprechend reagieren auch Dichlorvinylencarbonat und 1,3-Diacetyl-4-imidazolin-2-on mit 1. In keiner der untersuchten Reaktionen gibt es Hinweise auf die Bildung von Methylencyclopentan-Derivaten. Als Mechanismus für die Cycloadditionen wird ein primärer terminaler Angriff der triplettangeregten Komponenten an die Doppelbindung von 1 formuliert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 681-689 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Oxidation of Benzvalene to Bicyclo[1.1.0]butane-endo,endo-2,4-dicarbaldehyde with Singlet OxygenEven at -30°C benzvalene adds singlet oxygen to form the 1,2-dioxetane 2. Its constitution is proved by the transformation to tricyclo[3.1.0.02,6]hexane-cis-3,4-diol (5) with triphenylarsane and also by the cycloreversion, which, accompanied by chemiluminescence, leads to the title dialdehyde 3. The reduction of 3 with LiAlH4 gives the known alcohols 7-9. By means of the Wittig-Horner-Emmons olefination the α,β,α′,β′-unsaturated ester 10 is accessible, which on irradiation undergoes an intramolecular [2+2]-cycloaddition to yield a 4:1 mixture of the cyclobutane derivatives 11 and 12.
    Notes: Benzvalen addiert schon bei -30°C Singulettsauerstoff zum 1,2-Dioxetan 2, dessen Konstitution durch die Reduktion mit Triphenylarsan zum Tricyclo[3.1.0.02,6]hexan-cis-3,4-diol (5) und die unter Chemilumineszenz verlaufende Spaltung zum Titeldialdehyd 3 belegt wird. Die Reduktion von 3 mit LiAlH4 führt zu den bekannten Alkoholen 7-9. Der aus 3 durch Wittig-Horner-Emmons-Olefinierung zugängliche α,β,α′,β′-ungesättigte Ester 10 unterliegt beim Belichten einer intramolekularen [2+2]-Cycloaddition zum 4:1-Gemisch der Cyclobutanderivate 11 und 12.
    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...