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  • 2-hydroxytetrahydrofuran  (1)
  • 75.50.Mm  (1)
  • Ethidium  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    JETP letters 65 (1997), S. 160-165 
    ISSN: 1090-6487
    Keywords: 75.50.Mm ; 66.20.+d
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We report the first observation of the breakup of a rotating drop suspended in a viscous liquid. To produce the motion, a magnetic liquid is used as the material of the drop and the entire system is placed in a uniform, rotating, low-frequency magnetic field. The frequency dependence of the breakup of the drop into two smaller drops is investigated. A theoretical description is given for small Reynolds numbers. The drop is assumed to be ellipsoidal. The flow in the exterior and interior regions and the drag coefficient of the liquid ellipsoid with respect to rotational motion are calculated. A criterion for breakup of the drop is estimated and a comparison is made with experimental data.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Chemistry of heterocyclic compounds 36 (2000), S. 775-778 
    ISSN: 1573-8353
    Keywords: 2-hydroxytetrahydrofuran ; 4-hydroxybutanal ; 2,3-dihydrofuran ; tautomerism ; dehydration ; AM1 method ; concerted mechanism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The relative stability of 2-hydroxytetrahydrofuran and the tautomeric 4-hydroxybutanal was determined by the semi-empirical AM1 method. It was concluded that the cyclic tautomer predominates in the gas phase at 25°C. Vapor-phase dehydration of 2-hydroxytetrahydrofuran in the presence of porcelain and silica gel L leads to a quantitative yield of 2,3-dihydrofuran.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0952-3499
    Keywords: Sequence-specific photomodification ; Oligonucleotide derivatives ; Ethidium ; Azidoethidium ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Oligodeoxyribonucleotide derivatives containing ethidium or azidoethidium residues attached to 3′ and/or 5′ end were prepared. These derivatives formed tight specific complexes with complementary oligodeoxyribonucleotides where each attached ethidium residue led to an increase of complex Tm by 20-30°C. Tandem complexes of two oligodeoxyribonucleotides containing ethidium residues with an oligodeoxyribonucleotide having two adjacent complementary sequences for these Oligonucleotide were investigated. Photoinduced reactions of a number of ethidium and azidoethidium oligodeoxyribonucleotide derivatives with target complementary single-stranded and double-stranded oligo- and polydeoxyribonucleotides were investigated. The irradiation led to direct photocleavage of the target oligo- or polynucleotide, to formation of hidden (piperidine cleavable) modifications of the target of formation of covalent adducts between ethidium oligodeoxyribonucleotide derivative and the target. In a number of experiments, azidoethidium dyes were demonstrated to be considerably stronger photosensitizers than ethidium ones. Depending on the nature of the target (single- or double-stranded DNA) and on the irradiation conditions, the total damages to the target oligo- or polydeoxyribonucleotides ranged from 10-70% (for ethidium dyes) to 30-80% (for azidoethidium dyes).
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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