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  (4)
Collection
Keywords
Publisher
Years
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1118-1124 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Electronic Structure of Aromatic Amines: Photoelectron Spectra of 5,10-Dimethyl-5,10-dihydrophenazine, 5-Methyl-10-phenyl-5,10-dihydrophenazine, Phenoxazine and PhenothiazineThe photoelectron spectra of the title compounds 1-4 have been measured, and the lower ionization potentials have been assigned on the basis of a CNDO calculation. The slope of the onset of the first band in the spectra is related to the geometry of the molecule.
    Notes: Die Photoelektron-Spektren der Titelverbindungen 1-4 wurden gemessen. Eine Zuordnung der Ionisationspotentiale wird aufgrund eines LCMO-Modells und CNDO/2-Rechnungen vorgenommen. Aus dem Anstieg der Bande der ersten Ionisation wird eine Diskussion der Molekülgeometrien abgeleitet.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 67 (1984), S. 953-958 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: IR-spectroscopic investigations of light-induced rearrangement reactions of nitrosooxymethane (CH3ONO3), nitrosooxyethane (CH3CH2ONO) and N,N-dimethylnitrosamine ((CH3)2NNO) in low-temperature rare-gas matrices have established that these molecules are transformed in two photolysis steps to the previously unknown C-nitroso compounds nitrosomethanol (CH2(OH)(NO)), 1-nitrosoethanol (CH3CH(OH)(NO)), and methyl(nitrosomethyl)amine CH2(NO)(NH)(CH3). Evidence for a similar rearrangement reaction has been advanced for N-Nitrosopyrrolidine which is converted to C-nitrosopyrrolidine . The matrix-isolation technique in combination with wavelength-selective irradiation allowed to trap and characterize an intermediate of rearrangement which revealed to be nitroxyl (HNO) complex (CH2…HNO, CH3CHO…HNO, CH3N = CH2…HNO, and ). Since these findings have a close resemblance with rearrangement reactions of more complex nitrosooxy compounds, nitrosamines, or nitrosohydrazines used in organic synthesis, it is suggested that also in these reactions nitroxyl is present as an intermediate species.
    Additional Material: 3 Tab.
    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
    Helvetica Chimica Acta 64 (1981), S. 989-995 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photodecomposition of dimethylnitrosamine in the gas phase ( ∼ 1 Torr) has been investigated following irradiation into the S1 (nπ*) ← S0 (363.5 nm) and S2 (ππ*) ← S0 (248.1 nm) transitions at room temperature. With a quantum yield of unity, excitation into the S1 state yields the fragments (CH3)2N⋅ and NO which then recombine leaving no photoproducts. The addition of O2 results in only one photoproduct, (CH3)2NNO2. Irradiating into the S2 state, the products CH2=N—CH3, (CH2=N—CH3)3, CH2=NOH, N2O, NO, H2, and N2 were identified by capillary gas chromatography mass spectrometry. In the presence of N2 as a buffer gas the photoproducts are only CH2=N—CH3, (CH2=N—CH3)3, N2O, and H2. For both excitation conditions a mechanism is proposed involving cleavage of the N, N-bond as the main primary photolytic process.
    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
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 64 (1981), S. 2048-2055 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It has been demonstrated that the triplet lifetime of nonemitting molecules in the dilute vapor phase - even for complex triplet decays - can be accurately determined by means of time-resolved triplet-triplet (T-T) energy transfer to a strong emitter molecule. Besides the test molecules 1-butyne-3-one and benzaldehyde the lifetime of the vibrationally relaxed nonemitting T1(nπ*) state of cycloheptanone, τ=63 ± 5 µs at ∼0.5 Torr, together with its energy transfer rate constant to biacetyl, kET=(1.80±0.08) x 106 s-1 Torr-1, have been measured.
    Additional Material: 5 Ill.
    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...