Photodissociation and photochemistry of V⁺ (H₂O)n, n = 1–4, in the 360–680 nm region

The photodissociation and photochemistry of V⁺ (H₂O)n, n = 1–4, was studied in the 360–680 nm region in
 a Fourier transform ion cyclotron resonance mass spectrometer. The light of a high pressure mercury arc lamp was
 filtered with band pass filters, with center wavelengths from 360...

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Veröffentlicht in:Физика низких температур
Datum:2012
Hauptverfasser: Scharfschwerdt, B., van der Linde, C., Balaj, O.P., Herber, I., Schütze, D., Beyer, M.K.
Format: Artikel
Sprache:Englisch
Veröffentlicht: Фізико-технічний інститут низьких температур ім. Б.І. Вєркіна НАН України 2012
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Online Zugang:https://nasplib.isofts.kiev.ua/handle/123456789/117423
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Назва журналу:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Zitieren:Photodissociation and photochemistry of V⁺ (H₂O)n, n = 1–4, in the 360–680 nm region / B. Scharfschwerdt, C. van der Linde, O.P. Balaj,
 I. Herber, D. Schütze, M.K. Beyer // Физика низких температур. — 2012. — Т. 38, № 8. — С. 905-911 . — Бібліогр.: 47 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
Beschreibung
Zusammenfassung:The photodissociation and photochemistry of V⁺ (H₂O)n, n = 1–4, was studied in the 360–680 nm region in
 a Fourier transform ion cyclotron resonance mass spectrometer. The light of a high pressure mercury arc lamp was
 filtered with band pass filters, with center wavelengths from 360 to 680 nm in steps of 20 nm. The bandwidth of
 the filters, defined as full width at half maximum, was 10 nm. Photodissociation channels are loss of water molecules,
 as well as loss of atomic or molecular hydrogen, which may be accompanied by loss of water molecules.
 The most intense absorptions are red shifted with increasing hydration. Theoretical spectra are calculated with
 time dependent density functional theory. Calculations reproduce all features of the experimental spectra, including
 the red shift with increasing hydration shell and the overall pattern of strong and weak absorptions.
ISSN:0132-6414