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Pregled bibliografske jedinice broj: 23364

Reaction of aquachromium(II) ions with 2, 2'-bipyrimidine. A pulse radiolysis study


Bonifačić, Marija; Lovrić, Jasna; Orhanović, Mato
Reaction of aquachromium(II) ions with 2, 2'-bipyrimidine. A pulse radiolysis study // Journal of the Chemical Society. Dalton transactions, 17 (1998), 2879-2885 doi:10.1039/a803697g (međunarodna recenzija, članak, znanstveni)


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Naslov
Reaction of aquachromium(II) ions with 2, 2'-bipyrimidine. A pulse radiolysis study

Autori
Bonifačić, Marija ; Lovrić, Jasna ; Orhanović, Mato

Izvornik
Journal of the Chemical Society. Dalton transactions (0300-9246) 17 (1998); 2879-2885

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
excited states ; pulse radiolysis ; radicals

Sažetak
Chromium(II) ion was generated from hexaamminochromium(III) and hydrated electrons in the presence of 2, 2'-bipyridine (bpm). The reaction of hexaamminochromium(III) with e- (aq) has k = 4.9 E10 (1/Ms) at 25 °C. The hexaaminochromium(II) so produced loses all the ammonia ligands with k > 1 E5 (1/s). A product complex with an absorption maximum at around 350 nm was formed in the reaction of chromium(II) ion and bpm. In the presence of a moderate excess of bpm an equilibrium is established on the 0.1 ms timescale with K(app) = k(f) [bpm]/k(b). Both the forward (k(f)) and back (k(b)) reactions are pH dependent in the range 3.5 to 8.6. The UV spectra of the reaction product(s) indicate that the absorbing product contains chromium(III) and bipyrimidine radical ligand. The first acid dissociation constant of chromium(II) ion was determined as 1.4 E5 M. On the 0.1 ms timescale, chromium(III) and bipyrimidine radical ligand is stable but undergoes changes at longer times. The protonated bpm molecule is reduced by 1-hydoxy-1-methylethyl radicals, yielding a diprotonated bpm radical. No reaction was observed between hexaaquochromium(III) and diprotonated bpm radical in pulse radiolysis experiments, which places the rate constant for this reaction at < 2 E6 (1/Ms).

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekti:
00980604

Ustanove:
Institut "Ruđer Bošković", Zagreb

Profili:

Avatar Url Jasna Lovrić (autor)

Avatar Url Mato Orhanović (autor)

Avatar Url Marija Bonifačić (autor)

Poveznice na cjeloviti tekst rada:

doi pubs.rsc.org pubs.rsc.org

Citiraj ovu publikaciju:

Bonifačić, Marija; Lovrić, Jasna; Orhanović, Mato
Reaction of aquachromium(II) ions with 2, 2'-bipyrimidine. A pulse radiolysis study // Journal of the Chemical Society. Dalton transactions, 17 (1998), 2879-2885 doi:10.1039/a803697g (međunarodna recenzija, članak, znanstveni)
Bonifačić, M., Lovrić, J. & Orhanović, M. (1998) Reaction of aquachromium(II) ions with 2, 2'-bipyrimidine. A pulse radiolysis study. Journal of the Chemical Society. Dalton transactions, 17, 2879-2885 doi:10.1039/a803697g.
@article{article, author = {Bonifa\v{c}i\'{c}, Marija and Lovri\'{c}, Jasna and Orhanovi\'{c}, Mato}, year = {1998}, pages = {2879-2885}, DOI = {10.1039/a803697g}, keywords = {excited states, pulse radiolysis, radicals}, journal = {Journal of the Chemical Society. Dalton transactions}, doi = {10.1039/a803697g}, volume = {17}, issn = {0300-9246}, title = {Reaction of aquachromium(II) ions with 2, 2'-bipyrimidine. A pulse radiolysis study}, keyword = {excited states, pulse radiolysis, radicals} }
@article{article, author = {Bonifa\v{c}i\'{c}, Marija and Lovri\'{c}, Jasna and Orhanovi\'{c}, Mato}, year = {1998}, pages = {2879-2885}, DOI = {10.1039/a803697g}, keywords = {excited states, pulse radiolysis, radicals}, journal = {Journal of the Chemical Society. Dalton transactions}, doi = {10.1039/a803697g}, volume = {17}, issn = {0300-9246}, title = {Reaction of aquachromium(II) ions with 2, 2'-bipyrimidine. A pulse radiolysis study}, keyword = {excited states, pulse radiolysis, radicals} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


Citati:





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