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Pregled bibliografske jedinice broj: 1002790

Photoelimination of Nitrogen from Adamantane and Pentacycloundecane (PCU) Diazirines: Spectroscopic Study and Supramolecular Control


Šumanovac, Tatjana; Alešković, Marija; Šekutor, Marina; Matković, Marija; Baron, Thibaut; Mlinarić-Majerski; Bohne, Cornelia; Basarić, Nikola
Photoelimination of Nitrogen from Adamantane and Pentacycloundecane (PCU) Diazirines: Spectroscopic Study and Supramolecular Control // Photochemical & photobiological sciences, 18 (2019), 1806-1822 doi:10.1039/C9PP00124G (međunarodna recenzija, članak, znanstveni)


Naslov
Photoelimination of Nitrogen from Adamantane and Pentacycloundecane (PCU) Diazirines: Spectroscopic Study and Supramolecular Control

Autori
Šumanovac, Tatjana ; Alešković, Marija ; Šekutor, Marina ; Matković, Marija ; Baron, Thibaut ; Mlinarić-Majerski ; Bohne, Cornelia ; Basarić, Nikola

Izvornik
Photochemical & photobiological sciences (1474-905X) 18 (2019); 1806-1822

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

Ključne riječi
Diazirines ; carbenes ; photochemistry ; supramolecular chemistry ; laser flash photolysis

Sažetak
Photochemical reactivity of pentacycloundecane (PCU) and adamantane diazirines was investigated by preparative irradiations in different solvents, laser flash photolysis (LFP) and quantum chemical computations. In addition, formation of inclusion complexes for diazirines with cucurbit[7]uril, β- and γ-cyclodextrin (β- and γ-CD) were investigated by 1H NMR spectroscopy, isothermal microcalorimetry and circular dichroism spectroscopy, followed by investigation of photochemical reactivity of the formed complexes. Diazirines undergo efficient photochemical elimination of nitrogen (ΦR > 0.5) and deliver the corresponding singlet carbenes. Singlet carbenes react in intra- and intermolecular reactions and we found a rare singlet carbene pathway in CH3OH involving protonation and formation of a carbocation, detected due to the specific rearrangement of the pentacycloundecane skeleton. Singlet diazirines undergo intersystem crossing and deliver triplet carbenes that react with oxygen to form ketones which were isolated after irradiation. Our main finding is that the formation of diazirine inclusion complexes with β-CD and γ-CD changes the relative ratio of singlet vs. triplet pathways, with singlet carbene products being dominant from the chemistry of the irradiated complexes. Our combined theoretical and experimental studies provide new insights into the supramolecular control of carbene reactivity which has possible applications for the control of product distribution by solvent effects and choice of constrained media.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekt / tema
HRZZ-IP-2014-09-6312 - Supramolekulska kontrola fotokemijskih reakcija eliminacije (Nikola Basarić, )

Ustanove
Institut "Ruđer Bošković", Zagreb

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
  • MEDLINE


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