Journalartikel

Generation and reactivity of vinyltelluryl radical


AutorenlisteKeul, Felix; Mardyukov, Artur

Jahr der Veröffentlichung2022

Seiten15129-15134

ZeitschriftPhysical Chemistry Chemical Physics

Bandnummer24

Heftnummer24

ISSN1463-9076

eISSN1463-9084

DOI Linkhttps://doi.org/10.1039/d2cp01658c

VerlagRoyal Society of Chemistry


Abstract
Vinyltelluryl radical was prepared by high-vacuum flash pyrolysis from the corresponding divinylditelluride and trapped in an argon matrix at 10 K. The title compound was characterized by IR and UV/Vis spectroscopy, and all experimental data match well with density functional theory at the UB3LYP/def2-QZVPP level. According to UB3LYP/def2-QZVPP computations, the spin density is mainly localized on the Te atom. The vinylogy principle for the vinyltelluryl radical is not applicable due to the lack of delocalization of spin density. Upon irradiation of the matrix with light (lambda = 365 nm), the vinyltelluryl radical rearranges to a H-TeMIDLINE HORIZONTAL ELLIPSISacetylene complex. Doping the matrix with molecular oxygen leads to the hitherto unknown vinyltelluro peroxy radical. The latter isomerizes to the more thermodynamically stable vinyltelluroyl radical by irradiation with light at lambda = 523 nm.



Zitierstile

Harvard-ZitierstilKeul, F. and Mardyukov, A. (2022) Generation and reactivity of vinyltelluryl radical, Physical Chemistry Chemical Physics, 24(24), pp. 15129-15134. https://doi.org/10.1039/d2cp01658c

APA-ZitierstilKeul, F., & Mardyukov, A. (2022). Generation and reactivity of vinyltelluryl radical. Physical Chemistry Chemical Physics. 24(24), 15129-15134. https://doi.org/10.1039/d2cp01658c



Schlagwörter


ELECTRONIC-STRUCTUREINITIATORSLASER-INDUCED FLUORESCENCEMOLECULAR-BEAMPHOTOLYSISPOLYMERIZATIONVINOXY


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