Croatica Chemica Acta, Vol. 74 No. 2, 2001.
Izvorni znanstveni članak
Ab initio Theoretical Investigation of a Formal Alkene-Enedione Intramolecular [2 + 2] Photocyclization
Alan P. Marchand
; Department of Chemistry, University of North Texas, Denton, Texas 76203-5070, USA
Trevor D. Power
; Department of Chemistry, University of North Texas, Denton, Texas 76203-5070, USA
Hendrik G. Kruger
; School of Pure & Applied Chemistry, University of Natal, Durhan 4001, South Africa
Sažetak
Irradiation of 1 with visible light results in intramolecular [2 + 2] photocyclization to afford the corresponding pentacyclic cage diketone, i.e. pentacyclo [5.4.0.02,6.03,10.05,9]undecane-8,11-dione (2). The mechanism of this reaction has been scrutinized by using ab initio theoretical methods. The results of these calculations provide new evidence which supports earlier suggestions that alkene-enedione photocyclizations may actually proceed via a diradical stepwise mechanism through the triplet excited state rather than as concerted [2 + 2] cycloadditions.
Ključne riječi
photocyclization; intramolecular photocyclization; diketone; ab initio
Hrčak ID:
131812
URI
Datum izdavanja:
2.4.2001.
Posjeta: 671 *