30336-05-1Relevant articles and documents
Substituent Effects in the Photochemistry of 5-Aryl-3,3-diphenyl-2(3H)-furanones. Steady-State and Laser Flash Photolysis Studies
Pratapan, S.,Ashok, K.,Cyr, D.R.,Das, P.K.,George, M.V.
, p. 5826 - 5831 (1988)
The photochemistry of a series of 5-aryl-3,3-diphenyl-2(3H)-furanones, containing electron-releasing as well as electron-withdrawing para substituents on the phenyl group at theC5 position, has been investigated by steady-state photolysis, prod
Photochemical and Thermal Transformations of 2(3H)-Furanones and Bis(benzofuranones). A Laser Flash Photolysis study
Lohray, B. B.,Kumar, C. V.,Das, P. K.,George, M. V.
, p. 7352 - 7359 (2007/10/02)
Transformations of the 2(3H)-furanones 1-4 and bis(benzofuranones) 16-18 under steady-state photolysis and thermolysis are reported.Irradiation of 1 in benzene gives a mixture of the decarbonylated product 5 (62percent) and the cyclized phenanthrene derivative 10 (15percent).Similar results were obtained when the photolysis of 1 was carried out in methanol and acetone.Irradiation of 2 in benzene and methanol gave exclusively the decarbonylation product 6, whereas, in acetone, a mixture of the rearranged lactone 13 and and its cyclized product, 15, was obtained.Irradiation of both 3 and 4 gave the cyclized products 11 and 12, respectively.In contrast, the photolysis of the bis(benzofuranone) 16 in cyclohexane gave 3-phenylbenzo-2-(3H)-furanone (25), whereas the photolysis in methanol led to a mixture of methyl α-(2-hydroxyphenyl)phenylacetate (34) and 3-hydroxy-3-phenylbenzo-2(3H)-furanone (31).Similar results were obtained in the irradiation of 17 and 18.Neat thermolysis of furanones 1-3 at 350-450 deg C gave the decarbonylated products 5, 6, and 37 in 36-80 percent yields, whereas furanone 4 underwent facile isomerization to 5-benzyl-3,4,5-triphenyl-2(5H)-furanone (38), upon refluxing in diphenyl ether (ca. 255 deg C).Heating of bis(benzofuranones) 16-18 in refluxing cumene (ca. 150 deg C) gave the corresponding furanones 25-27 in 62-68 percent yields.Laser flash photolysis of furanones 1-4 at 248 and 337 nm leads to absorption spectral changes that can be explained in terms of singlet-mediated decarbonylation (φ = 0.3 for 2 in methanol, λex = 248 nm) and cyclization, i.e., dihydrophenanthrene formation (φ = 0.1-0.5 for 1, 3, and 4 in benzene and methanol, λex = 337 nm).The triplets of the furanones generated under energy-transfer sensitization by benzophenone in benzene are relatively long lived (r = 1.2-12 μs) and exhibit absorption maxima at 330-370 nm (εmax = (11-14) * 103 M-1 cm-1); these spectral and kinetic features appear to be characteristic of the styrene and cis-stilbene chromophores, constrained into planar configurations.Upon laser flash photolysis at 248 nm in methanol, bis(benzofuranones) 16-18 undergo facile fragmentation to the corresponding radicals 19-21, characterized by sharp and intense absorption maxima at ca. 330 nm, in addition to broad and weak absorption band systems at 500-600 nm; these radical species are the primary intermediates implicated in the formation of various final products in the course of steady-state photolysis of 16-18 under different conditions.
