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Title: Photorearrangements of bridgehead-aryl-substituted dibenzobarrelenes. Steady-state and laser flash photolysis studies

Journal Article · · Journal of Organic Chemistry; (United States)
DOI:https://doi.org/10.1021/jo00291a039· OSTI ID:5974479
;  [1];  [2]; ;  [3];  [4]
  1. Indian Inst. of Tech., Kanpur (India)
  2. Univ. of Notre Dame, IN (United States) Indian Inst. of Tech., Kanpur (United States)
  3. Univ. of Notre Dame, IN (United States)
  4. Regional Research Lab., Trivandrum (India) Univ. of Notre Dame, IN (United States) Indian Inst. of Tech., Kanpur (India)

Examples of a novel di-{pi}-methane rearrangement of 9-aryl-substituted dibenzobarrelenes containing 1,2-dibenzoylalkene moieties (1a-f) are presented. Steady-state irradiation of the dibenzobarrelenes 1a-f in benzene gives the regioselectively formed dibenzopentalenofurans, 5a-f, in excellent yields (74-90%). The structure of the bromo derivative 5f was confirmed through X-ray crystallographic analysis. Controlled irradiation of 1b, a representative example, at low temperatures suggests that the dibenzopentalenofurans (5a-f) are formed through the thermal isomerization of the corresponding dibenzosemibullvalenes 6a-f, which, in turn, arise through a di-{pi}-methane type of rearrangement. Laser flash photolysis (337.1 nm) of 1a-f in benzene gives rise to transient phenomena, attributable to dibenzobarrelenes triplets ({phi}{sup T} = 0.2-0.5). These transients are characterized by broad and diffuse absorption spectra and possess short lifetimes (0.13-0.19 {mu}s). They are readily quenched by oxygen, HTEMPO (4-hydroxy-2,2,6,6-tetramethylpiperidinyl-1-oxy), ferrocene, and {beta}-carotene, with rate constants in the limit of diffusion control (10{sup 8}-10{sup 10} M{sup {minus}1} s{sup {minus}1}).

OSTI ID:
5974479
Journal Information:
Journal of Organic Chemistry; (United States), Vol. 55:4; ISSN 0022-3263
Country of Publication:
United States
Language:
English