39763-18-3Relevant academic research and scientific papers
Ultraviolet and Polarized Infrared Spectroscopy of Matrix-Isolated Cyclobutadiene and Its Isotopomers
Arnold, Bradley R.,Michl, Josef
, p. 13348 - 13354 (2007/10/02)
The UV and polarized IR spectra of argon matrix isolated cyclobutadiene and its 1-d-, 1,2-d2-, 1,4-d2-, 1-13C-, 1,2-13C2-, and 1,4-13C2- labeled derivatives are reported.Above 250 nm, the UV spectrum contains no peaks with an extinction coefficient larger than 10 L M-1 cm-1, but a weak absorption tail extends throughout the UV region.The absorption rises abruptly below 250 nm.The IR peak positions mostly agree with previous reports where these are available.Photoalignment studies support the symmetry assignment of fundamental vibrations and prove that the two Kekule forms interconvert rapidly even at 10 K.The spectral and photochemical effe ts of the presence of an adjacent CO2 molecule in the cyclobutadiene matrix site are elucidated.Its presence causes a substantial retardation of the photofragmentation of cyclobutadiene into two acetylenes.This is attributed to accelerated vibrational energy loss from the cyclobutadiene absorber.
The Photo-isomerization of Cyclopentadienone O-Oxide Isolated in Low Temperature Matrices
Dunkin, Ian R.,Shields, Charles J.
, p. 154 - 156 (2007/10/02)
Discrepancies in recent reports from different laboratories on the i.r. spectrum of matrix-isolated cyclopentadienone O-oxide have now been reconciled by showing that two distinct isomers may be formed from cyclopentadienylidene and O2, and that one, a carbonyl oxide, may be converted photolytically into the other, a dioxirane.
Cyclopentadienone O-Oxide: A Highly Labile Intermediate in the Matrix Reaction between Cyclopentadienylidene and Oxygen
Bell, Gordon A.,Dunkin, Ian R.
, p. 1213 - 1215 (2007/10/02)
Cyclopentadienylidene reacts with oxygen in low-temperature matrices, giving a photolabile intermediate, the i.r. spectrum of which suggests that it is the carbonyl oxide, cyclopentadienone O-oxide.
