Reactions of laser ablated Be atoms with O2: Infrared spectra of beryllium oxides in solid argon

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Abstract
Pulsed-laser ablated beryllium atoms codeposited with O2 in excess argon at 10 K yielded new beryllium–oxygen molecules. The initial reaction to make BeO is endothermic, but activation energy is provided by hyperthermal Be atoms. A strong band at 1572.9 cm−1 and a weak band at 398.9 cm−1 gave oxygen isotopic shifts consistent with a BeO diatomic molecule and are assigned to the O2–BeO complex analogous to the Ar–BeO complex. A sharp band at 1413.2 cm−1 exhibited an oxygen isotopic triplet with 16,18O2 and shifts appropriate for linear OBeO. A nearly coincident band at 1412.4 cm−1 gave an isotopic doublet and shifted in agreement with linear BeOBe. Quantum chemical calculations at the second-order many-body perturbation theory [MBPT(2)] level predict 3Σ ground states and ν3 fundamentals at 1422.5 and 1418.2 cm−1 for OBeO and BeOBe, respectively, in excellent agreement with the observed values. Three bands at 1131.2, 866.3, and 522.4 cm−1 increased together on photolysis, yielded isotopic triplets, and agreed with MBPT(2) calculations for rhombic Be2O2. A sharp photosensitive band at 988.6 cm−1 gave oxygen isotopic shifts consistent with another linear OBeO species and is tentatively assigned to the molecular anion. An intense band at 1465.1 cm−1 that appeared on annealing gave oxygen isotopic shifts in agreement with calculations for linear BeOBeO. Two bands at 1288.9 and 1264.1 cm−1 appeared on photolysis and gave isotopic triplets and shifts that are in excellent agreement with calculations for branched BeBeO2. Annealing produced bands at 871.8 and 436.1 cm−1 that decreased on photolysis and are assigned to BeO3.

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