Observation and Characterization of the Hg-O Diatomic Molecule: A Matrix-Isolation and Quantum-Chemical Investigation.

Mercuric oxide is a well-known and stable solid, but the diatomic molecule Hg-O is very fragile and does not survive detection in the gas phase. However, laser ablation of Hg atoms from a dental amalgam alloy target into argon or neon containing about 0.3 % of 16 O2 or of 18 O2 during their condensation into a cryogenic matrix at 4 K allows the formation of O atoms which react on annealing to make ozone and new IR absorptions in solid argon at 521.2 cm-1 for Hg-16 O or at 496.4 cm-1 for Hg-18 O with the oxygen isotopic frequency ratio 521.2/496.4=1.0499. Solid neon gives a 529.0 cm-1 absorption with a small 7.8 cm-1 blue shift. CCSD(T) calculations found 594 cm-1 for Hg16 O and 562 cm-1 for Hg18 O (frequency ratio=1.0569). Such calculations usually produce harmonic frequencies that are slightly higher than the anharmonic (observed) values, which supports their relationship. These observed frequencies have the isotopic shift predicted for Hg-O and are within the range of recent high-level frequency calculations for the Hg-O molecule. Spectra for the related mercury superoxide and ozonide species are also considered for the first time.

Matrix Infrared Spectroscopic Studies of B-NCCN, B-η2-(NC)-CN, NCBCN, CNBCN, CNBNC, and High-Order Products Produced in Reactions of Boron Atoms with Cyanogen.

The products in reactions of laser-ablated boron atoms with cyanogen in excess argon have been identified via investigation of the matrix spectra and their variation on photolysis, annealing, and isotopic substitutions. DFT calculations have been performed for the plausible products and reaction paths, providing helpful guides. B-NCCN and B-η2-(NC)-CN were observed in the original deposition spectra, but they disappear on photolysis with λ > 220 nm while more stable NCBCN, CNBCN, and CNBNC were produced. Besides these primary products, high-order products [(NC)2B-NCCN, (CN)(NC)B-NCCN, (CN)2B-NCCN, and (NC)2B-B(CN)2] were also observed, which increased in the later stage of annealing. Our calculations show that initially produced B-NCCN is interconvertible to B-η2-(NC)-CN and the more stable boron cyanide and isocyanide, consistent with the observed results. The formation of high-order products demonstrates that boron highly prefers the trivalent state in reactions with cyanogen, similar to aluminum.

Matrix Infrared Spectroscopic and Theoretical Investigations of M···NCCN, M···CNCN, M···C(N)CN, NCMCN, CNMNC, CNMCN, and [M···NCCN]+ Produced in the Reactions of Group 11 Metal Atoms with Cyanogen.

Reactions of group 11 metals with cyanogen, N≡C-C≡N, in excess argon and neon have been carried out, and the products were identified via examination of the matrix spectra and their variation upon photolysis, annealing, and isotopic substitutions. Density functional theory calculations provided helpful information for the plausible products and reaction paths. While M···NCCN and M···CNCN were observed in all three metal systems, the cyanide and isocyanide products (NCMCN, NCMNC, and CNMNC) were identified only in the Cu reactions, and M···C(N)CN was identified in the Cu and Au spectra. Intrinsic reaction coordinate calculation results along with the observed spectral variation upon photolysis and annealing suggest that Cu···C(N)CN was the pathway to cyanide and isocyanide. The product absorptions with exceptionally high C-N stretching frequencies in the Au system have been tentatively assigned to a cation [Au···NCCN+]. The group 11 metal cyanides and isocyanides that require two chemical bonds to the central metal are energetically favorable only in the lightest metal system.