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A. R. W. McKellar

Publications and source records attributed to A. R. W. McKellar.

28 records · Page 2Linked to original sources

Spectra of the D2O dimer in the O-D fundamental stretch region: vibrational dependence of tunneling splittings and lifetimes

The fundamental O-D stretch region (2600 - 2800 cm-1) of the fully deuterated water dimer, (D2O)2, is studied using a pulsed supersonic slit jet source and a tunable optical parametric oscillator source. Relatively high spectral resolution (0.002 cm-1) enables all six dimer tunneling components to be observed, in most cases, for the acceptor asymmetric O-D stretch, the donor free O-D stretch, and the donor bound O-D stretch vibrations. The dominant acceptor switching tunneling splittings are observed to decrease moderately in the excited O-D stretch states, to roughly 75% of their ground state values, whereas the smaller donor-acceptor interchange splittings show more dramatic and irregular decreases. Excited state predissociation lifetimes, as determined from observed line broadening, show large variations (0.2 to 5 nanoseconds) depending on vibrational state, K-value, and tunneling symmetry. Another very weak band is tentatively assigned to a combination mode involving an intramolecular O-D stretch plus an intermolecular twist overtone. Asymmetric O-D stretch bands of the mixed isotopologue dimers D2O-DOH and D2O-HOD are also observed and analyzed.

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Infrared bands of CS2 dimer and trimer at 4.5 cm-1

We report observation of new infrared bands of (CS2)2 and (CS2)3 in the region of the CS2 ν1+ ν3 combination band (at 4.5 cm-1) using a quantum cascade laser. The complexes are formed in a pulsed supersonic slit-jet expansion of a gas mixture of carbon disulfide in helium. We have previously shown that the most stable isomer of (CS2)2 is a cross-shaped structure with D2d symmetry and that for (CS2)3 is a barrel-shaped structure with D3 symmetry. The dimer has one doubly degenerate infrared-active band in the ν1+ ν3 region of the CS2 monomer. This band is observed to have a rather small vibrational shift of -0.846 cm-1. We expect one parallel and one perpendicular infrared-active band for the trimer but observe two parallel and one perpendicular bands. Much larger vibrational shifts of -8.953 cm-1 for the perpendicular band and -8.845 cm-1 and +16.681 cm-1 for the parallel bands are observed. Vibrational shifts and possible vibrational assignments, in the case of the parallel bands of the trimer, are discussed using group theoretical arguments.

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The N2O-CS2 dimer is cross-shaped

The infrared spectrum of the cross-shaped van der Waals complex N2O-CS2 is observed in the region of the N2O nu1 fundamental band (~2220 cm-1) using a tuneable diode laser to probe a pulsed supersonic slit jet expansion. Both 14N- and 15N-substituted species are studied. Analysis of their spectra establishes that this dimer has a cross-shaped structure, similar to its isoelectronic cousin CO2-CS2. This is the first spectroscopic observation of N2O-CS2, and the molecular parameters determined here should be useful for detection of its pure rotational microwave spectrum.

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Infrared spectra of Rg1,2 - C6H6 complexes, Rg = He, Ne, Ar

Infrared spectra of Rg1,2 - C6H6 complexes (Rg = He, Ne, Ar) are observed in the region of the nu12 fundamental of C6H6 using a pulsed supersonic jet expansion and a tunable optical parametric oscillator laser source. The mixed trimer He - Ne - C6H6 is also detected. Four bands are analyzed for each complex, namely nu12 itself (~3048 cm-1) and three linked combination bands (~3079, 3100, and 3102 cm-1). The results are consistent with previous ultraviolet and microwave results, with Ne2 - C6H6 and He - Ne - C6H6 being analyzed spectroscopically here for the first time.

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Infrared spectrum and intermolecular potential energy surface of the CO-O2 dimer

Only a few weakly-bound complexes containing the O2 molecule have been characterized by high resolution spectroscopy, no doubt due to the complications added by the oxygen molecule's unpaired electron spin. Here we report an extensive infrared spectrum of CO-O2, observed in the CO fundamental band region using a tunable quantum cascade laser to probe a pulsed supersonic jet expansion. The rotational energy level pattern derived from the spectrum consists of stacks of levels characterized by the total angular momentum, J, and its projection on the intermolecular axis, K. Five such stacks are observed in the ground vibrational state, and ten in the excited state (v(CO) = 1). They are divided into two groups, with no observed transitions between groups. The groups correspond to different projections of the O2 electron spin, and correlate with the two lowest rotational states of O2, (N, J) = (1, 0) and (1, 2). The rotational constant of the lowest K = 0 stack implies an effective intermolecular separation of 3.82 Angstroms, but this should be interpreted with caution since it ignores possible effects of electron spin. A new high-level 4-dimensional potential energy surface is developed for CO-O2, and rotational energy levels are calculated for this surface, ignoring electron spin. By comparing calculated and observed levels, it is possible to assign detailed quantum labels to the observed level stacks.

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Infrared spectra of C2H4 dimer and trimer

Spectra of ethylene dimers and trimers are studied in the nu11 and (for the dimer) nu9 fundamental band regions of C2H4 (~2990 and 3100 cm-1) using a tunable optical parametric oscillator source to probe a pulsed supersonic slit jet expansion. The deuterated trimer has been observed previously, but this represents the first rotationally resolved spectrum of (C2H4)3. The results support the previously determined cross-shaped (D2d) dimer and barrel-shaped (C3h or C3) trimer structures. However, the dimer spectrum in the nu9 fundamental region of C2H4 is apparently very perturbed and a previous rotational analysis is not well verified.

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The He2 - OCS complex: comparison between theory and experiment

OCS is an ideal probe for quantum solvation effects in cold helium clusters. He2-OCS is the "second step" in going from a single OCS molecule to a large doped superfluid helium cluster. Here assignment of the spectrum of He2-OCS is significantly extended to higher values of J, K, and vt (the low frequency torsional vibration). The observation of a new infrared band, OCS nu1 + nu3, taken together with the known nu1 band, enables assignments to be verified by comparing ground state combination differences. Relatively straightforward scaling of previously calculated theoretical energy levels gives a remarkably good fit to experiment

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Infrared observation of OC-C2H2, OC-(C2H2)2 and their isotopologues

The fundamental band for the OC-C2H2 dimer and two combination bands involving the intermolecular bending modes nu9 and nu8 in the carbon monoxide CO stretch region are re-examined. Spectra are obtained using a pulsed supersonic slit jet expansion probed with a mode-hop free tunable infrared quantum cascade laser. Analogous bands for OC-C2D2 and the fundamental for OC-DCCH as an impurity are also observed and analysed. A much weaker band in the same spectral region is assigned to a new mixed trimer, CO-(C2H2)2. The trimer band is composed uniquely of a-type transitions, establishing that the CO monomer is nearly aligned with the a-inertial axis. The observed rotational constants agree well with ab initio calculations and a small inertial defect value indicates that the trimer is planar. The structure is a compromise between the T-shaped structure of free acetylene dimer and the linear geometry of free OC-C2H2. A similar band for the fully deuterated isotopologue CO-(C2D2)2 confirms our assignment.

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Three new infrared bands of the He-OCS complex

Three new infrared bands of the weakly-bound He-OCS complex are studied, using tunable lasers to probe a pulsed supersonic slit jet expansion. They correspond to the (0400) <-- (0000), (1001)<-- (0000), and (0401) <-- (0000) transitions of OCS at 2105, 2918, and 2937 cm-1, respectively. The latter band is about 7900 times weaker than the previously studied OCS nu1 fundamental. Vibrational shifts relative to the free OCS monomer are found to be additive. Since carbonyl sulfide has previously been shown to be a valuable probe of superfluid quantum solvation effects in helium clusters and droplets, the present results could be useful for future studies of vibrational effects in such systems.

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A molecular superfluid: non-classical rotations in doped para-hydrogen clusters

Clusters of para-hydrogen (pH2) have been predicted to exhibit superfluid behavior, but direct observation of this phenomenon has been elusive. Combining experiments and theoretical simulations, we have determined the size evolution of the superfluid response of pH2 clusters doped with carbon dioxide (CO2). Reduction of the effective inertia is observed when the dopant is surrounded by the pH2 solvent. This marks the onset of molecular superfluidity in pH2. The fractional occupation of solvation rings around CO2 correlates with enhanced superfluid response for certain cluster sizes.

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