The linear triatomic [ZnBi2](4-) found in the diamagnetic K4ZnBi2 was prepared as the first discrete Zn-Bi Zintl cluster anion in the neat solid state from the unique K-Zn-Bi system. The tetraanionic trimer has sixteen valence electrons isovalent with CO2, accounting for its nearly linear triatomic structure (Zn-Bi-Zn, 177.3(3)°) and multiple Zn[double bond, length as m-dash]Bi bonds revealed by the unprecedentedly short bond length (2.553(3) Å) and DFT π-bonding analyses, on the basis of the established 16-electron counting rule for a linear triatomic species. The VASP theoretical calculations reveal that K4ZnBi2 is a narrow gap direct semiconductor that is expected to present promising optical properties.
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http://dx.doi.org/10.1039/c3dt53419g | DOI Listing |
J Phys Chem Lett
December 2024
Raymond and Beverly Sackler Faculty of Exact Sciences, School of Chemistry, Tel Aviv University, Tel Aviv 6997801, Israel.
The "l-Doubling" phenomenon emanates from the coupling between molecular rotations and perpendicular vibrations (bending modes) in polyatomic molecules. This elusive phenomenon has been largely discarded in laser-induced molecular alignment. Here we explore and unveil the ramifications of l-Doubling on the coherent rotational dynamics of linear triatomic molecules at ambient temperatures and above.
View Article and Find Full Text PDFMolecules
August 2024
Institute of Fundamental Physics (IFF-CSIC), CSIC, Serrano 123, 28006 Madrid, Spain.
We present a computational investigation on the structural arrangements and energetic stabilities of small-size protonated argon clusters, Ar nH +. Using high-level ab initio electronic structure computations, we determined that the linear symmetric triatomic ArH +Ar ion serves as the molecular core for all larger clusters studied. Through harmonic normal-mode analysis for clusters containing up to seven argon atoms, we observed that the proton-shared vibration shifts to lower frequencies, consistent with measurements in gas-phase IRPD and solid Ar-matrix isolation experiments.
View Article and Find Full Text PDFJ Chem Phys
September 2024
Department of Chemistry, School of Science, Tokyo Institute of Technology, 2-12-1, Ookayama, Meguro-ku, Tokyo 152-8550, Japan.
We report a quantum mechanical method for calculating the momentum distributions of constituent atoms of polyatomic molecules in rotational-vibrational eigenstates. Application of the present theory to triatomic molecules in the rovibrational ground state revealed that oscillatory changes appear on the proton momentum distribution in the nonlinear H2O molecule, while no such modulation is present in the case of an oxygen atom in the linear CO2 molecule. The atomic momentum distributions were analyzed in detail by means of a rigid rotor model, and it was found that the oscillation originates from the quantum-mechanical delocalization of the target atom with respect to the other atoms.
View Article and Find Full Text PDFPhys Chem Chem Phys
May 2024
Chemistry Department, Queen's University, Kingston, Ontario K7L 3N6, Canada.
In this paper, we propose a new two-step strategy for computing ro-vibrational energy levels and wavefunctions of a triatomic molecule and apply it to CO. A two-step method [J. Tennyson and B.
View Article and Find Full Text PDFJ Phys Chem A
April 2024
Hangzhou Institute of Advanced Studies, Zhejiang Normal University, 1108 Gengwen Road, Hangzhou 311231, Zhejiang, P. R. China.
The wavelength-dependent dynamics of the O(D) channel, formed by photoexcitation of CO to the Δ state at 143.53-153.03 nm, is investigated by using the time-sliced velocity-mapped ion imaging method.
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