The unusual quadruple bonding of nitrogen in ThN.

Nitrogen has five valence electrons and can form a maximum of three shared electron-pair bonds to complete its octet, which suggests that its maximum bond order is three. With a joint anion photoelectron spectroscopy and quantum chemistry investigation, we report herein that nitrogen presents a quadruple bonding interaction with thorium in ThN. The quadruple Th≣N bond consists of two electron-sharing Th-N π bonds formed between the Th-6dxz/6dyz and N 2px/2py orbitals, one dative Th←N σ bond and one weak Th←N σ bonding interaction formed between Th-6dz2 and N 2s/2pz orbitals. The ThC molecule has also been investigated and proven to have a similar bonding pattern as ThN. Nonetheless, due to one singly occupied σ-bond, ThC is assigned a bond order of 3.5. Moreover, ThC has a longer bond length as well as a lower vibrational frequency in comparison with ThN.

The additional nitrogen atom breaks the uranyl structure: a combined photoelectron spectroscopy and theoretical study of NUO2.

We report a joint photoelectron spectroscopic and relativistic quantum chemistry study on gaseous NUO2-. The electron affinity (EA) of the neutral NUO2 molecule is reported for the first time with a value of 2.602(28) eV. The U-O and U-N stretching vibrational modes for the ground state and the first excited state are observed for NUO2. The geometric and electronic structures of both the anions and the corresponding neutrals are investigated by relativistic quantum chemistry calculations to interpret the photoelectron spectra and to provide insights into the nature of the chemical bonding. Both the ground state of the anion and neutral are calculated to be planar structures with C2v symmetry. Unlike the "T"-shape structure of UO3 which has a quasi-linear O-U-O angle, both the ground-state geometries of the anion and neutral have O-U-O bond angles of around 90°. The significant contraction of the O-U-O bond angle indicates the strong interaction between the U and N atoms compared with the "additional" oxygen in UO3. The chemical bonding calculation indicates that multiple bonding of U(VI) can occur in NUO2- and NUO2, and the UVI-N bond is significantly more covalent than the U-O bond. The current experimental and theoretical results reveal the difference between the U-N and U-O bond in the unified molecular system, and expand our understanding of the bonding capacities of actinide elements with the nitrogen atom.

Probing the electronic structure and Au-C bonding in AuC2nH (n = 4-7) using photoelectron imaging spectroscopy and quantum chemical calculations.

We report a combined experimental and theoretical study on the structures and chemical bonding of AuC2nH (n = 4-7) using photoelectron imaging and quantum chemical calculations. All the ground states of anions and neutral AuC2nH have a linear geometry. The electron affinities (EAs) are measured to be 2.063(5), 2.157(5), 2.220(5), and 2.267(5) eV for AuC2nH, n = 4-7, respectively. The photoelectron imaging data of AuC8H- and AuC10H- reveal major vibrational progressions in the Au-C stretching modes. The ground state stretching frequencies of the titled neutral molecules are 226, 193, 177, and 128 cm-1, respectively. By comparing the experimental ß value and theoretical molecular orbital analysis, we confirm that the CAM-B3LYP method is more suitable for describing the properties of such unsaturated long chains organogold clusters. The experimental and CAM-B3LYP methods give a big picture of the trend in EAs of AuC2nH. This shows that the EA value becomes larger with an increase in the carbon chain length, and it also shows a slow increment for larger n. The NRT analysis shows that the change of the Au-C bond order is not obvious as the number of carbon atoms increases, and the covalent character dominates the Au-C chemical bonds in these neutral species. The current study provides a wealth of electronic structure information about long-chain AuC2nH- (n = 4-7) and their corresponding neutral counterparts.

A combined photoelectron-imaging spectroscopic and theoretical investigation on the electronic structure of the VO2H anion.

The electronic structure and vibrational spectrum of the VO2H anion are explored by combining photoelectron imaging spectroscopy and density functional theoretical (DFT) calculations. The electron affinity (EA) of VO2H is determined to be 1.304 ± 0.030 eV from the vibrationally resolved photoelectron spectrum acquired at 1.52 eV (814 nm). The anisotropy parameter (ß) for the EA defined peak is measured to be 1.63 ± 0.10, indicating that it is the 17a' (4s orbital of the vanadium atom) electron attachment leading to the formation of the ground state of the VO2H anion. The vibrational fundamentals ν 1, ν 3, ν 4 and ν 5 are obtained for the neutral ground state. Experimental assignments are confirmed by energies from electronic structure calculations and Franck-Condon (FC) spectral simulations. These simulations support assigning the anion ground state as the results obtained from the B3LYP method. In addition, the molecular orbitals and bonding involved in the anionic VO2H cluster are also examined based on the present theoretical calculations.

Probing the Hydrogen Bonding in Microsolvated Clusters of Au1,2-(Solv)n (Solv = C2H5OH, n-C3H7OH; n = 1-3 for Au-; n =1 for Au2-).

The microsolvation of gold anions in different alcohol solvents is demonstrated by the combination of anion photoelectron spectroscopy and quantum chemical calculations on the Au1,2-(Solv)n (Solv = C2H5OH, n-C3H7OH; n = 1-3 for Au-; n = 1 for Au2-). The microsolvation structures of these clusters and their corresponding neutrals are assigned by comparing calculations with experiments. In terms of overall regularity, the increasing solvation number (n) and carbon chain extension both can increase the stability of the anion. When n ≥ 2, these clusters have low-energy isomers, where conventional hydrogen bonds (HBs) compete with nonconventional HBs (NHBs). NHBs are dominant when n ≤ 2 and when n is increased, vice versa. Interestingly, a variety of theoretical calculations show that after the hydroxy H atom of the ethanol molecule forms a weak ionic HB with Au-, there are two lowest conformations of ethanol, trans and gauche, which could be coexisting in the molecular beams. Some theoretical methods also suggest that the gauche isomer is more stable than the trans one, which indicates that Au- may exist as a gold gauche effect similar to fluorine.

Candidate for Laser Cooling of a Negative Ion: High-Resolution Photoelectron Imaging of Th

Laser cooling is a well-established technique for the creation of ensembles of ultracold neutral atoms or positive ions. This ability has opened many exciting new research fields over the past 40 years. However, no negatively charged ions have been directly laser cooled because a cycling transition is very rare in atomic anions. Efforts of more than a decade currently have La^{-} as the most promising candidate. We report on experimental and theoretical studies supporting Th^{-} as a new promising candidate for laser cooling. The measured and calculated electron affinities of Th are, respectively, 4901.35(48) cm^{-1} and 4832 cm^{-1}, or 0.607 690(60) and 0.599 eV, almost a factor of 2 larger than the previous theoretical value of 0.368 eV. The ground state of Th^{-} is determined to be 6d^{3}7s^{2} ^{4}F_{3/2}^{e} rather than 6d^{2}7s^{2}7p ^{4}G_{5/2}^{o}. The consequence of this is that there are several strong electric dipole transitions between the bound levels arising from configurations 6d^{3}7s^{2} and 6d^{2}7s^{2}7p in Th^{-}. The potential laser-cooling transition is ^{2}S_{1/2}^{o}↔^{4}F_{3/2}^{e} with a wavelength of 2.6 µm. The zero nuclear spin and hence lack of hyperfine structure in Th^{-} reduces the potential complications in laser cooling as encountered in La^{-}, making Th^{-} a new and exciting candidate for laser cooling.

Probing Chemical Bonding and Electronic Structures in ThO- by Anion Photoelectron Imaging and Theoretical Calculations.

Because of renewed research on thorium-based molten salt reactors, there is growing demand and interest in enhancing the knowledge of thorium chemistry both experimentally and theoretically. Compared with uranium, thorium has few chemical studies reported up to the present. Here we report the vibrationally resolved photoelectron imaging of the thorium monoxide anion. The electron affinity of ThO is first reported to be 0.707 ± 0.020 eV. Vibrational frequencies of the ThO molecule and its anion are determined from Franck-Condon simulation. Spectroscopic evidence is obtained for the two-electron transition in ThO-, indicating the strong electron correlation among the (7sσ)2(6dδ)1 electrons in ThO- and the (7sσ)2 electrons in ThO. These findings are explained by using quantum-chemical calculations including spin-orbit coupling, and the chemical bonding of gaseous ThO molecules is analyzed. The present work will enrich our understanding of bonding capacities with the 6d valence shell.