We have observed images of MgI fragment ions produced in ultraviolet laser photodissociation of mass-selected MgICH ions at 266 nm. Split distribution almost perpendicular to the polarization direction of the photolysis laser was observed in the photofragment image. Potential energy curves of MgICH were obtained by theoretical calculations. Among these curves, the excited complex ion dissociated along almost repulsive potentials with several avoided crossings, which was connected to MgI + CH. In the ground state of MgICH, the CHI was bonded with Mg from the iodine side, and the Mg-I-C bond angle was calculated to be 101.1°. The theoretical results also indicated that the dissociation occurred after the 5A' ← 1A' photoexcitation, where the transition dipole moment was almost parallel to the Mg-I bond axis. The MgI and CH fragments dissociated each other parallel to the direction connecting those center-of-masses, which was 67° with respect to the transition dipole moment of 5A' ← 1A' photoexcitation. Therefore, the fragment recoil direction was assumed to approach perpendicular tendency against the polarization direction under the fast dissociation process. However, calculated potential energy curves showed a complicated reaction pathway for MgI production, including nonadiabatic processes, although the experimental results indicated the fast dissociation reaction.
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http://dx.doi.org/10.1021/acs.jpca.8b01944 | DOI Listing |
J Am Chem Soc
January 2025
School of Chemistry and Molecular Engineering, State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing Tech University, Nanjing 211816, China.
ArBO ( = 1-3) complexes have been prepared and subjected to spectroscopic characterization in the gas phase. Mass-selected infrared photodissociation spectroscopy, in combination with theoretical calculations, reveals the coexistence of two nearly isoenergetic structural isomers in ArBO. One isomer entails two equivalent Ar atoms chemically bound to BO, while the other features an ArBO core ion accompanied by a weakly tagging argon atom.
View Article and Find Full Text PDFJ Phys Chem A
September 2024
Sterling Chemistry Laboratory, Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States.
We demonstrate a method to determine the structures of the primary photodissociation products from a cryogenically cooled parent ion. In this approach, a target ion is cooled by a pulse of buffer gas and tagged in a 20 K Paul trap. The cold ion is then photodissociated by pulsed (∼5 ns) UV laser excitation, and the ionic products are trapped, cooled, and tagged by introduction of a second buffer gas pulse in the same trap.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2024
Institut für Optik und Atomare Physik, Technische Universität Berlin, Berlin 10623, Germany.
The low electronegativity of Si gives rise to a variety of nonconventional intermolecular interactions in clusters of silanes and their derivatives, which have not been well characterized yet. Herein, we characterize the structures of various isomers of bare and Ar-tagged SiHOHSiH dimers composed of protonated silanol and silane by infrared photodissociation (IRPD) of mass-selected ions and dispersion-corrected density functional calculations (B3LYP-D3/aug-cc-pVTZ). The analysis of the IRPD spectra recorded in the OH stretch range reveals the competition between two types of nonconventional hydrogen bonds (H-bonds).
View Article and Find Full Text PDFPhys Chem Chem Phys
August 2024
MOE Key Laboratory of Laser Life Science & Guangdong Provincial Key Laboratory of Laser Life Science, Guangzhou Key Laboratory of Spectral Analysis and Functional Probes, College of Biophotonics, South China Normal University, Guangzhou 510631, China.
Benzonitrile (BN, CHCN) has been detected in the cold molecular cloud Taurus molecular cloud-1 (TMC-1) in 2018, which is suggested to be a precursor in the formation of more complex nitrogen-containing aromatic interstellar compounds. In this study, we utilized mass-selected infrared (IR) photodissociation spectroscopy and quantum chemical calculations to investigate the structures and gaseous ion-molecule reactions of benzonitrile-ammonia (BN-NH) and benzonitrile-methylamine (BN-MA) clusters. The spectral observations indicate that the cyclic hydrogen bonding structure predominates in both neutral clusters.
View Article and Find Full Text PDFJ Phys Chem A
March 2024
School of Chemical Science and Engineering, Shanghai Key Laboratory of Chemical Assessment and Sustainability, Tongji University, 1239 Siping Road, Shanghai 200092, China.
The transition-metal-boron bonding interactions and geometric structures of heterodinuclear transition metal carbonyl cluster cations BM(CO) (M = Co, Ni, and Cu) are studied by a combination of the infrared photodissociation spectroscopy and density functional theory calculations at the B3LYP/def2-TZVP level. The BCu(CO) and BCo(CO) cations are characterized as an (CO)B-M(CO) structure involving an σ-type (OC)B → M(CO) dative bonding with end-on carbonyls, while for BNi(CO) complexes with a bridged carbonyl, a 3c-2e bond involving the 5σ electrons of the bridged carbonyl and an electron-sharing bond between the B(CO) fragment and the Ni(CO) subunits were revealed. Moreover, the fundamental driving force of the exclusive existence of a bridged carbonyl group in the boron-nickel complexes has been demonstrated to stem from the desire of the B and Ni centers for the favorable 8- and 18-electron structures.
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