Singly and multiply charged molecular ions are found in diverse environments and hold relevance for a wide range of research areas like combustion chemistry, accelerator physics, atmospheric sciences, plasma physics, astrophysics etc. Molecular dications are of special significance as they can be generated and studied comparatively easily in laboratory experiments. And they have enabled exploration of new and exciting phenomenon such as hydrogen migration, inter-atomic Coulombic decay, plasmonic excitations, orbital tomography etc. The lifetime of a molecular dication is one of its fundamental characteristics, whose measurement contributes to strengthening ab initio calculations and in predicting the concentration of its dissociation products. Most of the already reported lifetimes of molecular dications are in the range of nanoseconds to seconds and metastable states with lifetimes of the order of picoseconds have only been theoretical predicted and an experimental verification is pending. We present a method of measuring subrotational lifetimes of molecular dications formed in three-body sequential breakup of polyatomic molecular precursors. Specifically, we have measured the subrotational lifetime of [Formula: see text] , which is formed as an intermediate in the three-body sequential fragmentation of [Formula: see text]. The lifetime against dissociation is determined to be a fraction of the rotational period of [Formula: see text] and is of the order of few picoseconds. The method proposed is general and is not restricted to triatomic precursors.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7679410PMC
http://dx.doi.org/10.1038/s41598-020-77408-0DOI Listing

Publication Analysis

Top Keywords

molecular dications
12
[formula text]
12
subrotational lifetime
8
lifetime molecular
8
molecular ions
8
lifetimes molecular
8
order picoseconds
8
three-body sequential
8
molecular
7
technique measurement
4

Similar Publications

The formation of following the double ionization of small organic compounds via a roaming mechanism, which involves the generation of H and subsequent proton abstraction, has recently garnered significant attention. Nonetheless, a cohesive model explaining trends in the yield of characterizing these unimolecular reactions is yet to be established. We report yield and femtosecond time-resolved measurements following the strong-field double ionization of CHX molecules, where X = OD, Cl, NCS, CN, SCN, and I.

View Article and Find Full Text PDF

Non vertical ionization-dissociation model for strong IR induced dissociation dynamics of [Formula: see text].

Sci Rep

January 2025

School of Physics and Information Technology, Shaanxi Normal University, Xi'an, 710062, Shaanxi, People's Republic of China.

Electron-nuclear coupling plays a crucial role in strong laser induced molecular dissociation dynamics. The interplay between electronic and nuclear degrees of freedom determines the pathways and outcomes of molecular fragmentation. However, a full quantum mechanical treatment of electron-nuclear dynamics is computationally intensive.

View Article and Find Full Text PDF

De Novo Design of Aminopropyl Quaternary Ammonium-Functionalized Covalent Organic Frameworks for Enhanced Polybenzimidazole Anion Exchange Membranes.

Small

January 2025

State Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, School of Chemical Engineering, Dalian University of Technology, Dalian, 116024, China.

Quaternary ammonium functionalized covalent organic frameworks (COFs) have great potential to enhance hydroxide transport owing to crystalline ordered 1D nanochannels, however, suffer from limited quaternary ammonium functional monomers and poor membrane-forming ability. In this work, a novel aminopropyl quaternary ammonium-functionalized COF (DCOF) is designed and synthesized via a bottom-up strategy. The self-supporting DCOF membrane exhibits high crystallinity with a dense and orderly arrangement of quaternary ammonium groups (IEC, 2.

View Article and Find Full Text PDF
Article Synopsis
  • - Glutathione (GSH) is an important tripeptide that protects cells from oxidative stress and removes toxic heavy metals, with the study focusing on its coordination with metals essential for biological redox processes: Zn, Cu, and Fe.
  • - Using infrared multiple photon dissociation (IRMPD) spectroscopy, researchers identified complexes formed between these metals and deprotonated GSH, revealing significant differences in metal coordination preferences based on experimental and theoretical vibrational spectra.
  • - The findings highlight common spectral features among the metal complexes while also indicating that the cysteine component of glutathione plays a crucial role in coordinating with these metals, which is relevant for understanding their biochemical functions.
View Article and Find Full Text PDF

Cyclo[4]pyrrole with - direct linkages.

Chem Sci

November 2024

Division of Applied Chemistry, Faculty of Engineering, Hokkaido University Kita 13, Nishi 8, Kita-ku Sapporo Hokkaido 060-8628 Japan

A cyclo[4]pyrrole bearing pyrrole C()-C() direct linkages, a contracted porphyrin analogue with no -carbon bridge, was synthesized from an oligoketone-related precursor. X-ray crystallography and StrainViz analysis revealed a non-planar structure with a total strain of 20.8 kcal mol.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!