Collisions between cold polar molecules represent a fascinating research frontier but have proven hard to probe experimentally. We report measurements of inelastic cross sections for collisions between nitric oxide (NO) and deuterated ammonia (ND) molecules at energies between 0.1 and 580 centimeter, with full quantum state resolution. At energies below the ~100-centimeter well depth of the interaction potential, we observed backward glories originating from peculiar U-turn trajectories. At energies below 0.2 centimeter, we observed a breakdown of the Langevin capture model, which we interpreted in terms of a suppressed mutual polarization during the collision, effectively switching off the molecular dipole moments. Scattering calculations based on an ab initio NO-ND potential energy surface revealed the crucial role of near-degenerate rotational levels with opposite parity in low-energy dipolar collisions.

Download full-text PDF

Source
http://dx.doi.org/10.1126/science.adf9836DOI Listing

Publication Analysis

Top Keywords

dipolar collisions
8
quantum state-resolved
4
state-resolved molecular
4
molecular dipolar
4
collisions
4
collisions decades
4
decades energy
4
energy collisions
4
collisions cold
4
cold polar
4

Similar Publications

Merging two molecular beams of ND3 up to the Liouville limit.

Rev Sci Instrum

September 2024

Radboud University Nijmegen, Institute for Molecules and Materials, Heijendaalseweg 135, 6525 AJ Nijmegen, The Netherlands.

In low-energy collisions between two dipolar molecules, the long-range dipole-dipole interaction plays an important role in the scattering dynamics. Merged beam configurations offer the lowest collision energies achievable, but they generally cannot be applied to most dipole-dipole systems as the electrodes used to merge one beam would deflect the other. This paper covers the design and implementation of a merged electrostatic guide whose geometry was numerically optimized for ND3-ND3 and ND3-NH3 collisions.

View Article and Find Full Text PDF

The ion trap mass spectrometer offers a unique advantage over other mass spectrometers by enabling multistage tandem mass spectrometry analysis with a single mass analyzer. It is employed to generate fragment ions through collision-induced dissociation (CID) usually by applying alternating current (AC) signals to a pair of electrodes for dipole excitation. The process of achieving double-stage tandem mass spectrometry analysis (MS/MS) in the mass spectrometer involves successive stages of injection, cooling, isolation, excitation, and scanning.

View Article and Find Full Text PDF

Purpose: Progress toward developing a novel radiocontrast agent for determining pO in tumors in a clinical setting is described. The imaging agent is designed for use with electron paramagnetic resonance imaging (EPRI), in which the collision of a paramagnetic probe molecule with molecular oxygen causes a spectroscopic change which can be calibrated to give the real oxygen concentration in the tumor tissue.

Procedures: The imaging agent is based on a nanoscaffold of aluminum hydroxide (boehmite) with sizes from 100 to 200 nm, paramagnetic probe molecule, and encapsulation with a gas permeable, thin (10-20 nm) polymer layer to separate the imaging agent and body environment while still allowing O to interact with the paramagnetic probe.

View Article and Find Full Text PDF

Ions stored in an electrodynamic ion trap can be forced from the center of the ion trap to regions of higher radio frequency (RF) electric fields by exposing them to a dipolar DC (DDC) potential applied across opposing electrodes. Such ions absorb power from the trapping RF field, resulting in increased ripple motion at the frequency of the trapping RF. When a bath gas is present, ions undergo energetic collisions that result in "RF-heating" sufficient to induce fragmentation.

View Article and Find Full Text PDF
Article Synopsis
  • A commercial quadrupole/time-of-flight mass spectrometer was modified to enhance its ability to study high mass ions (>100 kDa) by applying dipolar AC and DC voltages in its quadrupole arrays.
  • This modification facilitates advanced ion manipulation techniques, including resonance excitation for ion activation, selective isolation, and simultaneous storage of ions with opposite charges.
  • Performance evaluations using ions from nano-electrospray ionization showed the instrument could detect ions as large as 400,000 Da, although efficiency dropped significantly for ions above 250,000 Da due to detector and transfer limitations.
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!