Hexapole-Oriented Asymmetric-Top Molecules and Their Stereodirectional Photodissociation Dynamics

TL;DR

This study demonstrates the first successful orientation of a complex asymmetric-top molecule, 2-bromobutane, using a hexapolar electric filter combined with a homogeneous field, and explores its photodissociation dynamics.

Contribution

It introduces a novel method for orienting complex asymmetric-top molecules with heavy atoms, enabling detailed stereodirected photodissociation studies.

Findings

Successful orientation of 2-bromobutane achieved

New velocity and angular distribution features observed

Enhanced understanding of photodissociation dynamics

Abstract

Molecular orientation is a fundamental requisite in the study of stereodirected dynamics of collisional and photoinitiated processes. In this last decade, variable hexapolar electric filters have been developed and employed for the rotational-state selection and the alignment of molecules of increasing complexity, for which main difficulties are their mass, their low symmetry and the very dense rotational manifold. In this work, for the first time, a complex molecule such as 2-bromobutane, an asymmetric-top containing a heavy atom (the bromine), has been successfully oriented by a weak homogeneous field placed downstream the hexapolar filter. Efficiency of the orientation has been characterized experimentally, by combining time-of-flight measurements and a slice-ion-imaging detection technique. The application is described to the photodissociation dynamics of the oriented 2-bromobutane, which was carried out at a laser wavelength of 234 nm, corresponding to the breaking of the C Br bond. The Br photofragment is produced in both the ground Br (2P3/2) and the excited Br (2P1/2) electronic states and both channels are studied by the slice imaging technique, revealing new features in the velocity and angular distributions with respect to previous investigations on non-oriented molecules.