Abstract
The multi-photon dissociation and Coulomb explosion of ethyl bromide C2H5Br under near-infrared (800 nm) femtosecond laser field are experimentally investigated by a DC-sliced ion imaging technique. The sliced images of fragment ions C2H5+, Br+, CH3+, CH2Br+, H2+ and C2H3Br+ are obtained, and their dissociative pathways are assigned by observing their corresponding kinetic energy release (KER) and angular distribution. It is shown that low-KER components of these fragment ions result from multi-photon dissociation of singly charged parent ion C2H5Br+, while high-KER components come from Coulomb explosion of doubly charged parent ion C2H5Br2+. It is also shown that the precursor species [C2H5+...Br+] has a longer lifetime than [C2H3Br+...H2+] and [CH3...CH2Br+]. In addition, the probable H2 and H2+ elimination channels are theoretically simulated by Gaussian 09 software packages, and the results show that the former is an asynchronous process while the latter is a synchronous process.
| Original language | English |
|---|---|
| Pages (from-to) | 37078-37084 |
| Number of pages | 7 |
| Journal | RSC Advances |
| Volume | 5 |
| Issue number | 46 |
| DOIs | |
| State | Published - 2015 |