Ultrafast x-rays from high harmonic generation make possible new studies in molecular dynamics, for example of dynamics induced by ionizing radiation. I discuss our work on dynamics in polyatomic molecules, and other recent results.OCIS codes: (020.0020)Atomic and molecular physics; (300.6530)Spectroscopy, Ultrafast; (320.7120)Ultrafast PhenomenaIn general, when a small molecule is ionized by a high-energy photon, a large amount of energy deposited into the system can lead to very rapid dissociation dynamics. However, despite its relevance, for example, to the fact that cosmic radiation levels influence Ozone levels in Earth's stratosphere,[1] studies of photoionization-induced molecular dynamics are rare because of the lack of appropriate experimental tools. Two key developments have changed this picture, making such studies now possible: 1) the development of femtosecond/attosecond sources of ionizing radiation employing the high harmonic generation (HHG) process; and 2) the development of sophisticated coincidence detection techniques that allow specific dissociation pathways to be identified in data. This has made possible in recent years a new area of study in radiation femtochemistry. [2,3] Some of our recent work has focused on understanding fundamental issues in energy redistribution in diatomic and triatomic systems following photoionization. In triatomic molecules, we have studied N 2 O[4] and O 3 using timeresolved attosecond XUV (43 eV) and femtosecond IR pump/probe spectroscopy in combination with COLTRIMS 3D coincidence momentum imaging. In ozone, by comparing the time-resolved O 3 and O 2 fragmentation yields and kinetic energy releases (KER), we find that triatomic molecules show a remarkable ability to efficiently store excess energy in internal vibrational motion, as opposed to seeing this energy in the KER of the Coulomb-exploding fragments. This contrasts strongly with the case of diatomic molecules, where the fragments are atoms and this is not possible. We have also found that it is possible to influence dissociation branching ratios by using strong laser fields during the fist few tens-of-fs following photoionization, both setting the timescale for this energy partition in rapidly-dissociating systems and providing a mechanism for further understanding.In these experiments, XUV light at hν=43 eV is well above the double ionization threshold of O 3 ( fig. 1a). Upon the ionization, an O 3 2+ ion Coulomb explodes through an O 2 + + O + fragmentation channel, releasing a kinetic energy that reflects an internuclear separation of an O-O bond at the instant of ionization (fig 1b). By using ion/electron coincidence 3D momentum imaging (COLTRIMS), we can selectively observe the O 2 + + O + fragmentation channel. Fig. 1c shows a photo-ion photo-ion coincidence (PIPICO) time-of-flight spectrum that reveals two dominant fragmentation channels (Coulomb exploding Ozone and residual Oxygen gases). Figure 2 shows time-resolved KER and yield spectra of O 3 and O 2 in a presence of relatively delayed XUV (f...