Formation of N-bearing complex organic molecules in molecular clouds: Ketenimine, acetonitrile, acetaldimine, and vinylamine via the UV photolysis of CH ice
arXiv:2405.07855
Abstract
The solid-state CH chemistry in interstellar HO-rich ice has been proposed to explain astronomically observed complex organic molecules (COMs), including ketene (CHCO), acetaldehyde (CHCHO), and ethanol (CHCHOH), toward early star-forming regions. This formation mechanism is supported by recent laboratory studies and theoretical calculations for the reactions of CH+OH/H. However, the analog reaction of CH+NH forming N-bearing species has been suggested to have a relatively low rate constant that is orders of magnitude lower than the value of CH+OH. This work extends our previous laboratory studies on O-bearing COM formation to investigate the interactions between CH and NH ice triggered by cosmic ray-induced secondary UV photons under molecular cloud conditions. Experiments were performed in an ultra-high vacuum chamber to investigate the UV photolysis of the CH:NH ice mixture at 10 K. The studied ice chemistry of CH with NH radicals and H atoms resulting from the UV photodissociation of NH leads to the formation of several N-bearing COMs, including vinylamine (CHCHNH), acetaldimine (CHCHNH), acetonitrile (CHCN), ketenimine (CHCNH), and tentatively ethylamine (CHCHNH). The experimental results show an immediate and abundant CHCHNH yield as the first-generation product, which is further converted into other chemical derivatives. The effective destruction and formation cross-section values of parent species and COMs were derived, and we discuss the chemical links among these molecules and their astronomical relevance.
22 pages, 9 figures