Recently, Lattelais et al. (2009) have interpreted aggregated observations of molecular isomers to suggest that there exists a minimum energy principle, such that molecular formation will favor more stable molecular isomers for thermodynamic reasons.
To test the predictive power of this principle, we have fully characterized the spectra of the three isomers of C$_{3}$H$_{2}$O toward the well known molecular region Sgr B2(N). Evidence for the detection of the isomers cyclopropenone (c-C$_{3}$H$_{2}$O) and propynal (HCCCHO) is presented, along with evidence for the non-detection of the lowest zero-point energy isomer, propadienone (CH$_2$CCO). We interpret these observations as evidence that chemical formation pathways, which may be under kinetic control, have a more pronounced effect on final isomer abundances than thermodynamic effects such as the minimum energy principle.
Pety et al. (2012) recently reported the detection of several transitions of an unknown carrier in the Horsehead PDR and attribute them to l-C3H+. Here, we have tested the predictive power of their fit by searching for, and identifying, the previousl
y unobserved J=1-0 and J=2-1 transitions of the unknown carrier (B11244) towards Sgr B2(N) in data from the publicly available PRIMOS project. Also presented here are observations of the J=6-5 and J=7-6 transitions towards Sgr B2(N) and Sgr B2(OH) using the Barry E. Turner Legacy Survey and results from the Kaifu et al. (2004) survey of TMC-1. We calculate an excitation temperature and column density of B11244 of ~10 K and ~10^13 cm-2 in Sgr B2(N) and ~79 K with an upper limit of < 1.5 x 10^13 cm-2 in Sgr B2(OH) and find trace evidence for the cations presence in TMC-1. Finally, we present spectra of the neutral species in both Sgr B2(N) and TMC-1, and comment on the robustness of the assignment of the detected signals to l-C3H+.
