Gas-phase-synthesized chromium-benzene 1:2 sandwich cation complexes [Cr+(benzene)(2)] were soft-landed on a self-assembled monolayer (SAM) of fluorinated alkanethiol (C10F-SAM) at a hyperthermal collision energy of similar to 20 eV. The adsorption properties and thermal stability of the soft-landed complexes were studied with infrared reflection absorption spectroscopy (IRAS) and temperature-programmed desorption (TPD). The landed complexes were neutralized due to charge transfer from the SAM substrate, but their native sandwich structure remained intact. The hyperthermal collision event resulted in the penetration of the incoming complexes into the C10F-SAM matrix. The embedded complexes then tended to orient their molecular axes approximately along the surface normal. This orientational preference is measurably different from that of complexes isolated in alkanethiol SAM matrices, a discrepancy that might be caused by a repulsive interaction between the pi cloud of the capping benzene rings of the complex and the side-chain CF2 groups of the fluorocarbon chains in the C10F-SAM matrix. The thermal desorption study showed that the complexes supported inside the C10F-SAM could resist thermal desorption until the high-temperature region of similar to 320 K, a persistence revealing a large desorption activation energy (similar to 190 kJ/mol).