Conformational change is an important concept in chemistry and physics. In the present work, we study conformations of formic acid (HCOOH, FA) and report the preparation and identification of the complex of the higher-energy conformer cis-PA with N-2 in an argon matrix. The cis-F center dot center dot center dot N-2 complex was synthesized by combining annealing and vibrational excitation of the ground-state trans-FA in a FA/N-2/Ar matrix. The assignment is based on IR spectroscopic measurements and ab initio calculations. The cis-FA center dot center dot center dot N-2 complex decay in an argon matrix is much slower compared with the cis-FA monomer. In agreement with the experimental observations, the calculations predict a substantial increase in the stabilization barrier for the cis-FA center dot center dot center dot N-2 complex compared with the uncomplexed cis-FA monomer. A number of solvation effects in an argon matrix are computationally estimated and discussed. The present results on the cis-FA center dot center dot center dot N-2 complex show that intermolecular interaction can stabilize intrinsically unstable conformers, as previously found for some other cis-FA complexes.