We report the crystallization of a subsitutionally doped organic conductor based on a host lattice composed of spiro-bis(phenalenyl)boron radicals. Co-crystallization of solutions of spiro-bis(9-oxidophenalenone)boron radical [PLY(O,O)](2)B mixed with selected amounts of spiro-bis(9-oxidophenalenone)beryllium [PLY(O,O)](2)Be leads to the formation of a series of solid-state solutions of composition [PLY(O,O)](2)B(1-x)Bex. The dopant molecules [PLY(O,O)](2)Be serve to introduce holes into the lattice of spins provided by the [PLY(O,O)](2)B radicals and lead to a systematic increase in the conductivity while decreasing the activation energy of the conduction process and leaving the solid-state structure relatively unperturbed. While the energies of the hole sites are expected to be high, the results are consistent with the interpretation of the electronic structure of [PLY(O,O)](2)B in terms of the resonating valence bond model.