We investigated the selective excitation of localized surface plasmons by structured light. We derive selection rules using group theory and propose a fitting integral to quantify the contribution of the eigenmodes to the absorption spectra. Based on the result we investigate three nano oligomers of different symmetry (trimer, quadrumer, and hexamer) in detail using finite-difference time-domain simulations. We show that by controlling the incident light polarization and phase pattern we are able to control the absorption and scattering spectra. Additionally, we demonstrate that the fitting between the incident light and the oligomer modes may favor a number of modes to oscillate. Dark modes produce strong changes in the absorption spectrum and bright modes in the scattering spectrum. The experimental precision (axial shift error) may be on the same order as the oligomer diameter making the orbital angular momentum selection rules robust enough for experimental observation
