A combination of normal-incidence x-ray standing-wave ͑NIXSW͒ spectroscopy, x-ray photoelectron spectroscopy ͑XPS͒, scanning tunneling microscopy ͑STM͒, and density-functional theory ͑DFT͒ has been used to investigate the interaction of a number of phthalocyanine molecules ͑specifically, SnPc, PbPc, and CoPc͒ with the Ag͑111͒ surface. The metal-surface distances predicted by the DFT calculations for SnPc/Ag͑111͒ ͑2.48 Å͒ and CoPc/Ag͑111͒ ͑2.88 Å͒ are in good agreement with our NIXSW experimental results for these systems ͑2.31Ϯ 0.09 and 2.90Ϯ 0.05 Å, respectively͒. Good agreement is also found between calculated partial density-of-states plots and STM images of CoPc on Ag͑111͒. Although the DFT and Pb 4f NIXSW results for the Pb-Ag͑111͒ distance are similarly in apparently good agreement, the Pb 4f core-level data suggest that a chemical reaction between PbPc and Ag͑111͒ occurs due to the annealing procedure used in our experiments and that the similarity of the DFT and Pb 4f NIXSW values for the Pb-Ag͑111͒ distance is likely to be fortuitous. We interpret the Pb 4f XPS data as indicating that the Pb atom can detach from the PbPc molecule when it is adsorbed in the "Pb-down" position, leading to the formation of a Pb-Ag alloy and the concomitant reduction in Pb from a Pb 2+ state ͑in bulklike films of PbPc͒ to Pb 0 . In contrast to SnPc, neither PbPc nor CoPc forms a well-ordered monolayer on Ag͑111͒ via the deposition and annealing procedures we have used. Our DFT calculations show that each of the phthalocyanine molecules donate charge to the silver surface, and that back donation from Ag to the metal atom ͑Co, Sn, or Pb͒ is only significant for CoPc.