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We investigated the electronic structures of the 5 Ruddlesden-Popper series SrIrO (=1, 2, and ) using optical spectroscopy and first-principles calculations. As 5 orbitals are spatially more extended than 3 or 4 orbitals, it has been widely accepted that correlation effects are minimal in 5 compounds. However, we observed a bandwidth-controlled transition from a Mott insulator to a metal as we increased . In addition, the artificially synthesized perovskite SrIrO showed a very large mass enhancement of about 6, indicating that it was in a correlated metallic state.

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