Abstract

Penning ionization electron spectra (PIES) and ultraviolet photoelectron spectra (UPS) have been measured for ultrathin (3–10 Å) bis(1,2-benzoquinonedioximato)platinum(II) (Pt(bqd) 2) films to investigate the molecular aggregation and electronic structure. Upon vapor deposition onto a cooled graphite (0 0 0 1) surface, Pt(bqd) 2 forms either of two films A and B with completely different spectra. The PIES of film A exhibits enhanced bands due to π and platinum 5d ⊥ (d xz , d yz or d z 2 )-derived MOs while that of film B is characterized by overwhelming bands due to oxygen nonbonding MOs, which indicates that the molecule lies flat in film A but the molecular short axis stands in film B. Moreover, the UPS features of film A do not correspond to those of film B and are essentially the same as those of an amorphous film prepared on a cooled metal surface. Nevertheless, films A and B afford almost the same features in both PIES and UPS when annealed to room temperature: the PIES become rather smooth to provide somewhat enhanced π and d ⊥-derived bands whereas the UPS obtain an increased number of distinct bands. From these observations, it is considered that the electronic structure of a Pt(bqd) 2 molecule is modified through the intermolecular interactions of the d ⊥-derived MOs, which operate differently depending on the molecular aggregation.

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