Adsorbed structures of naphthalene on Cu(111) have been studied using low temperature scanning tunneling microscope (LT-STM) and low energy electron diffraction (LEED). Starting from single molecules, three kinds of long-range ordered superstructures, ( 5 3 × 5 3)R30°, (2 3 × 3)rect-1C 10 H 8 , and ( -4 1 1 -4 ) are observed depending on the molecular concentrations and the substrate temperatures during molecular adsorption.One of the self-assembled ordered phases with a (5 3 × 5 3) R30°periodicity is chiral in adsorptioninduced arrangement though a single naphthalene molecule itself has no inherent chirality. In STM images, isolated single molecules appear as depressions whereas the molecules are seen as protrusions in self-assembled layers. Coverage dependent two-photon photoemission (2PPE) spectra show that the adsorption-induced occupied states is formed at around Cu 3d bands, and this results in the enhanced tunneling of occupied state images in assembled layers.

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A mixture of 2,2,6,6-tetramethyl-1-piperidinyloxyl (TEMPO) radical and 2,2,6,6-tetramethyl-1-piperidine (TEMP) was included into organic 1-D nanochannels of tris(o-phenylenedioxy)cyclotriphosphazene (TPP) crystal. Dilution of the paramagnetic TEMPO radical was achieved with excess TEMP, thereby isolating a TEMPO molecule in the nanochannel. For inclusion compounds of TPP with TEMPO and TEMP (TEMPO/all guest compounds = 0.017, and 0.15), temperature-dependent electron spin resonance (ESR) spectra were observed to investigate their molecular dynamics and orientation. In the temperature range from 112 K to room temperature, the spectra depended remarkably on the temperature. Temperature dependence was well interpreted by uniaxial rotation, suggesting that TEMPO molecules undergo uniaxial rotation about a channel axis with a molecular orientation in which the N-O bond in the nitroxide group is perpendicular to the channel axis. The activation energy of uniaxial rotation was evaluated as 4.5 +/- 0.3 kJ mol(-1).

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