We investigated the adsorption of three related cyano-functionalizedt etraphenyl porphyrin derivativeso n Cu(111)b ys canningt unneling microscopy (STM) in ultrahigh vacuum (UHV) with the goalt oi dentify the role of the cyano group and the central Cu atom for the intermolecular and supramolecular arrangement. The porphyrin derivatives studied were Cu-TCNPP,C u-cisDCNPP,a nd 2H-cisDCNPP,t hat is, Cu-5,10,15,20-tetrakis-(p-cyano)-phenylporphyrin, Cumeso-cis-di(p-cyano)-phenylporphyrin and 2H-meso-cis-di(pcyano)-phenylporphyrin, respectively.S tartingf rom different structures obtained after deposition at room temperature, all three molecules form the same long-range ordered hexagonal honeycomb-type structure with triangular pores and three molecules per unit cell. For the metal-free 2H-cisDCNPP,t his occurs only after self-metalation upon heating. The structure-forming elements are pores with ad istance of 3.1 nm, formed by triangles of porphyrins fused together by cyano-Cu-cyano interactions with Cu adatoms. This finding leads us to suggest that two cyano-phenyl groups in the "cis"p ositioni st he minimum prerequisite to form ah ighly ordered 2D porous molecular pattern.T he experimental findings are supported by detailed density functional theory calculations to analyze the driving forces that lead to the formation of the porous hexagonal honeycombtype structure.

We studied the adsorption and reaction behavior of the ionic liquid (IL) 1,3-dimethylimidazolium bis[(trifluoromethyl)sulfonyl]imide ([C1C1Im][Tf2N]) on Cu(111) using non-contact atomic force microscopy (nc-AFM), scanning tunneling microscopy (STM), and angle-resolved X-ray photoelectron spectroscopy (ARXPS) in ultrahigh vacuum as a function of temperature, supported by density-functional theory (DFT) calculations. Our nc-AFM results for sub-monolayer IL films show that at 200 K, the IL self-assembles into highly ordered islands, with cations and anions arranged next to each other in a checkerboard–type phase. After extended annealing at 300 K, the structure transforms first to a hexagonal phase and then to a porous honeycomb phase. Simultaneously, many small, disordered islands are formed. Complementary ARXPS reveals no IL desorption until 300 K. However, a significant fraction of the IL is converted to a new species as deduced from new, strongly shifted peaks that develop in the XP spectra at around 275 K and grow with annealing time at 300 K. We correlate the remaining unshifted peaks to the ordered phases observed in nc-AFM and the shifted peaks to decomposition products, which appear as disordered islands in nc-AFM and STM. Upon further heating to 360 K, about 50% of the anions or their decomposition products desorb from the surface, while cation-related fragments mostly remain on the surface. From DFT, we obtain additional information on the structure of the ordered phases and the interaction of the IL with the substrate.

We study the interaction and metalation reaction of a free base 5,10,15,20‐terakis(4‐cyanophenyl)porphyrin (2HTCNPP) with post‐deposited Zn atoms and the targeted reaction product Zn‐5,10,15,20‐terakis(4‐cyanophenyl)porphyrin (ZnTCNPP) on a Ag(111) surface. The investigations are performed with scanning tunneling microscopy at room temperature after Zn deposition and subsequent heating. The goal is to obtain further insights in the metalation reaction and the influence of the cyanogroups on this reaction. The interaction of 2HTCNPP with post‐deposited Zn leads to the formation of three different 2D ordered island types that coexist on the surface. All contain a new species with a bright appearance, which increases with the amount of post‐deposited Zn. We attribute this to metastable SAT (“sitting atop”) complexes formed by Zn and the macrocycle, that is, an intermediate in the metalation reaction to ZnTCNPP, which occurs upon heating to 500 K. Interestingly, the activation barrier for the successive reaction of the SAT complex to the metalated ZnTCNPP species can also be overcome by a voltage pulse applied to the STM tip.

We investigated the adsorption of 2H-5,10,15,20-tetracyanophenyl-tetrabenzoporphyrin (2H-TCNPTBP) molecules on Cu(111) by scanning tunneling microscopy in ultrahigh vacuum at room temperature. Three types of network structures are observed to coexist on the surface. The first two, a porous Kagome lattice and a porous quadratic structure, are stabilized by cyano–Cu–cyano bonds with Cu adatoms; the third is a close-packed hexagonal network, with much weaker intermolecular H-bonds and dipole–dipole interactions of oppositely oriented cyano end groups. The coexistence of the three structures is attributed to very similar energetics. While the two metal-coordinated porous structures with identical molecular density are stabilized by the energy gain due to the network formation, the hexagonal network compensates the weaker intermolecular interactions by a factor of 2.3 higher molecular density; furthermore, kinetic stabilization might play a role. Our results show that cyano functionalization of benzoporphyrins gives rise to unusual two-dimensional self-assembled lattice structures.

The adsorption behavior and the mobility of 2H‐Tetranaphthylporphyrin (2HTNP) on Cu(111) was investigated by scanning tunneling microscopy (STM) at room temperature (RT). The molecules adsorb, like the structurally related 2HTPP, in the “inverted” structure with the naphthyl plane restricted to an orientation parallel to the Cu surface. The orientation of the four naphthyl groups yields altogether 16 possible conformations. Due to the existence of rotamer pairs, 10 different appearances are expected on the surface, and all of them are identified by STM at RT. Most interestingly, the orientation of the naphthyl groups significantly influences the diffusion behavior of the molecules on Cu(111). We identify three different groups of conformers, which are either immobile, medium or fast diffusing at RT. The mobility seems to decrease with increasing size of the footprint of the conformers on the surface.

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We investigated the adsorption behavior of a mixture of six 2H‐tetrakis‐(3, 5‐di‐tert‐butylphenyl)(x)benzoporphyrins (2H‐diTTBP(x)BPs, x=0, 1, 2‐cis, 2‐trans, 3, and 4) on Ag(111), Cu(111) and Cu(110) at room temperature by scanning tunneling microscopy (STM) under ultra‐high vacuum conditions. On Ag(111), we observe an ordered two‐dimensional square phase, which is stable up to 400 K. On Cu(111), the same square phase coexists with a stripe phase, which disappears at 400 K. In contrast, on Cu(110), 2H‐diTTBP(x)BPs adsorb as immobile isolated molecules or dispersed short chains along the [1 0] substrate direction, which remain intact up to 450 K. The stabilization of the 2D supramolecular structures on Ag(111) and Cu(111), and of the 1D short chains on Cu(110) is attributed to van der Waals interactions between the tert‐butyl and phenyl groups of neighboring molecules. From high‐resolution STM, we can assign all six 2H‐diTTBP(x)BPs within the ordered structures. Moreover, we deduce a crown shape quadratic conformation on Ag(111) and Cu(111), an additional saddle‐shape on Cu(111), and an inverted structure and a quadratic appearance on Cu(110). The different conformations are attributed to the different degree of interaction of the iminic nitrogen atoms of the isoindole and pyrrole groups with the substrate atoms.

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