Probing the spatial and momentum distribution of confined surface states in a metal coordination network.

The Shockley surface state on Cu(111) reacts sensitively to the perturbation by molecular adsorbates on the surface. In the porous structure of a metal-coordinated molecular network on Cu(111), the surface state is confined to a series of discrete states. Energy and momentum of eigenstates in the pores are related to both the energy dispersion of the free surface state and the geometric and energetic details of the confining barrier formed by the molecular network. The penetration of the confined state into the barrier is found to be sensitive to the constituting architectural elements.

Controlling the dimensionality of on-surface coordination polymers via endo- or exoligation.

The formation of on-surface coordination polymers is controlled by the interplay of chemical reactivity and structure of the building blocks, as well as by the orientating role of the substrate registry. Beyond the predetermined patterns of structural assembly, the chemical reactivity of the reactants involved may provide alternative pathways in their aggregation. Organic molecules, which are transformed in a surface reaction, may be subsequently trapped via coordination of homo- or heterometal adatoms, which may also play a role in the molecular transformation. The amino-functionalized perylene derivative, 4,9-diaminoperylene quinone-3,10-diimine (DPDI), undergoes specific levels of dehydrogenation (-1 H2 or -3 H2) depending on the nature of the present adatoms (Fe, Co, Ni or Cu). In this way, the molecule is converted to an endo- or an exoligand, possessing a concave or convex arrangement of ligating atoms, which is decisive for the formation of either 1D or 2D coordination polymers.

Covalent assembly of a two-dimensional molecular "sponge" on a Cu(111) surface: confined electronic surface states in open and closed pores.

We present a new class of on-surface covalent reactions, formed between diborylene-3,4,9,10-tetraaminoperylene and trimesic acid on Cu(111), which gives rise to a porous 2D-'sponge'. This aperiodic network allowed the investigation of the dependence of electron confinement effects upon pore size, shape and even in partial confinement.

Magnetic exchange coupling of a synthetic Co(II)-complex to a ferromagnetic Ni substrate.

On-surface assembly of a spin-bearing and non-aromatic porphyrin-related synthetic Co(II)-complex on a ferromagnetic Ni thin film substrate and subsequent magnetic exchange interaction across the interface were studied by scanning tunnelling microscopy (STM), X-ray absorption spectroscopy (XAS), X-ray magnetic circular dichroism (XMCD) and density functional theory +U (DFT + U) calculations.

Chirality transfer in 1D self-assemblies: influence of H-bonding vs metal coordination between dicyano[7]helicene enantiomers.

Chiral recognition as well as chirality transfer in supramolecular self-assembly and on-surface coordination is studied for the enantiopure 6,13-dicyano[7]helicene building block. It is remarkable that, with this helical molecule, both H-bonded chains and metal-coordinated chains can be formed on the same substrate, thereby allowing for a direct comparison of the chain bonding motifs and their effects on the self-assembly in experiment and theory. Conformational flexure and both adsorbate/adsorbent and intermolecular interactions can be identified as factors influencing the chiral recognition at the binding site. The observed H-bonded chains are chiral, however, the overall appearance of Cu-coordinated chains is no longer chiral. The study was performed via scanning tunneling microscopy, X-ray-photoelectron spectroscopy and density functional theory calculations. We show a significant influence of the molecular flexibility and the type of bonding motif on the chirality transfer in the 1D self-assembly.

Ammonia coordination introducing a magnetic moment in an on-surface low-spin porphyrin.

Amazing ammonia: The molecular spin state of Ni(II) porphyrin, supported on a ferromagnetic Co surface, can be reversibly switched between spin-off (S = 0) and spin-on (S = 1) states upon coordination and decoordination of the gaseous ligand NH3, respectively (see picture). This finding clearly indicates the possible use of the system as a single-molecule-based magnetochemical sensor and in spintronics.

Two-dimensional supramolecular electron spin arrays.

A bottom-up approach is introduced to fabricate two-dimensional self-assembled layers of molecular spin-systems containing Mn and Fe ions arranged in a chessboard lattice. We demonstrate that the Mn and Fe spin states can be reversibly operated by their selective response to coordination/decoordination of volatile ligands like ammonia (NH3).