One of the main goals of molecular electronics is to achieve electronic functions from devices consisting of tailored organic molecules connecting two metal electrodes. The fabrication of nanometre-scale spaced electrodes still results in expensive, and often scarcely reproducible, devices. On the other hand, the 'conductance' of long organic molecules--generally dominated by the tunnelling mechanism--is very poor. Here, we show that by incorporating a large number of metal centres into rigid molecular backbones we can obtain very long (up to 40 nm) and highly 'conductive' molecular wires. The metal-centre molecular wires are assembled in situ on metal surfaces via a sequential stepwise coordination of metal ions by terpyridine-based ligands. They form highly ordered molecular films of elevated mechanical robustness. The electrical properties, characterized by a junction based on Hg electrodes, indicate that the 'conductance' of these metal-centre molecular wires does not decrease significantly even for very long molecular wires, and depends on the nature of the incorporated redox centre. The outstanding electrical and mechanical characteristics of these easy-to-assemble molecular systems open the door to a new generation of molecular wires, able to bridge large-gap electrodes, and to form robust films for organic electronics.

Protein adsorption plays a key role in the biological response to implants. We report how nanoscale topography, chemistry, crystallinity, and molecular chain anisotropy of ultrahigh molecular weight polyethylene (UHMWPE) surfaces affect the protein assembly and induce lateral orientational order. We applied ultraflat, melt drawn UHMWPE films to show that highly oriented nanocrystalline lamellae influence the conformation and aggregation into network structures of human plasma fibrinogen by atomic force microscopy with unprecedented clarity and molecular resolution. We observed a transition from random protein orientation at low concentrations to an assembly guided by the UHMWPE surface nanotopography at a close to full surface coverage on hydrophobic melt drawn UHMWPE. This assembly differs from the arrangement at a hydrophobic, on the nanoscale smooth UHMWPE reference. On plasma-modified, hydrophilic melt drawn UHMWPE surfaces that retained their original nanotopography, the influence of the nanoscale surface pattern on the protein adsorption is lost. A model based on protein-surface and protein-protein interactions is proposed. We suggest these nanostructured polymer films to be versatile model surfaces to provide unique information on protein interactions with nanoscale building blocks of implants, such as nanocrystalline UHMWPE lamellae. The current study contributes to the understanding of molecular processes at polymer biointerfaces and may support their future design and molecular scale tailoring.

No abstract

Methyl isobutyrate is plasma‐polymerized varying the precursor flow rate (Φp), the working pressure (p) and the radiofrequency power injected in the discharge (PRF). Through the use of an experimental design, PRF reveals to be the key parameter regarding the incorporation of oxygen‐based functionalities in the plasma polymer films (PPFs). Combining the use of X‐ray photoelectron spectroscopy (XPS), time‐of‐flight secondary ion mass spectrometry (ToF‐SIMS) and principal component analysis (PCA), our results demonstrate that an increase of PRF (i) lowers the incorporation of the precursor ester groups within the PPFs and (ii) amplifies the PPF crosslinking density (χ). A correlation between the PPF physico‐chemistry and the plasma composition is established using residual gas analysis mass spectrometry. It is shown that an increase of PRF increases both the extent of the precursor fragmentation and the production of non‐reactive oxygen‐based species in the plasma that do not contribute to the PPF growth. Incidentally, in the PRF range studied, the total amount of oxygen‐based functionalities incorporated in the PPFs (at.%O) varies from 23.9 to 10.1 at.%.

A strategy for creating a general-purposes surface functionalization platform is reported, based on direct attachment of phosphate groups onto hydroxylated surfaces and subsequent formation of a terpyridine-based monolayer. Such a platform is suitable for the construction, onto technologically relevant oxide surfaces, of single- and multilayer structures of interest in technological applications. In particular, the paper describes the successful attachment of 4-(2,2':6',2''-terpyridine-4-yl)benzenephosphonic acid (1, PPTP) onto a SiO(2) surface previously functionalized by means of Zr-phosphate groups. Two alternative anchoring strategies of the PPTP were explored: (i) a direct one-step way, implying no protection of terpyridinic functionality, and (ii) a three-step way, implying protection and successive deprotection of this group. It was found that, in the first case, the PPTP ligand anchoring to the Zr-containing phosphate layer takes place by means of terpyridinic group. At variance of this, in the second case, due to the protection of the terpyridinic functionality, the anchoring process takes place through the phosphonic group, making the terpyridinic moiety available for further reactions, i.e., multilayer constructs. X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS) were used to study the functionalized surfaces, providing information on coverage, chemical structure, and stoichiometry of the various functionalized layers and, among the others, clear evidence of the PPTP linkage and orientation.