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Metal-tetraphenyl-porphyrin (M-TPP) molecules typically self-assemble forming square-like superlattices, as dictated by their shape. The dependence of the adsorption properties on the central atom is systematically studied for Co-, Ni-, and Zn-TPP adsorbed on oxygen passivated Fe(001), namely the Fe(001)-p(1 x 1)O surface. It is found by low energy electron diffraction (LEED) and scanning tunneling microscopy (STM) that despite the weak molecule-substrate interaction, preserving many features of quasi-free molecules, the self-assembled structure switches from the (5 x 5)R37 degrees superlattice of Co-TPP and Ni-TPP to the plain (5 x 5) of Zn-TPP. Ab initio calculations based on density functional theory (DFT) are used to investigate the adsorption properties of the different molecules and the possible overlayers formed. Adsorption energies, structures, and electronic properties are reported, discussing the bonding mechanisms and the magnetic character. Only moderate energy differences are found, suggesting that subtle effects may steer the selection of the structure among overlayers with similar properties although differing substantially as for the LEED and STM experimental results.

Metal-tetraphenyl-porphyrin (M-TPP) molecules typically self-assemble forming square-like superlattices, as dictated by their shape. The dependence of the adsorption properties on the central atom is systematically studied for Co-, Ni-, and Zn-TPP adsorbed on oxygen passivated Fe(001), namely the Fe(001)- p (1 × 1) O surface. It is found by low energy electron diffraction (LEED) and scanning tunneling microscopy (STM) that despite the weak molecule–substrate interaction, preserving many features of quasi-free molecules, the self-assembled structure switches from the (5 × 5) R 37 ° superlattice of Co-TPP and Ni-TPP to the plain (5 × 5) of Zn-TPP. Ab initio calculations based on density functional theory (DFT) are used to investigate the adsorption properties of the different molecules and the possible overlayers formed. Adsorption energies, structures, and electronic properties are reported, discussing the bonding mechanisms and the magnetic character. Only moderate energy differences are found, suggesting that subtle effects may steer the selection of the structure among overlayers with similar properties although differing substantially as for the LEED and STM experimental results.

In this study, we provided the detailed characterizations of our recent HRP-AuNPs/PEDOT:BSA/Pt biosensor, constructed through a simple fabrication procedure with improved stability and good sensitivity. Raman and Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy not only confirmed the synthesis of conductive PEDOT where BSA was the template for the polymerization, but also provided further insights into the stable immobilization of AuNP on the PEDOT:BSA film. Scanning electron microscopy revealed that the attachment of AuNPs were stable under a high salt environment. The current technology demonstrates a feasible procedure to form a functional AuNPs/PEDOT:BSA film that has potential applications in the fabrication of various biosensors and electric devices.

Encoding and manipulating information through the spin degrees of freedom of individual magnetic molecules or atoms is one of the central challenges in the continuing trend towards molecular/atomic scale electronics. With their large magnetic moment and long spin relaxation time, single-molecule magnets (SMMs) are of special importance in this emerging field. Their electrical addressing at the molecular level appears now well within reach using STM methods, which require to organize SMMs on a conducting surface. In this chapter, we present a critical overview of the latest achievements in the deposition of SMMs as monolayers or submonolayers on native or prefunctionalized surfaces. Special emphasis is placed on the selection and design of molecular structures that withstand solution or vapour-phase processing and that maintain their magnetic functionality on a surface. Chemical strategies to control the strength of molecule–substrate interaction and the molecular orientation on the surface are also illustrated. Rewardingly, these efforts have shown that the distinctive properties of SMMs, i.e. slow spin relaxation and quantum tunnelling of the magnetic moment, persist in metal-wired molecules.

The old concept of complementarity, connected with the process of molecular recognition represents a simple approach to understanding molecular assembling. The noncovalent interactions governing (self)assemblies are fundamental to supramolecular chemistry and crystal engineering. Among noncovalent interactions governing molecular assembling, hydrogen bonding plays the leading role. A few examples of molecular assembling relevant to life processes and (bio)nano materials reveal the importance of this phenomenon. Systematic analysis of hydrogen bonding patterns, as a function of proton donor and acceptor properties, and stereochemical parameters, including chirality, is presented for a large number of di(amino acid) and di(amino alcohol) derivatives with oxalyl, phthaloyl, and fumaroyl bridges. Particular attention will be given to the molecular topology of such hydrogen bonded assemblies in terms of crystal engineering.