Dysprosium-directed metallosupramolecular network on graphene/Ir(111) (CHEM. COMMUN. 2021)

The interest in exploiting the unique properties of lanthanides has led to the recent design of two-dimensional coordination networks incorporating f-block elements on metallic surfaces. In order to take this field to the next step of progression, it is necessary to electronically decouple these two-dimensional architectures from the metallic surface…

Continue reading

From high quality packing to disordered nucleation or phase separation in donor/acceptor interfaces: ClAlPc-C60 on Au(111) (PHYS. CHEM. CHEM. PHYS. 2021)

The dramatic consequences that the orientation adopted by the molecular dipoles, in diverse arrays of chloroaluminum phthalocyanine (ClAlPc) on Au(111), have on the ulterior adsorption and growth of C60 are explored by means of an all scanning probe microscopy approach. The unidirectional downwards organization of the molecular dipoles at the first…

Continue reading

Lanthanide-porphyrin species as Kondo irreversible switches through tip-induced coordination chemistry (NANOSCALE 2021)

Metallosupramolecular chemical protocols are applied to in situ design dysprosium porphyrin complexes on Au(111) by sequential deposition of 2H-4FTPP species and Dy, resulting in the production of premetallated Dy-2H-4FTPP, partially metallated Dy-1H-4FTPP and fully metallated Dy-0H-4FTPP complexes, as determined by scanning tunneling microscopy (STM) and density functional theory (DFT) calculations. A zero…

Continue reading

A Trapezoidal Octacyanoquinoid Acceptor Forms Solution and Surface Products by Antiparallel Shape Fitting with Conformational Dipole Momentum Switch (ANGEW. CHEM. 2021)

A new compound (1) formed by two antiparallelly disposed tetracyano thienoquinoidal units has been synthesized and studied by electrochemistry, UV/Vis-NIR, IR, EPR, and transient spectroscopy. Self-assembly of 1 on a Au(111) surface has been investigated by scanning tunneling microscopy. Experiments have been rationalized by quantum chemical calculations. 1 exhibits a…

Continue reading

Surfaces open new routes: unexpected formation of m-PANI oligomers from p-aminophenol (ANGEW. CHEM. 2020)

Surfaces never fail to surprise. Once more, they have demonstrated that chemistry on 2D metallic surfaces behaves differently to that on solution (3D). We have shown that highly unspecific solution-based Michael addition transforms into highly selective when carried out on a Pt(111) surface. In this way, we are able to…

Continue reading

Surface symmetry and reactivity rule the room-temperature adsorption of p-aminophenol (J. Phys. Chem. C 2020)

Molecular chemisorption on metal surfaces has attracted great interest over the past decades. Both the characteristics of the adsorbed molecules and the surface properties govern the chemisorption processes. We have studied the role of the nature and symmetry of different metallic surfaces, Cu(110), Cu(111) and Pt(111), on the room-temperature adsorption…

Continue reading

Inducing Intermolecular C-C Covalent Bonds between PAHs by Exposure to Atomic Hydrogen (JACS 2019)

The ESISNA group, in collaboration with the Nanotech@surfaces group from Empa (Switzerland), has demonstrated the catalytic role that atomic hydrogen can play in the formation of new intermolecular C-C covalent bonds on relatively inert surfaces. For this purpose, we have annealed a Au(111) surface, previously covered with different PAHs, in…

Continue reading

ESISNA at the «On-Surface Synthesis» international workshop 2018

On-surface synthesis is nowadays a promising and potential strategy for the development of novel nanomaterials. This approach allows not only to achieve materials of different dimensionalities such as 0D nanoobjects, 1D nanowires or even 2D networks for diverse applications but also the possibility to manipulate the molecules at the atomic…

Continue reading

On-surface chemistry: synthesis of azine derivatives with acceptor behaviour (Angew. Chem. 2018)

On-surface chemistry is a potential strategy focused on obtaining and developing novel nanomaterials of different dimensionalities with atomic precision. The growth mechanism is based on a bottom-up approach where molecular building blocks are evaporated onto a surface. Therefore, choosing the appropriate surface and precursor we are able to build and…

Continue reading

On-surface chemistry: (cyclo)dehydrogenation of PAH catalysed by coinage metal surfaces (Phys. Chem. Chem. Phys. 2017)

New nanoarchitectures can be built from polycyclic aromatic hydrocarbons (PAH) by exploiting the catalytic properties of some metal surfaces. Actually, this bottom-up approach allows the formation of nanostructures with different dimensionality from the same precursor as a consequence of the diffusion of the PAH on the surface. Thus, by selecting…

Continue reading