Mohamed El Garah
University of Strasbourg
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Mohamed El Garah.
ACS Nano | 2014
Marco Di Giovannantonio; Mohamed El Garah; Josh Lipton-Duffin; Vincent Meunier; Luis Cardenas; Yannick Fagot Revurat; Albano Cossaro; Alberto Verdini; Dmitrii F. Perepichka; Federico Rosei; G. Contini
We provide insight into surface-catalyzed dehalogenative polymerization, analyzing the organometallic intermediate and its evolution into planar polymeric structures. A combined study using scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy (XPS), low energy electron diffraction (LEED), near-edge X-ray absorption fine structure (NEXAFS) spectroscopy and first-principles calculations unveils the structural conformation of substrate-bound phenylene intermediates generated from 1,4-dibromobenzene precursors on Cu(110), showing the stabilizing role of the halogen. The appearance of covalently bonded conjugated structures is followed in real time by fast-XPS measurements (with an acquisition time of 2 s per spectrum and heating rate of 2 K/s), showing that the detaching of phenylene units from the copper substrate and subsequent polymerization occur upon annealing above 460 ± 10 K.
Nature Chemistry | 2014
Artur Ciesielski; Mohamed El Garah; Sébastien Haar; Petr Kovaříček; Jean-Marie Lehn; Paolo Samorì
Dynamic covalent chemistry relies on the formation of reversible covalent bonds under thermodynamic control to generate dynamic combinatorial libraries. It provides access to numerous types of complex functional architectures, and thereby targets several technologically relevant applications, such as in drug discovery, (bio)sensing and dynamic materials. In liquid media it was proved that by taking advantage of the reversible nature of the bond formation it is possible to combine the error-correction capacity of supramolecular chemistry with the robustness of covalent bonding to generate adaptive systems. Here we show that double imine formation between 4-(hexadecyloxy)benzaldehyde and different α,ω-diamines as well as reversible bistransimination reactions can be achieved at the solid/liquid interface, as monitored on the submolecular scale by in situ scanning tunnelling microscopy imaging. Our modular approach enables the structurally controlled reversible incorporation of various molecular components to form sophisticated covalent architectures, which opens up perspectives towards responsive multicomponent two-dimensional materials and devices.
Angewandte Chemie | 2015
Sara Bonacchi; Mohamed El Garah; Artur Ciesielski; Martin Herder; Simone Conti; Marco Cecchini; Stefan Hecht; Paolo Samorì
Here we report for the first time a submolecularly resolved scanning tunneling microscopy (STM) study at the solid/liquid interface of the in situ reversible interconversion between two isomers of a diarylethene photoswitch, that is, open and closed form, self-assembled on a graphite surface. Prolonged irradiation with UV light led to the in situ irreversible formation of another isomer as by-product of the reaction, which due to its preferential physisorption accumulates at the surface. By making use of a simple yet powerful thermodynamic model we provide a quantitative description for the observed surface-induced selection of one isomeric form.
Small | 2016
Artur Ciesielski; Mohamed El Garah; Stefano Masiero; Paolo Samorì
The self-assembly of small organic molecules interacting via non-covalent forces is a viable approach towards the construction of highly ordered nanostructured materials. Among various molecular components, natural and unnatural nucleobases can undergo non-covalent self-association to form supramolecular architectures with ad hoc structural motifs. Such structures, when decorated with appropriate electrically/optically active units, can be used as scaffolds to locate such units in pre-determined positions in 2D on a surface, thereby paving the way towards a wide range of applications, e.g., in optoelectronics. This review discusses some of the basic concepts of the supramolecular engineering of natural and unnatural nucleobases and derivatives thereof as well as self-assembly processes on conductive solid substrates, as investigated by scanning tunnelling microscopy in ultra-high vacuum and at the solid/liquid interface. By unravelling the structure and dynamics of these self-assembled architectures with a sub-nanometer resolution, a greater control over the formation of increasingly sophisticated functional systems is achieved. The ability to understand and predict how nucleobases interact, both among themselves as well as with other molecules, is extremely important, since it provides access to ever more complex DNA- and RNA-based nanostructures and nanomaterials as key components in nanomechanical devices.
Langmuir | 2010
Mohamed El Garah; Frank Palmino; Frédéric Chérioux
The formation of compact and large-scale self-assembled monolayers (SAMs) adsorbed on a mica surface has been achieved by insertion of alkyl chains on azobenzene derivatives, leading to strong intermolecular van der Waals interactions and hydrogen bonding. The reversible photoswitching of monolayers was investigated by monitoring the variation of the thickness of the SAMs during the cis-trans isomerization of the azobenzene cores with an atomic force microscope (AFM). The absence of covalent bonds between molecules and substrate induces a molecular diffusion which leads to the complete isomerization of the molecules constituting the SAMs.
Journal of the American Chemical Society | 2015
Mohamed El Garah; Nicolas Marets; Matteo Mauro; Alessandro Aliprandi; Sara Bonacchi; Luisa De Cola; Artur Ciesielski; Véronique Bulach; Mir Wais Hosseini; Paolo Samorì
The self-assembly of multiple molecular components into complex supramolecular architectures is ubiquitous in nature and constitutes one of the most powerful strategies to fabricate multifunctional nanomaterials making use of the bottom-up approach. When spatial confinement in two dimensions on a solid substrate is employed, this approach can be exploited to generate periodically ordered structures from suitably designed molecular tectons. In this study we demonstrate that physisorbed directional periodic arrays of monometallic or heterobimetallic coordination polymers can be generated on a highly oriented pyrolitic graphite surface by combinations of a suitably designed directional organic tecton or metallatecton based on a porphyrin or nickel(II) metalloporphyrin backbone bearing both a pyridyl unit and a terpyridyl unit acting as coordinating sites for CoCl2. The periodic architectures were visualized at the solid/liquid interface with a submolecular resolution by scanning tunneling microscopy and corroborated by combined density functional and time-dependent density functional theory calculations. The capacity to nanopattern the surface for the first time with two distinct metallic centers exhibiting different electronic and optical properties is a key step toward the bottom-up construction of robust multicomponent and, thus, multifunctional molecular nanostructures and nanodevices.
Small | 2016
Mohamed El Garah; Arezoo Dianat; Andrea Cadeddu; Rafael Gutierrez; Marco Cecchini; Timothy R. Cook; Artur Ciesielski; Peter J. Stang; Gianaurelio Cuniberti; Paolo Samorì
A joint experimental and computational study is reported on the concentration-dependant self-assembly of a flat C3 -symmetric molecule on a graphite surface. As a model system a tripodal molecule, 1,3,5-tris(pyridin-3-ylethynyl)benzene, has been chosen, which can adopt either C3h or Cs symmetry when planar, as a result of pyridyl rotation along the alkynyl spacers. Density functional theory (DFT) simulations of 2D nanopatterns with different surface coverage reveal that the molecule can generate different types of self-assembled motifs. The stability of fourteen 2D patterns and the influence of concentration are analyzed. It is found that ordered, densely packed monolayers and 2D porous networks are obtained at high and low concentrations, respectively. A concentration-dependent scanning tunneling microscopy (STM) investigation of this molecular self-assembly system at a solution/graphite interface reveals four supramolecular motifs, which are in perfect agreement with those predicted by simulations. Therefore, this DFT method represents a key step forward toward the atomically precise prediction of molecular self-assembly on surfaces and at interfaces.
Chemistry-an Asian Journal | 2013
Mohamed El Garah; Josh Lipton-Duffin; Jennifer M. MacLeod; Rico Gutzler; Frank Palmino; Vincent Luzet; Frédéric Chérioux; Federico Rosei
The supramolecular self-assembly of brominated molecules was investigated and compared on Cu(110) and Cu(110)-O(2×1) surfaces under ultrahigh vacuum. By using scanning tunnelling microscopy, we show that brominated molecules form a disordered structure on Cu(110), whereas a well-ordered supramolecular network is observed on the Cu(110)-O(2×1) surface. The different adsorption behaviors of these two surfaces are described in terms of weakened molecule-substrate interactions on Cu(110)-O(2×1) as opposed to bare Cu(110). The effect of oxygen-passivation is to suppress debromination and it can be a convenient approach for investigating other self-assembly processes on copper-based substrates.
ACS Nano | 2011
Mohamed El Garah; Younes Makoudi; Eric Duverger; Frank Palmino; Alain Rochefort; Frédéric Chérioux
The formation of a large scale pattern on Si(111)-7 × 7 reconstruction is still a challenge. We report herein a new solution to achieve this type of nanostructuration by using of zwitterionic molecules. The formation of a large-scale pattern is successfully obtained due to the perfect match between the molecular geometry and the surface topology and to electrostatic interactions between molecules and surface. The adsorption is described by high-resolution scanning tunneling microscopy (STM) images and supported by density functional theory and STM calculations.
ChemPhysChem | 2009
Mohamed El Garah; Younes Makoudi; Frank Palmino; Eric Duverger; Philippe Sonnet; Laurent Chaput; André Gourdon; Frédéric Chérioux
Metalloporphyrins represent a class of flexible molecules with a nearly square planar core conformation and a two dimensional conjugated p-electron delocalization. Due to their interesting physicochemical properties, metalloporphyrins adsorbed on a surface can be used in many technological applications such as molecular electronics, light-harvesting arrays for solar energy generation, catalysts, sensors, etc. The fine determination of the conformation and arrangement of adsorbed molecules on a surface are key points, since they are strongly related to the physical and chemical properties of the final organic–inorganic interfaces. They are changed by the subtle balance of internal deformation and substrate–molecule interactions, leading to a conformational adaptation of the molecule on the substrate lattice. These features are even more relevant in semiconductors than in metals because the moleculesemiconductor interactions are usually greater than molecule– metal interactions. Although scanning tunneling microscopy (STM) is a remarkable tool to investigate individual adsorbed molecules on semiconductors, experimental STM images of metalloporphyrins were achieved only on metals and only an unique very recent article investigates theoretically the adsorption of a metalloporphyrin on a Si(111)-H surface. Herein, we report the first experimental investigation at room temperature of the adsorption of Cu-5,10,15,20-tetrakis(3,5-di-tert-butylphenyl) porphyrin (Cu-TBPP) as a model of metalloporphyrin on a passivated silicon based surface (Si(111)-B) using STM and by theoretical calculations in order to fully understand the conformational adaptation of the Cu-TBPP on a Si(111)-B surface.