Dr. Marco Servalli

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Marco graduated in October 2016 and stayed with us as a postdoctoral scientist until the end of January 2018.

 

Marco Servalli
Marco Servalli

Research Interests

My research interests are mainly synthesis oriented. By making use of palladium-mediated cross-coupling reactions, I am developing a series of macrocyclic propeller-shaped monomers with anthracene-based photoreactive units for the synthesis of two-dimensional polymers (Fig. 1).

1,8-diazaanthracene based propeller-shaped monomers
Figure 1: The 1,8-diazaanthracene based propeller-shaped monomers 1 and 2 and the anthracene-based hydrocarbon monomer 3. While monomers of type 1 are still in the preparation process, 2 and 3 have been fully characterised.

Due to the high symmetry, rigidity and lack of amphiphilicity, these monomers are best suited for the topochemical synthesis of 2D-polymers (single crystal approach). This already-established method in our group, involves the crystallization of the monomers into lamellar single crystals; In each layer the photoreactive anthracene units stack face-to-face and can react with each other topochemically upon photoirradiation (the connection chemistry is the well-known anthracene dimerisation via [4+4]-cycloaddition), converting the layers into the corresponding 2D-polymers. Subsequent exfoliation of the obtained 2D-crystal allows the isolation of single molecular sheets (Fig. 2).

Polymerisation concept
Figure 2: Polymerisation concept with the three key steps of the topochemical approach. The connection chemistry is the well-studied dimerization of anthracene and 1,8-diazaanthracene via [4+4] cycloaddition
Crystal structure
Figure 3: Crystal structure of the ODCB solvate of monomer 3 (top) and crystal structure of the TCE solvate of monomer 2 (bottom) showing also the packing of a layer.

Monomers 1 and 2 are particularly interesting because they carry functional groups, providing the chance of synthesising a new class of functionalisable 2D-polymers (Fig. 4)

2D-polymers
Figure 4: 2D-polymers carrying functional groups could open the road for defined pores and surface functionalisation.

Apart from the topochemical approach, we are also exploring in collaboration with PD Dr. Markus Lackinger (TU München), a way of synthesising 2D-polymers by self-assembly of the monomers on surfaces. Ideally the monomer would self-assemble on a surface upon sublimation into the desired honeycomb structure (much like in the crystal approach); photoirradiation and subsequent etching of the surface would result into the isolation of the 2D-polymer (Fig. 5).

Principle of 2D-polymer synthesis
Figure 5: Principle of 2D-polymer synthesis by self-assembly on a surface.

Publications

Tip-enhanced Raman spectroscopy for structural analysis of two-dimensional covalent monolayers synthesized on water and on Au (111)
Liqing Zheng, Marco Servalli, A. Dieter Schlüter and Renato Zenobi
Chemical Science, vol. 10: no. 42, pp. 9673-9678, London: Royal Society of Chemistry, 2019.
Photochemical Creation of Covalent Organic 2D Monolayer Objects in Defined Shapes via a Lithographic 2D Polymerization
Marco Servalli, Kemal Celebi, Payam Payamyar, Liqing Zheng, Miroslav Položij, Benjamin Lowe, Agnieszka Kuc, Tobias Schwarz, Kerstin Thorwarth, Andreas Borgschulte, Thomas Heine, Renato Zenobi and A. Dieter Schlüter
ACS Nano, vol. 12: no. 11, pp. 11294-11306, Columbus, OH: American Chemical Society (ACS), 2018.
Photochemical Single-Crystal-to-Single-Crystal (SCSC) Reactions of Anthraphane to Dianthraphane and Poly1Danthraphane
Marco Servalli, Michael Solar, Nils Trapp, Michael Wörle and A. Dieter Schlüter
Crystal Growth & Design, vol. 17: no. 12, pp. 6510-6522, Washington, DC: American Chemical Society, 2017.
A Library of Single Crystal Structures of a D-Symmetric Hydrocarbon Cyclophane: a Comprehensive Packing Study of Anthraphane from 30 Solvents
Marco Servalli, Nils Trapp, Michael Solar and A. Dieter Schlüter
Crystal Growth & Design, vol. 17: no. 6, pp. 3419-3432, Washington, DC: American Chemical Society, 2017.
Anthraphane: An Anthracene-Based, Propeller-Shaped D3h-Symmetric Hydrocarbon Cyclophane and Its Layered Single Crystal Structures
Marco Servalli, Nils Trapp, Michael Woerle and Frank-Gerrit Klaerner
The Journal of Organic Chemistry, vol. 81: no. 6, pp. 2572-2580, Washington DC, USA: American Chemical Society, 2016.
Propeller-Shaped D3h-Symmetric Macrocycles with Three 1,8-Diazaanthracene Blades as Building Blocks for Photochemically Induced Growth Reactions
Marco Servalli, Luzia Gyr, Junji Sakamoto and A. Dieter Schlüter
European Journal of Organic Chemistry, vol. 2015: no. 20, pp. 4519-4523, Weinheim: Wiley, 2015.
Approaching two-dimensional copolymers: Photoirradiation of anthracene- And diaza-anthracene-bearing monomers in Langmuir monolayers
P. Payamyar, M. Servalli, T. Hungerland, A.P. Schütz, Z. Zheng, A. Borgschulte and A. Dieter Schlüter
Macromolecular Rapid Communications, vol. 36: no. 2, pp. 151-158, Weinheim: Wiley, 2015.
Minimally invasive characterization of covalent monolayer sheets using tip-enhanced raman spectroscopy
Lothar Opilik, Payam Payamyar, Jacek Szczerbinski, Andri P. Schütz, Marco Servalli, Tim Hungerland, A. Dieter Schlüter and Renato Zenobi
ACS Nano, vol. 9: no. 4, pp. 4252-4259, Columbus, OH: American Chemical Society, 2015.
AuI Catalysis on a Coordination Polymer: A Solid Porous Ligand with Free Phosphine Sites
Jiri Vaclavik, Marco Servalli, Christian Lothschütz, Jakub Szlachetko, Marco Ranocchiari and Jeroen A. van Bokhoven
ChemCatChem, vol. 5: no. 3, pp. 692-696, Weinheim: Wiley, 2013.
Fine tuning of gold electronic structure by IRMOF post-synthetic modification
J. Sa, J. Szlachetko, E. Kleymenov, C. Lothschütz, M. Nachtegaal, M. Ranocchiari, O.V. Safonova, M. Servalli, G. Smolentsev and Jeroen A. van Bokhoven
RSC Advances, vol. 3: no. 30, pp. 12043-12048, London: Royal Society of Chemistry, 2013.
Fast and high yield post-synthetic modification of metal-organic frameworks by vapor diffusion
Marco Servalli, Marco Ranocchiari and Jeroen A. van Bokhoven
Chemical Communications, vol. 48: no. 13, pp. 1904-1906, Cambridge, UK: Royal Society of Chemistry, 2012.
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