journal article·2018-11-27

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, A. Dieter Schlüter

ACS Nano· Volume 12· Issue 11
Publisher page

Abstract

In this work we prepare Langmuir-Blodgett monolayers with a trifunctional amphiphilic anthraphane monomer. Upon spreading at the air/water interface, the monomers self-assemble into 1 nm-thin monolayer islands, which are highly fluorescent and can be visualized by the naked eye upon excitation. In situ fluorescence spectroscopy indicates that in the monolayers, all the anthracene units of the monomers are stacked face-to-face forming excimer pairs, whereas at the edges of the monolayers, free anthracenes are present acting as edge groups. Irradiation of the monolayer triggers [4 + 4]-cycloadditions among the excimer pairs, effectively resulting in a two-dimensional (2D) polymerization. The polymerization reaction also completely quenches the fluorescence, allowing to draw patterns on the monomer monolayers. More interestingly, after transferring the monomer monolayer on a solid substrate, by employing masks or the laser of a confocal scanning microscope, it is possible to arbitrarily select the parts of the monolayer that one wants to polymerize. The unpolymerized regions can then be washed away from the substrate, leaving 2D macromolecular monolayer objects of the desired shape. This photolithographic process employs 2D polymerizations and affords 1 nm-thin coatings.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Supramolecular Self-Assembly in Materials · Covalent Organic Framework Applications · Luminescence and Fluorescent Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Laboratory of Polymer Chemistry, Department of Materials, ETH Zurich, Vladimir-Prelog-Weg 5, 8093 Zurich, Switzerland

John A. Paulson School of Engineering and Applied Sciences, Harvard University, 9 Oxford Street, Cambridge, Massachusetts 02138, United States

Laboratory of Organic Chemistry, Department of Chemistry and Applied Biosciences, ETH Zurich, Vladimir-Prelog-Weg 3, 8093 Zurich, Switzerland

Wilhelm-Ostwald-Institut für Physikalische und Theoretische Chemie, Universität Leipzig, Linnéstrasse 2, 04103 Leipzig, Germany

Theoretische Chemie, Technische Universität Dresden, Bergstraße 66b, 01062 Dresden, Germany

Abteilung Ressourcenökölogie, Forschungsstelle Leipzig, Helmholtz-Zentrum Dresden-Rossendorf, Permosenstrasse 15, 04318 Leipzig, Germany

ScopeM, Institute of Biochemistry, ETH Zurich, Otto-Stern-Weg 3, Zurich 8093, Switzerland

Advanced Analytical Technologies, Empa, Swiss Federal Laboratories for Materials Science and Technology, Überlandstrasse 129, 8600 Dübendorf, Switzerland

References (56)

Show source-provided references
1. 10.1002/anie.20080186310.1002/anie.200801863 ↗
2. 10.1146/annurev-matsci-070616-12404010.1146/annurev-matsci-070616-124040 ↗
3. 10.1038/nchem.162810.1038/nchem.1628 ↗
4. 10.1063/PT.3.392110.1063/PT.3.3921 ↗
5. 10.1038/nnano.2017.7210.1038/nnano.2017.72 ↗
6. 10.1126/science.aab053010.1126/science.aab0530 ↗
7. 10.1038/nphoton.2016.1510.1038/nphoton.2016.15 ↗
8. 10.1126/science.aac943910.1126/science.aac9439 ↗
9. 10.1002/adma.20170241510.1002/adma.201702415 ↗
10. 10.1038/nchem.126510.1038/nchem.1265 ↗
11. 10.1038/nchem.200810.1038/nchem.2008 ↗
12. 10.1021/ja404351p10.1021/ja404351p ↗
13. 10.1038/nchem.200710.1038/nchem.2007 ↗
14. 10.1021/jacs.6b1185710.1021/jacs.6b11857 ↗
15. 10.1002/adma.20130470510.1002/adma.201304705 ↗
16. 10.1021/ja512018j10.1021/ja512018j ↗
17. 10.1002/anie.20150847310.1002/anie.201508473 ↗
18. 10.1021/mz400597k10.1021/mz400597k ↗
19. 10.1002/anie.20170714010.1002/anie.201707140 ↗
20. Payamyar P. · 2018 · 18110.1016/B978-0-12-409547-2.13119-1 ↗
21. 10.1021/acsnano.5b0062910.1021/acsnano.5b00629 ↗
22. 10.1002/anie.20170380010.1002/anie.201703800 ↗
23. 10.1038/srep0250610.1038/srep02506 ↗
24. 10.1038/ncomms1346110.1038/ncomms13461 ↗
25. 10.1021/ja312380b10.1021/ja312380b ↗
26. 10.1002/anie.20180493710.1002/anie.201804937 ↗
27. 10.1002/adma.20170122010.1002/adma.201701220 ↗
28. 10.1002/anie.20110066910.1002/anie.201100669 ↗
29. 10.1002/marc.20130062410.1002/marc.201300624 ↗
31. 10.1038/ncomms771310.1038/ncomms7713 ↗
32. 10.1107/S160057671800282010.1107/S1600576718002820 ↗
33. Odian G. · 200410.1002/047147875X ↗
34. 10.1002/lpor.20081006110.1002/lpor.200810061 ↗
35. 10.1116/1.180295510.1116/1.1802955 ↗
36. 10.1038/srep0017510.1038/srep00175 ↗
37. 10.1021/cr980130e10.1021/cr980130e ↗
38. 10.1021/acs.joc.6b0020910.1021/acs.joc.6b00209 ↗
39. 10.1002/chem.20180251310.1002/chem.201802513 ↗
40. 10.1021/acs.cgd.7b0036710.1021/acs.cgd.7b00367 ↗
41. 10.1021/acs.cgd.7b0118410.1021/acs.cgd.7b01184 ↗
42. 10.1016/j.tet.2004.08.03610.1016/j.tet.2004.08.036 ↗
43. 10.1002/1099-0690(200212)2002:23<3927::AID-EJOC3927>3.0.CO;2-R10.1002/1099-0690(200212)2002:23<3927::AID-EJOC3927>3.0.CO;2-R ↗
44. 10.1021/ar800148f10.1021/ar800148f ↗
45. 10.1039/P2993000079910.1039/P29930000799 ↗
46. 10.1021/ja00435a02710.1021/ja00435a027 ↗
47. 10.1039/a801821i10.1039/a801821i ↗
48. 10.1039/b006013p10.1039/b006013p ↗
49. 10.1021/ja051701510.1021/ja0517015 ↗
50. 10.1039/b719637g10.1039/b719637g ↗
51. 10.1021/la904299n10.1021/la904299n ↗
52. 10.1103/PhysRevLett.52.21610.1103/PhysRevLett.52.216 ↗
53. 10.1021/ja303890510.1021/ja3038905 ↗
54. 10.1002/ejoc.20150049610.1002/ejoc.201500496 ↗
55. 10.1021/jacs.6b0545610.1021/jacs.6b05456 ↗
56. 10.1039/c2nr11458e10.1039/c2nr11458e ↗