journal article·2017Open access

Hierarchical self-assembly of enantiopure and racemic helicenes at the liquid/solid interface: from 2D to 3D

Hai Cao, Andrea Minoia, Inge De Cat, Johannes Seibel, Deepali Waghray, Zhi Li, David Cornil, Kunal S. Mali, Roberto Lazzaroni, Wim Dehaen, Steven De Feyter

Nanoscale· Volume 9· Issue 45

Abstract

The performance of organic nanostructures is closely related to the organization of the functional molecules. Frequently, molecular chirality plays a central role in the way molecules assemble at the supramolecular level. Herein we report the hierarchical self-assembly of benzo-fused tetrathia[7]helicenes on solid surfaces, from a single surface-bound molecule to well-defined microstructures, using a combination of various characterization techniques assisted by molecular modeling simulations. Similarities as well as discrepancies are revealed between homochiral and heterochiral aggregations by monitoring the hierarchical nucleation of helicenes on surfaces, where the impact of enantiopurity, concentration and adsorbate-substrate interaction on molecular organization are disclosed.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Surface Chemistry and Catalysis · Synthesis and Properties of Aromatic Compounds · Supramolecular Self-Assembly in Materials

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

Affiliations

Department of Chemistry

Division of Molecular Imaging and Photonics

KU Leuven–University of Leuven

3001 Leuven

Belgium

Laboratory for Chemistry of Novel Materials

Université de Mons-UMONS

B-7000 Mons

Division of Molecular Design and Synthesis

References (44)

Show source-provided references
1. Katsonis · J. Mater. Chem. · 2008 · 18 · 206510.1039/b718170a ↗
2. Wang · Chem. Soc. Rev. · 2013 · 42 · 293010.1039/C2CS35332F ↗
3. Liu · Chem. Rev. · 2015 · 115 · 730410.1021/cr500671p ↗
4. Brock · J. Am. Chem. Soc. · 1991 · 113 · 981110.1021/ja00026a015 ↗
5. Oda · Nature · 1999 · 399 · 56610.1038/21154 ↗
6. Zhu · Chem. – Eur. J. · 2010 · 16 · 803410.1002/chem.201000595 ↗
7. Verbiest · Science · 1998 · 282 · 91310.1126/science.282.5390.913 ↗
8. Kaseyama · Angew. Chem., Int. Ed. · 2011 · 50 · 368410.1002/anie.201007849 ↗
9. Kumar · Angew. Chem., Int. Ed. · 2015 · 54 · 594310.1002/anie.201500292 ↗
10. Nuckolls · J. Am. Chem. Soc. · 1998 · 120 · 954110.1021/ja982025s ↗
11. Phillips · J. Am. Chem. Soc. · 2001 · 123 · 1189910.1021/ja011706b ↗
12. Pop · J. Am. Chem. Soc. · 2013 · 135 · 1717610.1021/ja408350r ↗
13. Pop · Chem. Commun. · 2016 · 52 · 1243810.1039/C6CC06706A ↗
14. Zou · J. Am. Chem. Soc. · 2014 · 136 · 57810.1021/ja409796b ↗
15. Pérez-Garcíaa · Chem. Soc. Rev. · 2002 · 31 · 34210.1039/B201099M ↗
16. Pérez-García · Chem. Soc. Rev. · 2007 · 36 · 94110.1039/B610714A ↗
17. Elemans · Chem. Soc. Rev. · 2009 · 38 · 72210.1039/b800403j ↗
18. Raval · Chem. Soc. Rev. · 2009 · 38 · 70710.1039/b800411k ↗
19. Haq · Nat. Chem. · 2009 · 1 · 40910.1038/nchem.295 ↗
20. Ernst · Phys. Status Solidi B · 2012 · 249 · 205710.1002/pssb.201248188 ↗
21. Shen · Chem. Rev. · 2012 · 112 · 146310.1021/cr200087r ↗
22. Fasel · Nature · 2006 · 439 · 44910.1038/nature04419 ↗
23. Seibel · J. Phys. Chem. C · 2014 · 118 · 2913510.1021/jp504673g ↗
24. Stöhr · Angew. Chem., Int. Ed. · 2011 · 50 · 998210.1002/anie.201102627 ↗
25. Shchyrba · J. Am. Chem. Soc. · 2013 · 135 · 1527010.1021/ja407315f ↗
26. Taniguchi · Surf. Sci. · 2000 · 454–456 · 100510.1016/S0039-6028(00)00174-6 ↗
27. Taniguchi · Surf. Sci. · 2002 · 507–510 · 45810.1016/S0039-6028(02)01285-2 ↗
28. Taniguchi · J. Mol. Catal. A: Chem. · 2003 · 199 · 6510.1016/S1381-1169(03)00019-0 ↗
29. Ernst · Acc. Chem. Res. · 2016 · 49 · 118210.1021/acs.accounts.6b00110 ↗
30. Ernst · Nano Lett. · 2015 · 15 · 538810.1021/acs.nanolett.5b01762 ↗
31. Parschau · Angew. Chem., Int. Ed. · 2015 · 54 · 1442210.1002/anie.201507590 ↗
32. Mairena · ACS Nano · 2017 · 11 · 86510.1021/acsnano.6b07424 ↗
33. Seibel · J. Am. Chem. Soc. · 2013 · 135 · 743410.1021/ja402012j ↗
34. Hauke · J. Phys. Chem. C · 2012 · 116 · 463710.1021/jp2102258 ↗
35. Rahe · J. Phys. Chem. C · 2010 · 114 · 154710.1021/jp911287p ↗
36. Balandina · Chem. Commun. · 2013 · 49 · 220710.1039/c3cc37159j ↗
37. Waghray · Org. Lett. · 2011 · 13 · 551610.1021/ol202236r ↗
38. D. B. Amabilino , in Supramolecular Chemistry at Surfaces , RSC Publishing , Cambridge , 2016 , pp. 340–34110.1039/9781782622161 ↗
39. Palermo · Angew. Chem., Int. Ed. · 2007 · 46 · 442810.1002/anie.200700416 ↗
40. Ivasenko · Chem. Commun. · 2009 · 119210.1039/b819532c ↗
41. Pensa · Acc. Chem. Res. · 2012 · 45 · 118310.1021/ar200260p ↗
42. Love · Chem. Rev. · 2005 · 105 · 110310.1021/cr0300789 ↗
43. Buimaga-Iarinca · Theor. Chem. Acc. · 2014 · 133 · 150210.1007/s00214-014-1502-9 ↗
44. Brock · J. Am. Chem. Soc. · 1991 · 113 · 981110.1021/ja00026a015 ↗