Engineering of Linear Molecular Nanostructures by a Hydrogen-Bond-Mediated Modular and Flexible Host−Guest Assembly
Source abstract
Abstract
The formation of a desired nanostructure with concomitant patterns and functions is of utmost importance in the field of surface molecular engineering and nanotechnology. We here present a flexible host-guest assembly, which steers the formation of linear molecular nanostructures on surfaces by a hydrogen-bond-mediated assembly process. A linear monodendron molecular template with periodic hydrogen-bond binding sites is shown to accommodate a variety of molecules with pyridylethynyl terminals. The unit cell parameters in the transverse direction of the linear pattern can be tuned from 3.4 to 7.3 nm in response to the packing of the guest molecules with different sizes, shapes, and aggregation number. The introduction of hydrogen-bonding partners into the host template and into guest molecules is responsible for the steering of the linear pattern of guest molecules. The modular approach could greatly facilitate the ordering of guest molecules with desired functional moieties.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Surface Chemistry and Catalysis · Block Copolymer Self-Assembly · Supramolecular Self-Assembly in Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Chemistry, Chinese Academy of Sciences, and Beijing National Laboratory for Molecular Sciences, Beijing 100190, China
Graduate University of Chinese Academy of Sciences, Beijing 100064, China
Department of Chemistry, University of Utah, 315 South 1400 East, Salt Lake City, Utah 84112
Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry, East China Normal University, Shanghai 200062, China
References (46)
Show source-provided references
1. Lehn J. M. · Proc. Natl. Acad. Sci. U.S.A. · 2002 · 99 · 476310.1073/pnas.072065599 ↗
2. Tully D. C. · Chem. Commun. · 2001 · 122910.1039/b104290b ↗
3. Love J. C. · Chem. Rev. · 2005 · 105 · 110310.1021/cr0300789 ↗
4. Hoeben F. J. M. · Chem. Rev. · 2005 · 105 · 149110.1021/cr030070z ↗
5. Onclin S. · Angew. Chem., Int. Ed. · 2005 · 44 · 628210.1002/anie.200500633 ↗
6. Wan L. J. · Acc. Chem. Res. · 2006 · 39 · 33410.1021/ar0501929 ↗
7. Barth J. V. · Annu. Rev. Phys. Chem. · 2007 · 58 · 37510.1146/annurev.physchem.56.092503.141259 ↗
8. Wang D. · Phys. Chem. Chem. Phys. · 2008 · 10 · 646710.1039/b810304f ↗
9. Müllen K. · Acc. Chem. Res. · 2008 · 41 · 51110.1021/ar7001446 ↗
10. Sanchez L. · Chem. Rev. · 2009 · 109 · 208110.1021/cr800441b ↗
11. Cicoira F. · Top. Curr. Chem. · 2008 · 285 · 20310.1007/128_2008_2 ↗
12. Liang H. · Coord. Chem. Rev. · 2009 · 253 · 295910.1016/j.ccr.2009.07.028 ↗
13. Bonifazi D. · Chem.—Eur. J. · 2009 · 15 · 700410.1002/chem.200900900 ↗
14. Griessl S. · Single Mol. · 2002 · 3 · 2510.1002/1438-5171(200204)3:1<25::AID-SIMO25>3.0.CO;2-K ↗
15. Zwaneveld N. A. A. · J. Am. Chem. Soc. · 2008 · 130 · 667810.1021/ja800906f ↗
16. Xu W. · Small · 2009 · 5 · 195210.1002/smll.200900315 ↗
17. Zhou H. · J. Am. Chem. Soc. · 2007 · 129 · 1377410.1021/ja0742535 ↗
18. Kuhne D. · J. Am. Chem. Soc. · 2009 · 131 · 388110.1021/ja809946z ↗
19. Palma C. A. · J. Am. Chem. Soc. · 2009 · 131 · 1306210.1021/ja9032428 ↗
20. Theobald J. A. · Nature · 2003 · 424 · 102910.1038/nature01915 ↗
21. Pan G. B. · Angew. Chem., Int. Ed. · 2003 · 42 · 274710.1002/anie.200350432 ↗
22. Xu B. · Nano Lett. · 2005 · 5 · 220710.1021/nl051415r ↗
23. Mena-Osteritz E. · Adv. Mater. · 2006 · 18 · 44710.1002/adma.200501575 ↗
24. Stohr M. · Small · 2007 · 3 · 133610.1002/smll.200700099 ↗
25. Nishiyama F. · Adv. Mater. · 2007 · 19 · 11710.1002/adma.200601364 ↗
26. Yoshimoto S. · J. Am. Chem. Soc. · 2008 · 130 · 108510.1021/ja077407p ↗
27. Lu J. · J. Phys. Chem. B · 2004 · 108 · 516110.1021/jp037508j ↗
28. Kong X. H. · J. Phys. Chem. C · 2007 · 111 · 1738210.1021/jp074682p ↗
29. Meier C. · Angew. Chem., Int. Ed. · 2008 · 47 · 382110.1002/anie.200705527 ↗
30. Huang Y. L. · Small · 2010 · 6 · 7010.1002/smll.200901291 ↗
31. Madueno R. · Nature · 2008 · 454 · 61810.1038/nature07096 ↗
32. Li S. S. · Acc. Chem. Res. · 2009 · 42 · 24910.1021/ar800117j ↗
33. Li S. S. · J. Am. Chem. Soc. · 2007 · 129 · 926810.1021/ja0733282 ↗
34. Chen T. · J. Am. Chem. Soc. · 2010 · 132 · 132810.1021/ja907220f ↗
35. Gong J. R. · J. Am. Chem. Soc. · 2006 · 128 · 1238410.1021/ja062533z ↗
36. Furukawa S. · Angew. Chem., Int. Ed. · 2007 · 46 · 283110.1002/anie.200604782 ↗
37. Silien C. · Angew. Chem., Int. Ed. · 2009 · 48 · 334910.1002/anie.200806267 ↗
38. Adisoejoso J. · Angew. Chem., Int. Ed. · 2009 · 48 · 735310.1002/anie.200900436 ↗
39. Zhang X. · J. Phys. Chem. C · 2009 · 113 · 1619310.1021/jp9058356 ↗
40. Zhang X. · Chem.—Eur. J. · 2009 · 15 · 966910.1002/chem.200901618 ↗
41. Steiner T. · Angew. Chem., Int. Ed. · 2002 · 41 · 4810.1002/1521-3773(20020104)41:1<48::AID-ANIE48>3.0.CO;2-U ↗
42. Gong J. R. · Chem. Mater. · 2003 · 15 · 309810.1021/cm030289u ↗
43. Kuehl C. J. · J. Am. Chem. Soc. · 2001 · 123 · 963410.1021/ja0114355 ↗
44. Schweiger M. · J. Org. Chem. · 2005 · 70 · 486110.1021/jo050469i ↗
45. Lee J. · J. Am. Chem. Soc. · 2009 · 131 · 1202810.1021/ja903330j ↗
46. Yang H. B. · J. Am. Chem. Soc. · 2006 · 128 · 1001410.1021/ja063377z ↗