journal article·2016-07-26

Dehalogenative Homocoupling of Terminal Alkynyl Bromides on Au(111): Incorporation of Acetylenic Scaffolding into Surface Nanostructures

Qiang Sun, Liangliang Cai, Honghong Ma, Chunxue Yuan, Wei Xu

ACS Nano· Volume 10· Issue 7
Publisher page

Abstract

On-surface C-C coupling reactions of molecular precursors with alkynyl functional groups demonstrate great potential for the controllable fabrication of low-dimensional carbon nanostructures/nanomaterials, such as carbyne, graphyne, and graphdiyne, which demand the incorporation of highly active sp-hybridized carbons. Recently, through a dehydrogenative homocoupling reaction of alkynes, the possibility was presented to fabricate surface nanostructures involving acetylenic linkages, while problems lie in the fact that different byproducts are inevitably formed when triggering the reactions at elevated temperatures. In this work, by delicately designing the molecular precursors with terminal alkynyl bromide, we introduce the dehalogenative homocoupling reactions on the surface. As a result, we successfully achieve the formation of dimer structures, one-dimensional molecular wires and two-dimensional molecular networks with acetylenic scaffoldings on an inert Au(111) surface, where the unexpected C-Au-C organometallic intermediates are also observed. This study further supplements the database of on-surface dehalogenative C-C coupling reactions, and more importantly, it provides us an alternative efficient way for incorporating the acetylenic scaffolding into low-dimensional surface nanostructures.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Surface Chemistry and Catalysis · Graphene research and applications · Covalent Organic Framework Applications

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

Affiliations

Tongji−Aarhus Joint Research Center for Nanostructures and Functional Nanomaterials, College of Materials Science and Engineering, Tongji University, Caoan Road 4800, Shanghai 201804, People’s Republic of China

Funding

Ministry of Education of the People's Republic of China · National Natural Science Foundation of China

References (49)

Show source-provided references
1. 10.1021/acs.accounts.5b0017410.1021/acs.accounts.5b00174 ↗
2. 10.1038/nmat288510.1038/nmat2885 ↗
3. 10.1002/adma.20090262310.1002/adma.200902623 ↗
4. 10.1126/science.123818710.1126/science.1238187 ↗
5. 10.1021/nn402278910.1021/nn4022789 ↗
6. 10.1021/ja404039t10.1021/ja404039t ↗
7. 10.1021/ja312303a10.1021/ja312303a ↗
8. 10.1038/ncomms229110.1038/ncomms2291 ↗
9. 10.1002/anie.20120859710.1002/anie.201208597 ↗
10. 10.1038/nnano.2007.34610.1038/nnano.2007.346 ↗
11. 10.1021/ja503387510.1021/ja5033875 ↗
12. 10.1126/science.121183610.1126/science.1211836 ↗
13. 10.1039/C4CC05482B10.1039/C4CC05482B ↗
14. 10.1021/ja501680n10.1021/ja501680n ↗
15. 10.1039/b718865j10.1039/b718865j ↗
16. 10.1038/nature0719310.1038/nature07193 ↗
17. 10.1038/nature0921110.1038/nature09211 ↗
18. 10.1021/ja511995r10.1021/ja511995r ↗
19. 10.1021/nn401948e10.1021/nn401948e ↗
20. 10.1021/ja510292b10.1021/ja510292b ↗
21. 10.1038/nnano.2014.18410.1038/nnano.2014.184 ↗
22. 10.1038/srep0098310.1038/srep00983 ↗
23. 10.1021/nn502864210.1021/nn5028642 ↗
24. 10.1038/nchem.89110.1038/nchem.891 ↗
25. 10.1002/anie.20130061010.1002/anie.201300610 ↗
26. 10.1021/ja204956b10.1021/ja204956b ↗
27. 10.1039/C5CC04317D10.1039/C5CC04317D ↗
28. 10.1039/c4cc02757d10.1039/c4cc02757d ↗
29. 10.1039/C6CC01059H10.1039/C6CC01059H ↗
30. 10.1039/C5CP06459G10.1039/C5CP06459G ↗
31. 10.1002/chem.20150415210.1002/chem.201504152 ↗
32. 10.1002/anie.20141230710.1002/anie.201412307 ↗
33. 10.1021/jacs.5b1072510.1021/jacs.5b10725 ↗
34. 10.1021/acsnano.5b0180310.1021/acsnano.5b01803 ↗
35. 10.1021/ja501308s10.1021/ja501308s ↗
36. 10.1039/C4CC02859G10.1039/C4CC02859G ↗
37. 10.1039/c3cc40444g10.1039/c3cc40444g ↗
38. 10.1039/C4CC05235H10.1039/C4CC05235H ↗
39. 10.1021/jp203129f10.1021/jp203129f ↗
40. 10.1002/smll.20130301110.1002/smll.201303011 ↗
41. 10.1088/0034-4885/59/12/00410.1088/0034-4885/59/12/004 ↗
42. 10.1063/1.138949710.1063/1.1389497 ↗
43. 10.1103/PhysRevB.48.1311510.1103/PhysRevB.48.13115 ↗
44. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
45. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
46. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
47. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
48. 10.1002/jcc.2049510.1002/jcc.20495 ↗
49. 10.1103/PhysRevB.31.80510.1103/PhysRevB.31.805 ↗