journal article·2008-05-01

Suzuki Coupling of Aryl Organics on Diamond

Yu Lin Zhong, Kian Ping Loh, Anupam Midya, Zhi-Kuan Chen

Chemistry of Materials· Volume 20· Issue 9
Publisher page

Abstract

We demonstrate a facile method for the Suzuki coupling of aryl molecules on the diamond surface. This is a more versatile alternative compared to previous coupling methods based on alkene linkers because it opens up possibilities for the application of diamond in molecular electronics and photovoltaics. The diamond surface is premodified with aryldiazonium salt in order to functionalize it with aryl halide or aryl boronic acid, and these are then used as synthons in the subsequent Suzuki coupling to aryl molecules. This method is highly specific and can be used for the uninterrupted molecular conjugation of diamond to a large class of organic molecules. As a proof of concept, we also demonstrate a diamond−fullerene photocurrent converter by using Suzuki coupled oligothiophene as the conjugated linker between diamond (electron donor) and fullerene (electron acceptor).
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Research context

OpenAlex topics: Diamond and Carbon-based Materials Research · Molecular Junctions and Nanostructures · Semiconductor materials and devices

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Affiliations

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, and Institute of Materials Research and Engineering, 3 Research Link, Singapore 117602

References (46)

Show source-provided references
1. Strother T. · J. Am. Chem. Soc. · 2000 · 122 · 120510.1021/ja9936161 ↗
2. Gu H. · J. Phys. Chem. B · 2005 · 109 · 1361110.1021/jp050625p ↗
3. Liu Y. · Chem. Mater. · 2004 · 16 · 392410.1021/cm048875q ↗
4. Tsubota T. · Phys. Chem. Chem. Phys. · 2003 · 5 · 147410.1039/b210248j ↗
5. Yang W. · Nat. Mater. · 2002 · 1 · 25310.1038/nmat779 ↗
6. Hartl A. · Nat. Mater. · 2004 · 3 · 73610.1038/nmat1204 ↗
7. Zhong Y. L. · Langmuir · 2007 · 23 · 582410.1021/la063658k ↗
8. Chong K. F. · Langmuir · 2007 · 23 · 561610.1021/la070037y ↗
9. Wang J. · Diamond Relat. Mater. · 2006 · 15 · 27910.1016/j.diamond.2005.09.017 ↗
10. Zhou Y. L. · Electrochem. Commun. · 2006 · 8 · 181110.1016/j.elecom.2006.08.022 ↗
11. Shin D. · Electrochem. Commun. · 2006 · 8 · 84410.1016/j.elecom.2006.03.014 ↗
12. Baranton S. · J. Phys. Chem. B · 2005 · 109 · 2440110.1021/jp054513+ ↗
13. Lyskawa J. · Chem. Mater. · 2006 · 18 · 475510.1021/cm060752d ↗
14. Adenier A. · Chem. Mater. · 2005 · 17 · 49110.1021/cm0490625 ↗
15. Jiang D. · J. Am. Chem. Soc. · 2006 · 128 · 603010.1021/ja061439f ↗
16. Stewart M. P. · J. Am. Chem. Soc. · 2004 · 126 · 37010.1021/ja0383120 ↗
17. Corgier B. P. · J. Am. Chem. Soc. · 2005 · 127 · 1832810.1021/ja056946w ↗
18. Marwan J. · Chem. Mater. · 2005 · 17 · 239510.1021/cm047871i ↗
19. Price B. K. · J. Am. Chem. Soc. · 2005 · 127 · 1486710.1021/ja053998c ↗
20. Coulon E. · J. Org. Chem. · 2002 · 67 · 851310.1021/jo025880+ ↗
21. Kosynkin D. M. · Org. Lett. · 2001 · 3 · 993
22. Kuo T. C. · Electrochem. Solid-State Lett. · 1999 · 2 · 28810.1149/1.1390813 ↗
23. Wang J. · Langmuir · 2004 · 20 · 1145010.1021/la048740z ↗
24. Shin D. · Phys. Status Solidi A · 2006 · 203 · 324510.1002/pssa.200671402 ↗
25. Pinson J. · Chem. Soc. Rev. · 2005 · 34 · 42910.1039/b406228k ↗
26. Allongue P. · J. Electroanal. Chem. · 2003 · 550 · 16110.1016/S0022-0728(03)00076-7 ↗
27. Lud S. Q. · J. Am. Chem. Soc. · 2006 · 128 · 1688410.1021/ja0657049 ↗
28. Uetsuka H. · Langmuir · 2007 · 23 · 346610.1021/la063241e ↗
29. Miyaura N. · Chem. Rev. · 1995 · 95 · 245710.1021/cr00039a007 ↗
30. Cheng F. · Chem. Mater. · 2006 · 18 · 538910.1021/cm061736j ↗
31. Anariba F. · Anal. Chem. · 2003 · 75 · 383710.1021/ac034026v ↗
32. Maier F. · Phys. Rev. Lett. · 2000 · 85 · 347210.1103/PhysRevLett.85.3472 ↗
33. Ley L. · Physica B · 2006 · 376 · 26210.1016/j.physb.2005.12.068 ↗
34. Ristein J. · Science · 2006 · 313 · 105710.1126/science.1127589 ↗
35. Maier F. · Phys. Rev. B · 2001 · 64 · 16541110.1103/PhysRevB.64.165411 ↗
36. Chakrapani V. · Science · 2007 · 318 · 142410.1126/science.1148841 ↗
37. Shin D. · J. Am. Chem. Soc. · 2005 · 127 · 1123610.1021/ja052834t ↗
38. Allongue P. · J. Am. Chem. Soc. · 1997 · 119 · 20110.1021/ja963354s ↗
39. Yam C. M. · J. Colloid Interface Sci. · 2006 · 301 · 44110.1016/j.jcis.2006.05.040 ↗
40. Littke A. F. · J. Am. Chem. Soc. · 2000 · 122 · 402010.1021/ja0002058 ↗
41. Lü F. · Langmuir · 2006 · 22 · 84110.1021/la052866u ↗
42. Zhang S. · Langmuir · 2007 · 23 · 158410.1021/la062773s ↗
43. Bouvier P. · Electrochem. Solid-State Lett. · 2005 · 8 · E5710.1149/1.1979449 ↗
44. Mazura M. · Bioelectrochemistry · 2005 · 66 · 8910.1016/j.bioelechem.2004.04.005 ↗
45. Otsubo T. · J. Mater. Chem. · 2002 · 12 · 256510.1039/b203780g ↗
46. Hirayama D. · J. Am. Chem. Soc. · 2002 · 124 · 53210.1021/ja016703d ↗