journal article·2010-05-11

Indirect Grafting of Acetonitrile-Derived Films on Metallic Substrates

Avni Berisha, Catherine Combellas, Frédéric Kanoufi, Jean Pinson, Stéphane Ustaze, Fetah I. Podvorica

Chemistry of Materials· Volume 22· Issue 9
Publisher page

Abstract

Strongly bonded organic films with amino groups are obtained on gold, copper, and silicon surfaces by reduction of 2,6-dimethyl benzenediazonium in acetonitrile (ACN). The sterically hindered 2,6-dimethylphenyl radical is unable to attach to the surface, but it abstracts an hydrogen atom from ACN to give the cyanomethyl radical (·CH 2 CN) that reacts with the surface. A spontaneous reaction is also possible on copper. The film is characterized by IR spectroscopy, scanning electron microscopy, ellipsometry, water contact angles, and cyclic voltammetry. A mechanism is elaborated that accounts for the formation, grafting of the cyanomethyl radical, and finally formation of amino multilayers.
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Research context

OpenAlex topics: Molecular Junctions and Nanostructures · Conducting polymers and applications · Electrochemical sensors and biosensors

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Affiliations

Physico-Chimie des Electrolytes, des Colloides et Sciences Analytiques, ESPCI ParisTech, CNRS UMR 7195, 10 rue Vauquelin, 75231 Paris Cedex 05, France

Chemistry Department of Natural Sciences Faculty, University of Prishtina, rr. “Nëna Tereze” nr. 5, 10 000 Prishtina, Kosovo

Alchimer, 15 rue du Buisson aux Fraises, 91300, Massy, France

References (75)

Show source-provided references
1. Pinson J. · Chem. Soc. Rev. · 2005 · 34 · 42910.1039/b406228k ↗
2. Barrière F. · J. Solid State Electrochem. · 2008 · 12 · 123110.1007/s10008-008-0526-2 ↗
3. McCreery R., L. · Chem. Rev. · 2008 · 108 · 264610.1021/cr068076m ↗
4. Gooding J. J. · Electroanalysis · 2008 · 20 · 58210.1002/elan.200704124 ↗
5. Delamar M. · J. Am. Chem. Soc. · 1992 · 114 · 588310.1021/ja00040a074 ↗
6. Allongue P. · J. Am. Chem. Soc. · 1997 · 119 · 20110.1021/ja963354s ↗
7. Henry de Villeneuve C. · J. Phys. Chem. B · 1997 · 101 · 241510.1021/jp962581d ↗
8. Allongue P. · Electrochim. Acta · 1998 · 43 · 279110.1016/S0013-4686(98)00020-6 ↗
9. Adenier A. · J. Am. Chem. Soc. · 2001 · 123 · 454110.1021/ja003276f ↗
10. Chaussé A. · Chem. Mater. · 2002 · 14 · 39210.1021/cm011212d ↗
11. Adenier A. · Chem. Mater. · 2002 · 14 · 457610.1021/cm0211397 ↗
12. Bernard M. C. · Chem. Mater. · 2003 · 15 · 345010.1021/cm034167d ↗
13. Allongue P. · J. Electroanal. Chem. · 2003 · 550 · 16110.1016/S0022-0728(03)00076-7 ↗
14. Combellas C. · Langmuir · 2005 · 21 · 28010.1021/la048106l ↗
15. Adenier A. · Chem. Mater. · 2005 · 17 · 49110.1021/cm0490625 ↗
16. Combellas C. · Chem. Mater. · 2005 · 17 · 396810.1021/cm050339q ↗
17. Combellas C. · Chem. Mater. · 2006 · 18 · 202110.1021/cm052065c ↗
18. Adenier A. · Surf. Sci. · 2006 · 600 · 480110.1016/j.susc.2006.07.061 ↗
19. Podvorica F. I. · Electrochim. Acta · 2009 · 54 · 216410.1016/j.electacta.2008.10.017 ↗
20. Liu Y. C. · J. Am. Chem. Soc. · 1995 · 117 · 1125410.1021/ja00150a024 ↗
21. Liu Y. C. · Anal. Chem. · 1997 · 69 · 209110.1021/ac961305s ↗
22. DuVall S. H. · J. Am. Chem. Soc. · 2000 · 122 · 675910.1021/ja000227u ↗
23. Ranganathan S. · Nano Lett. · 2001 · 1 · 49110.1021/nl015566f ↗
24. Itoh T. · J. Am. Chem. Soc. · 2002 · 124 · 108910.1021/ja003875m ↗
25. Anariba F. · Anal. Chem. · 2003 · 75 · 383710.1021/ac034026v ↗
26. Hurley B. L. · J. Electrochem. Soc. · 2004 · 151 · B25210.1149/1.1687428 ↗
27. Anariba F. · Anal. Chem. · 2006 · 78 · 310410.1021/ac052042h ↗
28. Mahmoud A. M. · Anal. Chem. · 2009 · 81 · 697210.1021/ac901052v ↗
29. Saby C. · Langmuir · 1997 · 13 · 383710.1021/la961033o ↗
30. D’Amours M. · J. Phys. Chem B · 2003 · 107 · 481110.1021/jp027223r ↗
31. Baranton S. · J. Phys. Chem B · 2005 · 109 · 2440110.1021/jp054513+ ↗
32. Chamoulaud G. · Langmuir · 2004 · 20 · 498910.1021/la036285l ↗
33. Toupin B. · Langmuir · 2008 · 24 · 191010.1021/la702556n ↗
34. Cougnon C. · Angew. Chem., Int. Ed. · 2009 · 48 · 739510.1002/anie.200903092 ↗
35. Downard A. J. · Langmuir · 2000 · 16 · 968010.1021/la000866i ↗
36. Downard A. J. · Langmuir · 2001 · 17 · 558110.1021/la010499q ↗
37. Brooksby P. A. · Langmuir · 2004 · 20 · 503810.1021/la049616i ↗
38. Paulik M. G. · J. Phys. Chem. C · 2007 · 111 · 780810.1021/jp0706578 ↗
39. Downard A. J. · Langmuir · 2006 · 22 · 1073910.1021/la061148k ↗
40. Lehr J. · Langmuir · 2009 · 25 · 1350310.1021/la902002n ↗
41. Nielsen L. T. · J. Am. Chem. Soc. · 2007 · 129 · 188810.1021/ja0682430 ↗
42. Peng Z. · Chem. Mater. · 2008 · 20 · 606810.1021/cm800954t ↗
43. Malmos K. · J. Am. Chem. Soc. · 2009 · 131 · 1392610.1021/ja905919u ↗
44. Kariuki J. K. · Langmuir · 1999 · 15 · 653410.1021/la990295y ↗
45. Kariuki J. K. · Langmuir · 2001 · 17 · 594710.1021/la010415d ↗
46. Shewchuk D. M. · Langmuir · 2009 · 25 · 455610.1021/la8040083 ↗
47. Vase K. H. · Langmuir · 2007 · 23 · 378610.1021/la0629227 ↗
48. Matrab T. · Electrochem. Commun. · 2008 · 10 · 123010.1016/j.elecom.2008.06.006 ↗
49. Andrieux C. · J. Am. Chem. Soc. · 2003 · 125 · 1480110.1021/ja0374574 ↗
50. Wildgoose G. G. · Talanta · 2003 · 60 · 88710.1016/S0039-9140(03)00150-4 ↗
51. bBureau, C.; Pinson, J.Fr Pat 0510914, PCT WO2007048894 (to Alchimer).
52. Gomberg M. · J. Am. Chem. Soc. · 1924 · 45 · 233910.1021/ja01675a026 ↗
53. M’Halla F. · J. Am. Chem. Soc. · 1980 · 102 · 412010.1021/ja00532a023 ↗
54. Doppelt P. · Chem. Mater. · 2007 · 19 · 457010.1021/cm0700551 ↗
55. Combellas C. · J. Am. Chem. Soc. · 2008 · 130 · 857610.1021/ja8018912 ↗
56. Combellas C. · Langmuir · 2009 · 25 · 28610.1021/la8025792 ↗
57. Smith, M. B.; March, J.March’s Advanced Organic Chemistry,5thed.Wiley Interscience:New York, 2001; p510.
58. Socrates G. · 2008
59. Isse A. A. · J. Phys. Chem. A · 2004 · 108 · 418010.1021/jp036782a ↗
60. aThe reduction potential of the phenyl radical to its anion was measured by Andrieux,(20b)Ep= −0.64 V/SCE, and Vase,(20c)Ep= −0.95 V/SCE. The reduction potential of the 2,6-dimethyl phenyl radical should be slightly more negative because of the effect of the methyl groups.
61. Andrieux C. P. · J. Am. Chem. Soc. · 2003 · 125 · 1480110.1021/ja0374574 ↗
62. cVase, K.Ph.D. Thesis,University of Aarhus,Aarhus, Denmark, 2007.
63. aThe pKa of acetonitrile is 31.3(21b)and that of phenyllitium is about 43;(21c)therefore, the 2,6-dimethylbezene anion should be able to deprotonate acetonitrile to give the cyanomethyl anion.
64. Rossi L. · Mini-Rev. Org. Chem. · 2005 · 2 · 7910.2174/1570193052774135 ↗
65. cSmith, M. B.; March, J.March’s Advanced Organic Chemistry,5thed.Wiley Interscience:New York, 2001; p331.
66. Smith, M. B.; March, J.March’s Advanced Organic Chemistry,5thed.Wiley Interscience:New York, 2001; p1238.
67. aLund, H.Reduction of Azomethines in Organic Electrochemistry,4thed.Lund, H.; Hammerich, O., Eds.Marcel Dekker:New York, 2001, p435.
68. bReed, R. C.; Wightman, R. M.InEncyclopedia of Electrochemistry of the Elements;Bard, A. J.; Lund, H., Eds.Marcel Dekker:New York, Vol.XV.1, pp54.
69. Largeron M. · Org. Lett. · 2009 · 11 · 88310.1021/ol802885b ↗
70. Largeron M. · Chem. Eur. J. · 2008 · 14 · 99610.1002/chem.200700876 ↗
71. Smith, M. B.; March, J.March’s Advanced Organic Chemistry,5thed.Wiley Interscience:New York, 2001; p1177.
72. Tsubota T. · Phys. Chem. Chem. Phys. · 2002 · 4 · 388110.1039/b202345h ↗
73. Deniau G. · Chem. Mater. · 2006 · 18 · 542110.1021/cm060739t ↗
74. Tessier L. · Chem. Mater. · 2009 · 21 · 426110.1021/cm901430t ↗
75. Kim J. · Langmuir · 2010 · 26 · 259910.1021/la904027p ↗