journal article·2025-02-11Open access

Disulfide-Containing Nitrosoarenes: Synthesis and Insights into Their Self-Polymerization on a Gold Surface

Laura Nuić, Ana Senkić, Željka Car, Ena Asić, Nataša Vujičić, Marko Kralj, Ivana Biljan

Langmuir· Volume 41· Issue 5

Abstract

High Resolution Image Download MS PowerPoint Slide Disulfide-containing nitrosoarenes with [bis(4-nitrosobenzyl) disulfide, NOBnDS ( 1 )] or without [4-nitrosophenyl disulfide, NOPDS ( 2 ), and 1,2-bis(4′-nitroso-[1,1′-biphenyl]-4-yl)disulfane, NOBPDS ( 3 )] an alkyl spacer between the sulfur headgroup and the aromatic moiety (phenyl in NOPDS ( 2 ) or biphenyl in NOBPDS ( 3 )) were synthesized and used as precursors to form azodioxy thiolate films on Au(111) substrates. Due to the incorporated disulfide functionalities, these specifically designed nitrosoarenes are enabled to self-polymerize through azodioxy bonds on a gold surface. Thin films of NOBnDS ( 1 ), NOPDS ( 2 ), and NOBPDS ( 3 ) were prepared at different adsorption times via the solution-phase self-assembly of molecules onto the Au(111) surface and characterized by Raman spectroscopy, ellipsometry, water contact angle measurements, atomic force microscopy (AFM), and scanning tunneling microscopy (STM). For comparison, films of structurally analogous disulfide-containing nitro derivatives on Au(111), which can form only monolayer films, thus serving as a reference, were also fabricated and characterized. Raman spectra of NOBnDS ( 1 ), NOPDS ( 2 ), and NOBPDS ( 3 ) films on the Au(111) substrates revealed the presence of a N═N stretching band of the E -azodioxy group. Ellipsometry showed that nitrosoarenes form thicker films compared with their nitro counterparts, indicating the formation of azodioxy oligomer films. AFM revealed an island-like morphology of the nitrosoarene films, in contrast to the rather homogeneous one observed for the monolayer films of nitro derivatives. STM images of nitrosoarene films indicated the formation of poorly organized surface structures in which oligomer chains are possibly interdigitated and substantially tilted relative to the surface normal, which agrees with the relatively low values of the ellipsometry-derived thicknesses. The obtained results emphasized the influence of the substituent electronic effects on the on-surface formation of azodioxides and could be used for the future design of azodioxy thiolate films on gold surfaces.
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Research context

OpenAlex topics: Molecular Junctions and Nanostructures · Nanomaterials for catalytic reactions · Electrocatalysts for Energy Conversion

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

Affiliations

Department of Chemistry, Faculty of Science, University of Zagreb, Horvatovac 102A, HR-10000 Zagreb, Croatia

Center for Advanced Laser Techniques, Institute of Physics, Bijenička cesta 46, HR-10000 Zagreb, Croatia

Funding

European Regional Development Fund · Hrvatska Zaklada za Znanost · Croatian Government

References (100+)

Show source-provided references
1. 10.1021/cr000073110.1021/cr0000731 ↗
2. 10.1039/cs990190035510.1039/cs9901900355 ↗
3. 10.1016/j.ccr.2019.06.01110.1016/j.ccr.2019.06.011 ↗
4. Vančik H. · 201310.1007/978-94-007-6337-1 ↗
5. 10.1021/cr030004x10.1021/cr030004x ↗
6. 10.1039/b503212c10.1039/b503212c ↗
7. 10.1002/ajoc.20160024210.1002/ajoc.201600242 ↗
8. 10.1039/C4OB01033G10.1039/C4OB01033G ↗
9. 10.1016/j.freeradbiomed.2004.02.01810.1016/j.freeradbiomed.2004.02.018 ↗
10. 10.1016/j.freeradbiomed.2003.12.01310.1016/j.freeradbiomed.2003.12.013 ↗
11. 10.1016/j.bbagen.2013.03.03410.1016/j.bbagen.2013.03.034 ↗
12. 10.1016/j.jprot.2014.03.02310.1016/j.jprot.2014.03.023 ↗
13. 10.1021/ja106357w10.1021/ja106357w ↗
14. 10.1021/cr500520s10.1021/cr500520s ↗
15. 10.1039/a703760k10.1039/a703760k ↗
16. 10.1039/a708653i10.1039/a708653i ↗
17. 10.1002/mrc.126033071210.1002/mrc.1260330712 ↗
18. 10.1039/P2996000019110.1039/P29960000191 ↗
19. 10.1039/P2982000063710.1039/P29820000637 ↗
20. 10.1021/acs.jpca.7b1217910.1021/acs.jpca.7b12179 ↗
21. 10.1038/nchem.173010.1038/nchem.1730 ↗
22. 10.1016/j.polymer.2020.12323510.1016/j.polymer.2020.123235 ↗
23. 10.1039/D2TC00760F10.1039/D2TC00760F ↗
24. 10.1021/ma00074a01510.1021/ma00074a015 ↗
25. 10.1039/b500855g10.1039/b500855g ↗
26. 10.1021/acs.jpca.0c0838210.1021/acs.jpca.0c08382 ↗
27. 10.1007/s11224-018-1136-y10.1007/s11224-018-1136-y ↗
28. 10.1021/jp011528910.1021/jp0115289 ↗
29. 10.5562/cca171410.5562/cca1714 ↗
30. 10.1021/jo051236u10.1021/jo051236u ↗
31. 10.1039/C4CE01915F10.1039/C4CE01915F ↗
32. 10.1016/j.molstruc.2015.10.00910.1016/j.molstruc.2015.10.009 ↗
33. 10.5562/cca322010.5562/cca3220 ↗
34. 10.3390/cryst712037610.3390/cryst7120376 ↗
35. 10.1002/slct.20180386610.1002/slct.201803866 ↗
36. 10.1126/sciadv.adg607910.1126/sciadv.adg6079 ↗
37. 10.1016/j.heliyon.2023.e2178110.1016/j.heliyon.2023.e21781 ↗
38. 10.1039/C6CS00509H10.1039/C6CS00509H ↗
39. 10.3184/00368500578323846210.3184/003685005783238462 ↗
40. 10.1039/c0cs00139b10.1039/c0cs00139b ↗
41. 10.1039/C2TC00146B10.1039/C2TC00146B ↗
42. 10.1002/adma.20080326710.1002/adma.200803267 ↗
43. 10.1002/elan.20039001710.1002/elan.200390017 ↗
44. 10.1007/BF0270879810.1007/BF02708798 ↗
45. 10.1039/D0TC00388C10.1039/D0TC00388C ↗
46. 10.1039/b406037g10.1039/b406037g ↗
47. 10.2174/15680260878379092910.2174/156802608783790929 ↗
48. 10.1002/cphc.20160097910.1002/cphc.201600979 ↗
49. 10.3390/mi1205056510.3390/mi12050565 ↗
50. 10.1021/acsabm.9b0041710.1021/acsabm.9b00417 ↗
51. 10.1021/jp206547k10.1021/jp206547k ↗
52. 10.5562/cca202310.5562/cca2023 ↗
53. 10.1016/j.colsurfa.2018.05.02410.1016/j.colsurfa.2018.05.024 ↗
54. 10.1016/j.colcom.2021.10053910.1016/j.colcom.2021.100539 ↗
55. 10.1016/j.polymer.2023.12579510.1016/j.polymer.2023.125795 ↗
56. 10.1126/science.106029410.1126/science.1060294 ↗
57. 10.1063/1.154194310.1063/1.1541943 ↗
58. 10.1002/adma.20080163410.1002/adma.200801634 ↗
59. 10.1038/3504600010.1038/35046000 ↗
60. 10.1103/PhysRevLett.88.17680410.1103/PhysRevLett.88.176804 ↗
61. 10.1002/adma.20030609110.1002/adma.200306091 ↗
62. 10.1002/adma.20080326710.1002/adma.200803267 ↗
63. 10.1021/jp026846210.1021/jp0268462 ↗
64. 10.1063/1.12502710.1063/1.125027 ↗
65. 10.1063/1.141577110.1063/1.1415771 ↗
66. 10.1002/(SICI)1521-4095(200006)12:11<805::AID-ADMA805>3.0.CO;2-010.1002/(SICI)1521-4095(200006)12:11<805::AID-ADMA805>3.0.CO;2-0 ↗
67. 10.1002/1521-4095(200106)13:11<803::AID-ADMA806>3.0.CO;2-W10.1002/1521-4095(200106)13:11<803::AID-ADMA806>3.0.CO;2-W ↗
68. 10.1116/1.151466510.1116/1.1514665 ↗
69. 10.1016/j.susc.2005.02.02910.1016/j.susc.2005.02.029 ↗
70. 10.1016/j.progsurf.2003.12.00110.1016/j.progsurf.2003.12.001 ↗
71. 10.1039/C5NJ01885D10.1039/C5NJ01885D ↗
72. 10.1021/ol902186d10.1021/ol902186d ↗
73. 10.1055/s-2007-99080010.1055/s-2007-990800 ↗
74. 10.1002/chem.20140248710.1002/chem.201402487 ↗
75. 10.1016/j.tet.2007.02.10110.1016/j.tet.2007.02.101 ↗
76. 10.1021/jp507265k10.1021/jp507265k ↗
77. 10.1021/ja00142a02110.1021/ja00142a021 ↗
78. 10.1039/P2992000024310.1039/P29920000243 ↗
79. 10.1016/0584-8539(75)80050-X10.1016/0584-8539(75)80050-X ↗
80. 10.1021/acs.analchem.9b0264010.1021/acs.analchem.9b02640 ↗
81. 10.1039/C6CP02353C10.1039/C6CP02353C ↗
82. 10.1103/PhysRevLett.90.06610210.1103/PhysRevLett.90.066102 ↗
83. 10.1016/j.cplett.2004.02.10910.1016/j.cplett.2004.02.109 ↗
84. 10.1021/la702836r10.1021/la702836r ↗
85. 10.1039/b923628g10.1039/b923628g ↗
86. 10.1021/la980866710.1021/la9808667 ↗
87. 10.1021/ja00200a03910.1021/ja00200a039 ↗
88. 10.1021/ja047247710.1021/ja0472477 ↗
89. 10.1021/acs.langmuir.5b0210710.1021/acs.langmuir.5b02107 ↗
90. 10.1021/acs.langmuir.7b0192110.1021/acs.langmuir.7b01921 ↗
91. 10.1021/la001217+10.1021/la001217+ ↗
92. 10.1021/jp212193v10.1021/jp212193v ↗
93. 10.1021/la970098410.1021/la9700984 ↗
94. 10.1021/am509104z10.1021/am509104z ↗
95. 10.1039/C8NR07657J10.1039/C8NR07657J ↗
96. 10.1021/la053065u10.1021/la053065u ↗
97. 10.1021/jp037307f10.1021/jp037307f ↗
98. 10.1021/acs.jpcc.0c0150710.1021/acs.jpcc.0c01507 ↗
99. 10.1021/jp021981010.1021/jp0219810 ↗
100. 10.1021/la960777z10.1021/la960777z ↗