J. J. Gooding and S. Ciampi, Chem. Soc. Rev, vol.40, pp.2704-2718, 2011.

J. J. Gooding, Electroanalysis, vol.20, pp.573-582, 2008.

C. J. Love, L. A. Estroff, J. K. Kriebel, R. G. Nuzzo, and G. M. Whitesides, Chem. Rev, vol.105, pp.1103-1169, 2005.

C. Vericat, M. E. Vela, G. Benitez, P. Carro, and R. C. Salvarezza, Chem. Soc. Rev, vol.39, pp.1805-1834, 2010.

J. Pinson, F. Podvorica-;-b)-s.-mahouche-chergui, S. Gam-derouich, C. Mangeney, and M. H. Chehimi, Chem. Soc. Rev, vol.34, pp.4143-4166, 2005.

A. Adenier, C. Combellas, F. Kanoufi, J. Pinson, and F. I. Podvorica, Chem. Mater, vol.18, pp.2021-2029, 2006.

A. Mattiuzzi, I. Jabin, C. Mangeney, C. Roux, O. Reinaud et al., Nat. Commun, vol.3, p.1130, 2012.

, It was shown that propyl groups are the smallest possible for blocking the oxygen-through-the-annulus rotation of the aromatic units, see, Chem. Rev, vol.97, pp.1713-1734, 1997.

P. Blond, A. Mattiuzzi, H. Valkenier, L. Troian-gautier, J. Bergamini et al., Langmuir, vol.34, pp.6021-6027, 2018.

L. Troian-gautier, D. Martinez-tong, J. Hubert, F. Reniers, M. Sferrazza et al., J. Phys. Chem. C, vol.120, 2016.

L. Troian-gautier, H. Valkenier, A. Mattiuzzi, I. Jabin, N. Van-den-brande et al., Chem. Commun, vol.52, pp.10493-10496, 2016.

L. Santos, A. Mattiuzzi, I. Jabin, N. Vandencasteele, F. Reniers et al., J. Phys. Chem. C, vol.118, pp.15919-15928, 2014.

H. Valkenier, V. Malytskyi, P. Blond, M. Retout, A. Mattiuzzi et al., Langmuir, vol.33, pp.8253-8259, 2017.

G. De-leener, F. Evoung-evoung, A. Lascaux, J. Mertens, A. G. Porras-gutierrez et al., J. Electroanal. Chem, vol.138, pp.265-278, 2016.

T. Breton and A. J. Downard, Aust. J. Chem, vol.70, pp.960-972, 2017.

C. Cannizzo, M. Wagner, J. Jasmin, C. Vautrin, D. Doizi et al., Tetrahedron Lett, vol.55, pp.4315-4318, 2014.

J. Van-loon, A. Arduini, W. Verboom, R. Ungaro, G. J. Van-hummel et al., For seminal work, see: (a), Tetrahedron Lett, vol.30, pp.1633-1640, 1986.

R. Lavendomme, S. Zahim, G. De-leener, A. Inthasot, A. Mattiuzzi et al., Asian J. Org. Chem, vol.4, pp.710-722, 2015.

H. Shimizu, K. Iwamoto, K. Fujimoto, and S. Shinkai, Chem. Lett, p.2147, 1991.

, The term "iteroselectivity" refers to the selectivity that concerns the formation of products (i.e. iteromers) differing by the number of repeating chemical transformations they underwent, J. Org. Chem, vol.79, pp.6563-6570, 2014.

X. Chen, M. Ji, D. R. Fisher, and C. M. Wai, Synlett, vol.11, pp.1784-1786, 1999.

P. Timmerman, S. Harkema, G. J. Van-hummel, W. Verboom, and D. N. Reinhoudt, Note that the formation of oxidized products under nitration conditions was already reported on a related calix[4]arene, see, J. Incl. Phenom. Mol. Recognit. Chem, vol.16, pp.189-197, 1993.

J. Andersen, U. Madsen, F. Björkling, and X. Liang, Synlett, vol.14, pp.2209-2213, 2005.

C. Jaime, J. D. Mendoza, P. Prados, P. M. Nieto, and C. Sanchez, J. Org. Chem, vol.56, pp.3372-3376, 1991.

A. Inthasot, E. Brunetti, M. Lejeune, N. Ménard, T. Prangé et al., Chem. Eur. J, vol.22, pp.4855-4862, 2016.

J. Pinson and D. Bélanger, Chem. Soc. Rev, vol.40, pp.3995-4048, 2011.

S. H. Duvall and R. L. Mccreery, Anal. Chem, vol.71, pp.4594-4602, 1999.

H. Kawabata, M. Aoki, K. Murata, and S. Shinkai, Supramol. Chem, vol.2, pp.33-39, 1993.

X. Chen, M. Ji, D. R. Fisher, and C. M. Wai, Synlett, vol.11, pp.1784-1786, 1999.

, The efficient synthesis of a calix[4]arene-monodiazonium salt is described. The electrografting of this new compound on glassy carbon electrodes leads to a compact covalently-bound calix[4]arene layer. Surface Functionalization Volodymyr Malytskyi, Ludovic TroianGautier

C. Lagrost and I. Jabin,