We show, by complementary spectroscopic and STM analysis, that Cr7Ni derivatives are suitable to be sublimed in UHV conditions. Cr7Ni-bu weakly bonds to gold surface and can diffuse relatively freely on it, forming monolayers with hexagonal 2D packing. Conversely, by adding a functional thiol group to the central dibutylamine, a covalent bond between the molecule and surface gold adatoms is promoted, leading to a strong molecular grafting and the formation of a disordered monolayer. These two examples demonstrate the possibility to control the assembly of a large molecular complex, as rationalized by DFT calculations that establish different energy scales in the deposition processes. Moreover, low-temperature XMCD sprectra show that the magnetic features of Cr7Ni rings deposited in UHV on gold remain unchanged with respect to those of the corresponding bulk sample.

Self-Assembled Monolayer of Cr7Ni Molecular Nanomagnets by Sublimation

A Ghirri;V Corradini;V Bellini;R Biagi;U del Pennino;V De Renzi;M Affronte
2011

Abstract

We show, by complementary spectroscopic and STM analysis, that Cr7Ni derivatives are suitable to be sublimed in UHV conditions. Cr7Ni-bu weakly bonds to gold surface and can diffuse relatively freely on it, forming monolayers with hexagonal 2D packing. Conversely, by adding a functional thiol group to the central dibutylamine, a covalent bond between the molecule and surface gold adatoms is promoted, leading to a strong molecular grafting and the formation of a disordered monolayer. These two examples demonstrate the possibility to control the assembly of a large molecular complex, as rationalized by DFT calculations that establish different energy scales in the deposition processes. Moreover, low-temperature XMCD sprectra show that the magnetic features of Cr7Ni rings deposited in UHV on gold remain unchanged with respect to those of the corresponding bulk sample.
2011
Istituto Nanoscienze - NANO
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/234584
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