Two mononuclear DyIII complexes, [Dy(L1)(NCS)3] (Dy-EDA) and [Dy(L2)(NCS)3] (Dy-DAP), where L
n
(n = 1–2) corresponds to a macrocyclic
ligand derived
from 2,6-pyridinedicarboxaldehyde and ethylenediamine (L1) and 1,3-diaminepropane (L2) were immobilized on functionalized
silicon-based surfaces. This was achieved by the microcontact printing
(μCP) technique, generating patterns on a functionalized surface
via covalent bond formation through the auxiliary −NCS ligands
present in the macrocyclic complex species. With this strategy, it
was possible to control the position of the immobilized molecules
on the surface. Water contact angle measurements, X-ray photoelectron
spectroscopy (XPS), infrared reflection absorption spectra (IRRAS),
and atomic force microscopy (AFM) confirmed that the surfaces were
successfully functionalized. Furthermore, the optical properties in
a broad temperature range were investigated for the as-prepared compounds.
At room temperature, Dy-EDA was shown to emit in the
deep blue region (Commission Internationald’Eclairage (CIE):
(0.175, 0.128)), while Dy-DAP in the white region (CIE:
(0.252, 0.312)). The different CIE values were due to the contribution
of the strong emission of the ligand in the case of Dy-EDA. Besides, surface photoluminescence measurements showed that the
immobilized complexes retained their bulk emissive properties.