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                <title level="j">Inorganic Chemistry</title>
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                <term xml:lang="en">ELF and QTAIM topological analyses</term>
                <term xml:lang="en">Ag-N and Ag-Ag bond energies</term>
                <term xml:lang="en">DFT</term>
                <term xml:lang="en">Ethylamine</term>
                <term xml:lang="en">geometrical 2D/3D transition</term>
                <term xml:lang="en">Ag clusters</term>
                <term xml:lang="en">Energy</term>
                <term xml:lang="en">Metal clusters</term>
                <term xml:lang="en">Ligands</term>
                <term xml:lang="en">Silver</term>
                <term xml:lang="en">Mathematical methods</term>
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              <p>Amine ligands are expected to drive the organization of metallic centers as well as the chemical reactivity of silver clusters early growing during the very first steps of the synthesis of silver nanoparticles via an organometallic route. Density functional theory (DFT) computational studies have been performed to characterize the structure, the atomic charge distribution, and the planar two-dimensional (2D)/three-dimensional (3D) relative stability of small-size silver clusters (Agn, 2 ≤ n ≤ 7), with or without an ethylamine (EA) ligand coordinated to the Ag clusters. The transition from 2D to 3D structures is shifted from n = 7 to 6 in the presence of one EA coordinating ligand, and it is explained from the analysis of the Ag–N and Ag–Ag bond energies. For fully EA saturated silver clusters (Agn–EAn), the effect on the 2D/3D transition is even more pronounced with a shift between n = 4 and 5. Subsequent electron localization function (ELF) and quantum theory of atoms in molecules (QTAIM) topological analyses allow for the fine characterization of the dative Ag–N and metallic Ag–Ag bonds, both in nature and in strength. Electron transfer from ethylamine to the coordinated silver atoms induces an increase of the polarization of the metallic core.</p>
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