Journal
RUSSIAN CHEMICAL BULLETIN
Volume 71, Issue 6, Pages 1111-1122Publisher
SPRINGER
DOI: 10.1007/s11172-022-3511-5
Keywords
hypercoordinated silicon; substituted catecholate ligands; quantum chemical calculations; ionization potential; oxidation potential; electron localization function (ELF); average local ionization energy (ALIE)
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Funding
- Russian Foundation for Basic Research [19-2908021]
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The anionic complexes LSi(Cat(R))(2) were studied using quantum chemistry methods, and it was found that the substituents in the catecholate phenyl ring and the L group have weak influence on the geometry of the coordination environment of the silicon atom. The electron-withdrawing effect and the number of substituents in the catecholate ligands determine the ionization potentials. The formation of oxidized forms of the complexes is characterized by weakening of certain Si-O bonds and shortening of others. The analysis shows that one of the catecholate ligands is less sensitive to interaction with free radicals.
Anionic complexes LSi(Cat(R))(2) (L is a chelate N-methyl-N-(acetamido) methyl-C,O group or (2-oxo-1-hexahydroazepinyl)methyl-C,O group; Cat(R) is a substituted catecholate ligand) were studied by quantum chemistry at the PBE0/6-311G(d,p) and RI-MP2/def2-TZVPP levels with inclusion of nonspecific solvation using the PCM model. It was shown that the nature of substituents in the catecholate phenyl ring and the L group weakly influences the geometry of the coordination environment of the silicon atom. The higher the electron-withdrawing effect and the number of substituents in the catecholate ligands, the higher the vertical or adiabatic ionization potentials. It was established that the formation of oxidized forms of the complexes LSi(Cat(R))(2) is characterized by weakening of the Si-O bonds between the silicon atom and the Cat(R) (Cat(R)-2) ligand opposite to the Si-O bond with the group L and by shortening of the Si-O bonds between the silicon atom and the other catecholate ligand (Cat(R)-1). An analysis of the average local ionization energies and a topological analysis of the electron localization function showed the Cat(R)-2 ligand is less sensitive to the interaction with free radicals than Cat(R)-1 due to redistribution of electron density from the region of its oxygen atoms and phenyl ring.
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