Crystallographic and Computational Electron Density of d(x2-y2) Orbitals of Azo-Schiff Base Metal Complexes Using Conventional Programs

利用常规程序计算偶氮席夫碱金属配合物d(x2-y2)轨道的晶体学和计算电子密度

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Abstract

The crystal structures of two azobenzene derivative Schiff base metal complexes (new C(44)H(40)CuN(6)O(2) of P-1 and known C(44)H(38)MnN(6)O(7) of P2(1)/c abbreviated as Cu and Mn, respectively) were (re-)determined experimentally using conventional X-ray analysis to obtain electron density using a PLATON program. Cu affords a four-coordinated square planar geometry, while Mn affords a hexa-coordinated distorted octahedral geometry whose apical sites are occupied by an acetate ion and water ligands, which are associated with hydrogen bonds. The π-π or CH-π and hydrogen bonding intermolecular interactions were found in both crystals, which were also analyzed using a Hirshfeld surface analysis program. To compare these results with experimental results, a density functional theory (DFT) calculation was also carried out based on the crystal structures to obtain calculated electron density using a conventional Gaussian program. These results revealed that the axial Mn-O coordination bonds of Mn were relatively weaker than the in-plane M-N or M-O coordination bonds.

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