A computational investigation of polypyrrolic macrocyclic actinyl complexes: effects of explicit solvent coordination on structure, vibrational spectra and redox property

• Published in: Theoretical chemistry accounts Vol. 135; no. 8; pp. 1 - 9
• Main Authors: Qu, Ning, Zhong, Yu-Xi, Schreckenbach, Georg, Pan, Qing-Jiang
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.08.2016; Springer Nature B.V
• Subjects: Atomic/Molecular Structure and Spectra; Chemistry; Chemistry and Materials Science; Electron spin; Inorganic Chemistry; Macrocyclic compounds; Organic Chemistry; Physical Chemistry; Regular Article; Solvents; Tetrahydrofuran; Theoretical and Computational Chemistry; Reduction potentials; Solvation; Actinyl complexes; Relativistic DFT; Schiff-base polypyrrolic macrocycle
• ISSN: 1432-881X; 1432-2234
• DOI: 10.1007/s00214-016-1959-9

Eighteen actinyl complexes of a Schiff-base polypyrrolic macrocycle (H 4 L), [(Sol)(An m O 2 )(H 2 L)] n− (Sol = Vacant, pyridine (py) and tetrahydrofuran (THF); An=U, Np and Pu; m = VI and n = 0, m = V and n = 1) were investigated using relativistic density functional theory. Comparison of complexes with and without the explicit solvent coordination to the metal center, and changes in actinide element and metal oxidation state provide insight into their effects on structural and energetic properties of the complexes. Compared with those of the solvent-free complexes, the An=O bond lengths of the solvated complexes differ within 0.01 Å, and the deviation of the O=An=O angles is less than 1°. The H···O endo bonds are relatively sensitive to the explicit solvent coordination, showing the largest discrepancy of 0.05 Å. Charges and electron-spin densities of actinides are only slightly affected by the inclusion of the explicit solvent. Reduction potentials of actinyl complexes have been addressed, and their dependence on the bulk solvent polarity is being discussed, using a simple model based on the Born equation.