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Synthesis and Characterization of Isostructural Th(IV) and U(IV) Pyridine Dipyrrolide Complexes.
Valerio, Leyla R; Hakey, Brett M; Leary, Dylan C; Stockdale, Erin; Brennessel, William W; Milsmann, Carsten; Matson, Ellen M.
Afiliación
  • Valerio LR; Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
  • Hakey BM; Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
  • Leary DC; C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, West Virginia 26506, United States.
  • Stockdale E; Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
  • Brennessel WW; Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
  • Milsmann C; C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, West Virginia 26506, United States.
  • Matson EM; Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
Inorg Chem ; 63(21): 9610-9623, 2024 May 27.
Article en En | MEDLINE | ID: mdl-38377955
ABSTRACT
A series of pyridine dipyrrolide actinide(IV) complexes, (MesPDPPh)AnCl2(THF) and An(MesPDPPh)2 (An = U, Th, where (MesPDPPh) is the doubly deprotonated form of 2,6-bis(5-(2,4,6-trimethylphenyl)-3-phenyl-1H-pyrrol-2-yl)pyridine), have been prepared. Characterization of all four complexes has been performed through a combination of solid- and solution-state methods, including elemental analysis, single crystal X-ray diffraction, and electronic absorption and nuclear magnetic resonance spectroscopies. Collectively, these data confirm the formation of the mono- and bis-ligated species. Time-dependent density functional theory has been performed on all four An(IV) complexes, providing insight into the nature of electronic transitions that are observed in the electronic absorption spectra of these compounds. Room temperature, solution-state luminescence of the actinide complexes is presented. Both Th(IV) derivatives exhibit strong photoluminescence; in contrast, the U(IV) species are nonemissive.