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Merck
CN
  • Solid state π-π stacking and higher order dimensional crystal packing, reactivity, and electrochemical behaviour of salphenazine actinide and transition metal complexes.

Solid state π-π stacking and higher order dimensional crystal packing, reactivity, and electrochemical behaviour of salphenazine actinide and transition metal complexes.

Dalton transactions (Cambridge, England : 2003) (2016-08-19)
E E Hardy, M A Eddy, B A Maynard, A E V Gorden
摘要

Condensation of a 2,3-diaminophenazine or 2,3-diamino-2-quinoxalinol with two equivalents of 3,5-ditertbutylsalicylaldehyde affords new Schiff base ligands. Here, we describe and compare the synthesis, UV-Vis, electrochemical, solution, and solid state behaviour of the free base, salphenazine ligand [L(I)], and M[L(I)] complexes, where M = UO2(vi), Cu(ii), VO(iv), Zn(ii), Co(ii), and Ni(ii). The change in π-overlap and π-stacking between molecules and long-range ordering of the solid-state structure is vastly different depending on the size and electronic character of the metal. A sterically constrained μ-oxo Fe(iii) dimer complex is also reported.

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Sigma-Aldrich
2,3-二氨基吩嗪, 90%
Sigma-Aldrich
1,5-二氟-2,4-二硝基苯, 97%