Near-IR absorbing donor-acceptor ligand-to-ligand charge-transfer complexes of nickel(ii).

نویسندگان

  • Lindsay A Cameron
  • Joseph W Ziller
  • Alan F Heyduk
چکیده

A new series of square-planar nickel(ii) donor-acceptor complexes exhibiting ligand-to-ligand charge-transfer (LL'CT) transitions have been prepared. Whereas the use of a catecholate donor ligand in conjunction with a bipyridyl acceptor ligand affords a complex that absorbs throughout the visible region, the use of a azanidophenolate donor ligands in conjunction with a bipyridyl acceptor ligand affords complexes that absorbs well into the near-IR region of the solar spectrum. Three new complexes, (cat)Ni(bpy t Bu2) (1; (cat)2- = 3,5-di-tert-butyl-1,2-catecholate; bpy t Bu2 = 4,4'-di-tert-butyl-2,2'-bipyridine), (ap)Ni(bpy t Bu2) (2; (ap)2- = 4,6-di-tert-butyl-2-(2,6-diisopropylphenylazanido)phenolate), and (apPh)Ni(bpy t Bu2) (3; (apPh)2- = 10-(2,6-diisopropylphenylazanido)-9-phenanthrolate), have been prepared and characterized by structural, electrochemical, and spectroscopic methods. Whereas all three square-planar complexes show multiple reversible one-electron redox-processes and strong LL'CT absorption bands, in azanidophenolate complexes 2 and 3, the LL'CT absorption covers the near-IR region from 700-1200 nm. The electronic absorption spectra and ground state electrochemical data for 2 and 3 provide an estimate of their excited-state reduction potentials, E+/*, of -1.3 V vs. SCE, making them as potent as the singlet excited state of [Ru(bpy)3]2+.

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عنوان ژورنال:
  • Chemical science

دوره 7 3  شماره 

صفحات  -

تاریخ انتشار 2016