Co-existence of heterometallic Zn2Er and ZnEr arrayed chromophores for the sensitization of near-infrared (NIR) luminescence

With the Zn-Schiff-base [ZnL(Py)] from the simple Salen-type Schiff-base ligand H2L (H2L = N,N′-bis(salicylidene)ethylene-1,2-diamine) as the precursor, two co-crystallized heterometallic (Zn2Ln and ZnLn array) complexes [Zn2Ln(L)2(Py)2(NO3)2]·[ZnLn(L)(Py)(NO3)3(H2O)]·NO3·mMeOH·nS (Ln = Er(1), S = CH3CN, m = 2, n = 1 or Gd(2), S = H2O, m = 1, n = 3) were obtained by the further reaction with Ln(NO3)3·6H2O, respectively. The result of their photophysical properties shows the intramolecular effective energy transfer has been demonstrated in the Zn2Er and ZnEr arrayed complex 1, and the co-existence of different chromophores should be a potentially new way to the fine-tuning properties of NIR luminescence from Er3+ ions.

Two co-crystallized heterometallic (both Zn2Ln and ZnLn array) complexes 1–2 were obtained. The results of sensitization and the energy transfer of the Zn(II) blocks for the NIR luminescence of the Er3+ ion show that the co-existence of different chromophores is a potentially effective way to the fine-tuning properties of NIR luminescence from Er3+ ion.Figure optionsDownload as PowerPoint slide