Abstract
With the Zn-Schiff-base [ZnL(CH3CN)] from the pure Salen-type Schiff-base ligand H2L (H2L = N,N′-bis(salicylidene) phenylene-1,2-diamine) as the precursor, a hetero-trinuclear Zn2Nd complex [Zn2Nd(L)2(NO3)3(CH 3CN)2] (1) and a hetero-binuclear ZnNd complex [ZnNd(L)2Cl(DMF)] (2) are obtained by the further reaction with Nd(NO3)3•6H2O or NdCl3• 6H2O, respectively. The influence of structural differences of the two complexes on their photophysical properties shows the anionic inducement leads to the effective modulation of the NIR luminescent properties by the adjustment of the coordination sphere of the Nd3+ ions.
Original language | English |
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Pages (from-to) | 75-78 |
Number of pages | 4 |
Journal | Inorganic Chemistry Communications |
Volume | 14 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 2011 |
Scopus Subject Areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry
- Materials Chemistry
User-Defined Keywords
- Anionic inducement
- Modulation of NIR luminescence
- Sensitization and energy transfer
- ZnNd and ZnNd arrayed Schiff-base complexes