Abstract
The synthesis and structural characterization of a series of neutral Eu3+-containing macrocyclic complexes, Eu(4)-Eu(7), are reported. The synthetic pathway herein allows for the size and functionality of the macrocycle to be tailored in one step from a common precursor (N,N″-bis(p-isothiocyanatobenzylcarbamoylmethyl)diethylenetriamine-N, N′,N″-triacetic acid, (3) in high yield. The macrocyclic ligands 4-7 have within their structure a bis-amide derivative of diethylenetriaminepentaacetic acid (DTPA) functioning as the europium chelate that is bridged through thiourea groups by either a butyl (4), hexyl (5), octyl (6), or m-benzyl (7) linker. The two thiourea groups were designed into the host macrocycle to serve as hydrogen-bond donors to potential guest molecules that may alter the luminescence properties of the parent macrocycle. Characterization of the luminescence of Eu(4)-Eu(7) reveals an antenna effect from the ligand, and the luminescence lifetime data reveals the presence of one coordinated water molecule in aqueous solution.
Original language | English (US) |
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Pages (from-to) | 9829-9836 |
Number of pages | 8 |
Journal | Inorganic Chemistry |
Volume | 44 |
Issue number | 26 |
DOIs | |
State | Published - Dec 26 2005 |