The three novel pyridine-containing 12-membered macrocyclic ligands 1 ± 3 were synthesized. The coordinating arms are represented by three acetate moieties in 1 and 3 and by one acetate and two phosphonate moieties in 2. In all three ligands, the acetate arm in the distal position is substituted, wi
Synthesis and Relaxometric Properties of Gadolinium(III) Complexes of New Triazine-Based Polydentate Ligands
✍ Scribed by Lorenzo Tei; Marina Benzi; Filip Kielar; Mauro Botta; Camilla Cavallotti; Giovanni Battista Giovenzana; Silvio Aime
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- German
- Weight
- 288 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Two new derivatives based on an s‐triazine structural motif were synthesized by attaching two 2,2′‐hydrazinylidenebis[acetic acid] moieties to the triazine ring to reach an overall heptadenticity for the complexation of lanthanide(III) cations. The remaining reactive site was exploited for the substitution with a functionizable amino group (see H~4~L1) and a lipophilic moiety (see H~4~L2). Luminescence‐lifetime determinations revealed the presence of a single H~2~O molecule coordinated for [Eu(L1)]. A complete ^1^H‐NMR relaxometric study was carried out for the octacoordinated [Gd(L1)] and [Gd(L2)] complexes. A remarkably long H~2~O residence lifetime (^298^τ~M~=5.2 μs) was found by ^17^O‐NMR in the case of [Gd(L1)]. Micelle formation of the lipophilic complex [Gd(L2)] was evidenced, the critical micellization concentration (cmc) determined, and relaxometric properties of the system investigated.
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## Abstract A new synthetic route for preparing multidirectional ligands was developed by using 2,4,6‐trichloro‐1,3,5‐triazine (cyanuric chloride) as core. The reaction included the selective substitutions of 4‐aminobenzoic acid onto three chlorides of the triazine ring via a stepwise manner at 1:1
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