## Abstract A one‐pot synthetic route that allows functionalization of the 2,6‐bis(pyrazol‐1‐yl)pyridine backbone in the 4‐ and 4″‐pyrazole positions by direct H(4)‐pyrazole halogen exchange is described. The diiodo derivative in particular provides easy access to additional functionalities through
Lanthanide Complexes of Polyacid Ligands derived from 2, 6-bis(pyrazol-1-yl)pyridine, pyrazine, and 6, 6′-bis(pyrazol-1-yl)-2, 2′-bipyridine: Synthesis and luminescence properties
✍ Scribed by Juan Carlos Rodriguez-Ubis; Rosa Sedano; Gemma Barroso; Olga Juanes; Ernesto Brunet
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- German
- Weight
- 790 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
The synthesis of three novel pyrazole-containing complexing acids, N,N,N',N'-{ 2,6-bis[3-(aminomethyl)pyrdzol-l-yl]-4-methoxypyridine}tetrakis(acetic acid) (l), N,N,N',N'-{2,6-bis[3-(aininomethyl)pyrdzoI-1-yl]pyrazine}tetrakis(acetic acid) (2), and N,N,N',N'-{6,6'-bis[3-(aminomethyl)pyrazol-l-yl]-2,2-bipyridine)tetrakis(acetic acid) (3) is described. Ligands 1-3 formed stable complexes with Eu"', Tb"', Sm"', and Dy"' in H 2 0 whose relative luminescence yields, triplet-state energies, and emission decay lifetimes were measured. The number of H 2 0 molecules in the first coordination sphere of the lanthanide ion were also determined. Comparison of data from the Eu"' and Tb"' complexes of 1-3 and those of the parent trisheterocycle N,N,N',N'-{2,6-bis[3-(aminomethyl)pyrazol-1-yl]pyridine}tetrakis(acetic acid) showed that the modification of the pyridine ring for pyrazine or 2.2'bipyridine strongly modify the luminescence properties of the complexes. Me0 Substitution at C(4) of 1 maintain the excellent properties described for the parent compound and give an additional functional group that will serve for attaching the label to biomolecules in bioaffinity applications.
📜 SIMILAR VOLUMES
Page 2890 in ref. [1] : In the experimental procedures reported for the synthesis of 2,6-Bis(4-iodopyrazol-1-yl)pyridine ( 4) the iodinating agents HIO 3 and I 2 must be dissolved in acetic acid (CH 3 COOH), not in water (H 2 O), by using the same proportions as described in the text for both the sm
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The X-Ray structures of the 1:l copper(I1) complexes with racemic and optically active (+)-(R,R)-(2,6bis(pyrro1idin-2-y1)pyridine ((+)-bpp; (+)-I) were determined. Whereas the perchlorate 1 of the racemic complex contains the monomeric units with perfect C, symmetry, the sulfate of the optically act