The synthesis of chiral α-amino acid derived (1,2,3-triazol-4-yl)-picolinamide ( tzpa ) ligands 4–6 designed by combining the coordination properties two well-known ligand structures within a single unit is described.

The synthesis and study of the lanthanide luminescent 2,3-bis(1,2,3- triazol-4-yl)picolinamide (btp) based hydrogels F1 F2 is described where Tb( iii ) or Eu( are also used to crosslink btp units within polymers.

In the title compound, C(18)H(21)N(3)O(2)S·0.5H(2)O, the benzene ring makes dihedral angles of 88.59 (6) and 40.74 (8)° with the pyridine ring and the amide group, respectively. The water O atom lies on a twofold axis. In the crystal, the organic mol-ecules and the water mol-ecules are linked via O-H⋯O hydrogen bonds, while the organic mol-ecules are connected to each other via N-H⋯O hydrogen b...

Four 4-phthalimide derivatives of N-(3-chlorophenyl)-2-picolinamide were synthesized as potential ligands for the PET imaging of mGlu4 in the brain. Of these compounds, N-(3-chloro-4-(4-fluoro-1,3-dioxoisoindolin-2-yl)phenyl)-2-picolinamide (3, KALB001) exhibited improved binding affinity (IC50 = 5.1 nM) compared with ML128 (1) and was subsequently labeled with (18)F. When finally formulated in...

in this research, a pvc membrane electrode for manganese (ii) ions based on n-(2-picolinamidoethyl)picolinamide as neutral carrier was prepared. the electrode exhibits a nemstian responseover mn(ii) concentration range of (1.0 x10-5 t01.0 x 10-1m) with a slope of 29.3±0.5 mv perdecade of concentration with a working ph range of 4.0-9.0. it has a fast response time (

In this research, a PVC membrane electrode for Manganese (II) ions based on N-(2-Picolinamidoethyl)Picolinamide as neutral carrier was prepared. The electrode exhibits a Nemstian responseover Mn(II) concentration range of (1.0 x10-5 t01.0 X 10-1M) with a slope of 29.3±0.5 mV perdecade of concentration with a working pH range of 4.0-9.0. It has a fast response time (

A new palladium-catalyzed picolinamide (PA)-directed ortho-iodination reaction of ε-C(sp(2))-H bonds of γ-arylpropylamine substrates is reported. This reaction proceeds selectively with a variety of γ-arylpropylamines bearing strongly electron-donating or withdrawing substituents, complementing our previously reported PA-directed electrophilic aromatic substitution approach to this transformati...

The title compound, C(12)H(11)N(3)O(2), a hemiamidal, was synthesized by solvent-free aldol condensation at room temperature by grinding picolinamide with isonicotinaldehyde in a 1:1 molar ratio. In the mol-ecule, the two pyridine rings are inclined to one another by 58.75 (6)°. They are linked, at positions 2 and 4, by the hemiamidal bridge (-CO-NH-CHOH-). The NH-group H atom forms an intra-mo...