Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Pyridine macrocyclic ligands from

Ligand abbreviations bi = 2,2 -bi-2-imidazoline bt = 2,2 -bi-2-thiazoline bpy = 2,2 -bipyridine phen = 1,10-phenanthroline phy = l,10-phenanthroline-2-carbaldehyde phenylhydrazone bpp = 2,6-bis(pyrazol-3-yl)pyridine paptH = 2-(2-pyridylamino)-4-(2-pyridyl)thiazole 2-pic = 2-picolylamine L = macrocyclic ligand derived from condensation of 2,6-diacetylpyridine with 3,6-dioxaoctane-1,8-diamine Hjthpu = pyruvic acid thiosemicarbazone Hjthpx = pyridoxal thiosemicarbazone salen = dianion of W,iV -ethylenebis(salicylideneimine) H2fsa2en = dianion of fV,JV -ethylenebis(3-carboxysalicylaldimine). [Pg.64]

Among many different complexes that have been synthesized in attempt to mimic the structure and/or functionality of SODs (16-22), the most active SOD mimetics known to date are seven-coordinate Mn(II) complexes with macrocyclic ligands derived from C-substituted pentaazacyclopentadecane [15]aneNs and its pyridine derivative (Scheme 4) (12d,16a,23-25). Some of them possess SOD activity that exceeds the one of native mitochondrial MnSOD, and are the first SOD mimetics which entered clinical trials (12d,16a,23,26-28). A few Fe(III) complexes with the same type of ligands have also been studied and they are one of the best iron-based SOD catalysts (18). It should be stressed that the decomposition of superoxide catalyzed by these complexes has been quantified by direct stopped-fiow method, in the presence of a substantial superoxide excess over catalyst, as a reliable method for determining true SOD activity (29). [Pg.63]

Pyridine-2,6-dicarbaldehyde and 2,6-diacetylpyridine have been widely used in the template synthesis of imine chelates ranging in complexity from linear tridentates, such as (17),38 39 to macrocyclic structures with a range of ring sizes, such as (18).40-42 The in situ formation of macrocyclic ligands of this type depends upon the ring size and the strength of complexation of the triamine by the metal ion at the pH of the reaction. Related complexes with an additional donor atom attached to R2 have been synthesized also.43 44... [Pg.159]

ABSTRACT. A series of macrocyclic ligands related to hexaaza[is]-annulene form stable complexes with alkali metal and alkaline earth ions. A planar, substituent-solubilized "torand", consisting of multiply fused pyridine rings, has been synthesized and has been found to sequester calcium from a dilute source. [Pg.149]


See other pages where Pyridine macrocyclic ligands from is mentioned: [Pg.126]    [Pg.382]    [Pg.617]    [Pg.1206]    [Pg.187]    [Pg.75]    [Pg.74]    [Pg.336]    [Pg.569]    [Pg.577]    [Pg.130]    [Pg.128]    [Pg.116]    [Pg.197]    [Pg.337]    [Pg.559]    [Pg.1258]    [Pg.1268]    [Pg.441]    [Pg.3]    [Pg.229]    [Pg.133]    [Pg.238]    [Pg.83]    [Pg.1258]    [Pg.1268]    [Pg.389]    [Pg.145]    [Pg.1568]    [Pg.4712]    [Pg.4722]    [Pg.5442]    [Pg.5450]    [Pg.86]    [Pg.336]    [Pg.78]    [Pg.1604]    [Pg.232]    [Pg.250]    [Pg.310]    [Pg.116]    [Pg.17]    [Pg.87]    [Pg.206]   
See also in sourсe #XX -- [ Pg.18 , Pg.47 ]




SEARCH



Ligands pyridine

Macrocycles Macrocyclic ligands

Pyridines macrocyclic

© 2024 chempedia.info