178039-84-4Relevant articles and documents
Electrocatalytic carbon dioxide reduction by using cationic pentamethylcyclopentadienyl-iridium complexes with unsymmetrically substituted bipyridine ligands
Sypaseuth, Fanni D.,Matlachowski, Corinna,Weber, Manuela,Schwalbe, Matthias,Tzschucke, C. Christoph
, p. 6564 - 6571 (2015)
Eight [Ir(bpy)CpCl]+-type complexes (bpy= bipyridine, Cp=1,2,3,4,5-pentamethylcyclopentadienyl) containing differently substituted bipyridine ligands were synthesized and characterized. Cyclic voltammetry (CV) of the complexes in Ar-saturated a
ZnCl2 Capture Promotes Ethylene Polymerization by a Salicylaldiminato Ni Complex Bearing a Pendent 2,2′-Bipyridine Group
Smith, Abigail J.,Kalkman, Eric D.,Gilbert, Zachary W.,Tonks, Ian A.
, p. 2429 - 2432 (2016)
The effect of ZnCl2 additives on a series of (salicylaldiminato)Ni ethylene polymerization catalysts is reported. While ZnCl2 acts solely as a pyridine scavenger for simple imine catalyst frameworks such as the biphenylimine 4, in th
Synthesis, guest binding, and metal coordination of functionalized self-folding deep cavitands
Mettry, Magi,Moehlig, Melissa P.,Hooley, Richard J.
supporting information, p. 1497 - 1500 (2015/03/30)
A simple method to introduce donor functions to the upper rim of self-folding benzimidazole-based deep cavitands is described. The upper rim donors allow controlled noncovalent binding of suitably sized guest species via both self-complementary hydrogen bonding and space-filling interactions, and metal-mediated self-folding is possible if bidentate coordinators are incorporated.