Fluorogenic N,O-chelates built on a C2-symmetric aryleneethynylene platform: Spectroscopic and structural consequences of conformational preorganization and ligand denticity
摘要:
Using p-extended aryleneethynylene as a rigid structural skeleton, a C-2-symmetric bis(picolinate) ligand was prepared. Binding of zinc(II) or cadmium(II) ion to this formally tetradentate N2O2-chelate resulted in significant red-shifts and enhancement in emission. The metal-ligand interaction responsible for such structural change was investigated by isolation and characterization of a tetrazinc(II) complex, in which the picolinate group functions not only as terminal bidentate but also as bridging with its mu-1,3 carboxylate unit. (C) 2011 Elsevier B.V. All rights reserved.
Fluorogenic N,O-chelates built on a C2-symmetric aryleneethynylene platform: Spectroscopic and structural consequences of conformational preorganization and ligand denticity
摘要:
Using p-extended aryleneethynylene as a rigid structural skeleton, a C-2-symmetric bis(picolinate) ligand was prepared. Binding of zinc(II) or cadmium(II) ion to this formally tetradentate N2O2-chelate resulted in significant red-shifts and enhancement in emission. The metal-ligand interaction responsible for such structural change was investigated by isolation and characterization of a tetrazinc(II) complex, in which the picolinate group functions not only as terminal bidentate but also as bridging with its mu-1,3 carboxylate unit. (C) 2011 Elsevier B.V. All rights reserved.
Fluorogenic N,O-chelates built on a C2-symmetric aryleneethynylene platform: Spectroscopic and structural consequences of conformational preorganization and ligand denticity
作者:Byung Gyu Park、Maren Pink、Dongwhan Lee
DOI:10.1016/j.jorganchem.2011.07.007
日期:2011.12
Using p-extended aryleneethynylene as a rigid structural skeleton, a C-2-symmetric bis(picolinate) ligand was prepared. Binding of zinc(II) or cadmium(II) ion to this formally tetradentate N2O2-chelate resulted in significant red-shifts and enhancement in emission. The metal-ligand interaction responsible for such structural change was investigated by isolation and characterization of a tetrazinc(II) complex, in which the picolinate group functions not only as terminal bidentate but also as bridging with its mu-1,3 carboxylate unit. (C) 2011 Elsevier B.V. All rights reserved.