Metal-organic chains constructed from pre-organized N2S2 donor ligands
摘要:
Three new N2S2 donor ligands 1,1'-((2-(2-(phenylthio)phenylthio)phenyl)methylene)bis(3,5-R-1H-pyrazole), R = H (L-H), R = Me (L-Me), R = i-Pr (Li-Pr) have been prepared and characterized, These bifunctional ligands incorporate two distinct chelate donor systems, by virtue of the presence of bispyrazole and bis-thioether functions. The preferred conformation of these ligands is such that the N-2 and S-2 donor moieties may be oriented in opposite directions, thus favoring the formation of molecular chains when treated with AgBF4. The X-ray structures of Ag(I) complexes show that, depending on the steric hindrance present on the pyrazole rings, these ligands behave as kappa(4)-SSNN-mu bridging tetradentate (when R = H), or kappa(3)-SNN-mu bridging tridentate (when R = Me, i-Pr). Interestingly, [Ag(L-H)]BF4 crystallizes in the chiral space group P4(1), with the molecular chain that is folded around the 4(1) screw axis. (C) 2009 Elsevier Ltd. All rights reserved.
Metal-organic chains constructed from pre-organized N2S2 donor ligands
摘要:
Three new N2S2 donor ligands 1,1'-((2-(2-(phenylthio)phenylthio)phenyl)methylene)bis(3,5-R-1H-pyrazole), R = H (L-H), R = Me (L-Me), R = i-Pr (Li-Pr) have been prepared and characterized, These bifunctional ligands incorporate two distinct chelate donor systems, by virtue of the presence of bispyrazole and bis-thioether functions. The preferred conformation of these ligands is such that the N-2 and S-2 donor moieties may be oriented in opposite directions, thus favoring the formation of molecular chains when treated with AgBF4. The X-ray structures of Ag(I) complexes show that, depending on the steric hindrance present on the pyrazole rings, these ligands behave as kappa(4)-SSNN-mu bridging tetradentate (when R = H), or kappa(3)-SNN-mu bridging tridentate (when R = Me, i-Pr). Interestingly, [Ag(L-H)]BF4 crystallizes in the chiral space group P4(1), with the molecular chain that is folded around the 4(1) screw axis. (C) 2009 Elsevier Ltd. All rights reserved.
Three new N2S2 donor ligands 1,1'-((2-(2-(phenylthio)phenylthio)phenyl)methylene)bis(3,5-R-1H-pyrazole), R = H (L-H), R = Me (L-Me), R = i-Pr (Li-Pr) have been prepared and characterized, These bifunctional ligands incorporate two distinct chelate donor systems, by virtue of the presence of bispyrazole and bis-thioether functions. The preferred conformation of these ligands is such that the N-2 and S-2 donor moieties may be oriented in opposite directions, thus favoring the formation of molecular chains when treated with AgBF4. The X-ray structures of Ag(I) complexes show that, depending on the steric hindrance present on the pyrazole rings, these ligands behave as kappa(4)-SSNN-mu bridging tetradentate (when R = H), or kappa(3)-SNN-mu bridging tridentate (when R = Me, i-Pr). Interestingly, [Ag(L-H)]BF4 crystallizes in the chiral space group P4(1), with the molecular chain that is folded around the 4(1) screw axis. (C) 2009 Elsevier Ltd. All rights reserved.