Synthesis of a New Tetrapyridyl Ligand and the Characterization of Three Distinct Metal- and Hydrogen-Bonding Conformations
Abstract
The design, synthesis, and complexation characteristics of the ligand 1,2,4,5-tetrakis-(2‘-pyridylethynyl)benzene are described. Three distinct essentially planar conformations are demonstrated. Conformational flexibility allows the ligand to adopt an "in-in" conformation and complex silver(I) cations. On self-assembly with resorcinol, the ligand adopts an "out-out" conformation to accommodate the larger resorcinol molecule with pyridyl-hydroxyl hydrogen bonding. In contrast, an "in-out-in-out" conformation is adopted on complexation with 2,7-dinitrofluorenone through weak hydrogen bonds.
Department(s)
Chemistry and Biochemistry
Document Type
Article
DOI
https://doi.org/10.1021/cg0255974
Keywords
self organization, ligands, pyridyl, conformation, noncovalent interactions
Publication Date
2003
Recommended Citation
Bosch, Eric, Nate Schultheiss, Nigam Rath, and Marcus Bond. "Synthesis of a new tetrapyridyl ligand and the characterization of three distinct metal-and hydrogen-bonding conformations." Crystal growth & design 3, no. 2 (2003): 263-266.
Journal Title
Crystal growth & design