Supramolecular Architectures of Metal Complexes Controlled by a Strong π···π Stacking, 1,8-Naphthalimide Functionalized Third Generation Tris(pyrazolyl)methane Ligand
Autor: | Jacob J. Horger, Daniel L. Reger, Mark D. Smith, Eric Sirianni, Radu F. Semeniuc |
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Rok vydání: | 2009 |
Předmět: | |
Zdroj: | Crystal Growth & Design. 10:386-393 |
ISSN: | 1528-7505 1528-7483 |
DOI: | 10.1021/cg901000d |
Popis: | A new hetero-bifunctional ligand designed to form supramolecular structures with a combination of covalent and noncovalent forces has been prepared. The ligand, (1,8-naphthalimide)CH2C6H4CH2OCH2C(pz)3 (Ltris, pz = pyrazolyl ring), contains both a tris(pyrazolyl)methane coordination unit and a 1,8-naphthalimide strong π···π stacking unit. The reactions of iron(II), copper(II), and cadmium(II) tetrafluoroborate salts with 2 equiv of Ltris yield [Fe(Ltris)2](BF4)2 (1), [Cd(Ltris)2](BF4)2 (2), and [Cu(Ltris)2](BF4)2 (3), respectively. Vapor diffusion crystallization yielded two pseudopolymorphs for 1. In the solid-state structures of both forms, the iron is in an octahedral environment with bond distances expected for low-spin iron(II); both tris(pyrazolyl)methane donor sets are in a κ3-coordination mode with each Ltris ligand in a U-shaped, syn arrangement. In one pseudopolymorph, the 1,8-naphthalimide side chains are on the same side of the molecule when viewed down the metal axis (syn-1), twisted only 30° ... |
Databáze: | OpenAIRE |
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