4.7 Article

Orthogonal non-covalent binding forces in solid state supramolecular herringbone-shaped interlocked dimers. Pseudopolymorphism in [(ppy)Pd(mu-pz)](2) (ppy=2-(2-pyridyl)phenyl, pz = pyrazol-1-yl) complex

Journal

DALTON TRANSACTIONS
Volume -, Issue 43, Pages 9625-9636

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b910502f

Keywords

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Funding

  1. MICINN-Spain [CTQ2008-01402]
  2. Fundacion Seneca (Agencia de Ciencia y Tecnologia de la Region de Murcia) [04509/GERM/06]
  3. Programa de Ayudas a Grupos de Excelencia de la Region de Murcia, Plan Regional de Ciencia y Tecnologia

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The crystal structures of [(ppy)Pd(mu-pz)](2) (ppy = 2-(2-pyridyl)phenyl, pz = pyrazol-1-yl) ( 1) and two different solvatomorphs of it, [(ppy)Pd(mu-pz)](2)center dot 1/2 CH2Cl2 (2) and [(ppy)Pd(mu-pz)](2)center dot 1/2 CHCl3 (3) have been elucidated by powder (1 and 2) and single crystal (3) X-ray diffraction. In all of them two molecules fit together following a very similar pattern forming a dimer. All neutral dinuclear square-planar complexes having mu-pz or related bridges and planar aromatic ligands completing the coordination spheres found in the CSD show a similar arrangement to those observed in compounds 1-3, consisting of interlocked dimers following a herringbone-like pattern. A DFT study reveals the simultaneous action of pi,pi- and T-stacking interactions occurring as two sets of orthogonally oriented binding forces, as well as anagostic bonds overlapped with the latter.

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