Supramolecular Structures and Columnar Mesophase Induction in Nondiscoid Pyrazoles by Complexation to Rhodium(I)

Raquel Giménez,* Anabel Elduque,* José Antonio López, Joaquín Barberá, Emma Cavero, Ignacio Lantero, Luis A. Oro, and José Luis Serrano
Departamento de Qumica Orgnica and Departamento de Qumica Inorgnica, Facultad de CienciasInstituto de Ciencia de Materiales de Aragn, Universidad de Zaragoza-CSIC, 50009 Zaragoza, Spain
Inorg. Chem., 2006, 45 (25), pp 10363–10370
DOI: 10.1021/ic0614216
Publication Date (Web): November 15, 2006
Copyright © 2006 American Chemical Society
*

 To whom correspondence should be addressed. E-mail:  rgimenez@unizar.es (R.G.), anaelduq@unizar.es (A.E.).

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 Departamento de Química Orgánica.

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 Departamento de Química Inorgánica.

Abstract

Abstract Image

Several new cis-[RhCl(CO)2(Ln)] complexes have been prepared using different polycatenar pyrazole ligands (Ln) in order to obtain columnar liquid crystalline arrangements. The topology of the ligand plays an essential role, and a mesophase is induced at room temperature from a nonmesogenic pyrazole only when it is symmetrically substituted with six decyloxy chains. The single-crystal structure of a methoxy-substituted analogue, 3,5-bis(3,4,5-trimethoxyphenyl)pyrazole, is formed by globular tetrameric structures held together by H-bonding. However, parallel dimers are present in the corresponding cis-chlorodicarbonylrhodium(I) complex, a situation that explains the induction of a columnar mesophase in the decyloxy-substituted complex. The XRD pattern of the mesophase is consistent with a hexagonal symmetry in which the columns are formed by molecules assembled in an antiparallel mode. The crystal-to-mesophase transition was also detected by spectroscopic techniques as a shift in the IR carbonyl stretching bands and the appearance of a charge-transfer band in the absorption spectrum with thermochromic behavior.

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History

  • Published In Issue December 11, 2006
  • Received July 28, 2006

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