Transition Metals in Highly Correlated Discotic Phases: Designing Metallomesogens with Selected Intermolecular Organizations

Abstract

The diketonate Schiff-base complexes shown below were investigated, and the square planar derivatives (M=Ni, Cu, Pd) were found to display discotic hexagonal disordered phases (Dhd). The M=VO analogs are not liquid crystalline. None of the complexes can exhibit a disc-shape independently, and in the mesophase they must organize into a superstructure which on time average leads to antiparallel alignment of nearest neighbors. These discotic antiphases exhibit a number of important properties including low melting points, low viscosity, and close intermolecular contacts of 3.6A. Additionally when put between two untreated slides, these mesophases were found to readily align with the column axes perpendicular to the surfaces. The Cu and Ni complexes exhibited very similar mesophases and lattice constants whereas the Pd complexes displayed larger intercolumnar distances and higher clearing temperatures. The differences are ascribed to greater intermolecular associations displayed by the Pd complexes. X-ray diffraction studies revealed the Ni and the Cu complexes to have an additional halo centered at approx. 7.2A which may be the result of a doubling of the period along the column axes resulting from the antiparallel arrangement of the antiphase superstructure.

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Document Details

Document Type
Technical Report
Publication Date
Jan 08, 1994
Accession Number
ADA274695

Entities

People

  • Chung K. Lai
  • Hanxing Zheng
  • Timothy M. Swager

Organizations

  • University of Pennsylvania

Tags

DTIC Thesaurus Topics

  • Abstracts
  • Chemistry
  • Diffraction
  • Imines
  • Melting
  • Melting Point
  • Metals
  • Military Research
  • Pennsylvania
  • Phase Transformations
  • Superstructures
  • Transition Metals
  • Transitions
  • United States
  • United States Government
  • Viscosity
  • X-Ray Diffraction

Fields of Study

  • Chemistry

Readers

  • Materials Science and Engineering.
  • Organic Chemistry