4.5 Article

Self-ordering of organic-metal hybrid microstructures based on tetrathiafulvalene derivatives

期刊

SYNTHETIC METALS
卷 189, 期 -, 页码 42-46

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.synthmet.2013.12.023

关键词

Charge-transfer; Coordination complexes; Microstructures; Self-assembly

资金

  1. National Natural Science Foundation of China [21372136, 21104037]
  2. Ningbo Science and Technology Innovation Team [2011B82002]
  3. Ningbo University of Technology Innovation team
  4. SRF for ROCS, SEM

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Two divalent transition metal complexes of EDT-TTF-4-py (EDT-TTF-4-py = 4-ethylenedithiotetrathiafulvalenyl-pyridine) have been prepared and characterized in micro and bulk crystal forms. These hybrid microstructures were synthesized by coordinative self-assemble through a solution process. The isostructural Cu(hfac)(2) and Mn(hfac)(2) (hfac = hexafluoroacetylacetonate) complexes crystallize in the monoclinic space group P2(1)/c. Two pyridyl N atoms from two different molecules of EDT-TTF-4-py are coordinated in the trans configuration to the metal ion of M(hfac)(2) to form an octahedral complexes. The results of the elemental analysis, FT-IR, SEM-EDX and PXRD, show the chemical composition of the microstructures which are same as that of bulk crystals. Moreover, these two microstructure compounds are precursor for both conducting and magnetic materials. These investigations show the intriguing potentials of the coordinative bond in the development of multifunctional hybrid microstructures. (C) 2014 Elsevier B.V. All rights reserved.

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