4.5 Article

Two novel entangled metal-quinolone complexes with self-threading and polythreaded characters

Journal

INORGANICA CHIMICA ACTA
Volume 385, Issue -, Pages 170-177

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2012.01.056

Keywords

Metal-organic frameworks; Entangled networks; Hydrothermal synthesis; Crystal structure

Funding

  1. NSFC [20801044]
  2. China Postdoctoral Science Foundation [20080430205, 200902282]
  3. Science and Technology Foundation of Southwest University [SWUB2007035]
  4. Fundamental Research Funds for the Central Universities [XDJK2009B014]
  5. Program for Chongqing Excellent Talents in University

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Reactions of quinolones with metal salts in the presence of aromatic polycarboxylate ligands under hydrothermal conditions yield two novel entangled metal-quinolone complexes, namely [Cd-2(sar-aH) (2)(bpdc)(2)]center dot 4.5H(2)O (1) and [Mn(sara)(2)]center dot 2.5H(2)O (2), (saraH = sarafloxacin, bpdc = 4,4'-biphenyldicarboxylate). Their structures were determined by single-crystal X-ray diffraction analyses and further characterized by elemental analyses, IR spectra, X-ray powder diffraction, and TG analyses. Compound 1 is an uncommon 2D self-threading network, which represents the first entangled network constructed from mixed sarafloxacin and dicarboxylate ligands. Compound 2 exhibits a novel (2D -> 3D) polythreaded architecture that is constructed from 2D 4(4)-sql nets with side arms, which represents the first example of polythreaded metal-sarafloxacin complex. A comparison of the structures of 1 and 2 shows that the pH plays a crucial role in tuning the structures of the metal-quinolone complexes. Furthermore, the luminescent properties of compound 1 are discussed. (C) 2012 Elsevier B.V. All rights reserved.

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