Journal
MICROPOROUS AND MESOPOROUS MATERIALS
Volume 111, Issue 1-3, Pages 470-477Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.micromeso.2007.08.024
Keywords
metal coordination polymer; 2,6-naphthalenedicarboxylate; gas sorption; microporosity; magnetic property
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Two isostructural coordination polymers M-3(NDC)(3)(DMF)(4) (M = CO (1), Mn (2); H2NDC = 2,6-naphthalenedicarboxylic acid; DMF = N,N-dimethylformamide) were prepared through conventional and microwave-assisted solvothermal methods. Single crystal X-ray analysis indicated that both complexes crystallized in the monoclinic system with space group C2/c. Powder X-ray diffraction (PXRD) patterns of the bulk samples for the two complexes obtained from microwave-assisted solvothermal syntheses matched well with the simulated ones from the single crystal data as well as the ones prepared by conventional solvothermal method. These microporous cobalt(II) and manganese(II) coordination polymers undergo reversible structural change upon desolvating, giving stable microporous frameworks containing unsaturated metal sites, and resolvating. The desolvated complexes showed different nitrogen gas adsorption capabilities but very close hydrogen adsorption behaviors. Variable-temperature magnetic susceptibilities of I and 2 revealed the weak antiferromagnetic coupling between the adjacent metal ions bridged by carboxylate. (C) 2007 Elsevier Inc. All rights reserved.
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