4.7 Article

Two eight-connected self-penetrating porous metal-organic frameworks: configurational isomers caused by different linking modes between terephthalate and binuclear nickel building units

Journal

CRYSTENGCOMM
Volume 11, Issue 2, Pages 274-277

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b812643g

Keywords

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Funding

  1. National Natural Science Foundation of China [20703008, 20741003]
  2. Chang Jiang Scholars Program
  3. Program for Changjiang Scholars and Innovative Research Team in University [IRT0714]
  4. Science Foundation for Young Teachers of NENU [20070309]

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Two novel nanoporous metal-organic frameworks (MOFs) based on the same binuclear nickel secondary building units, {[Ni-2(H2O)(BDC)(2)(BIMB)(2)]center dot 6DMF}(n) (1) and {[Ni-2(H2O)(BDC)(2)(BIMB)(2)]center dot 5DMAc}(n) (2) (H2BDC terephthalic acid, BIMB 1,4-bis(1-imidazolyl) benzene and DMF = N,N'-dimethylformamide, DMAc = N,N'-dimethylacetamide) have been synthesized by self-assembly of Ni(NO3)(2)center dot 6H(2)O, BIMB and H2BDC in different solvents (DMF and DMAc), respectively. Different linking modes between terephthalate and binuclear nickel building units in 1 and 2 lead to an interesting phenomenon that their host frameworks are isomeric to each other and have the same three periodic eight-connected self-penetrating nets with novel 4(20).6(8) topology. Powder X-ray diffraction (PXRD) results indicate that 1 and 2 both have reversible framework transformations in an acetone/guest solvent molecule system.

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