| 1. |
- Abu-Youssef, Morsy A. M., et al.
(författare)
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New Polymeric Manganese Azide Derivatives with Quinazoline
- 2005
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Ingår i: European Journal of Inorganic Chemistry. - 1434-1948 .- 1099-0682. ; 2005:22, s. 4659 - 4664
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Tidskriftsartikel (refereegranskat)abstract
- Two new polymeric derivatives of the (azido)MnII system with formula [Mn(H2O)(μ-N3)(N3)(quinaz)2]n (1) and [Mn(μ-N3)2(quinaz)2]n (2) (quinaz = quinazoline) have been structurally and magnetically characterised. Compound 1 crystallises in the triclinic system, space group P-1, and consists of 1D chains with single end-to-end azido bridges. These chains give a two-dimensional supramolecular arrangement by means of H-bond interactions. Compound 2 crystallises in the monoclinic system, space group C2/c, and contains a square alternating 2D network bridged by azido ligands in the end-to-end coordination mode. Compound 2 exhibits some unusual features, such as the unprecedented linear coordination of the azido bridge. Magnetic analysis reveals moderate antiferromagnetic coupling, with J values in good agreement with the expected range, as a function of the Mn-N-N bond angles.
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| 2. |
- Abu-Youssef, Morsy A.M., et al.
(författare)
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Synthesis, Structure, and Magnetic Behavior of Two New 1D Polymeric Manganese Azido Complexes
- 2006
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Ingår i: European Journal of Inorganic Chemistry. ; 2006:16, s. 3177-3184
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Tidskriftsartikel (refereegranskat)abstract
- Two new MnII one-dimensional compounds with formulae [Mn(μ-N3)2(pyzamid)2]n (1) and [Mn2(3-ampy)4(μ-N3)2(N3)2(H2O)2]n, (2) (pyzamid = pyrazineamide and 3-ampy = 3-aminopyridine) were structurally and magnetically characterized. Compound 1 crystallizes in the monoclinic system, P2/c space group, and polymerizes through double end-on azido bridges giving 1D chains with the MnII atoms in a MnN6 environment. Compound 2 crystallizes in the triclinic system, P-1 space group, and consists of alternate [Mn(3-ampy)2(μ-N3)2(N3)2] and [Mn(3-ampy)2(μ-N3)2(H2O)2] octahedrons (MnN6 - MnN4O2 environments), linked by single end-to-end azido bridges. Both chains show very uncommon topologies. Attemps to obtain manganese/azido derivatives with the qux = quinoline-4-carboxylato anion gave the recently reported compound [Mn(μ-qux)2(μ-H2O)]n (3), which consists of a chain with only carboxylato and aqua bridges with the MnII atoms in a MnO6 slightly distorted octahedron. In good agreement with the expected behavior, magnetic susceptibility measurements show weak ferromagnetic interactions for 1, whereas compound 2 exhibits moderate antiferromagnetic coupling.
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| 3. |
- Winterlich, Meghan, et al.
(författare)
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A biocompatible ZnNa2-based metal-organic framework with high ibuprofen, nitric oxide and metal uptake capacity
- 2020
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Ingår i: Materials Advances. - : Royal Society of Chemistry (RSC). - 2633-5409. ; 1:7, s. 2248-2260
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Tidskriftsartikel (refereegranskat)abstract
- Metal organic frameworks (MOFs) have received significant attention in recent years in the areas of biomedical and environmental applications. Among them, mixed metal MOFs, although promising, are relatively few in number in comparison with their homometallic analogues. The employment of benzophenone-4,4'-dicarboxylic acid (bphdcH(2)) in mixed metal MOF chemistry provided access to a 3D MOF, [Na2Zn(bphdc)(2)(DMF)(2)](n) (NUIG1). NUIG1 displays a new topology and is a rare example of a mixed metal MOF based on 1D rod secondary building units. UV-vis, HPLC, TGA, XRPD, solid state NMR and computational studies indicated that NUIG1 exhibits an exceptionally high Ibuprofen (Ibu) and nitric oxide adsorption capacity. The MCF-7 cell line was used to assess the toxicity of NUIG1 and Ibu@NUIG1, revealing that both species are non-toxic (cell viability > 70%). NUIG1 exhibits good performance in the adsorption of metal ions (Co-II, Ni-II, Cu-II) from aqueous environments, as was demonstrated by UV-vis, EDX, ICP, SEM and direct and alternate current magnetic susceptibility studies. The colour and the magnetic properties of the M@NUIG1 species depend strongly on the kind and the amount of the encapsulated metal ion in the MOF pores.
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