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Get Free AccessTwo new open-framework yttrium oxalates have been prepared, for the first time, employing hydrothermal methods in the presence of organic amines. The crystal data for these oxalates are as follows: I, [C6N2H16]0.5[Y(H2O)(C2O4)2]·2H2O, triclinic, space group P(−1) (no. 2), a = 8.229(3), b = 9.739(1), c = 9.754(3) Å, α = 60.74(1), β = 72.36(1), γ = 84.67(1)°, V = 648.5(1) Å3, Z = 2, M = 377.1, Dcalc = 1.931 g cm-3, μ = 4.554 mm-1, Mo Kα, R1 = 0.054, wR2 = 0.13; II, [C5N2H12][Y(C2O4)2], monoclinic, space group Cc (no. 9), a = 11.552(1), b = 17.168(1), c = 8.719(1) Å, β = 130.64(1)°, V = 1312.1(1) Å3, Z = 2, M = 365.1, Dcalc = 1.848 g cm-3, μ = 4.48 mm-1, Mo Kα, R1 = 0.023, wR2 = 0.057. The Y atom is 9-coordinated in I, forming a D3h triply capped trigonal prism, and 8-coordinated in II, forming a square antiprism. The three-dimensional framework structures of I and II are built up by in-plane linkages between the Y and the oxalate moieties, forming layers with 12-membered honeycomb-like apertures, pillared by another oxalate in an out-of-plane manner. While I possesses channels along all the crystallographic directions, II has channels only in one direction. Adsorption studies indicate that water and methanol can be reversibly adsorbed in I.
Ramanathan Vaidhyanathan, Srinivasan Natarajan, Cnr Rao (2000). Three-Dimensional Yttrium Oxalates Possessing Large Channels. Chemistry of Materials, 13(1), pp. 185-191, DOI: 10.1021/cm000419o.
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Type
Article
Year
2000
Authors
3
Datasets
0
Total Files
0
Language
English
Journal
Chemistry of Materials
DOI
10.1021/cm000419o
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