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Crystal structures of several inorganic-organic hybrids solved from powder XRD (CROSBI ID 613394)

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Đerđ, Igor ; Kozlevčar, Bojan ; Kitanovski, Nives ; Borsan, N ; Kasunič, M ; Francetič, V ; Popović, Jasminka ; Nuskol, Marko ; Rocquefelte, Xavier ; Reedijk, J ; Crystal structures of several inorganic-organic hybrids solved from powder XRD // Acta crystallographica. Section A, Foundations and advances. 2014. str. C1-123-C1-123

Podaci o odgovornosti

Đerđ, Igor ; Kozlevčar, Bojan ; Kitanovski, Nives ; Borsan, N ; Kasunič, M ; Francetič, V ; Popović, Jasminka ; Nuskol, Marko ; Rocquefelte, Xavier ; Reedijk, J ;

engleski

Crystal structures of several inorganic-organic hybrids solved from powder XRD

When dealing with the crystal structure solving of low-crystalline materials, it is of paramount importance to combine DFT geometry optimization with direct-space methods in order to find the correct structural model. Particularly, in the case of inorganic-organic hybrids prepared by solvothermal route, finite dimensional single crystal is very difficult to obtain. Hence, we present several successfully elucidated crystal structures from the powder XRD of the low-crystalline inorganic-organic hybrids: Cr(HL)Cl3, HL=Hbdmpza (1), [1] VO(C10H7COO)2 (2), VO(C14H9COO)2 (3). All of these structures have been solved from powder XRD data, either from laboratory or synchrotron source, by combining direct-space methods (simulated annealing), DFT geometry optimization, and constraint Rietveld refinement. The solid compound 1 was isolated in acetonitrile by starting CrCl3·9H2O and HL only in a concentrated solution, from which microcrystalline aggregates precipitated. Additionally, the presence of a carboxylate proton in HL stabilizes the structure by H-bonds, but also enables adsorption of moisture. Other two hybrids were synthesized in o-xylene by reacting vanadium (V) triisopropoxide with 1-naphthalenecarboxylic [2] or 9-anthracenecarboxylic acid. [2] They contain one-dimensional chain of corner-sharing tetrahedra in the case of VO(C10H7COO)2 (Figure 1(a), (c)), and corner-sharing octahedra for VO(C14H9COO)2 (Figure 1(b), (d)) oriented along orthorhombic/monoclinic c-axis, respectively. While VO(C14H9COO)2 exhibits bidentate bridging binding of organic moiety to the metal center, VO(C10H7COO)2 shows monodentate mode as evidenced from DFT and infrared spectroscopy. The obtained crystal structures were further verified by direct methods (ab initio approach). I. D. acknowledges financial support from the Unity through Knowledge Fund (www.ukf.hr) of the Croatian Ministry of Science, Education and Sports (Grant Agreement No. 7/13).

Powder XRD ; hybrid materials

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Podaci o prilogu

C1-123-C1-123.

2014.

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objavljeno

Podaci o matičnoj publikaciji

Acta crystallographica. Section A, Foundations and advances

2053-2733

Podaci o skupu

International Union of Crystallography Congress (23 ; 2014)

pozvano predavanje

05.08.2014-12.08.2014

Montréal, Kanada

Povezanost rada

Fizika, Kemija

Indeksiranost