Syntheses and crystal structures of (18-crown-6)bis(perchlorato-O,O′)strontium and (18-crown-6)bis(perchlorato-O,O′)barium

Syntheses and crystal structures of (18-crown-6)bis(perchlorato-O,O′)strontium and... Two complexes, namely, (18-crown-6)bis(perchlorato-O,O′)strontium (I) and (18-crown-6)bis(perchlorato-O,O′)barium (II), are synthesized. Their crystal structures are determined by X-ray diffraction analysis. The structures of I (space group P21/c, a = 15.266 Å, b = 11.080 Å, c = 13.235 Å, β = 109.20°, Z = 4) and II (space group P21/n, a = 8.330 Å, b = 11.202 Å, c = 11.752 Å, β = 98.38°, Z = 2) are solved by a direct method and refined by the full-matrix least-squares method in the anisotropic approximation to R = 0.077 (I) and 0.041 (II) against 3714 (I) and 2478 (II) independent reflections (CAD-4 diffractometer, λMoK α radiation). Complex molecules [Sr(18C6)(ClO4)2] in the structure of I and [Ba(18C6)(ClO4)2] in II (in the inversion center)—are of the host-guest type. The Sr2+ or Ba2+ cation is localized in the center of a cavity of the 18-crown-6 ligand and coordinated by its all six O atoms. In compounds I and II, the coordination polyhedron of the Sr2+ and Ba2+ cations (coordination number 10) can be described as a distorted hexagonal bipyramid with two bifurcated vertices at two O atoms of two ClO 4 − ligands, which are disordered in I and II and each of them has two orientations. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Russian Journal of Coordination Chemistry Springer Journals

Syntheses and crystal structures of (18-crown-6)bis(perchlorato-O,O′)strontium and (18-crown-6)bis(perchlorato-O,O′)barium

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Publisher
Springer Journals
Copyright
Copyright © 2006 by Pleiades Publishing, Inc.
Subject
Chemistry; Inorganic Chemistry; Physical Chemistry
ISSN
1070-3284
eISSN
1608-3318
D.O.I.
10.1134/S1070328406090028
Publisher site
See Article on Publisher Site

Abstract

Two complexes, namely, (18-crown-6)bis(perchlorato-O,O′)strontium (I) and (18-crown-6)bis(perchlorato-O,O′)barium (II), are synthesized. Their crystal structures are determined by X-ray diffraction analysis. The structures of I (space group P21/c, a = 15.266 Å, b = 11.080 Å, c = 13.235 Å, β = 109.20°, Z = 4) and II (space group P21/n, a = 8.330 Å, b = 11.202 Å, c = 11.752 Å, β = 98.38°, Z = 2) are solved by a direct method and refined by the full-matrix least-squares method in the anisotropic approximation to R = 0.077 (I) and 0.041 (II) against 3714 (I) and 2478 (II) independent reflections (CAD-4 diffractometer, λMoK α radiation). Complex molecules [Sr(18C6)(ClO4)2] in the structure of I and [Ba(18C6)(ClO4)2] in II (in the inversion center)—are of the host-guest type. The Sr2+ or Ba2+ cation is localized in the center of a cavity of the 18-crown-6 ligand and coordinated by its all six O atoms. In compounds I and II, the coordination polyhedron of the Sr2+ and Ba2+ cations (coordination number 10) can be described as a distorted hexagonal bipyramid with two bifurcated vertices at two O atoms of two ClO 4 − ligands, which are disordered in I and II and each of them has two orientations.

Journal

Russian Journal of Coordination ChemistrySpringer Journals

Published: Sep 6, 2006

References

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