P–C bond cleavage-assisted lanthanide phosphate coordination polymers

Goura, Joydeb ; Walsh, James P. S. ; Tuna, Floriana ; Halder, Ritesh ; Maji, Tapas Kumar ; Chandrasekhar, Vadapalli (2015) P–C bond cleavage-assisted lanthanide phosphate coordination polymers Crystal Growth & Design, 15 (6). pp. 2555-2560. ISSN 1528-7483

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Official URL: https://pubs.acs.org/doi/abs/10.1021/cg5017005

Related URL: http://dx.doi.org/10.1021/cg5017005

Abstract

The reaction of lanthanide(III) salts with an organodiphosphonic acid under hydrothermal conditions resulted in a P–C bond cleavage affording [{Eu4(PO4)(PO4)0.5×4(PO4)0.25×4(H2 O)2}·6H2O]n (1), [{Dy4(PO4)(PO4)0.5×4(PO4)0.25×4(H2O)2}·6H2O]n (2), and [{Gd(PO4)0.5(PO4)0.5(H2O)3}·2H2O]n (3). 1 and 2 are porous 3D coordination polymers whose repeating units possess a dimeric motif. While one lanthanide ion in the dimer is eight-coordinate in a distorted square-antiprismatic geometry, the other is nine-coordinate and present in a distorted monocapped square-antiprismatic geometry. In contrast to 1 and 2, 3 possesses a 2D architecture; the asymmetric unit contains a monomeric GdIII center which is nine-coordinate in a distorted monocapped square-antiprismatic geometry.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:113125
Deposited On:29 May 2018 11:21
Last Modified:29 May 2018 11:21

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