Rajković, S.

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  • Rajković, S. (1)
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Coordination behaviour and two-dimensional-network formation in poly[[μ-aqua-diaqua-(μ5-propane-1,3-diyldinitrilo-tetra-acetato) -dilithium(I)-cobalt(II)] dihydrate]: The first example of an M II-1,3-pdta complex with a monovalent metal counter-ion

Rychlewska, Urszula; Warzajtis, B.; Đuran, Miloš; Radanović, Dušanka; Dimitrijević, M. D.; Rajković, S.

(2008)

TY  - JOUR
AU  - Rychlewska, Urszula
AU  - Warzajtis, B.
AU  - Đuran, Miloš
AU  - Radanović, Dušanka
AU  - Dimitrijević, M. D.
AU  - Rajković, S.
PY  - 2008
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/446
AB  - The title compound, {[CoLi2(C11H14N2O8) (H2O)3]·2H2O}n , constitutes the first example of a salt of the [M II(1,3-pdta)]2- complex (1,3-pdta is propane-1,3-diyldinitrilo-tetra-acetate) with a monopositive cation as counter-ion. Insertion of the Li+ cation could only be achieved through application of the ion-exchange column technique which, however, appeared unsuccessful with other alkali metals and the ammonium cation. The structure contains two tetra-hedrally coordinated Li+ cations, an octa-hedral [Co(1,3-pdta)]2- anion and five water mol-ecules, two of which are uncoordinated, and is built of two-dimensional layers extending parallel to the (010) lattice plane, the constituents of which are connected by the coordinate bonds. O - Hwater⋯O hydrogen bonds operate both within and between these layers. The crystal investigated belongs to the enanti-omeric space group P21 with only one () of two possible optical isomers of the [Co(1,3-pdta)]2- complex. A possible cause of enanti-omer separation during crystallization might be the rigidification and polarization of the [M(1,3-pdta)]2- core, resulting from direct coordination of Li + cations to three out of four carboxyl-ate groups constituting the 1,3-pdta ligand. The structure of (I) differs considerably from those of the other [M II(1,3-pdta)]2- complexes, in which the charge compensation is realized by means of divalent hexa-aqua complex cations. This finding demonstrates a significant structure-determining role of the counter-ions.
T2  - Acta Crystallographica Section C: Crystal Structure Communications
T1  - Coordination behaviour and two-dimensional-network formation in poly[[μ-aqua-diaqua-(μ5-propane-1,3-diyldinitrilo-tetra-acetato) -dilithium(I)-cobalt(II)] dihydrate]: The first example of an M II-1,3-pdta complex with a monovalent metal counter-ion
VL  - 64
IS  - 6
DO  - 10.1107/S0108270108010706
ER  - 
@article{
author = "Rychlewska, Urszula and Warzajtis, B. and Đuran, Miloš and Radanović, Dušanka and Dimitrijević, M. D. and Rajković, S.",
year = "2008",
abstract = "The title compound, {[CoLi2(C11H14N2O8) (H2O)3]·2H2O}n , constitutes the first example of a salt of the [M II(1,3-pdta)]2- complex (1,3-pdta is propane-1,3-diyldinitrilo-tetra-acetate) with a monopositive cation as counter-ion. Insertion of the Li+ cation could only be achieved through application of the ion-exchange column technique which, however, appeared unsuccessful with other alkali metals and the ammonium cation. The structure contains two tetra-hedrally coordinated Li+ cations, an octa-hedral [Co(1,3-pdta)]2- anion and five water mol-ecules, two of which are uncoordinated, and is built of two-dimensional layers extending parallel to the (010) lattice plane, the constituents of which are connected by the coordinate bonds. O - Hwater⋯O hydrogen bonds operate both within and between these layers. The crystal investigated belongs to the enanti-omeric space group P21 with only one () of two possible optical isomers of the [Co(1,3-pdta)]2- complex. A possible cause of enanti-omer separation during crystallization might be the rigidification and polarization of the [M(1,3-pdta)]2- core, resulting from direct coordination of Li + cations to three out of four carboxyl-ate groups constituting the 1,3-pdta ligand. The structure of (I) differs considerably from those of the other [M II(1,3-pdta)]2- complexes, in which the charge compensation is realized by means of divalent hexa-aqua complex cations. This finding demonstrates a significant structure-determining role of the counter-ions.",
journal = "Acta Crystallographica Section C: Crystal Structure Communications",
title = "Coordination behaviour and two-dimensional-network formation in poly[[μ-aqua-diaqua-(μ5-propane-1,3-diyldinitrilo-tetra-acetato) -dilithium(I)-cobalt(II)] dihydrate]: The first example of an M II-1,3-pdta complex with a monovalent metal counter-ion",
volume = "64",
number = "6",
doi = "10.1107/S0108270108010706"
}
Rychlewska, U., Warzajtis, B., Đuran, M., Radanović, D., Dimitrijević, M. D.,& Rajković, S.. (2008). Coordination behaviour and two-dimensional-network formation in poly[[μ-aqua-diaqua-(μ5-propane-1,3-diyldinitrilo-tetra-acetato) -dilithium(I)-cobalt(II)] dihydrate]: The first example of an M II-1,3-pdta complex with a monovalent metal counter-ion. in Acta Crystallographica Section C: Crystal Structure Communications, 64(6).
https://doi.org/10.1107/S0108270108010706
Rychlewska U, Warzajtis B, Đuran M, Radanović D, Dimitrijević MD, Rajković S. Coordination behaviour and two-dimensional-network formation in poly[[μ-aqua-diaqua-(μ5-propane-1,3-diyldinitrilo-tetra-acetato) -dilithium(I)-cobalt(II)] dihydrate]: The first example of an M II-1,3-pdta complex with a monovalent metal counter-ion. in Acta Crystallographica Section C: Crystal Structure Communications. 2008;64(6).
doi:10.1107/S0108270108010706 .
Rychlewska, Urszula, Warzajtis, B., Đuran, Miloš, Radanović, Dušanka, Dimitrijević, M. D., Rajković, S., "Coordination behaviour and two-dimensional-network formation in poly[[μ-aqua-diaqua-(μ5-propane-1,3-diyldinitrilo-tetra-acetato) -dilithium(I)-cobalt(II)] dihydrate]: The first example of an M II-1,3-pdta complex with a monovalent metal counter-ion" in Acta Crystallographica Section C: Crystal Structure Communications, 64, no. 6 (2008),
https://doi.org/10.1107/S0108270108010706 . .
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