<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>67(Pt 1)</volume><submitter>Guo ML</submitter><pubmed_abstract>The unit-cell parameters for the title mixed-metal coordination polymer, {[NiSr(C(3)H(2)O(4))(2)(H(2)O)(5)]·2H(2)O}(n), which is isostructural with its Co-containing analogue, were reported previously [Gil de Muro et al. (1999 ▶). Eur. J. Inorg. Chem. pp. 935-943]; the full crystal structure including a description of the hydrogen bonding is reported here. The Sr(2+) ion is bonded to five O atoms from three different malonate dianions and four water mol-ecules, displaying a distorted tricapped trigonal-prismatic coordination geometry. Two malonate dianions, two water mol-ecules and one Ni(2+) ion build up a dianionic [Ni(C(3)H(2)O(4))(2)(H(2)O)(2)](2-) unit incorporating a slightly distorted NiO(6) octa-hedron, which coordinates to three nearby Sr(2+) ions. This arrangement creates a metal-organic framework having a 20-membered ring with four Ni and six Sr atoms lying in the bc plane. The coordinated and uncoordinated water mol-ecules are responsible for the formation of two D5 hydrogen-bonded water chains within the 20-membered ring and they are linked into an R4 water cluster via two bifurcated O-H⋯(O,O) links.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>m19-20</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3050271</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Poly[[μ(2)-aqua-tetraaquadi-μ(3)-malonato-nickel(II)strontium(II)] dihydrate].</pubmed_title><pmcid>PMC3050271</pmcid><pubmed_authors>Lu CC</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Guo ML</pubmed_authors></additional><is_claimable>false</is_claimable><name>Poly[[μ(2)-aqua-tetraaquadi-μ(3)-malonato-nickel(II)strontium(II)] dihydrate].</name><description>The unit-cell parameters for the title mixed-metal coordination polymer, {[NiSr(C(3)H(2)O(4))(2)(H(2)O)(5)]·2H(2)O}(n), which is isostructural with its Co-containing analogue, were reported previously [Gil de Muro et al. (1999 ▶). Eur. J. Inorg. Chem. pp. 935-943]; the full crystal structure including a description of the hydrogen bonding is reported here. The Sr(2+) ion is bonded to five O atoms from three different malonate dianions and four water mol-ecules, displaying a distorted tricapped trigonal-prismatic coordination geometry. Two malonate dianions, two water mol-ecules and one Ni(2+) ion build up a dianionic [Ni(C(3)H(2)O(4))(2)(H(2)O)(2)](2-) unit incorporating a slightly distorted NiO(6) octa-hedron, which coordinates to three nearby Sr(2+) ions. This arrangement creates a metal-organic framework having a 20-membered ring with four Ni and six Sr atoms lying in the bc plane. The coordinated and uncoordinated water mol-ecules are responsible for the formation of two D5 hydrogen-bonded water chains within the 20-membered ring and they are linked into an R4 water cluster via two bifurcated O-H⋯(O,O) links.</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Dec</publication><modification>2025-04-05T00:32:09.352Z</modification><creation>2019-03-27T00:00:43Z</creation></dates><accession>S-EPMC3050271</accession><cross_references><pubmed>21522545</pubmed><doi>10.1107/S1600536809051782</doi><doi>10.1107/S1600536810049779</doi></cross_references></HashMap>