<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Albrecht R</submitter><pubmed_abstract>The reaction of Fe(NO3)3?9 H2O with KOH under hydroflux conditions at about 200?°C produces red crystals of K2-x Fe4O7-x (OH) x in a quantitative yield. In the crystal structure, edge-sharing [FeO6] octahedra form ?2[ Fe2O6] honeycomb nets. Pillars consisting of pairs of vertex-sharing [FeO4] tetrahedra link the honeycomb layers and form columnar halls in which the potassium ions are located. The trigonal (P 3? 1m) and the hexagonal (P63/mcm) polytypes of K2-x Fe4O7-x (OH) x show oriented intergrowth. The sub-stoichiometric potassium content (x?0.3) is compensated by hydroxide ions. K2-x Fe4O7-x (OH) x is an antiferromagnet above 2?K and its magnetic structure was determined by neutron powder diffraction. Under ambient conditions, K2-x Fe4O7-x (OH) x hydrolyzes and K2CO3???H2O forms gradually on the surface of the K2-x Fe4O7-x (OH) x crystals. Upon annealing at air at about 500?°C, the potassium atoms in the columnar halls start to order into a superstructure. The thermal decomposition of K2-x Fe4O7-x (OH) x proceeds via a topotactic transformation into K1+x' Fe11O17, adopting the rhombohedral ?'' or the hexagonal ?-aluminate-type structure, before ?-Fe2O3 is formed above 950?°C, which then converts into thermodynamically stable ?-Fe2O3.</pubmed_abstract><journal>ChemistryOpen</journal><pagination>74-83</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6345222</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Oxo-Hydroxoferrate K2-x Fe4O7-x (OH) x : Hydroflux Synthesis, Chemical and Thermal Instability, Crystal and Magnetic Structures.</pubmed_title><pmcid>PMC6345222</pmcid><pubmed_authors>Hunger J</pubmed_authors><pubmed_authors>Block T</pubmed_authors><pubmed_authors>Ruck M</pubmed_authors><pubmed_authors>Pottgen R</pubmed_authors><pubmed_authors>Doert T</pubmed_authors><pubmed_authors>Senyshyn A</pubmed_authors><pubmed_authors>Albrecht R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Oxo-Hydroxoferrate K2-x Fe4O7-x (OH) x : Hydroflux Synthesis, Chemical and Thermal Instability, Crystal and Magnetic Structures.</name><description>The reaction of Fe(NO3)3?9 H2O with KOH under hydroflux conditions at about 200?°C produces red crystals of K2-x Fe4O7-x (OH) x in a quantitative yield. In the crystal structure, edge-sharing [FeO6] octahedra form ?2[ Fe2O6] honeycomb nets. Pillars consisting of pairs of vertex-sharing [FeO4] tetrahedra link the honeycomb layers and form columnar halls in which the potassium ions are located. The trigonal (P 3? 1m) and the hexagonal (P63/mcm) polytypes of K2-x Fe4O7-x (OH) x show oriented intergrowth. The sub-stoichiometric potassium content (x?0.3) is compensated by hydroxide ions. K2-x Fe4O7-x (OH) x is an antiferromagnet above 2?K and its magnetic structure was determined by neutron powder diffraction. Under ambient conditions, K2-x Fe4O7-x (OH) x hydrolyzes and K2CO3???H2O forms gradually on the surface of the K2-x Fe4O7-x (OH) x crystals. Upon annealing at air at about 500?°C, the potassium atoms in the columnar halls start to order into a superstructure. The thermal decomposition of K2-x Fe4O7-x (OH) x proceeds via a topotactic transformation into K1+x' Fe11O17, adopting the rhombohedral ?'' or the hexagonal ?-aluminate-type structure, before ?-Fe2O3 is formed above 950?°C, which then converts into thermodynamically stable ?-Fe2O3.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2021-02-20T19:51:40Z</modification><creation>2019-03-26T22:43:48Z</creation></dates><accession>S-EPMC6345222</accession><cross_references><pubmed>30693170</pubmed><doi>10.1002/open.201800229</doi></cross_references></HashMap>