English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

The crystal structures of two polymorphic, hydrothermally synthesized cobalt selenite monohydrates, CoSeO 3  · H 2 O II ( a  = 568.1(1) pm,  b  = 476.7(1) pm,  c  = 1348.0(2) pm,  μ  = 101.37(1)°) and CoSeO 3  · H 2 O III ( a  = 477.2(1) pm,  b  = 1320.9(3) pm,  c  = 568.6(1) pm,  β  = 90.54(1)°), both  mP 32,  P 2 1 / n ,  Z  = 4, have been determined by single crystal X-ray diffraction. Both structures are built up from buckled  trans  layers  2  ∞ [CoSeO 3  · H 2 O] consisting of strongly distorted CoO 5 (H 2 O) octahedra and trigonal pyramidal SeO 3  2−  ions. The structures differ with respect to the stacking of the layers, which originates in their pseudosymmetry and in the stereochemical requirements of the selenite lone electron pair. Only intra-layer H bond schemes are built, i.e., the layers are held together by van der Waals interactions.

New polymorphic and pseudosymmetrical cobalt selenite monohydrates, CoSe0 3 · H 2 O II and CoSeO 3 · H 2 O III