Consecutive Single-Crystal-to-Single-Crystal Isomerization of Novel Octamolybdate Anions within a Microporous Hybrid Framework with Robust Water Sorption Properties

Abstract

The 3D hybrid framework [{Cu(cyclam)}₃ (κ-Mo₈ O₂₇ )] ⋅ 14H₂ O (1) (cyclam=1,4,8,11-tetraazacyclotetradecane) undergoes sequential single-crystal-to-single-crystal transformations upon heating to afford two different anhydrous phases (2 a and 3 a). These transitions modify the framework dimensionality and enable the isomerization of κ-octamolybdate (κ-Mo₈ ) anions into λ (2 a) and μ (3 a) forms through metal migration. Hydration of 3 a involves condensation of one water molecule to the cluster to afford the γ-Mo₈ isomer in 4, which dehydrates back into 3 a through the 6 a intermediate. In contrast, 2 a reversibly hydrates to form 5, exhibiting the same Mo₈ cluster as that of 1. It is remarkable that three of the Mo₈ clusters (κ, λ and μ) are new and that up to three different microporous phases can be isolated from 1 (2 a, 3 a, and 6 a). Water vapor sorption analyses show high recyclability and the highest uptake values for POM-based systems. The isotherms display an abrupt step at low humidity level desirable for humidity control devices or water harvesting in drylands.

Keywords: Microporous Materials; Polyoxometalates; Single-Crystal-to-Single-Crystal; Solid-State Isomerization; Water Sorption.