Magnetic switching in vapochromic oxalato-bridged 2D copper(II)-pyrazole compounds for biogenic amine sensing

A new two-dimensional (2D) coordination polymer of the formula {Cu(ox)(4-Hmpz)·1/3H2 O}n (1) (ox = oxalate and 4-Hmpz = 4-methyl-1H-pyrazole) has been prepared, and its structure has been determined by single-crystal X-ray diffraction. It consists of corrugated oxalato-bridged copper(II) neutral layers featuring two alternating bridging modes of the oxalate group within each layer, the symmetric bis-bidentate (µ-κ2 O1,O2:κ2 O2′,O1′) and the asymmetric bis(bidentate/monodentate) (µ4-κO1:κ2 O1,O2:κO2′:κ2 O2′,O1′) coordination modes. The three crystallographically independent six-coordinate copper(II) ions that occur in 1 have tetragonally elongated surroundings with three oxygen atoms from two oxalate ligands, a methylpyrazole-nitrogen defining the equatorial plane, and two other oxalate-oxygen atoms occupying the axial positions. The monodentate 4-Hmpz ligands alternatively extrude above and below each oxalate-bridged copper(II) layer, and the water molecules of crystallization are located between the layers. Compound 1 exhibits a fast and selective adsorption of methylamine vapors to afford the adsorbate of formula {Cu(ox)(4-Hmpz)·3MeNH2·1/3H2 O}n (2), which is accompanied by a concomitant color change from cyan to deep blue. Compound 2 transforms into {Cu(ox)(4-Hmpz)·MeNH2·1/3H2 O}n (3) under vacuum for three hours. The cryomagnetic study of 1–3 revealed a unique switching from strong (1) to weak (2 and 3) antiferromagnetic interactions. The external control of the optical and magnetic properties along this series of compounds might make them suitable candidates for switching optical and magnetic devices for chemical sensing.