Jin Wuk Lee

Microporous Lanthanide-Organic Frameworks with Open Metal Sites: Unexpected Sorption Propensity and Multifunctional Properties

Isostructural lanthanide-organic frameworks were prepared by a solvothermal reaction of the corresponding metal ions and the phosphine-oxide-based tricarboxylate ligand. The gravimetric gas uptake was unexpectedly increased when going from Nd(3+) to Gd(3+), which is associated with the enhanced surface areas and electrostatic interactions between exposed metal ions and gas molecules with quadrupole moments.

Magnetic metal–organic framework constructed from a paramagnetic metalloligand exhibiting a significant sorption and reversible magnetic conversions

A Co(II)-Cu(II) framework based on a paramagnetic metalloligand [Co(Tt)(2)] shows a permanent porosity with a record high surface area for magnetic MOFs as well as a reversible magnetic transformation between a paramagnetic-like state and a short-range magnetic order in the low-temperature regime upon solvation-desolvation cyclings.

Octacyanometalate-based ferrimagnetic MVMnIII (M = Mo, W) bimetallic chain racemates with slow magnetic relaxations

Cyanide-bridged M(V)-Mn(III) (M = Mo, W) bimetallic chain complexes with racemic spatial dispositions were constructed by self-assembling [M(CN)(8)](3-) precursors and Mn(III) Schiff bases. Antiferromagnetic couplings between spin centers within a chain result in a ferrimagnetic nature, and slow magnetic relaxations are observed as well.

One-Dimensional Cyanide-Bridged MnIIIWV Bimetallic Complexes: Metamagnetism, Spontaneous Resolution, and Slow Magnetic Relaxation

The reaction of [W(CN)(6)(bpy)](-) with the corresponding Mn Schiff bases led to the formation of two antiferromagnetic (1) and ferromagnetic (2) chains. The formation of the conglomerate (2) is associated with chiral induction by the enantiomeric chelate-ring conformation of the Mn Schiff base. Modulation of the linking groups in the Mn Schiff bases affects the interchain contacts, causing alteration of the magnetic behaviors from metamagnetism (1) to slow magnetic relaxation (2).

Cyanide-Bridged WVMnIII Single-Chain Magnet with Isolated MnIII Moieties Exhibiting Two Types of Relaxation Dynamics

A 5d-3d bimetallic compound was prepared by self-assembling [W(CN)(8)](3-) and the Mn(III) Schiff bases. This neutral complex consists of cyanide-linked W(V)Mn(III) anionic chains and isolated Mn(III) Schiff base cations. We demonstrate that two types of relaxation processes are involved in the system; the low-T dynamics may come from magnetic domain dynamics and the high-T relaxation stems from the anionic chain, revealing single-chain magnet character.

Cyanide-Bridged WVMnIII Bimetallic Chains Composed of a Blocked W Hexacyanide Precursor: Geometry-Related Magnetic Couplings and Magnetostructural Correlation

Five one-dimensional bimetallic W(V)Mn(III) complexes 1-5, consisting of [W(CN)6(bpy)](-) anions and [Mn(Schiff base)](+) cations, were prepared. The central coordination geometry around each W atom is determined as a distorted dodecahedron (DD) for 1 and 2, and a distorted square antiprism (SAPR) for 3-5. Magnetic analyses demonstrate that compounds 1, 4, and 5 exhibit antiferromagnetic interactions between magnetic centers, which are different from the ferromagnetic couplings in 2 and 3. For the distorted DD geometry, the Mn-N(ax) (ax = axial) bond length increases when moving from 1 to 2, with the Mn-N(ax)-C(ax) angle remaining constant. The elongation of the bond length is responsible for the reduction in orbital overlap and consequent ferromagnetic coupling in 2. In comparison, for 3-5 with the distorted SAPR geometry, given that the Mn-N(ax) bond lengths are similar across all the samples, the increase in the Mn-N(ax)-C(ax) angles accounts for the enhanced magnetic strength. Notably, a correlation between structure and magnetic exchange coupling is established for the first time in W(V)Mn(III) bimetallic systems based on the [W(CN)6(bpy)](-) precursor.

Designed cyanide- and phenoxide-bridged FeIIIMnIII single-molecule magnet constructed by highly blocked paramagnetic precursors

A tetranuclear Fe(III)(2)Mn(III)(2) compound was prepared using highly blocked precursors. The well-isolated molecular entity associated with appropriate magnetic anisotropy allows for single-molecule magnet behavior.

Syntheses, structures, and magnetic properties of cyano- and phenoxide-bridged Fe(III)–Mn(III) tetrameric assemblies formed by blocked fac-Fe tricyanide with aliphatic rings

Three tetranuclear clusters [(Tp(Me,mt3))Fe(CN)3Mn(L)]2 (1, L = 5-Clacphmen; 2, L = 5-Clsalen; 3, L = 5-MeOsalen; Tp(Me,mt3) = hydrotris(3-methyl-4,5-propylene-5-methylpyrazol-1-yl)borate) were prepared by assembling the fac-Fe tricyanide with the corresponding Mn Schiff bases. The assembled molecules are linked by cyanide and phenoxide bridges. Weak π-π contacts between molecules are evident in these clusters. Compounds 1-3 exhibit slow relaxation of the magnetization. The phenoxide linkers mediate ferromagnetic coupling between the Mn centers, which is ascribed to the long axial Mn-O* length. The overall magnetic exchange coupling nature of the Fe-C≡N-Mn route is accounted for by the important structural parameters of bridging pathways such as Mn-N(cyano) length, Mn-N(cyano)-C(cyano) angle, and C(eq)-Fe···Mn-N(eq) (eq = equatorial) torsion angle.