Host–Guest Hydrogen Bonding Varies the Charge‐State Behavior of Magnetic Sponges

Abstract

The electron-donor(D) and -acceptor(A)-assembled D2 A-layer framework [{Ru2 (m-FPhCO2 )4 }2 TCNQ(OMe)2 ]⋅nDCE (1-nDCE; m-FPhCO2 - =m-fluorobenzoate; TCNQ(OMe)2 =2,5-dimethoxyl-7,7,8,8-tetracyanoquinodimethane; DCE=1,2-dichloroethane) undergoes drastic charge-ordered state variations via three distinct states that are a two-electron-transferred state (2e-I), a charge-disproportionated state (1.5e-I), and a one-electron-transferred state (1e-I), depending on the degree of solvation by nDCE. The pristine form 1-4DCE has a paramagnetic 2e-I state, which eventually produces the solvent-free form 1 in 1.5e-I via an intermediate state 1-nDCE (n≤1) in 1e-I. Resolvation of 1 stabilizes 1-DCE, allowing it to switch between 1.5e-I and 1e-I, and to become ferrimagnetic with a Tc of 30 K (1.5e-I) and 88 K (1e-I). The stabilization of the 1e-I state of 1-DCE is due to the presence of host-guest hydrogen bonding that enables to suppress the electron-donation ability of D even in an identical framework with 1.