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Abstract This paper describes the use of a highly crystalline conductive 2D copper₃(hexaiminobenzene)₂(Cu₃(HIB)₂) as an ultrasensitive (limit of detection of 1.8 part‐per‐billion), highly selective, reversible, and low power chemiresistive sensor for nitric oxide (NO) at room temperature. The Cu₃(HIB)₂‐based sensors retain their sensing performance in the presence of humidity, and exhibit strong signal enhancement towards NO over other highly toxic reactive gases, such as NO₂, H₂S, SO₂, NH₃, CO, as well as CO₂. Mechanistic investigations of the Cu₃(HIB)₂‐NO interaction through spectroscopic analyses and density functional theory revealed that the Cu‐bis(iminobenzosemiquinoid) moieties serve as the binding sites for NO sensing, while the Ni‐bis(iminobenzosemiquinoid) MOF analog shows no noticeable response to NO. Overall, these findings provide a significant advance in the development of crystalline metal‐bis(iminobenzosemiquinoid)‐based conductive 2D MOFs as highly sensitive, selective, and reversible sensing materials for the low‐power detection of toxic gases. 

The integration of tunable magnetic properties and electrical conductivity within a single material presents significant opportunities for spintronic applications and quantum information processing. This paper describes the first systematic investigation of electrical conduction and magnetism in four novel isostructural electrically conductive metal−organic frameworks (cMOFs), Ln‐HHTP (Ln = Sm, Eu, Gd, Tb), constructed using lanthanide ions and hexahydroxytriphenylene (HHTP) ligands. These materials show tunable semiconducting properties arising from efficient interlayer charge transport, which can be modulated by the density of states of the metal centers. Ln‐HHTP cMOFs exhibit different magnetic properties, with magnetic interactions varying from antiferromagnetism in Tb‐HHTP to ferromagnetism in Gd‐HHTP and Sm‐HHTP. The magnetic properties in Ln‐HHTP are modulated by single‐ion anisotropies of Ln3+spins and inherent geometric frustration within the kagome lattice. Moreover, Gd‐HHTP and Tb‐HHTP demonstrate robust quantum tunneling of magnetization. This work advances the understanding of cMOF magnets and underscores their potential as tunable platforms for next‐generation spintronic and quantum technologies. 

Metallophthalocyanine (MPc)-linked conductive two-dimensional (2D) metal−organic frameworks (MOFs) hold tremendous promise as modular 2D materials in sensing, catalysis, and energy-related applications due to their combinatory bimetallic system from the MPc core and bridging metal nodes, endowing them with high electrical conductivity and multifunctionality. Despite significant advances, there is a gap in fundamental understanding regarding the periodic effects of metal nodes on the structural properties of MP-linked 2D MOFs. Herein, we report a series of highly crystalline MOFs wherein copper phthalocyanine (CuPc) is linked with Ni, Cu, and Zn nodes (CuPc-O-M, M: Ni, Cu, Zn). The prepared CuPc-O-M MOFs exhibit p-type semiconducting properties with an exceptionally high range of electrical conductivity. Notably, the differences in the 3d orbital configurations of the Ni, Cu, and Zn nodes in CuPc-O-M MOFs lead to perturbations of the interlayer stacking patterns of the 2D framework materials, which ultimately affect material properties, such as semiconducting band gaps and charge transport within the framework. The Cu2+ (3d9) metal node within the eclipsed interlayer stacking of CuPc-O-Cu MOF demonstrates excellent charge transport, which results in the smallest band gap of 1.14 eV and the highest electrical conductivity of 9.3 S m−1, while the Zn2+ (3d10) metal node within CuPc-O-Zn results in a slightly inclined interlayer stacking, leading to the largest band gap of 1.27 eV and the lowest electrical conductivity of 2.9 S m−1. These findings form an important foundation in the strategic molecular design of this class of materials for multifaceted functionality that builds upon the electronic properties of these materials. 

Thermally regenerative electrochemical cycles and thermogalvanic cells harness redox entropy changes (ΔSrc) to interconvert heat and electricity with applications in heat harvesting and energy storage. Their efficiencies depend on ΔSrc because it relates directly to the Seebeck coefficient, yet few approaches exist for controlling the reaction entropy. Here, we demonstrate the design principle of using highly charged molecular species as electrolytes in thermogalvanic devices. As a proof-of-concept, the highly charged Wells-Dawson ion [P2W18O62]6– exhibits a large ΔSrc (−195 J mol–1 K–1) and a Seebeck coefficient comparable to state-of-the-art electrolytes (−1.7 mV K–1), demonstrating the potential of linking the rich chemistry of polyoxometalates to thermogalvanic technologies.