In
emerging trends in our technology-dependent society, the applicability
of multifunctional coordination polymers (CPs) and metal–organic
frameworks is highly stimulating. In search of such chemical compounds,
a Mn(II), d5, based metal–organic framework (MOF),
{[Mn2(tdc)2(pcih)2(EtOH)]
n
} (1), has
been designed with the coordination of multidentate ligands tdc
2– (2,5-thiophene dicarboxylato)
and pcih (pyridine-4-carboxaldehyde isonicotinoylhydrazone).
The structure determination by single crystal X-ray diffraction has
revealed the formation of three-dimensional (3D) supramolecular architecture
via the combined nearly perpendicular bridging of pcih and tdc2–
ligands. A variable temperature
magnetic measurement of 1 shows weak antiferromagnetism
(χMT, 9.41 cm3 K mol–1 at 300 K) with two as good as “isolated” Mn(II) centers
(S = 5/2 with g ≈ 2.07).
Magnetic exchange is considered through 9/10 carboxylato bridged atoms
inclusively spanning two Mn(II) centers at a distance of 4.114 Å.
Interestingly, the 3D assembly of 1 exhibits electrical
conductivity in the semiconducting region (band gap, 3.72 eV; barrier
height, 0.65 eV; series resistance, 0.03 Ω). A Schottky barrier
diode feature is recorded at a threshold potential of 0.19 V and follows
a non-ohmic relation (I α V
2), and the conductivity is 3.42 × 10–5 S m–1. A galvanostatic charge–discharge
(GCD) experiment measures the moderate specific capacitance of 1 F/g
at a 2 mV/s scan rate.