The temperature-dependent dynamic properties of [CuII2(ADCOO)4(DMF)2]⋅(DMF)2 (1) and [CuII2(ADCOO)4(AcOEt)2] (2) crystals were examined by X-ray crystallography, 1H NMR spectroscopy, and measurements of the dielectric constants and magnetic susceptibilities (ADCOO=adamantane carboxylate, DMF=N,N-dimethylformamide, and AcOEt=ethyl acetate). In both crystals, four ADCOO groups bridged a binuclear CuIICuII bond, forming a paddle-wheel [CuII2(ADCOO)4] structure. The oxygen atoms of two DMF molecules in crystal 1 and two AcOEt molecules in crystal 2 were coordinated at axial positions of the [CuII2(ADCOO)4] moiety, forming [CuII2(ADCOO)4(DMF)2] and [CuII2(ADCOO)4(AcOEt)2], respectively. Two additional DMF molecules were included in the unit cell of crystal 1, whereas AcOEt was not included in the unit cell of crystal 2. The structural analyses of crystal 1 at 300 K showed three-fold rotation of the adamantyl groups, whereas rotation of the adamantyl groups of crystal 2 at 300 K was not observed. Thermogravimetric measurements of crystal 1 indicated a gradual elimination of DMF upon increasing the temperature above 300 K. The dynamic behavior of the crystallized DMF yielded significant temperature-dependent dielectric responses in crystal 1, which showed a huge dielectric peak at 358 K in the heating process. In contrast, only small frequency-dependent dielectric responses were observed in crystal 2 because of the freezing of the molecular rotation of the adamantyl groups. The magnetic behavior was dominated by the strong antiferromagnetic coupling between the two S=1/2 spins of the CuIICuII site, with magnetic exchange energies (J) of −265 K (crystal 1) and −277 K (crystal 2).