Abstract
An in-depth understanding of the physicochemical properties of the organic-inorganic hybrid [NH(3)(CH(2))(2)NH(3)](2)CdBr(6) whose structure corresponds to the formulation [NH(3)(CH(2))(2)NH(3)](2)CdBr(4)· 2Br is essential for its application in batteries, supercapacitors, and fuel cells. Therefore, this study aimed to determine the crystal structure, phase transition, structural geometry, and molecular dynamics of these complexes. Considering its importance, a single crystal of [NH(3)(CH(2))(2)NH(3)](2)CdBr(6) was grown; the crystal structure was found to be monoclinic. The phase transition temperatures were determined to be 443, 487, 517, and 529 K, and the crystal was thermally stable up to 580 K. Furthermore, the (1)H, (13)C, (14)N, and (113)Cd NMR chemical shifts caused by the local field surrounding the resonating nucleus of the cation and anion varied with increasing temperature, along with the surrounding environments of their atoms. In addition, (1)H spin-lattice relaxation time T(1ρ) and (13)C T(1ρ), which represent the energy transfer around the (1)H and (13)C atoms of the cation, respectively, varied significantly with temperature. Consequently, changes in the coordination geometry of Br around Cd in the CdBr(6) anion and the coordination environment around N (in the cation) were associated with changes in the N-H···Br hydrogen bond. The structural geometry revealed critical information regarding their basic mechanism of organic-inorganic hybrid compounds.