In the present work, characteristic properties of tetrabutylammonium bromide (TBAB) ionic clathrate hydrates structures were studied by single-crystal X-ray structure analysis. The structures of three different tetragonal TBAB ionic clathrate hydrates that were formed in our experiments were based on the same water lattice of tetragonal structure I (TS-I) differing in the ways of including bromide anions and arranging tetrabutylammonium cations. We demonstrated that (1) Br(-) can be included into the water lattice, replacing two water molecules, (2) the butyl group of the cation can be inserted not only in large T and P cavities but also in small D cavities of the water lattice TS-I, and (3) one of the reasons for polytypism of ionic clathrate hydrates on the basis of TS-I is the occurrence of alternative modes of arrangements of four-compartment cavities in adjacent layers of the water framework. The compositions of three TBAB ionic clathrate hydrates TBAB·38.1H2O, TBAB·32.5H2O, and TBAB·26.4H2O were determined by chemical analysis, and their enthalpies of fusion were measured by differential scanning calorimetry (DSC). From the obtained results, the enthalpies of the TBAB hydrate formation from TBAB and water were calculated thermodynamically.
Three ionic clathrate hydrates of different water content are formed in the binary system tetrabutylammonium chloride-water. The data on heats of fusion of these hydrates measured by DSC are presented. Single-crystal and powder X-ray diffraction studies of ionic clathrate hydrates of tetrabutylammonium chloride have been carried out. Structural justification of the occurrence of three different ionic clathrate hydrates derived from tetragonal structure-I in the (C(4)H(9))(4)NCl-H(2)O system has been found for the first time. A novel mode of hydrophilic inclusion of the halide anion with displacement of two hydrogen-bonded host water molecules has been revealed. Structural data obtained are indicative of the possibility of location of tetrabutylammonium cations in combined cavities formed with participation of D-voids.
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