TY - JOUR
T1 - Structural Disorder in Solidp-Iodotoluene
AU - Serrano-González, Heliodoro
AU - Harris, Kenneth D.M.
AU - Kitchin, Simon J.
AU - Alvarez-Larena, Angel
AU - Estop, Eugènia
AU - Alcobé, Xavier
AU - Tauler, Esperanza
AU - Labrador, Manuel
AU - Apperley, David C.
PY - 1999/3/1
Y1 - 1999/3/1
N2 - Single crystal X-ray diffraction studies have been carried out onp-iodotoluene at two temperatures (293 and 173 K) in order to explore the existence and temperature-dependence of orientational disorder in the crystal structure. In the average crystal structure at each temperature, the molecules are disordered between two orientations. The two orientations define a "head- tail" type of disorder in which the intramolecular CH3→I vectors are essentially antiparallel and the molecular planes are essentially coplanar. The structures at 293 and 173 K are essentially the same, except that there is a significant difference in the degree of disorder (the fractional occupancy of the minor molecular orientation is 0.17 at 293 K and 0.08 at 173 K). As the same crystal was used for the X-ray diffraction studies at both temperatures, the change in occupancy with temperature suggests that a mechanism exists for the molecular orientation to relax within the crystal. Solid state13C NMR results are also consistent with (although do not prove) the suggested dynamic interconversion between the two molecular orientations. Several aspects of the disorder in this system are discussed in detail, including an assessment of energetic aspects concerning the different molecular orientations within the crystal. © 1999 Academic Press.
AB - Single crystal X-ray diffraction studies have been carried out onp-iodotoluene at two temperatures (293 and 173 K) in order to explore the existence and temperature-dependence of orientational disorder in the crystal structure. In the average crystal structure at each temperature, the molecules are disordered between two orientations. The two orientations define a "head- tail" type of disorder in which the intramolecular CH3→I vectors are essentially antiparallel and the molecular planes are essentially coplanar. The structures at 293 and 173 K are essentially the same, except that there is a significant difference in the degree of disorder (the fractional occupancy of the minor molecular orientation is 0.17 at 293 K and 0.08 at 173 K). As the same crystal was used for the X-ray diffraction studies at both temperatures, the change in occupancy with temperature suggests that a mechanism exists for the molecular orientation to relax within the crystal. Solid state13C NMR results are also consistent with (although do not prove) the suggested dynamic interconversion between the two molecular orientations. Several aspects of the disorder in this system are discussed in detail, including an assessment of energetic aspects concerning the different molecular orientations within the crystal. © 1999 Academic Press.
U2 - 10.1006/jssc.1998.8110
DO - 10.1006/jssc.1998.8110
M3 - Article
SN - 0022-4596
VL - 143
SP - 285
EP - 295
JO - Journal of Solid State Chemistry
JF - Journal of Solid State Chemistry
ER -