A MOLECULAR-DYNAMICS SIMULATION OF THE PLASTIC PHASE OF HEXACHLOROETHANE

被引:6
作者
CRIADO, A [1 ]
MUNOZ, A [1 ]
机构
[1] UNIV SEVILLA,CSIC,DEPT FIS MAT CONDENSADA,E-41080 SEVILLE,SPAIN
关键词
D O I
10.1080/00268979400101601
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A molecular dynamics simulation of the plastic phase of the pseudooctahedral molecule C2Cl6 has been carried out using a 6-exp potential model taken from the literature. A plastic phase has been found for a temperature range which is in good agreement with experiment. The calculated thermal averages of the centre of mass displacements and the orientational cubic harmonics are also in good agreement with the experimental values. The calculated atomic orientational probability distribution shows maxima along the [100] and [111] directions for the Cl and C atoms, respectively, and the distribution is isotropic over a wide angular range about the maxima. An analysis of the instantaneous molecular positions shows that the molecules have a larger probability of rotating, and perform sudden reorientations around the [100] crystal directions. It has been found that the molecular C-C axis plays no important role in the molecular dynamics, which is identical to what is found for the plastic phase of the octahedral molecule SF6. A search has been made for the formation of linear clusters of molecules as suggested in the literature but these do not appear in the simulation. A correlated repulsion between molecules and their next-nearest neighbours has been found so that the molecules avoid close contacts of the chlorine atoms along the [100] directions by performing rotations about the [110] crystal directions. The single-molecule rotational potential is calculated and compared with the experimental one, showing that the potential energy barrier for molecular rotations about the [100] directions is considerably lower than for the [110] and [111] rotations. The single-molecule dynamics are also studied and the translational power spectrum reveals a strong translational-rotational coupling whereas the rotational spectrum shows an isotropic rotational diffusion behaviour. The molecules are found to librate around ideal positions for an average residence time of 54 ps between consecutive reorientational jumps.
引用
收藏
页码:815 / 833
页数:19
相关论文
共 26 条
[1]   INTERMOLECULAR POTENTIAL FUNCTION MODEL FOR CRYSTALLINE HEXACHLOROBENZENE [J].
BATES, JB ;
BUSING, WR .
JOURNAL OF CHEMICAL PHYSICS, 1974, 60 (06) :2414-2419
[2]   MOLECULAR-DYNAMICS SIMULATION OF THE PLASTIC PHASE OF SOLID METHANE [J].
BOUNDS, DG ;
KLEIN, ML ;
PATEY, GN .
JOURNAL OF CHEMICAL PHYSICS, 1980, 72 (10) :5348-5356
[3]   NEUTRON-DIFFRACTION STUDY OF THE PLASTIC PHASES OF POLYCRYSTALLINE SF6 AND CBR4 [J].
DOLLING, G ;
POWELL, BM ;
SEARS, VF .
MOLECULAR PHYSICS, 1979, 37 (06) :1859-1883
[4]   A MOLECULAR-DYNAMICS SIMULATION STUDY OF THE PLASTIC CRYSTALLINE PHASE OF SULFUR-HEXAFLUORIDE [J].
DOVE, MT ;
PAWLEY, GS .
JOURNAL OF PHYSICS C-SOLID STATE PHYSICS, 1983, 16 (31) :5969-5983
[5]  
DOVE MT, 1986, J MOL GRAPHICS, V4, P79
[6]   COLLECTIVE EXCITATIONS IN AN ORIENTATIONALLY FRUSTRATED SOLID - NEUTRON-SCATTERING AND COMPUTER-SIMULATION STUDIES OF SF6 [J].
DOVE, MT ;
PAWLEY, GS ;
DOLLING, G ;
POWELL, BM .
MOLECULAR PHYSICS, 1986, 57 (04) :865-880
[7]   A MOLECULAR-DYNAMICS SIMULATION STUDY OF THE ORIENTATIONALLY DISORDERED PHASE OF SULFUR-HEXAFLUORIDE [J].
DOVE, MT ;
PAWLEY, GS .
JOURNAL OF PHYSICS C-SOLID STATE PHYSICS, 1984, 17 (36) :6581-6599
[8]   ANION ORDERING IN ALKALI CYANIDE CRYSTALS [J].
FERRARIO, M ;
MCDONALD, IR ;
KLEIN, ML .
JOURNAL OF CHEMICAL PHYSICS, 1986, 84 (07) :3975-3985
[9]   THE DETERMINATION OF THE EFFECTIVE ROTATIONAL POTENTIAL IN THE PLASTIC PHASE OF C2CL6 FROM NEUTRON BRAGG SCATTERING DATA [J].
GERLACH, P ;
PRANDL, W ;
VOGT, K .
MOLECULAR PHYSICS, 1984, 52 (02) :383-397
[10]   SHORT-RANGE-ORDER CORRELATIONS IN THE ORIENTATIONALLY DISORDERED PHASE OF HEXACHLOROETHANE .1. DIFFUSE-X-RAY SCATTERING [J].
GERLACH, P ;
PRANDL, W .
ACTA CRYSTALLOGRAPHICA SECTION A, 1988, 44 :128-135