P. Ganal et al., STRUCTURAL INVESTIGATION OF MERCURY-INTERCALATED TITANIUM DISULFIDE .1. THE CRYSTAL-STRUCTURE OF HG1.24TIS2, Chemistry of materials, 7(6), 1995, pp. 1132-1139
X-ray powder and single-crystal diffraction have been used together wi
th thermogravimetric compositional analysis to determine the crystal s
tructure of the superstoichiometric intercalation compound Hg1.24TiS2
at ambient temperature. Hg1.24TiS2 forms an unusual (3 + 1)-dimensiona
l layered misfit compound, which can alternatively be described as int
erpenetrating three-dimensional TiS2 and Hg sublattices. The symmetry
of each sublattice can be described by the monoclinic space group C2/m
. These sublattices share commensurate a and c axes but are incommensu
rate with each other along the b axis [a = 5.9223(9) Angstrom, b(TiS2)
= 3.4076(2) Angstrom, b(Hg) = 2.7566(1) Angstrom, c = 8.862(1) Angstr
om, and beta = 102.33(3)degrees]. Hg forms infinite one-dimensional ch
ains within the nearly trigonal prismatic sulfur channels created by h
ost-layer restacking. The Hg chains exhibit metallic intrachain guest-
guest bonding, with a bond distance of 2.76 Angstrom. Comparison of th
e intrachain Hg-Hg bond distance to the Hg-n+-Hg-n+ bond distances for
compounds containing linear Hg chains with a known ionic valence indi
cates the intercalated Hg in Hg1.24TiS2 has very Little ionic characte
r. Unlike other transition-metal dichalcogenide intercalation compound
s that possess primarily ionic guest-host interactions, this compound
exhibits weak covalent guest-host interactions and very Little ionic c
harge transfer.