First examples of thallium chalcogenide cages. Syntheses, Se-77, Tl-203, and Tl-205 NMR study of the Tl4Se54- and Tl4Se64- anions, the X-ray crystal structure of (2,2,2-crypt-K+)(3)Tl5Se53-, and theoretical studies
J. Campbell et al., First examples of thallium chalcogenide cages. Syntheses, Se-77, Tl-203, and Tl-205 NMR study of the Tl4Se54- and Tl4Se64- anions, the X-ray crystal structure of (2,2,2-crypt-K+)(3)Tl5Se53-, and theoretical studies, INORG CHEM, 40(2), 2001, pp. 233-254
The Ti5S53- union has been obtained by extracting KTlSe in ethylenediamine
in the presence of 2,2,2-crypt. The salt, (2,2,2-erypt-K+)(3)Tl5Se53-, crys
tallizes in the triclinic system, space group P1, with Z = 2 and a = 11.676
(2) Angstrom, b = 16.017(3) Angstrom, c = 25.421(5) Angstrom, alpha = 82.32
(3)degrees, beta = 88.47(3)degrees, gamma = 69.03(3)degrees at -123 degrees
C. Two other mixed oxidation stale Tl-I/Tl-III unions, Tl4Se54- and Tl4Se64
-, have been obtained by extracting KTlSe into liquid NH3 in the presence o
f 2,2,2-crypt and have been characterized in solution by low-temperature Se
-77, Tl-203, and Tl-205 NMR soectroscopy and were shown to exist as a 1:1 e
quilibrium mixture at -40 degreesC. The couplings, (1)J(Tl-203.205-Se-77) a
nd (2)J((Tl-203.205Tl)-Tl-203.205), have been observed for Tl4Se54- and Tl4
Se64- and have been used to arrive at the solution structures of both anion
s. Structural assignments achieved by de: were achieved by detailed analyse
s and simulations of all spin multiplets that comprise the Tl-205.203 NMR s
pectra and that arise from natural abundance Tl-205,Tl-203 and Se-77 or enr
iched Se-77 isotopomer distributions: The structures of all three anions ar
e based on a Tl4Se4 cube in which Tl and Se atoms occupy alternate corners.
There are one and two exo-selenium atoms bonded to thallium in Tl4Se54- an
d Tl4Se64-, respectively, so that these thalliums are four-cooridinate and
possess a formal oxidation state of +3 and the remaining three-coordinate t
hallium atoms are in the +1 oxidation state. The structure of Tl5Se53- may
be formally regarded as an adduct in which Tl+ is coordinated to the unique
exo-selenium and to two seleniums in a cube face containing the Tl-III ato
m. The T4Se54-, Tl4Se64-, and Tl5Se53- anions and the presently unknown, bu
t structurally related, Tl4Se44- anion can be described as electron-precise
cages; Ab initio methods at the MP2 level of theory show that Tl4Se54-, Tl
4Se64-, and Tl5Se53- exhibit true minima and display geometrical parameters
that are in excellent agreement with their experimental cubanoid structure
s, and that Tl4Se44- is cube-shaped (T-d point symmetry). The gas-phase ene
rgetics associated with plausible routes to the formation and interconversi
ons of these anions have been determined by ab initio methods and assessed.
It is proposed that all three cubanoid anions are derived from the known T
l2Se22-, TlSe33-, Se-2(2-), and polyselenide anions that have been shown to
be present in the solutions they are derived from.