Synthesis and structures of bismuth(III) complexes involving thio- and seleno-ether ligands

Citation
Aj. Barton et al., Synthesis and structures of bismuth(III) complexes involving thio- and seleno-ether ligands, J CHEM S DA, (6), 2000, pp. 859-865
Citations number
25
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
ISSN journal
03009246 → ACNP
Issue
6
Year of publication
2000
Pages
859 - 865
Database
ISI
SICI code
0300-9246(2000):6<859:SASOBC>2.0.ZU;2-N
Abstract
Bismuth trihalides (BiX3, X = Cl, Br or I) reacted with a range of thio- an d seleno-ether ligands L-L in anhydrous MeCN solution to yield compounds wi th either a 1 : 1, 1 : 2 or 2 : 1 Bi : L-L ratio. Structural studies on [Bi Br3{MeE(CH2)(3)EMe}] (E = S or Se) and [BiCl3{MeSe(CH2)(3)SeMe}] revealed t hat all of these species adopt an infinite two-dimensional sheet array deri ved from planar Bi2X6 units linked by bridging dithio- or diseleno-ether li gands which occupy mutually trans co-ordination sites, giving a distorted o ctahedral geometry at Bi-III. The structure of [BiBr3{MeS(CH2)(2)SMe}(2)] r eveals a discrete molecular compound which adopts a 7-co-ordinate distorted pentagonal bipyramidal geometry involving two chelating MeS(CH2)(2)SMe lig ands. This arrangement is also found for the iodide analogue. Reaction of B iBr3 with the Ph-substituted ligand PhS(CH2)(2)SPh generated a very differe nt structural arrangement in which chains of almost mutually orthogonal Bi2 Br2 'rectangles' are crosslinked by bridging dithioether ligands to yield i nfinite sheets of formula [Bi2Br6{PhS(CH2)(2)SPh}]. With the tripodal ligan ds L-3 (MeC(CH2SMe)(3) or MeC(CH2SeMe)(3)) compounds of stoichiometry [BiX3 (L-3)] were obtained. The crystal structure of [BiCl3{MeC(CH2SeMe)(3)}] sho ws Bi2Cl6 subunits linked by bridging selenoether ligands to give a two-dim ensional sheet. Each selenoether tripod functions as a bidentate chelate to Bi and bridges to an adjacent Bi via the third Se-donor, giving a distorte d octahedral geometry at Bi-III. Although a rather poor quality structure, [Bi2I6{MeC(CH2SeMe)(3)}(2)] is not isostructural with its chloro analogue, but shows discrete dimers formed via Bi2I6 subunits, with each Bi also co-o rdinated to a bidentate Se tripod and two terminal I ligands. The third Se- donor on each ligand remains non-co-ordinating. The influence of the Bi-bas ed lone pair on the structures adopted by these complexes is discussed.