Synthesis, spectroscopic characterization and structural studies of dialkyl dithiophosphinate and N,N-dialkyl dithio- and monothio-carbamate derivatives of 1-iodo-1,1,2,3,4,5-hexahydrotellurophene

Citation
V. Garcia-montalvo et al., Synthesis, spectroscopic characterization and structural studies of dialkyl dithiophosphinate and N,N-dialkyl dithio- and monothio-carbamate derivatives of 1-iodo-1,1,2,3,4,5-hexahydrotellurophene, J ORGMET CH, 623(1-2), 2001, pp. 74-80
Citations number
35
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF ORGANOMETALLIC CHEMISTRY
ISSN journal
0022328X → ACNP
Volume
623
Issue
1-2
Year of publication
2001
Pages
74 - 80
Database
ISI
SICI code
0022-328X(20010330)623:1-2<74:SSCASS>2.0.ZU;2-A
Abstract
The synthesis of the organotellurium(IV) compounds [C4H8TeI(S2PMe2)] (2), [ C4H8TeI(S2PEt2)] (3), [C4H8TeI(S2CNC4H6)] (4) and [C4H8TeI(SOCNC5H10)] (6) was achieved. All of them were characterized by IR, H-1-, C-13-, P-31- and Te-125-NMR, mass spectroscopy, elemental analyses and single-crystal X-ray diffraction. In addition, the crystal and molecular structures of the previ ously known 1,1 -diiodotetrahydrotellurophene and [C4H8TeI(S2CNEt2)] (5) we re obtained. The geometry around Te(IV) is that of a sawhorse structure in which the lone pair is apparently stereochemically active and occupying an equatorial position in a distorted trigonal bipyramid. All the structures e xhibit different supramolecular associations. The intermolecular Te . . .S and Te . . . I interactions result in the formation of dimeric species in 4 , and in 1 and 6. respectively. The intermolecular Te . . .S bonds in 2, 3 and 5 lead to formation of one-dimensional polymers. (C) 2001 Elsevier Scie nce B.V. All rights reserved.