Issue 35, 2012

Isolation and molecular structures of novel organotellurium(iv) halides, oxyhalide and mixed halide

Abstract

The formation of chiral (R)-[2-(4-ethyl-2-oxazolinyl)phenyl]tellurium(IV) trihalides (trichloride (5), tribromide (6) and triiodide (7)) and (R)-[2-(4-ethyl-2-oxazolinyl)phenyl]tellurium(II) bromide (8) is described. The molecular structure of the first chiral organotellurium(IV) triiodide (7) is discussed. The most interesting feature of the structure of 5 is the observation of the shortest intramolecular Te⋯N distance for any organotellurium(IV) trichloride. Compounds 5 and 6 do not undergo electrophilic addition reaction with olefins. Attempted addition reaction of 6 with olefin in methanol leads to the isolation of the rare partially hydrolysed tellurium(IV) halide, methyl-2-(dibromooxotellurium)benzoate (9). Novel stable mixed halide 12 was isolated from the bromination of 11. DFT calculations indicate that both the isomers 12a and 12b have similar stability.

Graphical abstract: Isolation and molecular structures of novel organotellurium(iv) halides, oxyhalide and mixed halide

Supplementary files

Article information

Article type
Paper
Submitted
21 Mar 2012
Accepted
15 Jun 2012
First published
18 Jun 2012

Dalton Trans., 2012,41, 10707-10714

Isolation and molecular structures of novel organotellurium(IV) halides, oxyhalide and mixed halide

P. Rakesh, H. B. Singh and R. J. Butcher, Dalton Trans., 2012, 41, 10707 DOI: 10.1039/C2DT30645J

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements