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Synthesis and properties of the ditelluroethers m- and p-C6H4(CH2TeMe)(2) and their Te(IV) derivatives: crystal structures of PhTeI2(CH2)(3T)TeI2Ph, m-C6H4(CH2TeI2Me)(2) and p-C6H4(CH2TeI2Me)(2)

Synthesis and properties of the ditelluroethers m- and p-C6H4(CH2TeMe)(2) and their Te(IV) derivatives: crystal structures of PhTeI2(CH2)(3T)TeI2Ph, m-C6H4(CH2TeI2Me)(2) and p-C6H4(CH2TeI2Me)(2)
Synthesis and properties of the ditelluroethers m- and p-C6H4(CH2TeMe)(2) and their Te(IV) derivatives: crystal structures of PhTeI2(CH2)(3T)TeI2Ph, m-C6H4(CH2TeI2Me)(2) and p-C6H4(CH2TeI2Me)(2)
The new ditelluroethers m-C6H4(CH2TeMe)(2) and p-C6H4(CH2TeMe)(2) have been prepared in good yield from nucleophilic reaction of m- or p-C6H4(CH2Br)(2) and LiTeMe in THF solution. Reaction of the new ditelluroethers with MeI or I-2 affords the light yellow m- or p-C6H4(CH(2)TeMe(2)l)(2) or the red/orange m- or p-C6H4(CH2TeI2Me)(2), respectively in high yield. These compounds have been characterised by IR, H-1, C-13{H-1} and (12)'Te{(1) H} NMR spectroscopy and El mass spectrometry as appropriate. The crystal structures of the di-iodo, derivatives m-C6H4(CH(2)Tel(2)Me)(2), p-C6H4(CH2TeI2Me)(2) and the related Phl(2)Te(CH2)(3)Tel(2)Ph (prepared from PhTe(CH2)(3)TePh and diiodine in THF solution) are described. In each compound the TeI2 units are axial and significant intermolecular Te... I secondary contacts ( approximate to3.6-4.1 Angstrom) are evident, which link these covalent compounds into extended networks with each Te atom in a distorted 6-coordinate environment.
tellurium, x-ray structures, secondary interactions, molecular-structure, macrocycles, complexes, ligands, o-c6h4(ch2teme)(2), chemistry, me
0022-328X
1006-1013
Hesford, Matthew J.
0285a942-8dd9-4561-84fe-f4c6087d5c5f
Hill, Nicholas J.
c588ad7e-5668-46b9-b84a-791b664f37aa
Levason, William
e7f6d7c7-643c-49f5-8b57-0ebbe1bb52cd
Reid, Gillian
37d35b11-40ce-48c5-a68e-f6ce04cd4037
Hesford, Matthew J.
0285a942-8dd9-4561-84fe-f4c6087d5c5f
Hill, Nicholas J.
c588ad7e-5668-46b9-b84a-791b664f37aa
Levason, William
e7f6d7c7-643c-49f5-8b57-0ebbe1bb52cd
Reid, Gillian
37d35b11-40ce-48c5-a68e-f6ce04cd4037

Hesford, Matthew J., Hill, Nicholas J., Levason, William and Reid, Gillian (2004) Synthesis and properties of the ditelluroethers m- and p-C6H4(CH2TeMe)(2) and their Te(IV) derivatives: crystal structures of PhTeI2(CH2)(3T)TeI2Ph, m-C6H4(CH2TeI2Me)(2) and p-C6H4(CH2TeI2Me)(2). Journal of Organometallic Chemistry, 689 (6), 1006-1013. (doi:10.1016/j.jorganchem.2003.12.033).

Record type: Article

Abstract

The new ditelluroethers m-C6H4(CH2TeMe)(2) and p-C6H4(CH2TeMe)(2) have been prepared in good yield from nucleophilic reaction of m- or p-C6H4(CH2Br)(2) and LiTeMe in THF solution. Reaction of the new ditelluroethers with MeI or I-2 affords the light yellow m- or p-C6H4(CH(2)TeMe(2)l)(2) or the red/orange m- or p-C6H4(CH2TeI2Me)(2), respectively in high yield. These compounds have been characterised by IR, H-1, C-13{H-1} and (12)'Te{(1) H} NMR spectroscopy and El mass spectrometry as appropriate. The crystal structures of the di-iodo, derivatives m-C6H4(CH(2)Tel(2)Me)(2), p-C6H4(CH2TeI2Me)(2) and the related Phl(2)Te(CH2)(3)Tel(2)Ph (prepared from PhTe(CH2)(3)TePh and diiodine in THF solution) are described. In each compound the TeI2 units are axial and significant intermolecular Te... I secondary contacts ( approximate to3.6-4.1 Angstrom) are evident, which link these covalent compounds into extended networks with each Te atom in a distorted 6-coordinate environment.

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Published date: 15 March 2004
Keywords: tellurium, x-ray structures, secondary interactions, molecular-structure, macrocycles, complexes, ligands, o-c6h4(ch2teme)(2), chemistry, me

Identifiers

Local EPrints ID: 20228
URI: http://eprints.soton.ac.uk/id/eprint/20228
ISSN: 0022-328X
PURE UUID: 431b8af6-2f1e-483f-9e6f-505a5343b6f5
ORCID for William Levason: ORCID iD orcid.org/0000-0003-3540-0971
ORCID for Gillian Reid: ORCID iD orcid.org/0000-0001-5349-3468

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Date deposited: 21 Feb 2006
Last modified: 16 Mar 2024 02:43

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Contributors

Author: Matthew J. Hesford
Author: Nicholas J. Hill
Author: William Levason ORCID iD
Author: Gillian Reid ORCID iD

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