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Synthesis of Sterically Hindered Tellurophenols and the Structure of [Cd(μ‐TeC 6 H 2 M 3 ) 2 ] ∞
Author(s) -
Bochmann Manfred,
Coleman Andrew P.,
Webb Kevin J.,
Hursthouse Michael B.,
Mazid Muhammed
Publication year - 1991
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.199109731
Subject(s) - steric effects , tec , chemistry , crystallography , metal , stereochemistry , physics , organic chemistry , ionosphere , astronomy
Useful starting compounds for the synthesis of metal complexes are provided by the thermally sensitive and photosensitive tellurophenols 1 (R = Me, i Pr, t Bu). For instance, the methyl‐substituted compound 1 reacts with [Cd{N(SiMe 3 ) 2 } 2 ] to give [Cd(TeC 6 H 2 Me 3 ) 2 ] ∞ , whose linear one‐dimensional chain structure is due to the spatial bulk of the mesityl groups.

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