Systematic Structural Coordination Chemistry of p‐tert ‐Butyltetrathiacalix[4]arene: Further Complexes of Transition‐Metal Ions

Author:

Bilyk Alexander1,Dunlop John W.1,Fuller Rebecca O.12,Hall Annegret K.1,Harrowfield Jack M.13,Hosseini M. Wais4,Koutsantonis George A.1,Murray Ian W.1,Skelton Brian W.1,Stamps Robert L.2,White Allan H.1

Affiliation:

1. Chemistry M313, School of Biomedical, Biomolecular and Chemical Sciences, University of Western Australia, Crawley, Western Australia 6009

2. School of Physics M013, The University of Western Australia, Crawley, Western Australia 6009

3. Laboratoire de Chimie Supramoléculaire, Institut de Science et d'Ingénierie Supramoléculaires, Université de Strasbourg, 67083 Strasbourg, France

4. Laboratoire de Chimie de Coordination Organique, Institut Le Bel, Université de Strasbourg, 67000 Strasbourg, France

Publisher

Wiley

Subject

Inorganic Chemistry

Reference62 articles.

1. Transition metal and lanthanide cluster complexes constructed with thiacalix[n]arene and its derivatives

2. Note that we have restricted our considerations to homometallic complexes and cases where only solvent molecules or simple anions are bound to the transition metals in addition to the thiacalixarene. Various complexes containing other strong ligands are known. See for example

3. Mononuclear and Dinuclear Molybdenum and Tungsten Complexes of p-tert-Butyltetrathiacalix[4]arene and p-tert-Butyltetrasulfonylcalix[4]arene: Facile Cleavage of the Calixarene Ligand Framework by Nickel

4. Dinukleare Titankomplexe des Thiacalix[4]arens

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