Abstract
Depending on the ratio of the starting reagents, the interaction of [FcTeI] with Fe(CO)5 gave complex (Fc2Te2)Fe(CO)3I2 (1) bearing an Fc2Te2 ligand, or a dimeric complex [(CO)3IFe(μ-TeFc)]2 (2). An interaction of equimolar amounts of [CpFe(CO)2]2 and Fc2Te2 under the thermal conditions in toluene afforded CpFe(CO)2TeFc (3). Complex 3 can be easily halogenated at the Te center by elemental bromine and iodine to give monomeric CpFe(CO)2TeX2Fc (X = Br (4), I (5)). Complex 5 can be prepared alternatively via formal insertion of [FcTeI] into Fc-I bond of CpFe(CO)2I. Complex 3 readily substitutes one carbonyl in Fe(CO)4I2 to give the adduct CpFe(CO)2(μ-TeFc)Fe(CO)3I2 (6).
Original language | English |
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Pages (from-to) | 88-95 |
Number of pages | 8 |
Journal | Journal of Organometallic Chemistry |
Volume | 777 |
DOIs | |
State | Published - 1 Feb 2015 |
Externally published | Yes |
Keywords
- Electrochemistry
- Ferrocenyl
- Metal-chalcogenide
- Mössbauer spectroscopy
- Organotellurium
- X-ray diffraction
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
- Materials Chemistry