In chemistry, a transition metal ether complex is a coordination complex consisting of a transition metal bonded to one or more ether ligand. The inventory of complexes is extensive.[2] Common ether ligands are diethyl ether and tetrahydrofuran. Common chelating ether ligands include the glymes, dimethoxyethane (dme) and diglyme, and the crown ethers. Being lipophilic, metal-ether complexes often exhibit solubility in organic solvents, a property of interest in synthetic chemistry. In contrast, the di-ether 1,4-dioxane is generally a bridging ligand.
Bonding, structure, reactions
editEthers are L-type ligands. They are σ-donors that exert weak field ligands. They resemble water ligands as seen in aquo complexes. They do not, however, readily participate in hydrogen bonding. The ether oxygen is nearly trigonal planar in its complexes.[4]
Being weakly basic, ether ligands tend to be easily displaceable. Otherwise, ether ligands are relatively unreactive. Cyclic ethers such as thf can ring-open or even deoxygenated when bound to highly electrophilic metal halides. Thus treatment of tungsten hexachloride with one equivalent of thf gives 1,4-dichlorobutane:[5]
- WCl6 + OC4H8 → WOCl4 + ClCH2CH2CH2CH2Cl
At higher concentrations of thf, polytetrahydrofuran is produced.
Examples
editHomoleptic complexes
editEthers are relatively bulky ligands, thus homoleptic (i.e., all ligands being the same) ether complexes are uncommon. Examples often feature weakly coordinating anions such as BArF4− and Al(ORF)4−.
Metal halide complexes
editMetal chloride-tetrahydrofuran complexes are especially studied.[12] These compounds are often reagents because they are soluble in organic solvents as well as being anhydrous.
Formula of metal-chloride-ether complexes |
Coordination sphere |
color |
---|---|---|
TiCl4(thf)2 | TiO2Cl4 | yellow[13] |
TiCl3(thf)3 | TiO3Cl3 | blue[12] |
[TiCl3(thf)2]2 | TiO2Cl4 | green[14] |
ZrCl4(thf)2 | ZrO2Cl4 | white[12] |
HfCl4(thf)2 | HfO2Cl4 | white[12] |
VCl3(thf)3 | VO3Cl3 | pink[12] |
VCl3(thf)2]2 | VO2Cl4 | red[14] |
NbCl4(thf)2 | NbO2Cl4 | yellow[15] |
Ta3Cl9(thf)4 | TaO2Cl4 and TaOCl5[15] | |
CrCl3(thf)3 | CrO3Cl3 | pink[12][16] |
MoCl4(thf)2 | MoO2Cl4 | pink[17] |
MoCl4(Et2O)2 | MoO2Cl4 | beige[18] |
MoCl3(thf)3 | MoO3Cl3 | red[17] |
WCl4(Et2O)2 | WO2Cl4 | yellow[19] |
MnCl3(thf)3 | MnO3Cl3 | brown-purple[20] |
TcCl4(thf)2 | TcO2Cl4 | yellow[13] |
ReCl4(thf)2 | ReO2Cl4 | green[21] |
Fe4Cl8(thf)6 | FeO2Cl3, FeO2Cl4 | brown[22] |
FeCl3(thf)2 | FeO2Cl3[23] | the related diethyl ether complex is brown |
FeCl3(OEt2)2 | FeO2Cl3 | brown[11] |
Co4Cl8(thf)6 | CoO2Cl3, CoO2Cl4 | blue[24] |
[CoCl2(dme)]2 | CoO2Cl3[25] | |
NiCl2(dimethoxyethane)2 | NiCl2O4 | yellow[26] |
[Cu2Cl4(thf)3]n | CuO2Cl4, CuOCl4 | orange[27] |
ZnCl2(thf)2 | ZnO2Cl2 | white[16] |
Metal carbonyl complexes
edit- M(CO)5(thf) (M = Cr, Mo, W)[4]
- Mo(CO)3(diglyme)
References
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- ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
- ^ Duan, Zhiming; Zhang, Yan; Zhang, Bin; Zhu, Daoben (2009). "Crystal-to-Crystal Transformation from Antiferromagnetic Chains into a Ferromagnetic Diamondoid Framework". Journal of the American Chemical Society. 131 (20): 6934–6935. doi:10.1021/ja902101x. PMID 19402661.
- ^ a b Schubert, U.; Friedrich, P.; Orama, O. (1978). "Kristall- und molekülstruktur von pentacarbonyltetrahydrofuran-chrom(0)". Journal of Organometallic Chemistry. 144 (2): 175–179. doi:10.1016/S0022-328X(00)84160-1.
- ^ Bianchi, Sabrina; Bortoluzzi, Marco; Castelvetro, Valter; Marchetti, Fabio; Pampaloni, Guido; Pinzino, Calogero; Zacchini, Stefano (2016). "The reactivity of tungsten hexachloride with tetrahydrofuran and 2-methoxyethanol". Polyhedron. 117: 769–776. doi:10.1016/j.poly.2016.07.024. hdl:11568/803763.
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