Nickelocene
|
|
|||
| 200px | |||
| Names | |||
|---|---|---|---|
| IUPAC name
nickelocene
|
|||
| Other names
Bis(cyclopentadienyl) nickel(II)
|
|||
| Identifiers | |||
1271-28-9  |
|||
| ChEBI | CHEBI:30679 |
||
| RTECS number | QR6500000 | ||
| Properties | |||
| C10H10Ni | |||
| Molar mass | 188.88 g/mol | ||
| Appearance | Green crystals | ||
| Melting point | 171 to 173 °C (340 to 343 °F; 444 to 446 K) | ||
| insoluble | |||
| Structure | |||
| D5h, D5d | |||
| 0 D | |||
| Vapor pressure | {{{value}}} | ||
| Related compounds | |||
|
Related compounds
|
CoCp2, FeCp2 | ||
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|||
 verify (what is  ?) |
|||
| Infobox references | |||
Nickelocene is the organonickel compound with the formula Ni(η5-C5H5)2. Also known as bis(cyclopentadienyl)nickel or NiCp2, this bright green paramagnetic solid is of enduring academic interest,[1] although it yet has no practical applications.
Structure and bonding
Ni(C5H5)2 belongs to a group of organometallic compounds called metallocenes. Metallocenes usually adopt structures in which a metal ion is sandwiched between two parallel cyclopentadienyl (Cp) rings. This structure is relevant to the solubility in organic solvents and volatility. In the solid-state, the molecule has D5h symmetry, wherein the two rings are eclipsed.
The Ni center has a formal 2+ charge, and the Cp rings are usually assigned as cyclopentadienyl anions (Cp−), related to cyclopentadiene by deprotonation. The structure is similar to ferrocene. In terms of its electronic structure, three pairs of d electrons on nickel are allocated to the three d orbitals involved in Ni - Cp bonding: dxy, dx2–y2, dz2. One of the two remaining d-electrons resides in each of the dyz and dxz orbitals, giving rise to the molecule's paramagnetism, as manifested in the unusually high field chemical shift observed in its 1H NMR spectrum. With 20 valence electrons, nickelocene has the highest electron count of the transition metal metallocenes. Cobaltocene, Co(C5H5)2, with only 19 valence is, however, a stronger reducing agent, illustrating the fact that electron energy, not electron count determines redox potential.
Preparation
Nickelocene was first prepared by E. O. Fischer in 1953, shortly after the discovery of ferrocene, the first metallocene compound.[2] It has been prepared in a one-pot reaction, by deprotonating cyclopentadiene with ethylmagnesium bromide, and adding anhydrous nickel(II) acetylacetonate.[3] A modern synthesis entails treatment of anhydrous sources of NiCl2 with sodium cyclopentadienyl:[4]
-
- [Ni(NH3)6]Cl2 + 2 NaC5H5 → Ni(C5H5)2 + 2 NaCl + 6 NH3
Properties
Like many organometallic compounds, Ni(C5H5)2 does not tolerate extended exposure to air before noticeable decomposition.[5] Samples are typically handled with air-free techniques.
Most chemical reactions of nickelocene are characterized by its tendency to yield 18-electron products with loss or modification of one Cp ring.
- Ni(C5H5)2 + 4 PF3 → Ni(PF3)4 + organic products
The reaction with secondary phosphines follows a similar pattern:
-
- 2 Ni(C5H5)2 + 2 PPh2H → [Ni2(PPh2)2(C5H5)2] + 2 C5H6
Nickelocene can be oxidized to the corresponding cation, which contains Ni(III).
Gaseous Ni(C5H5)2 decomposes to a Ni mirror upon contact with a hot surface, releasing the hydrocarbon ligands as gaseous coproducts. This process has been considered as a means of preparing Ni films.
References
- ↑ Elschenbroich, C. ”Organometallics” (2006) Wiley-VCH: Weinheim. ISBN 978-3-527-29390-2
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Girolami, G. S.; Rauchfuss, T. B. and Angelici, R. J., Synthesis and Technique in Inorganic Chemistry, University Science Books: Mill Valley, CA, 1999.ISBN 0935702482
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
