Rhenium pentachloride

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Rhenium pentachloride
ReCl5structure.png
Names
IUPAC name
Rhenium pentachloride
Other names
Rhenium(V) chloride, Rhenium chloride, pentachlororhenium
Identifiers
13596-35-5 YesY
ChemSpider 75428
EC Number 237-042-6
Jmol 3D model Interactive image
PubChem 83602
Properties
ReCl5
Molar mass 363.471 g/mol
Appearance red-brown
Density 4.9 g/cm3, solid
Melting point 220 °C (428 °F; 493 K)
Boiling point N/A
Will react to decompose and release HCl (g)
Structure
Monoclinic, mP48; a = 0.924 nm, b = 1.154 nm, c = 1.203 nm, α = 90°, β = 109.1°, γ = 90° [1]
P21/c, No. 14
Octahedral
Hazards
Main hazards releases HCl upon hydrolysis
Safety data sheet MSDS
R/S statement R: 36, 37, 38
NFPA 704
Flammability (red): no hazard code Health code 1: Exposure would cause irritation but only minor residual injury. E.g., turpentine Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazard W: Reacts with water in an unusual or dangerous manner. E.g., cesium, sodiumNFPA 704 four-colored diamond
Related compounds
Other anions
Rhenium hexafluoride
Related compounds
Trirhenium nonachloride, rhenium tetrachloride, rhenium hexachloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Rhenium pentachloride is an inorganic compound of chlorine and rhenium. The compound has the formula Re2Cl10 but it is usually referred to as the pentachloride. It is a red-brown solid. It is the highest chloride of rhenium.

Structure and preparation[edit]

Rhenium pentachloride has a bioctahedral structure and can be formulated as Cl4Re(μ-Cl)2ReCl4. The Re-Re distance is 3.74 Å.[1] The motif is similar to that seen for tantalum pentachloride.

This compound was first prepared in 1933,[2] a few years after the discovery of rhenium. The preparation involves chlorination of rhenium at temperatures up to 900 °C.[3] The material can be purified by sublimation.

ReCl5 is one of the most oxidized binary chlorides of Re. With a d2 configuration, it could conceivably be further chlorinated, and indeed ReCl6 has been prepared, albeit indirectly from rhenium hexafluoride.[4] Rhenium heptafluoride is known but not the heptachloride.[5]

Uses and reactions[edit]

It degrades in air to a brown liquid.[6]

Although rhenium pentachloride has no commercial applications, it is of historic significance as one of the early catalysts for olefin metathesis.[7] Reduction gives Trirhenium nonachloride.

Oxygenation affords the Re(VII) oxychloride:[8]

ReCl5 + 3 Cl2O → ReO3Cl + 5 Cl2

References[edit]

  1. ^ a b Mucker, K. F.; Smith, G. S.; Johnson, Q. (1968). "The crystal structure of ReCl5". Acta Crystallographica Section B. 24 (6): 874. doi:10.1107/S0567740868003316. 
  2. ^ Geilmann, Wilhelm; Wrigge, Friedrich W.; Biltz, Wilhelm. (1933). "Rheniumpentachlorid". Z. anorg. allgem. Chem. (in German). 214 (3): 244. doi:10.1002/zaac.19332140304. 
  3. ^ Roger Lincoln, Geoffrey Wilkinson "Rhenium Pentachloride and Volatile Metal Chlorides by Direct Chlorination Using a Vertical-Tube Reactor" Inorganic Syntheses, 1980, Volume 20, Pages 41–43. doi:10.1002/9780470132517.ch11.
  4. ^ Tamadon, Farhad; Seppelt, Konrad (2013). "The Elusive Halides VCl5, MoCl6, and ReCl6". Angew. Chem. Int. Ed. 52: 767–769. doi:10.1002/anie.201207552. 
  5. ^ Stuart A. Macgregor and Klaus H. Moock "Stabilization of High Oxidation States in Transition Metals. 2.1 WCl6 Oxidizes [WF6]-, but Would PtCl6 Oxidize [PtF6]-? An Electrochemical and Computational Study of 5d Transition Metal Halides: [MF6]z versus [MCl6]z (M = Ta to Pt; z = 0, 1−, 2−)" pp 3284–3292. doi:10.1021/ic9605736
  6. ^ Edwards, D. A.; Ward, R. T. (1970). "Some reactions of rhenium(V) chloride". Journal of the Chemical Society a Inorganic Physical Theoretical: 1617. doi:10.1039/J19700001617. 
  7. ^ Ring-opening polymerization of endo and exo-dicyclopentadiene and their 7,8-dihydro derivatives, Hamilton, J.G.; Ivin, K.J.; Rooney, J.J. Journal of Molecular Catalysis 1986 , 36, 115.
  8. ^ Housecroft, C. E.; Sharpe, A. G. (2004). Inorganic Chemistry (2nd ed.). Prentice Hall. ISBN 978-0130399137. 

External links[edit]