To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
Languages
Recent
Show all languages
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

Oxotrichlorobis(triphenylphosphine)rhenium(V)

From Wikipedia, the free encyclopedia

Oxotrichlorobis(triphenyl­phosphine)rhenium(V)
Names
IUPAC name
Trichloridooxidobis(triphenylphosphane)rhenium(V)
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/2C18H15P.3ClH.O.Re/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;;;/h2*1-15H;3*1H;;/q;;;;;-2;/p-3
    Key: ZHLPLZVSIOQWFP-UHFFFAOYSA-K
  • C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.[O-2].[Cl-].[Cl-].[Cl-].[Re]
Properties
ReOCl3(PPh3)2
Molar mass 833.15 g/mol
Appearance yellow microcrystals
Melting point 205 °C (401 °F; 478 K)
not soluble in water
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Oxotrichlorobis(triphenylphosphine)rhenium(V) is the chemical compound with the formula ReOCl3(PPh3)2. This yellow, air-stable solid is a precursor to a variety of other rhenium complexes.[1] In this diamagnetic compound, Re has an octahedral coordination environment with one oxo, three chloro and two mutually trans triphenylphosphine ligands. The oxidation state of rhenium is +5 and its configuration is d2.

Synthesis

ReOCl3(PPh3)2 is commercially available, but it is readily synthesized by reaction of perrhenic acid with triphenylphosphine in a mixture of hydrochloric acid and acetic acid. In this reaction, Re(VII) is reduced to Re(V), and triphenylphosphine is oxidized to its oxide.

HReO4 + 3 HCl + 3 PPh3 → ReOCl3(PPh3)2 + Ph3PO + 2 H2O

The required perrhenic acid solution can be prepared in situ from rhenium(VII) oxide.

Uses

ReOCl3(PPh3)2 is a precursor to a variety of other oxo-, nitridio, and hydrido complexes. It converts to ReH7(PPh3)2 by a treatment with LiAlH4.[2]

ReOCl3(PPh3)2 catalyzes the selective oxidation of secondary alcohols by DMSO, producing the corresponding ketals.[3]

References

  1. ^ Johnson, N. P.; Lock, C. J. L.; Wilkinson, G. (1967). "Complexes of Rhenium(V)". Inorganic Syntheses. pp. 145–148. doi:10.1002/9780470132401.ch39. ISBN 978-0-470-13240-1. {{cite book}}: |journal= ignored (help)
  2. ^ K. Abdur-Rashid; A. J. Lough & R. H. Morris (2001). "Intra- and inter-ion-pair protonic-hydridic bonding in polyhydridobis(phosphine)rhenates". Canadian Journal of Chemistry. 79 (5–6): 964. doi:10.1139/cjc-79-5-6-964.
  3. ^ Pombeiro, A. J. L.; Fatima, M.; Crabtree, R. H. "Technetium and Rhenium: Inorganic & Coordination Chemistry" Encyclopedia of Inorganic Chemistry. John Wiley & Sons: New York, 2006. doi:10.1002/0470862106.ia237
This page was last edited on 23 September 2023, at 00:56
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.