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
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

Protactinium(V) bromide

From Wikipedia, the free encyclopedia

Protactinium(V) bromide
Names
IUPAC name
Protactinium(V) bromide
Identifiers
3D model (JSmol)
  • [Pa](Br)(Br)(Br)(Br)Br
Properties
PaBr5
Molar mass 630.556 g mol−1
Appearance red solid
Density 4.98 g/cm3
Structure
monoclinic[1][2]
P21/c , No. 14
Related compounds
Other anions
Protactinium(V) fluoride
Protactinium(V) chloride
Protactinium(V) iodide
Other cations
Praseodymium(III) bromide
Thorium(IV) bromide
Uranium(IV) bromide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Protactinium(V) bromide is an inorganic compound. It is a halide of protactinium, consisting of protactinium and bromine. It is radioactive and has a chemical formula of PaBr5, which is a red crystal of the monoclinic crystal system.[2][1]

YouTube Encyclopedic

  • 1/3
    Views:
    422
    252 370
    18 632
  • Protactinium
  • full detailed chemistry reduced syllabus | class 12th science | new indian era
  • 11th August Paper Analysis Shift 1 Questions from Mhtcet Shift 2 2022 😵‍💫 By :- #abhisheksir

Transcription

Preparation

Protactinium(V) bromide can be obtained by reacting protactinium(V) chloride with boron tribromide at 500 to 550 °C.[3]

3PaCl5 + 5BBr3 → 3PaBr5 + 5BCl3

It can also be obtained by reacting protactinium(V) oxide with aluminum bromide at 400 °C.[4]

Physical properties

Protactinium(V) bromide is an orange-red, crystalline, extremely moisture-sensitive solid that reacts violently with water and ammonia, but is persistent in absolutely dry air. It is insoluble in isopentane, dichloromethane and benzene, and in anhydrous acetonitrile is dissolves to form PaBr5•4CH3CN. It comes in several modifications. Below 400 °C as an α-modification and above 400 °C as a β-modification. The α-form has a monoclinic crystal structure of the space group P21/c (No. 14) and lattice parameters a = 1296 pm, b = 1282 pm, c = 992 pm, β = 108° and the β-form also has monoclinic crystal structure with space group P21/n (No. 14, position 2) and lattice parameters a = 838.5 pm, b = 1120.5 pm, c = 895.0 pm, β = 91.1°.[3] The β form exists as a dimer. At 400 °C in a vacuum, protactinium(V) bromide sublimes.[5] A γ-form, which has a β-uranium(V) chloride-type crystal structure, has also been detected.[6]

References

  1. ^ a b Brown, D.; Petcher, T. J.; Smith, A. J. (1968). "Crystal Structures of some Protactinium Bromides". Nature. 217 (5130): 737. Bibcode:1968Natur.217..737B. doi:10.1038/217737a0. S2CID 4264482.
  2. ^ a b Brown, D.; Petcher, T. J.; Smith, A. J. (1969). "The crystal structure of β-protactinium pentabromide". Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry. 25 (2): 178. doi:10.1107/S0567740869007357.
  3. ^ a b Georg Brauer (Hrsg.), unter Mitarbeit von Marianne Baudler u. a.: Handbuch der Präparativen Anorganischen Chemie. 3., umgearbeitete Auflage. Band I, Ferdinand Enke, Stuttgart 1975, ISBN 3-432-02328-6, S. 1177.
  4. ^ Advances in Inorganic Chemistry and Radiochemistry (in German), Academic Press, 1970, p. 31
  5. ^ D. Brown, T. J. Petcher, A. J. Smith: The crystal structure of β-protactinium pentabromide. In: Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry. 25, S. 178–182, doi:10.1107/S0567740869007357.
  6. ^ D. Brown: The polymorphism of protactinium pentabromide. In: Inorganic and Nuclear Chemistry Letters. 15, 1979, S. 219–223, doi:10.1016/0020-1650(79)80132-4.
This page was last edited on 5 January 2024, at 12:41
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.