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Praseodymium(III) fluoride

From Wikipedia, the free encyclopedia
Praseodymium(III) fluoride
Names
Other names
Praseodymium trifluoride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.033.853Edit this at Wikidata
EC Number
  • 237-254-9
UNII
  • InChI=1S/3FH.Pr/h3*1H;/q;;;+3/p-3
    Key: BOTHRHRVFIZTGG-UHFFFAOYSA-K
  • [F-].[F-].[F-].[Pr+3]
Properties
PrF3
Appearancegreen crystalline solid
Density6.267 g·cm−3[1]
Melting point1370 °C[2]
Hazards
GHS labelling:
GHS06: ToxicGHS07: Exclamation mark
Danger
H301,H311,H315,H319,H331,H335,H413
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Praseodymium(III) fluoride is aninorganic compound with theformula PrF3, being the most stablefluoride ofpraseodymium.

Preparation

[edit]

The reaction betweenpraseodymium(III) nitrate andsodium fluoride will obtain praseodymium(III) fluoride as a green crystalline solid:[3]

Pr(NO3)3 + 3 NaF → 3 NaNO3 + PrF3

There are also literature reports on the reaction betweenchlorine trifluoride and various oxides of praseodymium (Pr2O3, Pr6O11 and PrO2), where praseodymium(III) fluoride is the only product. The reaction betweenbromine trifluoride and praseodymium oxide left in the air for a period of time also produces praseodymium(III) fluoride, but the reaction is incomplete; the reaction betweenpraseodymium(III) oxalate hydrate and bromine trifluoride can obtain praseodymium(III) fluoride, and carbon is also produced from this reaction.[4] Praseodymium(III) fluoride can also be obtained by reacting praseodymium oxide andsulfur hexafluoride at 584 °C.[5]

Properties

[edit]

Physical

[edit]

Praseodymium(III) fluoride forms pale green crystals of trigonal system[6] (or hexagonal system[7]), space group P 3c1,[6] (or P 6/mcm[7]), cell parametersa = 0.7078 nm,c = 0.7239 nm, Z = 6, structure likecerium(III) fluoride (CeF3).

Chemical

[edit]

Praseodymium(III) fluoride is a green, odourless, hygroscopic solid that is insoluble in water.[8]

Uses

[edit]

Praseodymium(III) fluoride is used as a doping material for laser crystals.[9]

See also

[edit]

References

[edit]
  1. ^E. A. Krivandina, Z. I. Zhmurova, B. P. Sobolev, T. M. Glushkova, D. F. Kiselev, M. M. Firsova, A. P. Shtyrkova (October 2006). "Growth of R 1 − y Sr y F3 − y crystals with rare earth elements of the cerium subgroup (R = La, Ce, Pr, or Nd; 0 ≤ y ≤ 0.16) and the dependence of their density and optical characteristics on composition".Crystallography Reports.51 (5):895–901.doi:10.1134/S106377450605021X.ISSN 1063-7745.S2CID 189794019.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. ^H. von Wartenberg. The melting points of neodymium and praseodymium fluorides.Naturwissenschaften, 1941. 29: 771.ISSN 0028-1042.
  3. ^Lin Ma, Wei-Xiang Chen, Yi-Fan Zheng, Jie Zhao, Zhude Xu (May 2007)."Microwave-assisted hydrothermal synthesis and characterizations of PrF3 hollow nanoparticles".Materials Letters.61 (13):2765–2768.doi:10.1016/j.matlet.2006.04.124. Retrieved2019-03-26.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^Popov, Alexander I.; Glockler, George (Mar 1952)."Observations on the Fluorination of Praseodymium and Neodymium Compounds".Journal of the American Chemical Society.74 (5):1357–1358.Bibcode:1952JAChS..74R1357P.doi:10.1021/ja01125a521.ISSN 0002-7863.
  5. ^OPALOVSKII, A. A.; LOBKOV, E. U.; ERENBURG, B. G.; ZAKHAR'EV, YU. V.; SHINGAREV, V. G. (1973-01-16)."ChemInform Abstract: RK. VON SF6 MIT SELTENERDMETALLOXIDEN".Chemischer Informationsdienst.4 (3).doi:10.1002/chin.197303045.ISSN 0009-2975.
  6. ^abКнунянц И.Л. и др., ed. (1995).Химическая энциклопедия. Vol. 4. М.m: Советская энциклопедия.ISBN 5-85270-092-4.
  7. ^abНикольский Б.П. и др., ed. (1966).Справочник химика. Vol. 1 (2-е изд., испр ed.). М.-Л.: Химия.
  8. ^Praseodymium(III) fluoride at AlfaAesar, accessed on 2023-12-22 (PDF) (JavaScript required).[dead link]
  9. ^Shalibeik, Hotan (2007).Rare-earth-doped fiber lasers and amplifiers (1. Aufl ed.). Göttingen: Cuvillier.ISBN 978-3-86727-467-8.
Pr(II)
Pr(III)
Organopraseodymium(III) compounds
Pr(III,IV)
Pr(IV)
Pr(V)
Salts and covalent derivatives of thefluoride ion
HF?HeF2
LiFBeF2BF
BF3
B2F4
+BO3
CF4
CxFy
+CO3
NF3
FN3
N2F2
NF
N2F4
NF2
?NF5
+N
+NO3
OF2
O2F2
OF
O3F2
O4F2
?OF4
F2Ne
NaFMgF2AlF
AlF3
SiF4P2F4
PF3
PF5
+PO4
S2F2
SF2
S2F4
SF3
SF4
S2F10
SF6
+SO4
ClF
ClF3
ClF5
?ArF2
?ArF4
KFCaF
CaF2
ScF3TiF2
TiF3
TiF4
VF2
VF3
VF4
VF5
CrF2
CrF3
CrF4
CrF5
?CrF6
MnF2
MnF3
MnF4
?MnF5
FeF2
FeF3
FeF4
CoF2
CoF3
CoF4
NiF2
NiF3
NiF4
CuF
CuF2
?CuF3
ZnF2GaF2
GaF3
GeF2
GeF4
AsF3
AsF5
Se2F2
SeF4
SeF6
+SeO3
BrF
BrF3
BrF5
KrF2
?KrF4
?KrF6
RbFSrF
SrF2
YF3ZrF2
ZrF3
ZrF4
NbF4
NbF5
MoF4
MoF5
MoF6
TcF4
TcF
5

TcF6
RuF3
RuF
4

RuF5
RuF6
RhF3
RhF4
RhF5
RhF6
PdF2
Pd[PdF6]
PdF4
?PdF6
Ag2F
AgF
AgF2
AgF3
CdF2InF
InF3
SnF2
SnF4
SbF3
SbF5
TeF4
?Te2F10
TeF6
+TeO3
IF
IF3
IF5
IF7
+IO3
XeF2
XeF4
XeF6
?XeF8
CsFBaF2 LuF3HfF4TaF5WF4
WF5
WF6
ReF4
ReF5
ReF6
ReF7
OsF4
OsF5
OsF6
?OsF
7

?OsF
8
IrF2
IrF3
IrF4
IrF5
IrF6
PtF2
Pt[PtF6]
PtF4
PtF5
PtF6
AuF
AuF3
Au2F10
?AuF6
AuF5•F2
Hg2F2
HgF2
?HgF4
TlF
TlF3
PbF2
PbF4
BiF3
BiF5
PoF2
PoF4
PoF6
AtF
?AtF3
?AtF5
RnF2
?RnF
4

?RnF
6
FrFRaF2 LrF3RfDbSgBhHsMtDsRgCnNhFlMcLvTsOg
LaF3CeF3
CeF4
PrF3
PrF4
NdF2
NdF3
NdF4
PmF3SmF
SmF2
SmF3
EuF2
EuF3
GdF3TbF3
TbF4
DyF2
DyF3
DyF4
HoF3ErF3TmF2
TmF3
YbF2
YbF3
AcF3ThF2
ThF3
ThF4
PaF4
PaF5
UF3
UF4
UF5
UF6
NpF3
NpF4
NpF5
NpF6
PuF3
PuF4
PuF5
PuF6
AmF2
AmF3
AmF4
?AmF6
CmF3
CmF4
 ?CmF6
BkF3
BkF
4
CfF3
CfF4
EsF3
EsF4
?EsF6
FmMdF3No
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