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Protactinium(IV) chloride

From Wikipedia, the free encyclopedia
Protactinium(IV) chloride
Names
IUPAC name
Protactinium(IV) chloride
Identifiers
3D model (JSmol)
  • InChI=1S/4ClH.Pa/h4*1H;/q;;;;+4/p-4
    Key: YVRMMEYNJWFJEX-UHFFFAOYSA-J
  • [Pa](Cl)(Cl)(Cl)Cl
Properties
PaCl4
Molar mass372.848 g mol−1
Appearancechartreuse
Density4.72 g/cm3
Structure
tetragonal[1],tI20
I41/amd , No. 141
Related compounds
Otheranions
Protactinium(IV) fluoride
Protactinium(IV) bromide
Protactinium(IV) iodide
Othercations
Uranium(IV) chloride
Thorium(IV) chloride
Praseodymium(III) chloride
Related compounds
Protactinium(V) chloride
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Protactinium(IV) chloride is aninorganic compound. It is an actinide halide, a salt composed ofprotactinium andchlorine. It isradioactive, and has the chemical formula of PaCl4. It is a chartreuse-coloured (yellowish-green) crystal[1] of thetetragonal crystal system.

Preparation

[edit]

Protactinium(IV) chloride can be prepared by thereduction ofprotactinium(V) chloride:[2]

2 PaCl5 + H2 → 2 PaCl4 + 2 HCl
3 PaCl5 + Al → 3 PaCl4 + AlCl3

It can also be obtained by thechlorination ofprotactinium(IV) oxide:[2]

PaO2 + 2 CCl4 → PaCl4 + 2 COCl2

It can also be formed during the thermal decomposition of protactinium oxychloride at 500 °C in a vacuum:[3]

2 PaOCl2 → PaCl4 + PaO2

Properties

[edit]

Protactinium(IV) chloride is a chartreuse,hygroscopic, crystalline solid that can be sublimed at 400 °C in a vacuum. It is soluble in strongmineral acids, forming green solutions. The complex PaCl4·4CH3CN is formed withacetonitrile. It has atetragonalcrystal structure with thespace groupI41/amd (space group no. 141) and the lattice parametersa = 837.7 pm,c = 747.9 pm[2] of theuranium(IV) chloride type.[4]

References

[edit]
  1. ^abBrown D., Hall T.L., Moseley P.T (1973). "Structural parameters and unit cell dimensions for the tetragonal actinide tetrachlorides(Th, Pa, U, and Np) and tetrabromides (Th and Pa)".J. Chem. Soc., Dalton Trans. (6):686–691.doi:10.1039/DT9730000686.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. ^abcGeorg 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, pp. 1176.
  3. ^Harry Julius Emeleus, A. G. Sharpe (1970),ADVANCES IN INORGANIC CHEMISTRY AND RADIOCHEMISTRY (in German), Academic Press, p. 15,ISBN 978-0-08057861-3
  4. ^Lester R. Morss, Norman M. Edelstein, J. Fuger (Hrsg.): . Bände 1-6. Springer, Dordrecht 2010,ISBN 978-94-007-0211-0, S. 201 (English,[1] in Google Books).
Pa(II)
Pa(III)
Pa(IV)
Pa(V)
Salts and covalent derivatives of thechloride ion
HClHe
LiClBeCl2B4Cl4
B12Cl12
BCl3
B2Cl4
+BO3
C2Cl2
C2Cl4
C2Cl6
CCl4
+C
+CO3
NCl3
ClN3
+N
+NO3
ClxOy
Cl2O
Cl2O2
ClO
ClO2
Cl2O4
Cl2O6
Cl2O7
ClO4
+O
ClF
ClF3
ClF5
Ne
NaClMgCl2AlCl
AlCl3
Si5Cl12
Si2Cl6
SiCl4
P2Cl4
PCl3
PCl5
+P
S2Cl2
SCl2
SCl4
+SO4
Cl2Ar
KClCaCl
CaCl2
ScCl3TiCl2
TiCl3
TiCl4
VCl2
VCl3
VCl4
VCl5
CrCl2
CrCl3
CrCl4
MnCl2
MnCl3
FeCl2
FeCl3
CoCl2
CoCl3
NiCl2CuCl
CuCl2
ZnCl2GaCl
GaCl3
GeCl2
GeCl4
AsCl3
AsCl5
+As
Se2Cl2
SeCl2
SeCl4
BrClKr
RbClSrCl2YCl3ZrCl2
ZrCl3
ZrCl4
NbCl3
NbCl4
NbCl5
MoCl2
MoCl3
MoCl4
MoCl5
MoCl6
TcCl3
TcCl4
RuCl2
RuCl3
RuCl4
RhCl3PdCl2AgClCdCl2InCl
InCl2
InCl3
SnCl2
SnCl4
SbCl3
SbCl5
Te3Cl2
TeCl2
TeCl4
ICl
ICl3
XeCl
XeCl2
XeCl4
CsClBaCl2*LuCl3HfCl4TaCl3
TaCl4
TaCl5
WCl2
WCl3
WCl4
WCl5
WCl6
ReCl3
ReCl4
ReCl5
ReCl6
OsCl2
OsCl3
OsCl4
OsCl5
IrCl2
IrCl3
IrCl4
PtCl2
PtCl4
AuCl
(Au[AuCl4])2
AuCl3
Hg2Cl2
HgCl2
TlCl
TlCl3
PbCl2
PbCl4
BiCl3PoCl2
PoCl4
AtClRn
FrClRaCl2**LrCl3RfCl4DbCl5SgO2Cl2BhO3ClHsMtDsRgCnNhFlMcLvTsOg
 
*LaCl3CeCl3PrCl3NdCl2
NdCl3
PmCl3SmCl2
SmCl3
EuCl2
EuCl3
GdCl3TbCl3DyCl2
DyCl3
HoCl3ErCl3TmCl2
TmCl3
YbCl2
YbCl3
**AcCl3ThCl3
ThCl4
PaCl4
PaCl5
UCl3
UCl4
UCl5
UCl6
NpCl3
NpCl4
PuCl3AmCl2
AmCl3
CmCl3BkCl3CfCl3
CfCl2
EsCl2
EsCl3
FmCl2MdCl2NoCl2
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