Ytterbium(III) chloride

Ytterbium(III) chloride
Ytterbium(III) chloride
Names
IUPAC name
Ytterbium(III) chloride
Identifiers
CAS Number
  • 10361-91-8 ☒N
  • hydrate: 19423-87-1 ☒N
  • 19423-82-6 (non-specific) checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 55430 checkY
ECHA InfoCard 100.030.715 Edit this at Wikidata
EC Number
  • 233-800-5
PubChem CID
  • 9860484
UNII
  • IO29D13DLW checkY
CompTox Dashboard (EPA)
  • DTXSID0047117 Edit this at Wikidata
InChI
  • InChI=1S/3ClH.Yb/h3*1H;/q;;;+3/p-3 checkY
    Key: CKLHRQNQYIJFFX-UHFFFAOYSA-K checkY
  • InChI=1/3ClH.Yb/h3*1H;/q;;;+3/p-3
    Key: CKLHRQNQYIJFFX-DFZHHIFOAT
  • Cl[Yb](Cl)Cl
Properties
Chemical formula
YbCl3
Molar mass 279.40 g/mol
Appearance White powder
Density 4.06 g/cm3 (solid)
Melting point 854 °C (1,569 °F; 1,127 K)[1]
Boiling point 1,453 °C (2,647 °F; 1,726 K)[1]
Solubility in water
17 g/100 mL (25 °C)
Structure
Crystal structure
Monoclinic, mS16
Space group
C12/m1, No. 12
Related compounds
Other anions
Ytterbium(III) oxide
Other cations
Terbium(III) chloride, Lutetium(III) chloride
Supplementary data page
Ytterbium(III) chloride (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references
Chemical compound

Ytterbium(III) chloride (YbCl3) is an inorganic chemical compound. It reacts with NiCl2 to form a very effective catalyst for the reductive dehalogenation of aryl halides.[2] It is poisonous if injected, and mildly toxic by ingestion. It is an experimental teratogen, known to irritate the skin and eyes.

History

The synthesis of YbCl3 was first reported by Jan Hoogschagen in 1946.[3] It is now a commercially available source of Yb3+ ions and therefore of significant chemical interest.

Chemical properties

The valence electron configuration of Yb+3 (from YbCl3) is 4f135s25p6, which has crucial implications for the chemical behaviour of Yb+3. Also, the size of Yb+3 governs its catalytic behaviour and biological applications. For example, while both Ce+3 and Yb+3 have a single unpaired f electron, Ce+3 is much larger than Yb+3 because lanthanides become much smaller with increasing effective nuclear charge as a consequence of the f electrons not being as well shielded as d electrons.[4] This behavior is known as the lanthanide contraction. The small size of Yb+3 produces fast catalytic behavior and an atomic radius (0.99 Å) comparable to many biologically important ions.[4]

The gas-phase thermodynamic properties of this chemical are difficult to determine because the chemical can disproportionate to form [YbCl6]−3 or dimerize.[5] The Yb2Cl6 species was detected by electron impact (EI) mass spectrometry as (Yb2Cl5+).[5] Additional complications in obtaining experimental data arise from the myriad of low-lying f-d and f-f electronic transitions.[6] Despite these issues, the thermodynamic properties of YbCl3 have been obtained and the C3V symmetry group has been assigned based upon the four active infrared vibrations.[6]

Preparation

Anhydrous ytterbium(III) chloride can be produced by the ammonium chloride route.[7][8][9] In the first step, ytterbium oxide is heated with ammonium chloride to produce the ammonium salt of the pentachloride:

Yb2O3 + 10 NH4Cl → 2 (NH4)2YbCl5 + 6 H2O + 6 NH3

In the second step, the ammonium chloride salt is converted to the trichlorides by heating in a vacuum at 350-400 °C:

(NH4)2YbCl5 → YbCl3 + 2 HCl + 2 NH3

Reactions

YbCl3 is a paramagnetic Lewis acid, like many of the lanthanide chlorides. It gives rise to pseudocontact shifted NMR spectra, akin to NMR shift reagents

Applications in biology

Membrane biology has been greatly influenced by YbCl3, where39K+ and23Na+ ion movement is critical in establishing electrochemical gradients.[10] Nerve signaling is a fundamental aspect of life that may be probed with YbCl3 using NMR techniques. YbCl3 may also be used as a calcium ion probe, in a fashion similar to a sodium ion probe.[11]

YbCl3 is also used to track digestion in animals. Certain additives to swine feed, such as probiotics, may be added to either solid feed or drinking liquids. YbCl3 travels with the solid food and therefore helps determine which food phase is ideal to incorporate the food additive.[12] The YbCl3 concentration is quantified by inductively coupled plasma mass spectrometry to within 0.0009 μg/mL.[4] YbCl3 concentration versus time yields the flow rate of solid particulates in the animal's digestion. The animal is not harmed by the YbCl3 since YbCl3 is simply excreted in fecal matter and no change in body weight, organ weight, or hematocrit levels has been observed in mice.[11]

The catalytic nature of YbCl3 also has an application in DNA microarrays, or so called DNA “chips”.[13] YbCl3 led to a 50–80 fold increase in fluorescein incorporation into target DNA, which could revolutionize infectious disease detection (such as a rapid test for tuberculosis).[13]

References

  1. ^ a b Walter Benenson; John W. Harris; Horst Stöcker (2002). Handbook of Physics. Springer. p. 781. ISBN 0-387-95269-1.
  2. ^ Zhang, Yuankui; Liao, Shijian; Xu, Yun; Yu, Daorong; Shen, Qi (1997). "Reductive Dehalogenation of Aryl Halides by the Nanometric Sodium Hydride Using Lanthanide Chloride as Catalyst". Synth. Commun. 27 (24): 4327–4334. doi:10.1080/00397919708005057.
  3. ^ Hoogschagen, J. (1946). "The light absorption in the near infra red region of praseodymium, samarium and ytterbium solutions". Physica. 11 (6): 513–517. Bibcode:1946Phy....11..513H. doi:10.1016/S0031-8914(46)80020-X.
  4. ^ a b c Evans, C.H. (1990). Biochemistry of the Lanthanides. New York: Plenum. ISBN 978-1-4684-8750-3.
  5. ^ a b Chervonnyi, A.D.; Chervonnaya, N.A. (2004). "Thermodynamic Properties of Ytterbium Chlorides". Russ. J. Inorg. Chem. (Engl. Transl.). 49 (12): 1889–1897.
  6. ^ a b Zasorin, E. Z. (1988). "Structure of the rare-earth element trihalide molecules from electron diffraction and spectral data". Russ. J. Phys. Chem. (Engl. Transl.). 62 (4): 441–447. (Russian language version: Zh. Fiz. Khim. 62(4), pp. 883-895)
  7. ^ Brauer, G., ed. (1963). Handbook of Preparative Inorganic Chemistry (2nd ed.). New York: Academic Press.
  8. ^ Meyer, G. (1989). "The Ammonium Chloride Route to Anhydrous Rare Earth Chlorides—The Example of Ycl 3". The Ammonium Chloride Route to Anhydrous Rare Earth Chlorides-The Example of YCl3. Inorganic Syntheses. Vol. 25. pp. 146–150. doi:10.1002/9780470132562.ch35. ISBN 978-0-470-13256-2.
  9. ^ Edelmann, F. T.; Poremba, P. (1997). Herrmann, W. A. (ed.). Synthetic Methods of Organometallic and Inorganic Chemistry. Vol. VI. Stuttgart: Georg Thieme Verlag. ISBN 978-3-13-103021-4.
  10. ^ Hayer, M.K.; Riddell, F.G. (1984). "Shift reagents for 39K NMR". Inorganica Chimica Acta. 92 (4): L37–L39. doi:10.1016/S0020-1693(00)80044-4.
  11. ^ a b Shinohara, A.; Chiba, M.; Inaba, Y. (2006). "Comparative study of the behavior of terbium, samarium, and ytterbium intravenously administered in mice". Journal of Alloys and Compounds. 408–412: 405–408. doi:10.1016/j.jallcom.2004.12.152.
  12. ^ Ohashi, Y.; Umesaki, Y.; Ushida, K. (2004). "Transition of the probiotic bacteria, Lactobacillus casei strain Shirota, in the gastrointestinal tract of a pig". International Journal of Food Microbiology. 96 (1): 61–66. doi:10.1016/j.ijfoodmicro.2004.04.001. PMID 15358506.
  13. ^ a b Browne, K.A. (2002). "Metal ion-catalyzed nucleic acid alkylation and fragmentation". Journal of the American Chemical Society. 124 (27): 7950–7962. doi:10.1021/ja017746x. PMID 12095339.


  • v
  • t
  • e
Yb(II)
  • YbF2
  • YbCl2
  • YbBr2
  • YbI2
  • YbH2
  • YbS
Yb(III)
  • LaYbO3
  • Yb(acac)3
  • Yb(CH3COO)3
  • YbBr3
  • Yb(BrO3)3
  • YbCl3
  • Yb(CN)3
  • YbF3
  • Yb(OH)3
  • Yb(IO3)3
  • YbI3
  • Yb(NO3)3
  • YbN
  • Yb2(C2O4)3
  • Yb2O3
  • YbP
  • Yb2(SO4)3
  • Yb
    2
    S
    3
Other
  • v
  • t
  • e
Salts and covalent derivatives of the chloride ion
HCl He
LiCl BeCl2 B4Cl4
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
NaCl MgCl2 AlCl
AlCl3
Si5Cl12
Si2Cl6
SiCl4
P2Cl4
PCl3
PCl5
+P
S2Cl2
SCl2
SCl4
+SO4
Cl2 Ar
KCl CaCl
CaCl2
ScCl3 TiCl2
TiCl3
TiCl4
VCl2
VCl3
VCl4
VCl5
CrCl2
CrCl3
CrCl4
MnCl2
MnCl3
FeCl2
FeCl3
CoCl2
CoCl3
NiCl2 CuCl
CuCl2
ZnCl2 GaCl
GaCl3
GeCl2
GeCl4
AsCl3
AsCl5
+As
Se2Cl2
SeCl2
SeCl4
BrCl Kr
RbCl SrCl2 YCl3 ZrCl3
ZrCl4
NbCl3
NbCl4
NbCl5
MoCl2
MoCl3
MoCl4
MoCl5
MoCl6
TcCl3
TcCl4
RuCl2
RuCl3
RuCl4
RhCl3 PdCl2 AgCl CdCl2 InCl
InCl2
InCl3
SnCl2
SnCl4
SbCl3
SbCl5
Te3Cl2
TeCl2
TeCl4
ICl
ICl3
XeCl
XeCl2
XeCl4
CsCl BaCl2 * LuCl3 HfCl4 TaCl3
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
BiCl3 PoCl2
PoCl4
AtCl Rn
FrCl RaCl2 ** LrCl3 RfCl4 DbCl5 SgO2Cl2 BhO3Cl Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
 
* LaCl3 CeCl3 PrCl3 NdCl2
NdCl3
PmCl3 SmCl2
SmCl3
EuCl2
EuCl3
GdCl3 TbCl3 DyCl2
DyCl3
HoCl3 ErCl3 TmCl2
TmCl3
YbCl2
YbCl3
** AcCl3 ThCl3
ThCl4
PaCl4
PaCl5
UCl3
UCl4
UCl5
UCl6
NpCl3 PuCl3 AmCl2
AmCl3
CmCl3 BkCl3 CfCl3
CfCl2
EsCl2
EsCl3
FmCl2 MdCl2 NoCl2
  • v
  • t
  • e
La Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu
+4 CeF4 PrF4 NdF4 TbF4 DyF4
+3 LaF3
LaCl3
LaBr3
LaI3
CeF3
CeCl3
CeBr3
CeI3
PrF3
PrCl3
PrBr3
PrI3
NdF3
NdCl3
NdBr3
NdI3
PmF3
PmCl3
PmBr3
PmI3
SmF3
SmCl3
SmBr3
SmI3
EuF3
EuCl3
EuBr3
EuI3
GdF3
GdCl3
GdBr3
GdI3
TbF3
TbCl3
TbBr3
TbI3
DyF3
DyCl3
DyBr3
DyI3
HoF3
HoCl3
HoBr3
HoI3
ErF3
ErCl3
ErBr3
ErI3
TmF3
TmCl3
TmBr3
TmI3
YbF3
YbCl3
YbBr3
YbI3
LuF3
LuCl3
LuBr3
LuI3
+2 LaI2 CeI2 PrI2 NdF2
NdCl2
NdBr2
NdI2
SmF2
SmCl2
SmBr2
SmI2
EuF2
EuCl2
EuBr2
EuI2
GdI2 DyF2
DyCl2
DyBr2
DyI2
TmF2
TmCl2
TmBr2
TmI2
YbF2
YbCl2
YbBr2
YbI2