Ytterbium(III) chloride

Last updated
Ytterbium(III) chloride
Ytterbium(III) chloride.jpg
Aluminium-trichloride-crystal-3D-balls.png
Names
IUPAC name
Ytterbium(III) chloride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.715 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 233-800-5
PubChem CID
UNII
  • InChI=1S/3ClH.Yb/h3*1H;/q;;;+3/p-3 Yes check.svgY
    Key: CKLHRQNQYIJFFX-UHFFFAOYSA-K Yes check.svgY
  • InChI=1/3ClH.Yb/h3*1H;/q;;;+3/p-3
    Key: CKLHRQNQYIJFFX-DFZHHIFOAT
  • Cl[Yb](Cl)Cl
Properties
YbCl3
Molar mass 279.40 g/mol
AppearanceWhite 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]
17 g/100 mL (25 °C)
Structure
Monoclinic, mS16
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).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

Ytterbium(III) chloride (Yb Cl3) 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.

Contents

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]

Related Research Articles

<span class="mw-page-title-main">Erbium</span> Chemical element, symbol Er and atomic number 68

Erbium is a chemical element; it has symbol Er and atomic number 68. A silvery-white solid metal when artificially isolated, natural erbium is always found in chemical combination with other elements. It is a lanthanide, a rare-earth element, originally found in the gadolinite mine in Ytterby, Sweden, which is the source of the element's name.

The lanthanide or lanthanoid series of chemical elements comprises at least the 14 metallic chemical elements with atomic numbers 57–70, from lanthanum through ytterbium. In the periodic table, they fill the 4f orbitals. Lutetium is also sometimes considered a lanthanide, despite being a d-block element and a transition metal.

<span class="mw-page-title-main">Ytterbium</span> Chemical element, symbol Yb and atomic number 70

Ytterbium is a chemical element; it has symbol Yb and atomic number 70. It is a metal, the fourteenth and penultimate element in the lanthanide series, which is the basis of the relative stability of its +2 oxidation state. Like the other lanthanides, its most common oxidation state is +3, as in its oxide, halides, and other compounds. In aqueous solution, like compounds of other late lanthanides, soluble ytterbium compounds form complexes with nine water molecules. Because of its closed-shell electron configuration, its density, melting point and boiling point are much lower than those of most other lanthanides.

<span class="mw-page-title-main">Cerium(III) chloride</span> Chemical compound

Cerium(III) chloride (CeCl3), also known as cerous chloride or cerium trichloride, is a compound of cerium and chlorine. It is a white hygroscopic salt; it rapidly absorbs water on exposure to moist air to form a hydrate, which appears to be of variable composition, though the heptahydrate CeCl3·7H2O is known. It is highly soluble in water, and (when anhydrous) it is soluble in ethanol and acetone.

<span class="mw-page-title-main">Praseodymium(III) chloride</span> Chemical compound

Praseodymium(III) chloride is the inorganic compound with the formula PrCl3. Like other lanthanide trichlorides, it exists both in the anhydrous and hydrated forms. It is a blue-green solid that rapidly absorbs water on exposure to moist air to form a light green heptahydrate.

Neodymium(III) chloride or neodymium trichloride is a chemical compound of neodymium and chlorine with the formula NdCl3. This anhydrous compound is a mauve-colored solid that rapidly absorbs water on exposure to air to form a purple-colored hexahydrate, NdCl3·6H2O. Neodymium(III) chloride is produced from minerals monazite and bastnäsite using a complex multistage extraction process. The chloride has several important applications as an intermediate chemical for production of neodymium metal and neodymium-based lasers and optical fibers. Other applications include a catalyst in organic synthesis and in decomposition of waste water contamination, corrosion protection of aluminium and its alloys, and fluorescent labeling of organic molecules (DNA).

<span class="mw-page-title-main">Samarium(III) chloride</span> Chemical compound

Samarium(III) chloride, also known as samarium trichloride, is an inorganic compound of samarium and chloride. It is a pale yellow salt that rapidly absorbs water to form a hexahydrate, SmCl3.6H2O. The compound has few practical applications but is used in laboratories for research on new compounds of samarium.

<span class="mw-page-title-main">Europium(III) chloride</span> Chemical compound

Europium(III) chloride is an inorganic compound with the formula EuCl3. The anhydrous compound is a yellow solid. Being hygroscopic it rapidly absorbs water to form a white crystalline hexahydrate, EuCl3·6H2O, which is colourless. The compound is used in research.

<span class="mw-page-title-main">Dysprosium(III) chloride</span> Chemical compound

Dysprosium(III) chloride (DyCl3), also known as dysprosium trichloride, is a compound of dysprosium and chlorine. It is a white to yellow solid which rapidly absorbs water on exposure to moist air to form a hexahydrate, DyCl3·6H2O. Simple rapid heating of the hydrate causes partial hydrolysis to an oxychloride, DyOCl.

<span class="mw-page-title-main">Ytterbium(III) oxide</span> Chemical compound

Ytterbium(III) oxide is the chemical compound with the formula Yb2O3. It is one of the more commonly encountered compounds of ytterbium. It occurs naturally in trace amounts in the mineral gadolinite. It was first isolated from this in 1878 by Jean Charles Galissard de Marignac.

<span class="mw-page-title-main">Terbium(III,IV) oxide</span> Chemical compound

Terbium(III,IV) oxide, occasionally called tetraterbium heptaoxide, has the formula Tb4O7, though some texts refer to it as TbO1.75. There is some debate as to whether it is a discrete compound, or simply one phase in an interstitial oxide system. Tb4O7 is one of the main commercial terbium compounds, and the only such product containing at least some Tb(IV) (terbium in the +4 oxidation state), along with the more stable Tb(III). It is produced by heating the metal oxalate, and it is used in the preparation of other terbium compounds. Terbium forms three other major oxides: Tb2O3, TbO2, and Tb6O11.

<span class="mw-page-title-main">Erbium(III) chloride</span> Chemical compound

Erbium(III) chloride is a violet solid with the formula ErCl3. It is used in the preparation of erbium metal.

<span class="mw-page-title-main">Gadolinium(III) chloride</span> Chemical compound

Gadolinium(III) chloride, also known as gadolinium trichloride, is GdCl3. It is a colorless, hygroscopic, water-soluble solid. The hexahydrate GdCl3∙6H2O is commonly encountered and is sometimes also called gadolinium trichloride. Gd3+ species are of special interest because the ion has the maximum number of unpaired spins possible, at least for known elements. With seven valence electrons and seven available f-orbitals, all seven electrons are unpaired and symmetrically arranged around the metal. The high magnetism and high symmetry combine to make Gd3+ a useful component in NMR spectroscopy and MRI.

<span class="mw-page-title-main">Yttrium(III) chloride</span> Chemical compound

Yttrium(III) chloride is an inorganic compound of yttrium and chloride. It exists in two forms, the hydrate (YCl3(H2O)6) and an anhydrous form (YCl3). Both are colourless salts that are highly soluble in water and deliquescent.

<span class="mw-page-title-main">Lanthanum(III) chloride</span> Chemical compound

Lanthanum chloride is the inorganic compound with the formula LaCl3. It is a common salt of lanthanum which is mainly used in research. It is a white solid that is highly soluble in water and alcohols.

Lanthanide trichlorides are a family of inorganic compound with the formula LnCl3, where Ln stands for a lanthanide metal. The trichlorides are standard reagents in applied and academic chemistry of the lanthanides. They exist as anhydrous solids and as hydrates.

Erbium compounds are compounds containing the element erbium (Er). These compounds are usually dominated by erbium in the +3 oxidation state, although the +2, +1 and 0 oxidation states have also been reported.

Ytterbium compounds are chemical compounds that contain the element ytterbium (Yb). The chemical behavior of ytterbium is similar to that of the rest of the lanthanides. Most ytterbium compounds are found in the +3 oxidation state, and its salts in this oxidation state are nearly colorless. Like europium, samarium, and thulium, the trihalides of ytterbium can be reduced to the dihalides by hydrogen, zinc dust, or by the addition of metallic ytterbium. The +2 oxidation state occurs only in solid compounds and reacts in some ways similarly to the alkaline earth metal compounds; for example, ytterbium(II) oxide (YbO) shows the same structure as calcium oxide (CaO).

Lanthanide chlorides are a group of chemical compounds that can form between a lanthanide element and chlorine. The lanthanides in these compounds are usually in the +2 and +3 oxidation states, although compounds with lanthanides in lower oxidation states exist.

References

  1. 1 2 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. 1 2 3 Evans, C.H. (1990). Biochemistry of the Lanthanides. New York: Plenum. ISBN   978-1-4684-8750-3.
  5. 1 2 Chervonnyi, A.D.; Chervonnaya, N.A. (2004). "Thermodynamic Properties of Ytterbium Chlorides". Russ. J. Inorg. Chem. (Engl. Transl.). 49 (12): 1889–1897.
  6. 1 2 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. 1 2 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. 1 2 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.


This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.