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ytterbium(III) Chloride

YbCl3 salt

Properties

StateSolid (hygroscopic; commonly hydrated)
Colorwhite to pale yellow
SolubilityVery soluble in water; soluble in alcohols
Melting Point896 °C (anhydrous)

About ytterbium(III) Chloride

Ytterbium(III) chloride is a white-to-pale-yellow hygroscopic salt — anhydrous YbCl3 has a molar mass of 279.4 g/mol, but you almost never buy it that way. The bottle on the shelf is the heptahydrate or hexahydrate, because the anhydrous form is a pain to make from solution: dehydrating the hydrate in moist air gives YbOCl (the oxychloride) instead of clean YbCl3. To get genuinely anhydrous material you either vacuum-sublime it, heat the hydrate with NH4Cl under argon, or react Yb metal with Cl2 directly. In the solid state the Yb(III) center sits in a 9-coordinate tricapped trigonal prism, the typical geometry for the larger trivalent rare-earth cations. YbCl3 is the workhorse precursor for ytterbium chemistry: doped crystals, fiber-laser preforms, Yb(II) reduction studies (YbCl2 is reachable via sodium-naphthalenide reduction in THF), and — most usefully for the synthesis community — it is the starting material for ytterbium(III) triflate, the most popular water-tolerant Lewis acid catalyst in modern green chemistry.

Where you'll encounter it

If you've ever ordered a rare-earth chloride from Strem or Sigma-Aldrich for an organometallic project, you've likely opened a brown glass bottle of YbCl3·6H2O sitting in a desiccator, and watched it start to bead with water the moment the lid came off. In a synthesis lab, the most common job for YbCl3 is feeding the next bench over: you weigh out the hydrate, dissolve it in degassed water with triflic acid, and recover Yb(OTf)3 after evaporation and drying. In a laser-materials facility, YbCl3 is the dopant source that goes into the precursor melt for Yb:YAG single-crystal growth or into the modified-chemical-vapor-deposition (MCVD) process for Yb-doped silica fiber preforms — the same fibers that end up in 10-kilowatt cutting lasers on factory floors.

Common Uses

  • Precursor for synthesis of ytterbium(III) triflate Lewis-acid catalyst
  • Dopant feedstock for Yb:YAG single-crystal growth and Yb:silica fiber preforms
  • Starting material for organolanthanide complexes via salt metathesis
  • Source of Yb(II) reagents after reduction with sodium-naphthalenide in THF
  • Lanthanide reference standard in ICP-MS calibration of rare-earth analyses

Safety Information

GHS classification: Skin irritation Category 2 (H315), Eye irritation Category 2A (H319), STOT SE Category 3 respiratory tract irritation (H335). Acute oral toxicity is moderate (LD50 oral rat for related YbCl3·6H2O around 480 mg/kg). The hydrate releases small amounts of HCl on heating or contact with strong dehydrating reagents, so handle in a fume hood when sublimating or reacting with NH4Cl. There is no OSHA PEL specific to ytterbium compounds, but follow the general inert-dust limit of 15 mg/m3 total / 5 mg/m3 respirable. Standard PPE: nitrile gloves, splash goggles, lab coat. Store sealed under desiccant.

This safety summary is for educational reference only and may not be complete. It is not a substitute for Safety Data Sheets (SDS), medical advice, or professional chemical safety guidance. Always consult appropriate SDS and qualified professionals before handling chemicals.

Constituent Elements

Frequently Asked Questions

What is the molar mass of ytterbium(III) chloride?
Anhydrous YbCl3 is 279.4 g/mol — that's 173.05 g/mol for ytterbium plus three chlorines at 35.45 each. The commercially common hexahydrate YbCl3·6H2O comes in at 387.5 g/mol, and the heptahydrate at 405.5 g/mol, so always check which form you actually have on the bottle before scaling a stoichiometric reaction.
How is Yb(II) accessed from YbCl3?
Reduce YbCl3 to YbCl2 with sodium-naphthalenide or lithium-biphenyl in THF at room temperature, under rigorous inert atmosphere. The resulting Yb(II) species is a single-electron reductant in the same family as SmI2 — it does ketyl coupling, Barbier allylation, and selective 1,4-reduction of alpha,beta-unsaturated carbonyls. Yb(II) is more oxygen-sensitive than Sm(II) but has a slightly more negative reduction potential, which makes it the right choice for stubborn ketyl cyclizations.
Why is anhydrous YbCl3 hard to prepare?
Heating YbCl3 hydrates in air drives off HCl and gives ytterbium oxychloride YbOCl, not the anhydrous chloride. Clean dehydration needs either vacuum sublimation, NH4Cl-assisted dehydration under argon (the NH4Cl traps water as the ammonium salt and decomposes cleanly), or a direct route from Yb metal plus Cl2 at high temperature in a sealed tube.