vano
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Osmium chemistry
Hello! now I have a few ampoules of OsO4. I searched here but osmium chemistry is rare. I think what can I do with the oxide? I want something
interesting and I will take any advice.
![IMG-1505.jpg - 2.3MB](https://www.sciencemadness.org/whisper/files.php?pid=676452&aid=94715)
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DraconicAcid
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Leave it ampuled. It's named after the way it stinks for a reason.
Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
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vano
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Sorry, I don't understand, not very good at English. but maybe you meant its toxicity.
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Texium
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If you do open it, be very careful. It’s surprisingly volatile and extremely toxic. It really should only be handled in a fume hood. You can inhale
a deadly dose at concentrations lower than you can smell.
Not sure about inorganic osmium chemistry, but the oxide itself is used extensively in organic chemistry as a catalytic oxidant. It’s usually used
with a stoichiometric amount of a re-oxidant like NMO, hydrogen peroxide, or ferricyanide, due to its high cost and toxicity. Most commonly this is
used to convert alkenes into cis-diols, and it can be extended to convert alkenes to two aldehydes, similar to ozonolysis, by addition of periodate.
See here: https://en.m.wikipedia.org/wiki/Lemieux–Johnson_oxidation
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Texium
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The word “osmium” is derived from the Greek word for “smell” because
of the tetroxide’s strong, unpleasant odor.
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vano
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thank you! I will not work with it at home, of course in the laboratory. the best way is to crack it, put the broken ampoule in a solvent , and close
the bottle.
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DraconicAcid
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I did my thesis with compounds of rhodium and iridium, and some of my colleagues worked with osmium. One particular colleague would make large
batches of [PPN][HOs(CO)4] every few months- the entire lab would reek. Any piece of equipment (clamps, clips, etc) that he used would reek. I'd be
washing my hands an extra twelve times a day just because I'd accidentally pick up something that he had used.
Even years after he left, my supervisor would suggest that I try something with osmium, and I'd tell him to fuck off.
Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
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vano
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haha, that's bad. Now it's clear why you think about osmium like that.
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BromicAcid
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From my recollection the big issue is damage to the eye tissues due to exposure to the tetroxide. Just be aware, as others have mentioned it's
surprisingly volatile.
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vano
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Oh, i understand. Thanks for your advice!
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teodor
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If I had that I would try those sequences of preparations ("->" means that the left is the starting material for the right):
- OsO4 -> KOsO3N -> K2OsCl5N
- OsO4 -> (NH4)2[OsCl6] (or (NH4)2[OsBr6]) -> [Os(NH3)5(N2)]I2 -> [Os(NH3)5I]I2
- (NH4)2[OsCl6] (or (NH4)2[OsBr6]) -> [Os(NH3)6]I3 -> [Os(NH3)5(NO)]I3 -> [Os(OH)(NH3)4(NO)]I2 -> [OsI(NH3)4(NO)]I2 ("I" could be
substituted with Cl or Br)
All those preparations were published in "Inorganic syntheses" (vol. 5, 6, 16). Except for the issues with the toxicity (of the starting compound) all
those syntheses are relatively easy and they don't require any exotic equipment/techniques/chemicals.
The interesting part is that to get any compound from the right you must perform all intermediate syntheses which can be a long-term project.
[Edited on 5-9-2022 by teodor]
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Bedlasky
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Look at this book:
https://1lib.cz/book/2276103/0e932b
There is really detailed description of osmium chemistry.
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vano
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thank you everyone!
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teodor
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My favorite source of the information for Os chemistry is the 160+ pages article "RECENT ADVANCES IN OSMIUM CHEMISTRY" by PETER A. LAY and W. DEAN
HARMAN published in "Advances in inorganic chemistry vol. 37" @ 1991.
It is more comprehensive compared to Pergamon Press book, also it contains references to all previous publications.
You can find the book at the same (pirate) library.
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Yamato71
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OsO4 can instantly blind you if it or it's vapor contacts your eyes. Your corneas will turn irreversibly black due to reduction to metallic osmium
within the tissues. Osmium chemistry is one of my huge nopes.
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vano
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yes of course. but I want to work with tetravalent osmium. I will reduce it with thionyl chloride and then remove all air with a vacuum. I will make
this reaction in the lab and it will be safe.
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Keras
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Osmium tetroxide sole usage (in organic chemistry) is to transform a double bond into a gem-diol.
But this can be done also with potassium permanganate, which is orders of magnitude less toxic and dangerous for your eyes than OsO₄.
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Bedlasky
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Why with thionyl chloride? If you plan to do aqueous chemistry, you can use some common reducing agent (for example sulfite).
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njl
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Because he's badass
Reflux condenser?? I barely know her!
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vano
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I don't want to work with aqueous solutions, I want anhydrous tetrachloride to make organometallics in an organic solvent. also thyonyl chloride
reaction is something new and funny for me, i want to try it.
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woelen
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Then I suggest
that you first try experimenting with thionyl chloride and other chemicals than OsO4. Reactions with thionyl chloride can be quite violent and can
produce lots of fumes/gases. The produced fumes/gases usually are of the SO2/HCl kind and can be dealt with by the more experienced home chemist, but
if there are osmium-containing vapors in it as well, then that could lead to very nasty surprises.
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vano
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tetrachloride doesn't sublime. so when the reaction is finish, ill remove all gases with a vacuum.
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woelen
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Maybe you don't get OsCl4 vapors, but what if some unreacted OsO4-vapors escape? Can you be sure that this does not happen, or that you can contain
the Os completely. I know from experience that with experiments with SOCl2 it is almost impossible to contain all of the huge amounts of HCl-fumes and
SO2-gas, which can be produced. Breathing a whiff of SO2 or HCl, or getting stinging eyes of SO2 or HCl is unpleasant, but not fatal. But getting
fumes of OsO4 in your eyes may be very serious for the rest of your life.
I once did an experiment with RuO2, and took a little pinch of that (maybe a few mg) and left this in an erlenmeyer with bleach in it. This gave a
nice deep red solution. I put this away, without a cap. Several days later, I came back and saw that the liquid had become colorless, and there was a
big stain on the workbench around the erlenmeyer. When I removed the erlenmeyer, the surface under it was still clean, the rest is considerably
darker. This happened a year ago or so. The stain still is there, I cannot remove it from the workbench. I tell this as a demonstration of how
extremely easily stains are obtained from minute quantities. And this was with RuO4. OsO4 is worse!
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vano
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it is necessary to use exec thionyl chloride I think, it is an osmium oxide hydrate, so ill remove water also. I think the reaction will go at room
temperature, then I use a vacuum. I know that the water-thionyl chloride reaction produces HCl, which can form chloroosmic acid, but it must be small
contamination, but I can remove it with heating and a vacuum. It's good also that tetrachloride has 323C as the decomposition temperature.
there are some issues also, mostly theoretical for example SO2 as a bridging ligand, but I'm not thinking of such theoretical things, just low
possibility. the final step of synthesis must leave only tetrachloride.
also as I said I won't do the reaction in my homelab.
[Edited on 2-11-2022 by vano]
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Fleaker
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OsO4 is actually rather nasty, much worse in comparison to even RuO4.
The first thing one notices is a halo around the lights when working with it and the vapors are escaping.
Neither flask nor beaker.
"Kid, you don't even know just what you don't know. "
--The Dark Lord Sauron
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