Klute
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Synthesis of palladium nano-particules and their use in Suzuki coupling
I present the preparation of palladium nanoparticules and their use in Suzuki cross-coupling reaction.
Palladium nanoparticules are efficient heterogeneous catalysts for number of palladium-catalyzed reactions. Unlike precipitated particules, they are
active without dissolution or use of ligands.
To favor small particule size, a linear polymer (PolyVinylPyrrolidone, PVP, M: 40 000) is used to ensuregood distribution of the particules and to
prevent agglomeration.
Preparation of nano-particules of palladium
5,0mg (0,028 mmoles) of PdCl2, 0,5mL 2M HCl and 14,5mL milli-Q H2O are combined in an erlenmeyer flask. The suspension is stirred until complete
dissolution of th solids
The solution is then transfered to a 100mL RBF with 21mL dH2O, 14mL EtOH and 66,7mg PVP (Pd/PVP 1/20). The light orange solution is heated to reflux
for 2H, during which the solution turns dark brown/grey. The reaction is followed by UV-Vis, follwing the disaperance of a peak at 235nm ([PdCl4]-).
The nano particules are then cooled to room temp and used as is in the coupling reaction
Synthesis of biphenyl via Suzuki coupling
In a 250mL RBF are combined: 183,0mg (1,5mmol) phenylboronic acid, 78,5mg (0,5mmol) bromobenzene and 408,2mg (3mmol) sodium acetate trihydrate. 50mL
MeCn and 25mL dH2O are added, followed by the nanoparticules solution. The dark brown solution is heated to reflux for 30min.
The flask is then cooled down and extracted with 3x40mL pet ether. the xtracts are dried and evaporated at the rotavap. The biphenyl is obtained in a
yield of 43%.
I'm going to try using PD/C as a catalyst for this wonderfull reaction, as I haven't got any PdCl2 left.. I would like to get some more exotic boronic
acids, surely making then by grignard, as I only have a gram of phenylboronic acid left. I could always make it from bromobenzene, of which I have
enough.
Any suggestions on new substrates? I'd like to look into chiral products, with susbtitued arylbromide, I worked on a Suzuki coupling with
calixarene-phosphine ligands on chiral products, and I am going to work 2 to 4 months on this same reaction using chiral ferrocene-phosphine ligands!
Whoho very interesting!
Lets' revive the organometallic and catalysis spirit of SM!
EDIT: forgot the ref:
Size control of palladium nanoparticules and their crystals structures
T. Teranishi and M. Miyake
Chem. Mater.; 10, 594-600 (1998)
[Edited on 18-1-2010 by Klute]
\"You can battle with a demon, you can embrace a demon; what the hell can you do with a fucking spiritual computer?\"
-Alice Parr
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aonomus
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Hm, you have milliQ on tap there? Very nice.
I would think that the Suzuki coupling would be good for larger functionalized molecules, or perhaps a macrocyclization. If you used the Suzuki
coupling on smaller molecules as a substitute for a grignard reacting on a relatively plain molecule, it would seem like a bit of a waste.
Also, how do you plan on recovering the catalyst?
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Nicodem
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Beautiful ligand-free contribution and thanks a lot Klute.
The paper you refer to only gives the instructions to prepare the Pd nanoparticles. Is the application of the so prepared solution in the Suzuki
coupling your idea or you found similar examples in the literature?
You should however know, that with 5.6 mol% palladium and a threefold bromobenzene excess, a 43% yield leaves much to be optimized. It is known that
on similarly easy ortho-unsubstituted substrates even using the same amount of palladium on carbon (ligand-free) gives good results (biphasic
Na2CO3(aq) or K2CO3(aq) with toluene, THF or DME) even without bromoaromate excess. Perhaps the nanoparticles collapsed under the reaction conditions?
Have you noticed palladium black formation (the reaction mixture typically turns dark and sometimes a fine black precipitate forms when more Pd
catalyst is used)? If so, you might try using only tiny amounts of your palladium nanoparticles solution (<0.1 mol%). This is a now already known
trick to prevent ligand-free palladium(0) deactivation in Suzuki, Heck and other couplings (provided of course that you have reactive substrates:
ortho-unsubstituted, not electron rich aryl bromide/iodide). I know it is somewhat paradoxical and counterintuitive that the lower the catalyst
loading the better the results, but then again, here we talk about phosphineless situations. Check Adv. Synth. Catal., 346[7i], 1812–1817 for one such example.
…there is a human touch of the cultist “believer” in every theorist that he must struggle against as being
unworthy of the scientist. Some of the greatest men of science have publicly repudiated a theory which earlier they hotly defended. In this lies their
scientific temper, not in the scientific defense of the theory. - Weston La Barre (Ghost Dance, 1972)
Read the The ScienceMadness Guidelines!
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ANDLOS
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I want to ask plz can this be used in reduction of aromatic nitro group
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