the nickel looks brown and not yellow....you think it is ok? i will enter it to the glove-box after drying on high-vacuum,,,
and i will take NMR,,,,hope it is ok!
i just saw the message after i started the reaction
it goes really nice...i need to distill in one hour the thionyl chloride and put the nickel in a desiccator ...
soon i will have about 10 grams of nickel chloride,,,thank you
ohhh great,,,!! i will save some money for my supervisor by not ordering the anhydrous this way and i will have more metal to
try my experiments with! cool!!
ohh,,,cool,,,i just found this book now:
http://onlinelibrary.wiley.com/doi/10.1002/9780470132593.ch80/summary;jsessionid=3D3BD722D2E786D787F1E14197938DC0.d03t01
i dont have access to it,,, maybe we have it at the library,,,
thank you again:)
Hey,,,
someone here worked with NICKEL CHLORIDE HEXAHYDRATE? i have in the lab a big stock of it, but i wanna work with the dry nickel chloride!
it can be dried good enough on high vacuum and heat to work with moisture sensitive ligands? or i should order dried one?
The acetone is from the chloroform-D bottle we have,,,, someone contaminated it !
i will try to dry it more on the high vacuum..the problem is that it becomes like a tar and doesnt solidify
the solvents i used are :THF, acetone, DCM, water, Toluene
thank u
Dana
i will send you the NMR tomorrow when i will be at the Faculty, i dried it under vacuum and high temperature, it doesn't solidify yet...
have you tried this reaction before?
thank you for the help!
Dana
Hey all,,,
I have synthesised the compound 1,3-Diisopropylimidazolium chloride according to the patent procedure, and i have it by NMR, but it still contains contaminations, and
i get it as a brown tar insted of brown solid,,
what is the best method to wash this product? i washed few times with THF, but it still oily instead of solid!
thank you,,
Dana
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