subskune
Hazard to Self
Posts: 71
Registered: 30-4-2017
Member Is Offline
Mood: No Mood
|
|
Ideas to make long-chain alditols
Hey there,
I want to make some very long-chain alditols (sugar alcohols). Basically polymers.
The problem is: I have no idea how to start. The 1,2 Dihydroxyethylene does not exist in its -ene form. The route of how polyvinylalcohol is made does
not work, since the double bond is locked between two substitutents.
Any ideas?
|
|
Pumukli
National Hazard
Posts: 708
Registered: 2-3-2014
Location: EU
Member Is Offline
Mood: No Mood
|
|
Aren't these sugar-like compounds made from formaldehyde polymerized with Ca(OH)2? Are those something different?
Anyway, formaldehyde polymerization works best with a moderately strong base, hence Ca(OH)2 is used afaik.
|
|
Metacelsus
International Hazard
Posts: 2539
Registered: 26-12-2012
Location: Boston, MA
Member Is Offline
Mood: Double, double, toil and trouble
|
|
I thought formaldehyde polymerization gave polyoxymethylene: https://en.wikipedia.org/wiki/Polyoxymethylene
Although the polyols do have the right empirical formula, I don't think they would be the major product under base-catalyzed polymerization.
Doing some more research, I see this might also take place if calcium is present: https://en.wikipedia.org/wiki/Formose_reaction
It could make some short oligomers but it would require a considerable amount of optimization to get long chains.
|
|
Pumukli
National Hazard
Posts: 708
Registered: 2-3-2014
Location: EU
Member Is Offline
Mood: No Mood
|
|
Yes, Metacelsus, you are right. Subskune explicitely wants "very long chain" polyols, this Butlerov reaction may not yield it, even after several days
of condensations.
|
|
subskune
Hazard to Self
Posts: 71
Registered: 30-4-2017
Member Is Offline
Mood: No Mood
|
|
The wiki entry states that the resulting alcohols of the formose reaction are C2-6. I thought of something like 100+.
Onthe other hand formaldehyde is the monomer of the repeating group of this alditols. Maybe there is a fancy way of converting POM directly. Papers on
this topic are quite scarce.
|
|
Metacelsus
International Hazard
Posts: 2539
Registered: 26-12-2012
Location: Boston, MA
Member Is Offline
Mood: Double, double, toil and trouble
|
|
The issue with aldose chains longer than C5 is that they can cyclize, which stops them from growing longer.
I bet it would be possible to develop a specialized catalyst for making long chains, but it certainly wouldn't be easy.
What are you planning to use these for? There may be substitutes.
|
|
TGSpecialist1
Hazard to Self
Posts: 53
Registered: 24-12-2017
Member Is Offline
Mood: always tired
|
|
https://en.wikipedia.org/wiki/Vinylene_carbonate
Bottom of the page.
|
|
Metacelsus
International Hazard
Posts: 2539
Registered: 26-12-2012
Location: Boston, MA
Member Is Offline
Mood: Double, double, toil and trouble
|
|
Good idea! That should definitely work.
|
|
subskune
Hazard to Self
Posts: 71
Registered: 30-4-2017
Member Is Offline
Mood: No Mood
|
|
Thank you a lot!!! Exactly what I was looking for
|
|
TGSpecialist1
Hazard to Self
Posts: 53
Registered: 24-12-2017
Member Is Offline
Mood: always tired
|
|
Note that if you'll use organic peroxide as a polymerization catalyst then your final polymer will be terminated with aldehyde groups.
|
|