The synthesis of high value acrylic monomers is currently done industrially via cyanohydrin hydration using concentrated acids, resulting in large quantities of useless byproducts. This current process is energy intensive and lacks atom economy; therefore, alternative cyanohydrin hydration strategies are under investigation. Ideally, cyanohydrin hydration would be done using organometallic nitrile hydration catalysts. Cyanohydrin hydration with these catalysts is challenging, because it needs to be done at low temperatures and under acidic conditions to reduce cyanohydrin degradation and catalyst poisoning with cyanide.
This dissertation describes the reactivity of [Ru(#951; / 10000-01-01
| Identifer | oai:union.ndltd.org:uoregon.edu/oai:scholarsbank.uoregon.edu:1794/12362 |
| Date | January 2012 |
| Creators | Knapp, Spring Melody, Knapp, Spring Melody |
| Contributors | DeRose, Victoria |
| Publisher | University of Oregon |
| Source Sets | University of Oregon |
| Language | en_US |
| Detected Language | English |
| Type | Electronic Thesis or Dissertation |
| Rights | All Rights Reserved. |
Page generated in 0.0018 seconds