Catalysts in Organic Synthesis

1. Catalysts in Organic Synthesis Dr. Christoph, Phayao UniversityFeb. 2012

2. Commercial Applications

3. .... and many more industrial applications !

4. Top 20 synthetic chemicals produced in the US in 2004

5. Why catalysis ? In the chemical production there is a lot of waste produced in each synthesis. The amount of waste in kg per kg product is about: 1-5 kg waste for bulk chemicals 5 – 50 kg waste for fine chemicals 25 – 100 kg waste for pharmaceuticals

7. Why Catalysts ? – an example:

8. Types of catalyzed reactions • Hydrogenation = Reduction • Oxidation • Hydroformylation • Addition of HX to Olefins (esp. Hydration) • C-C bond formation

9. Catalyst = active site + support • Most often transition metals, finely distributed on a support. • “Inert” porous materials which • carry the metal atoms or ions. • Most often used are • Aluminumoxide • Titaniumoxide • Active Charcoal

10. Catalytic Cycles http://en.wikipedia.org/wiki/Catalytic_cycle

12. How to make a catalyst ? A common way is to use a transition metal salt (like AuCl3-) in solution and make a slow precipitation in aqueous solution (see demo video) If there is some support material in the reaction also, the metal “nanoparticles” could precipitate on the support like Al2O3 or TiO2.

13. Catalytic Steps (Homogenous Catalysis)

14. (a) Ligand coordination and dissociation Catalytic steps often require easy coordination of reactants to metal ions and equally easy loss of products. For this task, square-planar 16-el. Complexes are ideal because they are coordinatively unsaturated Especially Pd(II), Pt(II) and Rh(I) complexes are suitable For example the catalyst for the Wilkinson reaction(industrial hydrogenation of alkenes at mild conditions)

15. Exceptions to the 18-electron rule:

17. (b) Oxidative Addition Basic reaction: The new M-X and M-Y bonds are formed using: • the electron pair of the X-Y bond • one metal-centered lone pair The metal goes up in oxidation state (+2) X-Y formally gets reduced to X-, Y- Common for transition metals, rare for main-group metals Oxidative addition, reductive elimination

18. One reaction, multiple mechanisms Concerted addition, mostly with non-polar X-Y bonds • H2, silanes, alkanes, O2, ... • Arene C-H bonds more reactive than alkane C-H bonds (!) Intermediate A is a s-complex. Reaction may stop here if metal-centered lone pairsare not readily available. Final product expected to have cis X,Y groups. Oxidative addition, reductive elimination

19. Concerted addition, "arrested" Cr(PMe3)5: phosphines are better donors, weaker acceptors: full oxidative addition Cr(CO)5: coordinatively unsaturated, but metal-centered lone pairs not very available:s-complex Oxidative addition, reductive elimination

20. Which of the following can undergo oxidative addition of MeI? (Check ox.number of metal before and after reaction)

21. Which of the following will be MORE ACTIVE towards ox. addition of H2? The most electron-rich complex will be easiest to oxidize.

22. (c) Reductive Elimination Favoured by electron-poor metal centers !

23. Example:

24. How does it work ? Pd and Pt atoms have a high affinity for Hydrogen to form M-H bonds. • The hydrogen molecule can accept electron density from a d-orbital into the • σ* antibonding MO ! • the H-H bond becomes weaker and can easily split up. • (this works also for C-H bonds ! )

25. Unusual HIGH ox.number for Pt !

26. (d) Insertion / Migration Research showed that the X-group migrates to the unsaturated ligand U The reverse reaction is called beta-Hydrid-Elimination

27. “CO Insertion” – actually the Methylgroup migrates to the CO ! Note that the ox.number of Mn does NOT change !

30. Mindmap: “All in One” – made by http://www.spiderscribe.net

31. Part 2: Overview Basic industrial important reactions

33. (1) From crude oil to Olefins => CRACKING The ethene and propene are important materials for making plastics or producing other organic chemicals. The octane is one of the molecules found in petrol (gasoline). http://www.chemguide.co.uk/organicprops/alkanes/cracking.html

34. Catalytic Cracking – Zeolites as “Superacids” Mixed structure of Al2O3 and SiO2. Each Al(3+) needs an additional cation (like Na+ or H+) so that the charges are balanced ! Cation exchange is exploited in water softening, where alkali metals such as Na+ or K+ in zeolite framework are replaced by Ca2+ and Mg2+ ions from water.

35. Zeolites can protonate an alkane to give a carbocation or carbenium ion. (Haag-Dessau Mechanism, 1984) The carbonium ion then decomposes and forms smaller parts including double-bonds.

36. Base-catalyzed Production of Bio-Diesel Follow this link to watch the movie This is an example of a homogenous catalysis, where the catalyst (NaOH) is in the same phase as the product (vegetable oil). The byproducts and the catalyst have to be separated from this phase later.

37. Hydration of Alkenes => Alcohols (2) From olefins to alcohols => Hydration http://www.docbrown.info/page06/OrgMechs1b.htm The catalyst is an acid, so that a hydronium ion is formed that act as electrophil. To save material, in industrial scale we can use zeolites as acid catalyst instead of for example sulfuric acid.

38. (3) From alcohols to aldehydes=> Oxidation In industry, formaldehyde is produced on a large scale by oxidation of methanol (“Formox” process) over a catalyst of molybdenum and iron oxide. A mixture of air and methanol is vaporised and passed into catalyst-packed reactor tubes. The reaction which takes place at 350oC is highly exothermic and generates heat to provide steam for turbines and process heating. Another oxidation route significant in industry is the Wacker process, whereby ethylene is oxidized to acetaldehyde in the presence of copper and palladium catalysts. (see next) In the lab we can use dichromate as oxidation agent - to prevent formation of the carboxylic acid, we have to take the aldehyde product out by distilliation !

39. Hydroformylation At the end, it is a hydrogenation and CO insertion H2

40. (4) From aldehydes to carboxylic acids => Oxidation Compare the conventional way of oxidation with strong oxidizing agent to the reaction with molecular oxygen from air http://www.chemeddl.org/collections/TSTS/Stahl/Stahl9-12/Catalyticcyles.html

42. (5) From ketones to alcohols => Reduction Especially the metals Pd and Pt are suitable for this kind of reaction ! Example: intermediate for Ibuprofen

43. Hydrogenation The exact mechanism of heterogeneous processes is often not fully understood ! In a simplified way, a multiple bond can be hydrogenated by Pd or Pt atoms on a support:

44. Catalytic olefin hydrogenation (1)Homogenous catalysis • Usually with platinum metals. • e.g. Wilkinson's catalyst • Many chiral variations available. • Enantioselectivity • Rarely possible with early transition metals Oxidative addition, reductive elimination

45. Catalytic olefin hydrogenation (2) • Alternative mechanismfor metals not forminga "stable" hydride. • Requires oxidative addition,not observed forearly transition metals. Oxidative addition, reductive elimination

46. How does it work ? Pd and Pt atoms have a high affinity for Hydrogen to form M-H bonds. • The hydrogen molecule can accept electron density from a d-orbital into the • σ* antibonding MO ! • the H-H bond becomes weaker and can easily split up. • (this works also for C-H bonds ! )

47. In addition, transition metals can make covalent bonds to π-bonds of ligands: The π-MO of ethylene acts as electron donor, the antibonding π*-MO can accept electron density from a metal d-orbital (“backbonding”).

48. Thank you for your attention ! Please visit our class again and good luck for your exams !