Title page for ETD etd-01102002-163336

Type of Document Master's Thesis
Author Merrill, James Malcolm
URN etd-01102002-163336
Title Coordination Chemistry of Bis(diphenylphosphino)amine Ligands with Cobalt Carbonyl and the Intermolecular Catalyzed Pauson-Khand Reaction
Degree Master of Science
Department Chemistry
Advisory Committee
Advisor Name Title
Hanson, Brian E. Committee Chair
Deck, Paul A. Committee Member
Dillard, John G. Committee Member
  • phosphine ligands
  • asymmetric
  • homogeneous catalysis
  • Pauson-Khand
Date of Defense 2001-12-19
Availability unrestricted
Bis(diphenylphosphino)amine (PNP) ligands, prepared from (S)-(-)-1-methylbenzyl amine, (-)-cis-myrtanylamine, (S)-(-)-1,1-napthyl(ethyl)amine (PNP1 1a, PNP2 1b, and PNP3 1c respectively) and their cobalt carbonyl complexes are reported. In the absence of alkynes the PNP ligands chelate to the cobalt rather than bridging the two cobalt centers. Although the PNP ligands are chiral the crystal structures are best solved in centrosymmetric space groups with disorder at the chiral carbon with the exception of (PNP3)Co2(CO)6, 2c, which is solved in a non-centrosymmetric space group.

When the PNP ligand chelates to cobalt, as in 2, the compounds show activity for the catalytic Pauson-Khand reaction, whereas when the PNP ligand bridges, as in 3, the reaction precedes stiochiometrically. The use of these chiral ligands has not yet resulted in enantioselective catalytic Pauson-Khand cycloadditions. However, a small 15% e.e. was detected for the stiochiometric Pauson-Khand cycloaddition with 3c as the metal substrate.

  Filename       Size       Approximate Download Time (Hours:Minutes:Seconds) 
 28.8 Modem   56K Modem   ISDN (64 Kb)   ISDN (128 Kb)   Higher-speed Access 
  JamesMerrillmastersthesis.pdf 1.09 Mb 00:05:01 00:02:35 00:02:15 00:01:07 00:00:05

Browse All Available ETDs by ( Author | Department )

dla home
etds imagebase journals news ereserve special collections
virgnia tech home contact dla university libraries

If you have questions or technical problems, please Contact DLA.