Hydroformylation of olefins by water soluble and asymmetric cobalt and platinum complexes

Hydroformylation of olefins (OXO synthesis), one of the oldest organometallic catalytic reactions, continues to be of interest because of its commercial significance. Great interest recently has been placed on the development of immobilized homogeneous catalysts that combine the virtues of conventional heterogeneous and homogeneous catalysts. The objective of this dissertation is to investigate novel phosphine modified water soluble cobalt and platinum complexes as homogeneous and immobilized hydroformylation catalysts. The ligands include (1) Monodentate phosphines: P[ (CH₂ ) _n-C₆H₄-S0₃Na] ₃ (n = 0-3) and P[C₆H₄-NMe₃⁺BF₄⁻]₃; (2) Bidentate asymmetric phosphines: CHlRAPHOS(NMe₂)₄ (CHlRAPHOS = 2, 3-bis (diphenylphosphino) butane) , SKEWPHOS (NMe₂)₄ (SKEWPHOS = 2,4-bis(diphenylphospino)pentane), and DlOP(NMe₂)₄ (DlOP = 2,2-dimethyl-4,5-bis(diphenyl(phosphinomethyl)-1,3- dioxolane) ). These complexes were immobilized and/or recycled by four different methods: (1) Two phase catalysis; (2) Supported aqueous phase catalysis; (3) Catalyst supported on ion exchange resins; (4) Extraction of the catalyst from an organic phase into an aqueous phase. Catalytic results for the hydroformylation of a-olefins shows that nib (normal:branch of aldehyde product) ratio can be increased if proper alkyl-phosphine ligands are chosen. For example, as high as 18.5 of nib ratio was obtained in PtCl[P(C₆H₅)₃]₂-snCl₃ system and 5.6 in CO₂ (CO) ₆ [TRlMAPP] ₂ (TRlMAPP = trimethylamino-phenylphosphine) system. Metal leaching, from the aqueous phase to the organic phase during the catalytic reaction, was reduced by supporting the water soluble cobalt and platinum complexes onto a high surface area glass (CGP-350). For instance, 5.7% cobalt metal was found in the organic phase when CO₂(CO)₆(TPPTS)₂ was used under reaction conditions (TPPTS = triphenylphosphine trisulphonated salt). When the same cobalt complex was immobilized on glass, no cobalt metal leaching was observed. Asymmetric hydroformylation of styrene catalyzed by PtCl [SKEWPHOS (NMe₂) ₄] -SnCl₃ shows a very strong temperature dependence on optical selectivity. Enantiomeric excess (ee's) switches sign from <i><b>S</i></b> to <i><b>R</i></b> form at 57°C. At 25°C, there is 60.6% ee of <i><b>S</i></b> product, whereas 56.7% ee in favor of R product is observed at 100°C.

Name thesis:degree_name

Ph. D.

Level thesis:degree_level

doctoral

Discipline thesis:degree_discipline

Chemistry

Department dc:contributor.department

Chemistry

Grantor dc:publisher

Virginia Tech

Year dc:date.issued

1991

Author dc:creator

• Guo, Ipin

Chair dc:contributor.committeechair

• Hanson, Brian E.

Committee members dc:contributor.committeemember

• Anderson, Mark R.
• Davis, Mark E.
• Mason, John G.
• Merola, Joseph S.

Statement dc:rights

• In Copyright

Licence dc:rights.uri

• http://rightsstatements.org/vocab/InC/1.0/

Language dc:language.iso

en

Dc Identifier Other

etd-10142005-103047

OAI identifier oai:identifier

oai:vtechworks.lib.vt.edu:10919/39855