| Autor: |
Pawar GM; Lehrstuhl für Makromolekulare Stoffe und Faserchemie, Institut für Polymerchemie, Universität Stuttgart, Pfaffenwaldring 55, D-70550 Stuttgart, Germany., Weckesser J, Blechert S, Buchmeiser MR |
| Jazyk: |
angličtina |
| Zdroj: |
Beilstein journal of organic chemistry [Beilstein J Org Chem] 2010 Mar 23; Vol. 6, pp. 28. Date of Electronic Publication: 2010 Mar 23. |
| DOI: |
10.3762/bjoc.6.28 |
| Abstrakt: |
Norborn-5-ene-(N,N-dipyrid-2-yl)carbamide (M1) was copolymerized with exo,exo-[2-(3-ethoxycarbonyl-7-oxabicyclo[2.2.1]hept-5-en-2-carbonyloxy)ethyl]trimethylammonium iodide (M2) using the Schrock catalyst Mo(N-2,6-Me₂-C₆H₃)(CHCMe₂Ph)(OCMe(CF₃)₂)₂[Mo] to yield poly(M1-b-M2). In water, poly(M1-b-M2) forms micelles with a critical micelle-forming concentration (cmc) of 2.8 x 10⁻⁶ mol L⁻¹; Reaction of poly(M1-b-M2) with [Rh(COD)Cl]₂ (COD = cycloocta-1,5-diene) yields the Rh(I)-loaded block copolymer poly(M1-b-M2)-Rh containing 18 mg of Rh(I)/g of block copolymer with a cmc of 2.2 x 10⁻⁶ mol L⁻¹. The Rh-loaded polymer was used for the hydroformylation of 1-octene under micellar conditions. The data obtained were compared to those obtained with a monomeric analogue, i.e. CH₃CON(Py)₂RhCl(COD) (C1, Py = 2-pyridyl). Using the polymer-supported catalyst under micellar conditions, a significant increase in selectivity, i.e. an increase in the n:iso ratio was accomplished, which could be further enhanced by the addition of excess ligand, e.g., triphenylphosphite. Special features of the micellar catalytic set up are discussed. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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