Novel amphiphilic diphosphines: Synthesis, X-ray structure, rhodium complexes, use in hydroformylation, and rhodium recycling

被引:58
|
作者
Buhling, A
Kamer, PCJ
vanLeeuwen, PWNM
Elgersma, JW
Goubitz, K
Fraanje, J
机构
[1] UNIV AMSTERDAM,VANT HOFF RES INST,NL-1018 WV AMSTERDAM,NETHERLANDS
[2] UNIV AMSTERDAM,ANALYT CHEM LAB,AMSTERDAM INST MOL STUDIES,NL-1018 WV AMSTERDAM,NETHERLANDS
[3] UNIV AMSTERDAM,AMSTERDAM INST MOL STUDIES,DEPT CRYSTALLOG,NL-1018 WV AMSTERDAM,NETHERLANDS
关键词
D O I
10.1021/om970068w
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three novel amphiphilic diphosphines have been synthesized: bis[2-(phenyl(3-pyridyl)phosphino)ethyl] ether (POPpy) and bis[2-((4-((diethylamino)methyl)phenyl)phenylphosphino)ethyl]ether (POPam), based on bis[2-(diphenylphosphino)ethyl]ether (POP), and 4,6-bis[bis(4-((diethylamino)methyl)phenyl)phosphino]-10,10-dimethylxanthene (xantham), based on 4,6-bis(diphenylphosphino)-10,10-dimethylxanthene (Xantphos). The crystal structure of xantham has been determined. Solution structures of rhodium xantham complexes have been studied using NMR and IR spectroscopy. When POPam is used in the hydroformylation of oct-1-ene, a linear/branched ratio (l/b) of 7.3 is achieved (88% nonanal) without isomerization to oct-2-ene. The use of POPpy results in an activity that is twice as high, a higher l/b-ratio of 9, and 0.7% isomerization. When xantham is used in the hydroformylation of hex-1-ene, oct-1-ene, and dodec-1-ene (80 degrees C, 20 bar of syngas, toluene), l/b-ratios of 50 have been achieved (94% nonanal) together with 4% of isomerized octenes. The pH-dependent distribution characteristics of the free Ligands have been determined, and it is shown that POPpy, POPam, and xantham can be extracted for 40% from a Et2O solution into an aqueous solution of H2SO4 at pH values of, respectively, 2.5, 5, and 5. Rhodium recycling experiments using POPam and xantham show that rhodium can be extracted into an aqueous layer at pH 5-5.5 for more than 99.95%, as determined by ICP-AES analysis, which allows complete separation of the product aldehydes and catalyst. After neutralization of the aqueous phase containing protonated POPam with an aqueous solution of NaHCO3, only 65% of the rhodium can be re-extracted into fresh toluene. In the case of xantham, 98% of the rhodium is re-extracted. Pressurizing the recovered rhodium and excess xantham to 20 bar at 80 degrees C resulted in regeneration of the original active hydride complex, as judged by the retention of activity of up to 86%. POPpy has proved inappropriate for the recycling of rhodium.
引用
收藏
页码:3027 / 3037
页数:11
相关论文
共 50 条
  • [31] Rhodium(III) and palladium(II) complexes of some P-heterocycles; synthesis and X-ray structures
    Odinets, IL
    Vinogradova, NM
    Lyssenko, KA
    Golovanov, DG
    Petrovskii, PV
    Mastryukova, TA
    Szelke, H
    Szabó, NB
    Keglevich, G
    JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2005, 690 (03) : 704 - 712
  • [32] X-ray study of rhodium(III) sulfates
    Vorob'yova, S. N.
    Baidina, I. A.
    Alekseev, A. V.
    Belyaev, A. V.
    JOURNAL OF STRUCTURAL CHEMISTRY, 2009, 50 (06) : 1134 - 1142
  • [33] Synthesis and X-ray structures of water-soluble tris(hydroxymethyl)phosphine complexes of rhodium(I)
    Lorenzini, Fabio
    Patrick, Brian O.
    James, Brian R.
    DALTON TRANSACTIONS, 2007, (30) : 3224 - 3226
  • [34] (PENTAMETHYLCYCLOPENTADIENYL)RHODIUM AND IRIDIUM COMPLEXES .37. SYNTHESIS AND X-RAY STRUCTURE DETERMINATION OF BIS(MU3-METHYLIDYNE)TRIS[ETA5-PENTAMETHYLCYCLOPENTADIENYL)RHODIUM]
    DEMIGUEL, AV
    ISOBE, K
    BAILEY, PM
    MEANWELL, NJ
    MAITLIS, PM
    ORGANOMETALLICS, 1982, 1 (12) : 1604 - 1607
  • [35] Synthesis and structure of novel chiral oxazolinylferrocenes and oxazolinylferrocenylphosphines, and their rhodium(I)-complexes
    Nishibayashi, Y
    Segawa, K
    Arikawa, Y
    Ohe, K
    Hidai, M
    Uemura, S
    JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1997, 545 : 381 - 398
  • [36] Synthesis and crystal structure of a dinuclear rhodium complex. Catalytic activity of mono- and di-nuclear rhodium phosphite complexes in hydroformylation
    vandenBeuken, EK
    deLange, WGJ
    vanLeeuwen, PWNM
    Veldman, N
    Spek, AL
    Feringa, BL
    JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1996, (17): : 3561 - 3569
  • [37] X ray absorption and X-ray photoelectron spectroscopy of a rhodium colloid
    Rothe, J
    Pollmann, J
    Franke, R
    Hormes, J
    Bonnemann, H
    Brijoux, W
    Siepen, K
    Richter, J
    FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1996, 355 (3-4): : 372 - 374
  • [38] NOVEL RHODIUM ALKOXIDE COMPLEXES - STRUCTURE AND REACTIVITY
    KEGLEY, SE
    SCHAVERIEN, CJ
    BERGMAN, RG
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1987, 193 : 405 - INOR
  • [39] ELECTRONIC AND STERIC EFFECTS OF CHELATING DIPHOSPHINES ON THE STRUCTURE OF IRIDIUM COMPLEXES AND RHODIUM-CATALYZED
    CASEY, CP
    LIN, EJ
    PROFT, BR
    BEUTTENMILLER, EW
    MATTER, BA
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1995, 210 : 186 - INOR
  • [40] Novel rhodium complexes with N-pyrrolylphosphines: Attractive precursors of hydroformylation catalysts
    Trzeciak, AM
    Glowiak, T
    Grzybek, R
    Ziolkowski, JJ
    JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1997, (11): : 1831 - 1837