메뉴 건너뛰기




Volumn 58, Issue 7, 2012, Pages 2192-2201

Mechanistic model for kinetics of propene hydroformylation with Rh catalyst

Author keywords

Cyclohexyl diphenylphosphine; Hydroformylation; Kinetic modeling; Propene; Rhodium

Indexed keywords

CONCENTRATION-DEPENDENT; CYCLOHEXYL; DIPHENYLPHOSPHINE; EXPERIMENTAL DATA; EXPERIMENTAL OBSERVATION; ISOBUTYRALDEHYDE; KINETIC MODELING; KINETIC MODELS; KINETIC REGIME; LIGAND CONCENTRATION; MECHANISTIC MODELS; N-BUTYRALDEHYDE; NUMERICAL DATA; RH CATALYSTS; RHODIUM CATALYSTS; SEMI-BATCH; TRIPHENYL PHOSPHINES;

EID: 84862007699     PISSN: 00011541     EISSN: 15475905     Source Type: Journal    
DOI: 10.1002/aic.12746     Document Type: Article
Times cited : (8)

References (35)
  • 1
    • 0038683352 scopus 로고    scopus 로고
    • Concepts in homogeneous catalysis: the industrial view
    • Cornils B, Herrmann WA. Concepts in homogeneous catalysis: the industrial view. J Catal. 2003; 216: 23-31.
    • (2003) J Catal. , vol.216 , pp. 23-31
    • Cornils, B.1    Herrmann, W.A.2
  • 4
    • 0004247812 scopus 로고
    • Dordrecht: Reidel
    • 2. Dordrecht: Reidel, 1983.
    • (1983) 2
    • Sheldon, R.A.1
  • 7
    • 0000580987 scopus 로고    scopus 로고
    • Theoretical studies of some transition-metal-mediated reactions of industrial and synthetic importance
    • Torrent M, Sola M, Frenking G. Theoretical studies of some transition-metal-mediated reactions of industrial and synthetic importance. Chem Rev. 2000; 100: 439-493.
    • (2000) Chem Rev. , vol.100 , pp. 439-493
    • Torrent, M.1    Sola, M.2    Frenking, G.3
  • 9
    • 0005187574 scopus 로고    scopus 로고
    • Synthesis and reactions of alkyl cobalt and acyl cobalt tetracarbonyls
    • Heck RF. Synthesis and reactions of alkyl cobalt and acyl cobalt tetracarbonyls. Adv Organomet Chem. 1996; 4: 243-266.
    • (1996) Adv Organomet Chem. , vol.4 , pp. 243-266
    • Heck, R.F.1
  • 10
    • 84948293821 scopus 로고
    • Mechanism of the oxo reaction
    • Orchin M, Rupilius W. Mechanism of the oxo reaction. Catal Rev. 1972; 6: 85-131.
    • (1972) Catal Rev. , vol.6 , pp. 85-131
    • Orchin, M.1    Rupilius, W.2
  • 11
    • 46649113067 scopus 로고
    • Transition metal clusters in homogeneous catalysis
    • Suess-Fink G, Meister G. Transition metal clusters in homogeneous catalysis. Adv Organomet Chem. 1993; 35: 41-134.
    • (1993) Adv Organomet Chem. , vol.35 , pp. 41-134
    • Suess-Fink, G.1    Meister, G.2
  • 12
    • 0001212031 scopus 로고    scopus 로고
    • Catalytic conversions in water: environmentally attractive processes employing water soluble transition metal complexes
    • Papadogianakis G, Sheldon RA. Catalytic conversions in water: environmentally attractive processes employing water soluble transition metal complexes. New J Chem. 1996; 20: 175-185.
    • (1996) New J Chem. , vol.20 , pp. 175-185
    • Papadogianakis, G.1    Sheldon, R.A.2
  • 14
    • 33947299262 scopus 로고
    • Low-pressure system for producing normal aldehydes by hydroformylation of α-olefins
    • Pruett RL, Smith JA. Low-pressure system for producing normal aldehydes by hydroformylation of α-olefins. J Org Chem. 1969; 34: 327-330.
    • (1969) J Org Chem. , vol.34 , pp. 327-330
    • Pruett, R.L.1    Smith, J.A.2
  • 16
    • 34347271804 scopus 로고    scopus 로고
    • Hydroformylation of alkenes: an industrial view of the status and importance
    • Bohnen HW, Cornils B. Hydroformylation of alkenes: an industrial view of the status and importance. Adv Catal. 2002; 47: 1-64.
    • (2002) Adv Catal. , vol.47 , pp. 1-64
    • Bohnen, H.W.1    Cornils, B.2
  • 17
    • 0035970275 scopus 로고    scopus 로고
    • Kinetic modeling of homogeneous catalytic processes
    • Chaudhari RV, Seayad A, Jayasree S. Kinetic modeling of homogeneous catalytic processes. Catal Today. 2001; 66: 371-380.
    • (2001) Catal Today. , vol.66 , pp. 371-380
    • Chaudhari, R.V.1    Seayad, A.2    Jayasree, S.3
  • 20
    • 77956809530 scopus 로고
    • The kinetics of some industrial heterogeneous catalytic reactions
    • Temkin MI. The kinetics of some industrial heterogeneous catalytic reactions. Adv Catal. 1979; 28: 173-281.
    • (1979) Adv Catal. , vol.28 , pp. 173-281
    • Temkin, M.I.1
  • 22
    • 47749109871 scopus 로고    scopus 로고
    • Kinetic modeling of propene hydroformylation with Rh/TPP and Rh/CHDPP catalysts
    • Bernas A, Mäki-Arvela P, Lehtonen J, Salmi T, Murzin DY. Kinetic modeling of propene hydroformylation with Rh/TPP and Rh/CHDPP catalysts. Ind Eng Chem Res. 2008; 47: 4317-4324.
    • (2008) Ind Eng Chem Res. , vol.47 , pp. 4317-4324
    • Bernas, A.1    Mäki-Arvela, P.2    Lehtonen, J.3    Salmi, T.4    Murzin, D.Y.5
  • 23
    • 71649098584 scopus 로고    scopus 로고
    • Kinetic modeling of regioselectivity in alkenes hydroformylation over rhodium
    • Murzin DY, Bernas A, Salmi T. Kinetic modeling of regioselectivity in alkenes hydroformylation over rhodium. J Mol Catal A: Chem. 2010; 215: 148-154.
    • (2010) J Mol Catal A: Chem. , vol.215 , pp. 148-154
    • Murzin, D.Y.1    Bernas, A.2    Salmi, T.3
  • 25
    • 0033303388 scopus 로고    scopus 로고
    • Perspectives of rhodium organometallic catalysis. Fundamental and applied aspects of hydroformylation
    • 883-900.
    • Trzeciak AM, Ziolkowski JJ. Perspectives of rhodium organometallic catalysis. Fundamental and applied aspects of hydroformylation. Coord Chem Rev. 1999; 190-192: 883-900.
    • (1999) Coord Chem Rev. , pp. 190-192
    • Trzeciak, A.M.1    Ziolkowski, J.J.2
  • 26
    • 0006300735 scopus 로고
    • Intermediates or their analogues in hydroformylation of alkenes catalysed by hydridocarbonyltris-(triphenylphosphine)rhodium(I)
    • Yagupsky G, Brown CK, Wilkinson G. Intermediates or their analogues in hydroformylation of alkenes catalysed by hydridocarbonyltris-(triphenylphosphine)rhodium(I). Chem Commun. 1969; 1244-1245.
    • (1969) Chem Commun. , pp. 1244-1245
    • Yagupsky, G.1    Brown, C.K.2    Wilkinson, G.3
  • 27
    • 37049128684 scopus 로고
    • Further studies on hydridocarbonyltris(triphenylphosphine)rhodium(I); intermediate species in hydroformylation; rhodium and iridium Analogues
    • Yagupsky G, Brown CK, Wilkinson G. Further studies on hydridocarbonyltris(triphenylphosphine)rhodium(I); intermediate species in hydroformylation; rhodium and iridium Analogues. J Chem Soc A. 1970; 1392-1401.
    • (1970) J Chem Soc A. , pp. 1392-1401
    • Yagupsky, G.1    Brown, C.K.2    Wilkinson, G.3
  • 30
    • 37049124551 scopus 로고
    • Hydroformylation of alkenes by use of rhodium complex catalysts
    • Evans D, Osborn JA, Wilkonson G. Hydroformylation of alkenes by use of rhodium complex catalysts. J Chem Soc A. 1968; 3131-3142.
    • (1968) J Chem Soc A. , pp. 3131-3142
    • Evans, D.1    Osborn, J.A.2    Wilkonson, G.3
  • 31
    • 2142653402 scopus 로고
    • The reaction of hydridocarbonyltris-(triphenylphosphine)rhodium with carbon monoxide, and of the reaction products, hydridodicarbonylbis(triphenylphosphine)rhodium and dimeric species, with hydrogen
    • Evans D, Yagupsky G, Wilkinson G. The reaction of hydridocarbonyltris-(triphenylphosphine)rhodium with carbon monoxide, and of the reaction products, hydridodicarbonylbis(triphenylphosphine)rhodium and dimeric species, with hydrogen, J Chem Soc A. 1968; 2660-2665.
    • (1968) J Chem Soc A. , pp. 2660-2665
    • Evans, D.1    Yagupsky, G.2    Wilkinson, G.3
  • 33
    • 69249102369 scopus 로고    scopus 로고
    • Kinetics and mechanism of propene hydroformylation catalyzed by rhodium complexes with a diphosphite ligand
    • Rush SN, Noskov YuG, Kron TE, Korneeva GA. Kinetics and mechanism of propene hydroformylation catalyzed by rhodium complexes with a diphosphite ligand. Kinet Catal. 2009; 50: 557-566.
    • (2009) Kinet Catal. , vol.50 , pp. 557-566
    • Rush, S.N.1    Noskov, Y.2    Kron, T.E.3    Korneeva, G.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.