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Volumn 29, Issue 24, 2010, Pages 6723-6731

Oligomerization of ethylene using new tridentate iron catalysts bearing α-diimine ligands with pendant S and P donors

Author keywords

[No Author keywords available]

Indexed keywords

ACENAPHTHENEQUINONE; ACTIVE CATALYST; COORDINATION COMPOUNDS; CRYSTALLOGRAPHIC STUDIES; DIIMINE COMPLEXES; DIIMINE LIGAND; DONOR ATOMS; ETHYLENE OLIGOMERIZATIONS; IRON CATALYST; IRON CHLORIDES; IRON COMPLEX; P DONORS; PRECATALYSTS; PRIMARY AMINES; PRODUCT DISTRIBUTIONS; SCHIFF BASE CONDENSATION; SOLID-STATE STRUCTURES; STRUCTURAL VARIABILITY;

EID: 78650653553     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om1007743     Document Type: Article
Times cited : (50)

References (48)
  • 9
    • 78650676274 scopus 로고    scopus 로고
    • (BP Amoco) U.S. Patent 5968866
    • Wu, F.-J. (BP Amoco) U.S. Patent 5968866, 1999.
    • (1999)
    • Wu, F.-J.1
  • 18
    • 78650656310 scopus 로고
    • CPChem's proprietary 1-hexene process is based on Cr-pyrrole complexes.; (Phillips) U.S. Patent 5198563
    • CPChem's proprietary 1-hexene process is based on Cr-pyrrole complexes. Reagan, W. K.; Conroy, B. K. (Phillips) U.S. Patent 5198563, 1993.
    • (1993)
    • Reagan, W.K.1    Conroy, B.K.2
  • 20
    • 78650653423 scopus 로고    scopus 로고
    • (CPChem) U.S. Patent 7476775
    • Kreischer, B. E. (CPChem) U.S. Patent 7476775, 2009.
    • (2009)
    • Kreischer, B.E.1
  • 21
    • 78650668780 scopus 로고    scopus 로고
    • (CPChem) U.S. Patent 7396970
    • Battiste, D. R. (CPChem) U.S. Patent 7396970, 2008.
    • (2008)
    • Battiste, D.R.1
  • 26
    • 78650646936 scopus 로고    scopus 로고
    • Recent press releases have indicated that other companies are intent on producing 1-hexene via selective ethylene trimerization
    • Recent press releases have indicated that other companies are intent on producing 1-hexene via selective ethylene trimerization.
  • 27
    • 78650633590 scopus 로고    scopus 로고
    • ExxonMobil and Texas Petrochemicals can produce 1-butene by distillation from raffinate streams
    • ExxonMobil and Texas Petrochemicals can produce 1-butene by distillation from raffinate streams.
  • 28
    • 78650646712 scopus 로고    scopus 로고
    • Sasol extracts η±-olefins in the comonomer range by distilling them from Fischer-Tropsch hydrocarbon streams. Sasol has also employed successive hydroformylation, hydrogenation, and alcohol dehydration to convert the odd-carbon-number olefins to even-numbered comonomer olefins, i.e., 1-heptene into 1-octene
    • Sasol extracts η±-olefins in the comonomer range by distilling them from Fischer-Tropsch hydrocarbon streams. Sasol has also employed successive hydroformylation, hydrogenation, and alcohol dehydration to convert the odd-carbon-number olefins to even-numbered comonomer olefins, i.e., 1-heptene into 1-octene.
  • 29
    • 78650635523 scopus 로고
    • Dow has recently constructed a plant in Spain to prepare 1-octene from butadiene: (Dow) U.S. Patent 5254782
    • Dow has recently constructed a plant in Spain to prepare 1-octene from butadiene: Schaart, B. J.; Pelt, H. L.; Jacobsen, G. B. (Dow) U.S. Patent 5254782, 1993.
    • (1993)
    • Schaart, B.J.1    Pelt, H.L.2    Jacobsen, G.B.3
  • 33
    • 78650676051 scopus 로고    scopus 로고
    • (CPChem) U.S. Patent 7268096
    • Small, B. L.; Carney, M. J. (CPChem) U.S. Patent 7268096, 2007.
    • (2007)
    • Small, B.L.1    Carney, M.J.2
  • 34
    • 78650649396 scopus 로고    scopus 로고
    • (CPChem) U.S. Patent 7129304
    • Small, B. L.; Carney, M. J. (CPChem) U.S. Patent 7129304, 2006.
    • (2006)
    • Small, B.L.1    Carney, M.J.2
  • 35
    • 78650639346 scopus 로고    scopus 로고
    • (CPChem) U.S. Patent 7271121
    • Small, B. L.; Carney, M. J. (CPChem) U.S. Patent 7271121, 2007.
    • (2007)
    • Small, B.L.1    Carney, M.J.2
  • 42
    • 0004072929 scopus 로고
    • Wiley: New York,; Coll
    • Kuhn, W. E. Organic Syntheses; Wiley: New York, 1943; Coll. Vol. 2, p 447.
    • (1943) Organic Syntheses , vol.2 , pp. 447
    • Kuhn, W.E.1
  • 43
    • 18444366072 scopus 로고    scopus 로고
    • V. 3.60; Rigaku Corporation and Rigaku/MSC
    • CrystalStructure V. 3.60; Rigaku Corporation and Rigaku/MSC, 2004.
    • (2004) CrystalStructure
  • 44
    • 0004150157 scopus 로고    scopus 로고
    • V. 6.10; Bruker AXS: Madison, WI
    • SHELXTL V. 6.10; Bruker AXS: Madison, WI, 2000.
    • (2000) SHELXTL
  • 45
    • 78650669269 scopus 로고    scopus 로고
    • V5.054; Bruker Analytical X-ray Systems: Madison, WI
    • SMART V5.054; Bruker Analytical X-ray Systems: Madison, WI, 2001.
    • (2001) SMART
  • 46
    • 84977289324 scopus 로고
    • An empirical correction for absorption anisotropy
    • An empirical correction for absorption anisotropy: Blessing, R. Acta Crystallogr. 1995, A51, 33-38
    • (1995) Acta Crystallogr. , vol.51 , pp. 33-38
    • Blessing, R.1
  • 47
    • 78650673008 scopus 로고    scopus 로고
    • V6.45; Bruker Analytical X-Ray Systems: Madison, WI
    • SAINT+ V6.45; Bruker Analytical X-Ray Systems: Madison, WI, 2003.
    • (2003) SAINT+
  • 48
    • 0004150157 scopus 로고    scopus 로고
    • V6.14; Bruker Analytical X-Ray Systems: Madison, WI
    • SHELXTL V6.14; Bruker Analytical X-Ray Systems: Madison, WI, 2000.
    • (2000) SHELXTL


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.