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Volumn 321, Issue 1-2, 2010, Pages 71-76

Alkylalumination of arylacetylene catalyzed by zirconocene catalysts supported on solid materials

Author keywords

Modified SiO2; Supported zirconocene catalyst; Zr catalyzed alkylalumination

Indexed keywords

ANIONIC MOIETIES; ARYL ACETYLENES; CATALYTIC SYSTEM; CO CATALYSTS; HIGH ACTIVITY; METHYLALUMINOXANE; MONTMORILLONITE K10; OLEFIN POLYMERIZATION; SOLID MATERIAL; SOLVENT EFFECTS; SUPPORTING MATERIAL; TERMINAL ALKYNE; ZIRCONOCENE CATALYST; ZIRCONOCENES;

EID: 77949287800     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2010.02.004     Document Type: Article
Times cited : (3)

References (104)
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    • For recent reviews related to zirconocene catalyzed polymerization
    • For recent reviews related to zirconocene catalyzed polymerization:
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    • For recent reviews on zirconocene-catalyzed organic reactions in general:
  • 32
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    • For recent reviews related to the application of zirconocene-catalyzed alkylalumination in organic synthesis
    • For recent reviews related to the application of zirconocene-catalyzed alkylalumination in organic synthesis:
  • 47
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    • For reviews on supported ziroconocene catalysts
    • For reviews on supported ziroconocene catalysts:
  • 49
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    • (2000) Metallocene-Based Polyolefins , pp. 173
    • Chien, J.C.W.1
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    • (2000) Metallocene-Based Polyolefins , pp. 201
    • Hlatky, G.G.1
  • 52
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    • Y. Suga, Y. Maruyama, E. Isobe, T. Suziki, F. Shimizu, EP 0511 665 A2 (1992), to Mitsubishi Kasei Corporation.
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    • 77949302759 scopus 로고    scopus 로고
    • For some recent reports related to the application of zirconocene-catalyzed alkylalumination in organic synthesis
    • For some recent reports related to the application of zirconocene-catalyzed alkylalumination in organic synthesis:
  • 99
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    • For a related study see
    • For a related study see:
  • 102
    • 77949291439 scopus 로고    scopus 로고
    • Styrene 2c is favored over 2b because of a favorable interaction between the Lewis acidic zirconium atom and the aryl group in the zirconacycle precursor to 2c.
    • Styrene 2c is favored over 2b because of a favorable interaction between the Lewis acidic zirconium atom and the aryl group in the zirconacycle precursor to 2c.
  • 104
    • 77949283703 scopus 로고    scopus 로고
    • 2 for 24 h, a mixture of styrenes 2b-e and acetylene 1 was obtained (2b: 34%, 2c: 7%, 2d: 1%, 2e: 0.4%, 1: 12%).
    • 2 for 24 h, a mixture of styrenes 2b-e and acetylene 1 was obtained (2b: 34%, 2c: 7%, 2d: 1%, 2e: 0.4%, 1: 12%).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.