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Bonding Energies and Structural Study of Alkylaluminium

Bonding Energies and Structural Study of Alkylaluminium
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摘要 Neutral aluminium alkyls are well known to act as ethylene oligomerization and polymerization catalysts and cocatalysts.On the basis of the full optimization of alkylaluminium compounds with Gaussian 98 program package at the B3LYP/6-31G** level,the selected structures and bonding energies were investigated extensively.The geometries and bonding energies of AlR3(R = H,CH3,C2H5,C3H7,C4H9) and Al(C2H5)2R'(R' = C2H5,C3H7,C4H9,C5H11,C6H13) were investigated extensively,and we found that,along with the prolongation of carbon chains the terminal C-C bond is shortened gradually until to a constant value of about 0.1532 nm in C4H9;and the bonding energy almost remains constant.The dative bonding of C2H4 to Al(C2H5)3,whose bonding energy is only 15.30 kJ/mol,is very weak. Neutral aluminium alkyls are well known to act as ethylene oligomerization and polymerization catalysts and cocatalysts.On the basis of the full optimization of alkylaluminium compounds with Gaussian 98 program package at the B3LYP/6-31G** level,the selected structures and bonding energies were investigated extensively.The geometries and bonding energies of AlR3(R = H,CH3,C2H5,C3H7,C4H9) and Al(C2H5)2R'(R' = C2H5,C3H7,C4H9,C5H11,C6H13) were investigated extensively,and we found that,along with the prolongation of carbon chains the terminal C-C bond is shortened gradually until to a constant value of about 0.1532 nm in C4H9;and the bonding energy almost remains constant.The dative bonding of C2H4 to Al(C2H5)3,whose bonding energy is only 15.30 kJ/mol,is very weak.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2010年第6期833-838,共6页 结构化学(英文)
基金 supported by the National Natural Science Foundation of China (No. 10674099)
关键词 ALKYLALUMINIUM bonding energy molecular geometry steric effect alkylaluminium,bonding energy,molecular geometry,steric effect
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  • 1Bruce, M.; Gibson, V. C.; Redshaw, C.; Solan, G. A.; White, A. J. P.; Williams, D. J. Chem. Commun. 1998, 2523-2524.
  • 2Hill, A. F. Organotransition Metal Chemistry; Wiley-InterScience, New York 2002.
  • 3Kissin, Y. V. Alkene Polymer&ation Reactions with Transition Metal Catalysts; Elsevier, Amsterdam 2008.
  • 4Ziemkowska, W. Polyhedron 2002, 21,281-286.
  • 5Yang, X. E; Ni, X. F.; Shen, Z. Q. Chem. J. Chinese U. 2006, 27, 1561-1565.
  • 6Soga, K; Uozumi, T.; Saito, M.; Shiono, T. Macromol. Chem. Phys. 2003, 195, 1503-1515.
  • 7Scmikolcnova, N. V.; Zakharov, V. A. Macromol. Chem. Phys. 2003, 198, 2889-2897.
  • 8Guan, Z.; Zheng, Y.; Jiao, S. K. Acta Polym. Sin. 2001, 799-802.
  • 9Li, G L.; Dong, W. M.; Jiang, L. S.; Zhang, X. Q.; Wang, F. S. ChineseJ. Catal. 2005, 26, 879-883.
  • 10Zhong, C. E; Gao, M. Z.; Mao, B. Q. ActaPolym. Sin. 2006, 141-145.

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