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|Title:||Ligand effect on ethylene trimerisation with [NNN]-heteroscorpionate pyrazolyl Cr(III) catalysts||Authors:||Zhang, J.
|Issue Date:||2009||Citation:||Zhang, J., Li, A., Hor, T.S.A. (2009). Ligand effect on ethylene trimerisation with [NNN]-heteroscorpionate pyrazolyl Cr(III) catalysts. Dalton Transactions (42) : 9327-9333. ScholarBank@NUS Repository. https://doi.org/10.1039/b909685j||Abstract:||Cr(III) complexes with [NNN]-heteroscorpionate pyrazolyl ligands of the type Pz'2CHX (Pz' = pyrazol-l-yl (Pz), or 3,5-dimethylpyrazol-1-yl (PzMe); X = N-containing heterocyclic ring or amine CH 2NR1R2; R1, R2 = H or alkyl) have been prepared. Upon activation with MAO, they are active for selective ethylene trimerisation to 1-hexene. The effects of the hetero-functional group and chelate ring size on the catalytic performance have been examined. The pre-catalysts with an N-heterocycle substituent show highest activity [32400-53000 g/(g Cr h-1)] and total C6 selectivities (>97.6%) as well as 1-hexene selectivity (>96.0%) among hexenes. The X-ray single-crystal crystallographic analysis of CrCl 3[PzMe 2CH2NCH2Ph] and CrCl3[PzMe 2CH2NCH2Fc] (Fc = ferrocenyl) shows a tridentate coordination on the fac-octahedral Cr(III) sphere with the Cr-N bond length dependent on the N-substituent. © 2009 The Royal Society of Chemistry.||Source Title:||Dalton Transactions||URI:||http://scholarbank.nus.edu.sg/handle/10635/94147||ISSN:||14779226||DOI:||10.1039/b909685j|
|Appears in Collections:||Staff Publications|
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