Ni(ii) complexes bearing pyrrolide-imine ligands with pendant N-, O- and S-donor groups: synthesis, structural characterization and use in ethylene oligomerization. Issue 111 (26th October 2015)
- Record Type:
- Journal Article
- Title:
- Ni(ii) complexes bearing pyrrolide-imine ligands with pendant N-, O- and S-donor groups: synthesis, structural characterization and use in ethylene oligomerization. Issue 111 (26th October 2015)
- Main Title:
- Ni(ii) complexes bearing pyrrolide-imine ligands with pendant N-, O- and S-donor groups: synthesis, structural characterization and use in ethylene oligomerization
- Authors:
- Pinheiro, A. C.
Virgili, A. H.
Roisnel, T.
Kirillov, E.
Carpentier, J.-F.
Casagrande, O. L. - Abstract:
- Abstract : Nickel complexes bearing pyrrolide-imine ligands with pendant N-, O- and S-donor groups have been synthesized and their catalytic behavior in ethylene oligomerization has been investigated. Abstract : A series of new Ni(ii ) complexes of general formula {L}NiCl [Ni1, L = 2-(C4 H3 N-2′-CHN)C2 H4 NHPh;Ni2, L = 5- tert -butyl-2-(C4 H2 N-2′-CHN)C2 H4 NHPh;Ni3, L = 2-(C4 H3 N-2′-CHN)C2 H4 OPh;Ni4, L = 2-(C4 H3 N-2′-CHN)C6 H4 -2′-OPh;Ni5, L = 2-(C4 H3 N-2′-CHN)C6 H4 -2′-SPh;Ni6, L = 2-(C4 H3 N-2′-CHN)CH2 C6 H4 -2′-OMe] were prepared and fully characterized. All nickel precatalysts, activated with methylaluminoxane (MAO), exhibited moderate to good activities for ethylene oligomerization [TOF = 6.1–71.3 × 10 3 mol (C2 H4 ) (mol (Ni) −1 h −1 )] and producing high selectivities for 1-butene (68.3–94.0 wt%). The catalytic performance was substantially affected by the ligand environment regarding the pendant oxygen- and sulfur-donor groups, and the substituents on the pyrrolide group. Activation of nickel precatalystNi3 with ethylaluminum sesquichloride (Et3 Al2 Cl3, EASC) instead of MAO produced a significantly more productive catalyst system thanNi2 /MAO (TOF = 153 700 vs. 43 500 mol (C2 H4 ) (mol (Ni) −1 h −1 )); however, the 1-butene selectivity was drastically reduced, attaining only 53 wt% with a concomitant production of larger amounts of internal butenes (38 wt%). Under optimized conditions ([Ni] = 10 μmol, 30 °C, oligomerization time = 20 min, 20 bar ethylene,Abstract : Nickel complexes bearing pyrrolide-imine ligands with pendant N-, O- and S-donor groups have been synthesized and their catalytic behavior in ethylene oligomerization has been investigated. Abstract : A series of new Ni(ii ) complexes of general formula {L}NiCl [Ni1, L = 2-(C4 H3 N-2′-CHN)C2 H4 NHPh;Ni2, L = 5- tert -butyl-2-(C4 H2 N-2′-CHN)C2 H4 NHPh;Ni3, L = 2-(C4 H3 N-2′-CHN)C2 H4 OPh;Ni4, L = 2-(C4 H3 N-2′-CHN)C6 H4 -2′-OPh;Ni5, L = 2-(C4 H3 N-2′-CHN)C6 H4 -2′-SPh;Ni6, L = 2-(C4 H3 N-2′-CHN)CH2 C6 H4 -2′-OMe] were prepared and fully characterized. All nickel precatalysts, activated with methylaluminoxane (MAO), exhibited moderate to good activities for ethylene oligomerization [TOF = 6.1–71.3 × 10 3 mol (C2 H4 ) (mol (Ni) −1 h −1 )] and producing high selectivities for 1-butene (68.3–94.0 wt%). The catalytic performance was substantially affected by the ligand environment regarding the pendant oxygen- and sulfur-donor groups, and the substituents on the pyrrolide group. Activation of nickel precatalystNi3 with ethylaluminum sesquichloride (Et3 Al2 Cl3, EASC) instead of MAO produced a significantly more productive catalyst system thanNi2 /MAO (TOF = 153 700 vs. 43 500 mol (C2 H4 ) (mol (Ni) −1 h −1 )); however, the 1-butene selectivity was drastically reduced, attaining only 53 wt% with a concomitant production of larger amounts of internal butenes (38 wt%). Under optimized conditions ([Ni] = 10 μmol, 30 °C, oligomerization time = 20 min, 20 bar ethylene, [Al]/[Ni] = 250), precatalystNi3 led to a TOF = 55 900 mol (C2 H4 ) (mol (Ni) −1 h −1 ) and 82.8 wt% selectivity for 1-butene. … (more)
- Is Part Of:
- RSC advances. Volume 5:Issue 111(2015)
- Journal:
- RSC advances
- Issue:
- Volume 5:Issue 111(2015)
- Issue Display:
- Volume 5, Issue 111 (2015)
- Year:
- 2015
- Volume:
- 5
- Issue:
- 111
- Issue Sort Value:
- 2015-0005-0111-0000
- Page Start:
- 91524
- Page End:
- 91531
- Publication Date:
- 2015-10-26
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5ra16782e ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1118.xml