Please use this identifier to cite or link to this item:
https://doi.org/10.1021/om0701322
DC Field | Value | |
---|---|---|
dc.title | A strange nickel(I)-nickel(0) binuclear complex and its unexpected ethylene oligomerization | |
dc.contributor.author | Weng, Z. | |
dc.contributor.author | Teo, S. | |
dc.contributor.author | Liu, Z.-P. | |
dc.contributor.author | Andy Hor, T.S. | |
dc.date.accessioned | 2014-10-16T08:19:23Z | |
dc.date.available | 2014-10-16T08:19:23Z | |
dc.date.issued | 2007-06-04 | |
dc.identifier.citation | Weng, Z., Teo, S., Liu, Z.-P., Andy Hor, T.S. (2007-06-04). A strange nickel(I)-nickel(0) binuclear complex and its unexpected ethylene oligomerization. Organometallics 26 (12) : 2950-2952. ScholarBank@NUS Repository. https://doi.org/10.1021/om0701322 | |
dc.identifier.issn | 02767333 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/93012 | |
dc.description.abstract | The unusual heterovalent bimetallic Ni1-Ni0 complex {[η-C5H4CH=N(C6F5)]Fe[η- C5H4PPh2]}2Ni2(Cl) (2) was isolated from the reaction between [η-C5H4CH= N(C6F5)]Fe[η-C5H4PPh 2] (1) and Ni(COD)2 in the presence of AlEtCl2 or AlCl3. Complex 2 has been crystallographically characterized and theoretically analyzed; it is catalytically active (TOF 90 500) and selective (91%) toward the formation of C4 oligomers from ethylene (300 psi) at 30 °C, the only other significant isomer formed being C6. © 2007 American Chemical Society. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/om0701322 | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1021/om0701322 | |
dc.description.sourcetitle | Organometallics | |
dc.description.volume | 26 | |
dc.description.issue | 12 | |
dc.description.page | 2950-2952 | |
dc.description.coden | ORGND | |
dc.identifier.isiut | 000246764400002 | |
Appears in Collections: | Staff Publications |
Show simple item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.