Abstract
We report the selective dimerization of propylene to branched hexenes using Ni-MFU-4l, a solid catalyst prepared by cation exchange. Analysis of the resulting product distribution demonstrates that the selectivity arises from 2,1-insertion and slow product reinsertion, mechanistic features reproduced by a molecular nickel tris-pyrazolylborate catalyst. Characterization of Ni-MFU-4l by X-ray absorption spectroscopy provides evidence for discrete, tris-pyrazolylborate-like coordination of nickel, underscoring the small-molecule analogy that can be made at metal-organic framework nodes.
Original language | English (US) |
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Pages (from-to) | 1681-1683 |
Number of pages | 3 |
Journal | Organometallics |
Volume | 36 |
Issue number | 9 |
DOIs | |
State | Published - May 8 2017 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry