Abstract
The enantioselectivity found in homogeneous isospecific Ziegler–Natta catalysts for the insertion of 1‐alkenes in metal–deuterium or in metalisobutyl bonds is discussed from a theoretical point of view. Nonbonded energy calculations, based on a model of the catalytic site previously proposed by us, indicate that the strong enantioselectivity found in the insertion of 1‐alkenes in a metal–isobutyl bond is drastically reduced in the presence of a metal–deuterium bond. In particular, a weak enantioselectivity in favour of a monomer coordinated with the opposite chirality (lower for the case of 1‐butene, higher for the case of styrene) is shown to occur in the latter case.
Original language | English (US) |
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Pages (from-to) | 299-306 |
Number of pages | 8 |
Journal | Chirality |
Volume | 3 |
Issue number | 4 |
DOIs | |
State | Published - 1991 |
Externally published | Yes |
Keywords
- 1‐pentene
- conformational analysis
- metallocene/methylalumoxane systems
- nonbonded interactions
- styrene
ASJC Scopus subject areas
- Drug Discovery
- Analytical Chemistry
- Spectroscopy
- Catalysis
- Pharmacology
- Organic Chemistry