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Phosphine and N-heterocyclic carbene ligands on Pt(II) shift selectivity from ethylene hydrophenylation toward benzene vinylation

Journal Article · · Journal of Organometallic Chemistry
 [1];  [2];  [3];  [3];  [3];  [2];  [3]
  1. Univ. of Virginia, Charlottesville, VA (United States); University of Virginia
  2. Brigham Young Univ., Provo, UT (United States)
  3. Univ. of Virginia, Charlottesville, VA (United States)

In this study, a series of Pt(II) complexes of the type ([(L~L)Pt(L')(Ph)][BAr'4] (L~L = 1,2-bis(dimethylphosphino)ethane, 1,2-bis(diphenylphosphino)ethane, (N-pyrrolyl)2P(CH2)2P(N-pyrrolyl)2, 1,3-bis(diphenylphosphino)propane, 1,1'-bis(diphenylphosphino)ferrocene, (bis-(diphenylphosphino)methyl)methylamine, 8-(diisopropylphosphino)quinoline, 1,1'-methylene-3,3'-di-tert-butylimidazol-2,2'-diylidine); L' = THF or NCMe) has been synthesized and fully characterized. These complexes were screened as catalysts for ethylene hydrophenylation to yield ethylbenzene. All of the complexes exhibited selectivity for styrene production with low catalytic turnover. DFT calculations have been used to model reactivity of the [(dmpe)Pt(L')(Ph)][BAr'4] (dmpe = 1,2-bis(dimethylphosphino)ethane). It is shown that selective styrene formation is a result of a calculated ΔΔG of 5 kcal/mol for the benzene C–H activation step in the catalytic cycles for styrene versus ethylbenzene formation.

Research Organization:
Univ. of Virginia, Charlottesville, VA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22). Chemical Sciences, Geosciences & Biosciences Division
Grant/Contract Number:
SC0000776
OSTI ID:
1607459
Alternate ID(s):
OSTI ID: 1343326
Journal Information:
Journal of Organometallic Chemistry, Journal Name: Journal of Organometallic Chemistry Journal Issue: C Vol. 793; ISSN 0022-328X
Publisher:
ElsevierCopyright Statement
Country of Publication:
United States
Language:
English

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