Evidence map›Paper›PMID 25945516›Full record

ArticleJournal of the American Chemical Society2015

Mechanistic significance of the si-o-pd bond in the palladium-catalyzed cross-coupling reactions of arylsilanolates.

Steven A Tymonko, Russell C Smith, Andrea Ambrosi, Michael H Ober, Hao Wang, Scott E Denmark

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Kinetic Analysis of Transmetalation at Prototypical NickelAngewandte Chemie (International ed. in English) · 2026
    Article
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  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Understanding Site Selectivity in the Palladium-Catalyzed Cross-Coupling of Allenylsilanolates.Synlett : accounts and rapid communications in synthetic organic chemistry · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Article
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  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Steven A TymonkoRoger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, Illinois 61801, United States.
Russell C SmithRoger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, Illinois 61801, United States.
Andrea AmbrosiRoger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, Illinois 61801, United States.
Michael H OberRoger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, Illinois 61801, United States.
Hao WangRoger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, Illinois 61801, United States.
Scott E DenmarkRoger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, Illinois 61801, United States.

Funding

Organosilicon-Based Cross-Coupling ReactionsR01GM063167 · NIGMS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI DENMARK, SCOTT ERIC · 2002 to 2009
$2.5M
NIGMS NIH HHS GM R01-63167NIGMS NIH HHS R01 GM063167
6 · The paper itself

Abstract

Through the combination of reaction kinetics (both stoichiometric and catalytic), solution- and solid-state characterization of arylpalladium(II) arylsilanolates, and computational analysis, the intermediacy of covalent adducts containing Si-O-Pd linkages in the cross-coupling reactions of arylsilanolates has been unambiguously established. Two mechanistically distinct pathways have been demonstrated: (1) transmetalation via a neutral 8-Si-4 intermediate that dominates in the absence of free silanolate (i.e., stoichiometric reactions of arylpalladium(II) arylsilanolate complexes), and (2) transmetalation via an anionic 10-Si-5 intermediate that dominates in the cross-coupling under catalytic conditions (i.e., in the presence of free silanolate). Arylpalladium(II) arylsilanolate complexes bearing various phosphine ligands have been isolated, fully characterized, and evaluated for their kinetic competence under thermal (stoichiometric) and anionic (catalytic) conditions. Comparison of the rates for thermal and anionic activation suggested, but did not prove, that intermediates containing the Si-O-Pd linkage were involved in the cross-coupling process. The isolation of a coordinatively unsaturated, T-shaped arylpalladium(II) arylsilanolate complex ligated with t-Bu3P allowed the unambiguous demonstration of the operation of both pathways involving 8-Si-4 and 10-Si-5 intermediates. Three kinetic regimes were identified: (1) with 0.5-1.0 equiv of added silanolate (with respect to arylpalladium bromide), thermal transmetalation via a neutral 8-Si-4 intermediate; (2) with 1.0-5.0 equiv of added silanolate, activated transmetalation via an anionic 10-Si-5 intermediate; and (3) with >5.0 equiv of added silanolate, concentration-independent (saturation) activated transmetalation via an anionic 10-Si-5 intermediate. Transition states for the intramolecular transmetalation of neutral (8-Si-4) and anionic (10-Si-5) intermediates have been located computationally, and the anionic pathway is favored by 1.8 kcal/mol. The energies of all intermediates and transition states are highly dependent on the configuration around the palladium atom.

Indexed as

AnionsBromidesCatalysisHydrocarbons, AromaticKineticsLigandsModels, MolecularPalladiumSilanesThermodynamicsAnionsBromidesHydrocarbons, AromaticLigandsPalladiumSilanes

Identifiers

PMID25945516
PMCPMC4442671

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.