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Record W2031049312 · doi:10.1021/ja992987e

The Mechanism of Carbon−Carbon Bond Activation in Cationic 6-Alkylcyclohexadienyl Ruthenium Hydride Complexes

2000· article· en· W2031049312 on OpenAlexaff
Christina M. Older, Jeffrey M. Stryker

Bibliographic record

VenueJournal of the American Chemical Society · 2000
Typearticle
Languageen
FieldChemistry
TopicAsymmetric Hydrogenation and Catalysis
Canadian institutionsUniversity of Alberta
Fundersnot available
KeywordsChemistryRutheniumCationic polymerizationHydrideMechanism (biology)Carbon fibersReinforced carbon–carbonCarbon–carbon bondPhotochemistryPolymer chemistryOrganic chemistryCatalysisMetal

Abstract

fetched live from OpenAlex

Carbon−carbon bond activation in cationic 6- endo -methyl-η 5 -cyclohexadienyl and 6- exo -methyl-η 5 -cyclohexadienyl ruthenium hydride complexes has been investigated. Contrary to expectations, it is the 6- exo -methyl complex and not the stereoisomeric 6- endo -methyl complex that undergoes selective carbon−carbon bond activation under exceptionally mild conditions, quantitatively converting the 6- exo -methyl substituent and the hydride ligand to methane. The mechanism of the activation reaction involves dissociation of protic acid from the agostic starting complex by reaction with a weak base (typically water), followed by protolytic activation of the alkyl group, with “back-side” assistance from the nucleophilic metal center. Under the same conditions, the corresponding 6- endo -methyl isomer undergoes selective dehydrogenation rather than demethylation, despite the proximity of the endo -methyl substituent to the metal center. For both exo and endo isomers, the cationic ruthenium hydride intermediates were determined by spectroscopic analysis to adopt fluxional agostic structures. The agostic complexes are kinetically stable at room temperature under rigorously anhydrous conditions but convert quantitatively to cationic η 6 -arene products in the presence of a Brønsted base. The rates of both carbon−carbon bond activation and dehydrogenation are dependent on the identity and concentration of the base and suppressed in the presence of excess acid. The protolytic mechanism for carbon−carbon bond activation is supported by deuterium-labeling studies and by the reactivity of the neutral complexes toward Lewis acids and one-electron oxidants. This mechanism is shown to be relevant to carbon−carbon bond activation reactions observed in less-substituted 6- exo -methyl-η 5 -cyclohexadienyl complexes and in a steroid-derived 6,6-disubstituted-η 5 -cyclohexadienyl complex, representative of previously reported cases of dealkylative ligand aromatization. The low kinetic barrier for the protolytic dealkylation mechanism is contrasted to the comparatively high activation barriers reported for carbon−carbon bond activation reactions that occur in structurally related systems that cannot access a protolytic pathway. This investigation provides a consistent basis for rationalizing this potentially important but poorly understood class of metal-mediated reactions.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.007
Threshold uncertainty score0.335

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.006
GPT teacher head0.226
Teacher spread0.219 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations32
Published2000
Admission routes1
Has abstractyes

Explore more

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