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Record W1974425403 · doi:10.1021/ja994378c

The Mechanism of Methane Elimination in B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Initiated Monocyclopentadienyl-Ketimide Titanium and Related Olefin Polymerization Catalysts

2000· article· en· W1974425403 on OpenAlexaff
Suobo Zhang, Warren E. Piers, Xiaoliang Gao, Masood Parvez

Bibliographic record

VenueJournal of the American Chemical Society · 2000
Typearticle
Languageen
FieldChemistry
TopicOrganoboron and organosilicon chemistry
Canadian institutionsNova Chemicals (Canada)University of Calgary
Fundersnot available
KeywordsChemistryYield (engineering)AlkylMedicinal chemistryCatalysisAlkylationOlefin fiberLigand (biochemistry)Derivative (finance)StereochemistryOrganic chemistry

Abstract

fetched live from OpenAlex

A new class of monocyclopentadienyl titanium olefin polymerization catalysts and their activation with B(C 6 F 5 ) 3 is reported herein. Dichlorides Cp[ t Bu(R)C N]TiCl 2 {Cp = C 5 H 5, R = t Bu ( 1a ); Cp = C 5 Me 5, R = t Bu ( 2a ); Cp = C 5 Me 4 SiMe 3, R = t Bu ( 3a ); Cp = C 5 Me 5, R = CH 2 SiMe 3 ( 4a ); Cp = C 5 Me 5, R = Me ( 5a )} were prepared in 50−92% yield from CpTiCl 3 and t Bu(R)C NLi. Analogous dimethyl compounds 1b − 5b were prepare via methylation of dichlorides a using MeMgBr in 89−92% yield. Dimethyl compound 6b (L = C 5 Me 5, R = CH(SiMe 3 ) 2 ) was prepared directly from Cp*TiMe 3 and t Bu[(Me 3 Si) 2 CH]C NH in 40% yield. Dynamic 1 H NMR studies showed that the ketimide ligands in compounds b rotate rapidly about Ti−N on the NMR time scale, with a Δ G ‡ of 9.6(6) kcal mol - 1 or less. The mixed alkyl compound Cp*[ t Bu(R)C N]Ti(CH 3 )CH 2 SiMe 3 {R = t Bu ( 7 )} was prepared via alkylation of the corresponding methyl chloride derivative with BrMgCH 2 SiMe 3 . When treated with B(C 6 F 5 ) 3, compounds 1b − 6b are rapidly converted into the ion pairs {Cp[ t Bu(R)C N]TiCH 3 } + [H 3 C(B(C 6 F 5 ) 3 ] -, 1c − 6c; mixed alkyl compound 7 yields the ion pair [Cp*( t Bu 2 C N)TiCH 2 SiMe 3 ] + [H 3 C(B(C 6 F 5 ) 3 ] -, 7c, exclusively. Multinuclear NMR experiments show that ion pairing is tight in these compounds and that ketimide ligand rotation is occurring with a slightly higher barrier in comparison to the neutral derivatives b . Ion pairs 1c − 5c undergo a decomposition process involving loss of methane and producing the neutral compounds Cp[ t Bu(R)C N]Ti(C 6 F 5 )[CH 2 B(C 6 F 5 ) 2 ], 1d − 5d . The X-ray crystal structure of 1d has been determined. Active cationic compounds are not regenerated from neutral compounds d in the presence of B(C 6 F 5 ) 3 and thus this reaction is a potential deactivation pathway for these particular ion pairs. Detailed kinetic studies on the decomposition of 2c show the reaction to be first order in [ 2c ] with activation parameters of Δ H ‡ = 20.6(8) kcal mol - 1 and Δ S ‡ = −8.5(10) eu, corresponding to Δ G ‡ 298 of 23.1(8) kcal mol - 1 . A substantial kinetic isotope effect of k H / k D = 9.1(6) was measured using d 6 - 2c . Further mechanistic experiments, including crossover and examination of alkane elimination from mixed alkyl ion pair 7c, point to a σ-bond metathesis mechanism for the production of compounds d . The implications of our results for other, related catalyst systems are discussed.

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 machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation 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 score0.002
Threshold uncertainty score0.004

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

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 head0.217
Teacher spread0.211 · 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 source (direct Gemma or distilled Codex), 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

Citations135
Published2000
Admission routes1
Has abstractyes

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Same venueJournal of the American Chemical SocietySame topicOrganoboron and organosilicon chemistryFrench-language works237,207