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Record W2041836626 · doi:10.1039/b908737k

Frustrated Lewis pairs derived from N-heterocyclic carbenes and Lewis acids

2009· article· en· W2041836626 on OpenAlexaff
P.A. Chase, A.L. Gille, Thomas M. Gilbert, Douglas W. Stephan

Bibliographic record

VenueDalton Transactions · 2009
Typearticle
Languageen
FieldChemistry
TopicOrganoboron and organosilicon chemistry
Canadian institutionsUniversity of Toronto
Fundersnot available
KeywordsFrustrated Lewis pairLewis acids and basesDeprotonationChemistryBoraneAdductCarbeneBoranesMedicinal chemistrySalt (chemistry)Amine gas treatingBoronStereochemistryOrganic chemistryCatalysisIon

Abstract

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The chemistry of frustrated Lewis pairs derived from N-heterocyclic carbenes and a number of Lewis acids has been probed. The combination of 1,3-bis[2,6-(di-iso-propyl)phenyl]-1,3-imidazol-2-ylidene (IDipp) (1) with B(C6F5)3 was shown to give the classical Lewis acid-base adduct (IDipp)B(C6F5)3 (2) which was unreactive. In contrast, the combination 1,3-di-tert-butyl-1,3-imidazol-2-ylidene (3) with B(C6F5)3 proved to form a frustrated Lewis pair, and reacts with H2 to give the salt [ItBuH][HB(C6F5)3] (4) in high yield. In a similar fashion, addition of (3) to a series of amine-borane adducts including H3NB(C6F5)3 (5), PhH2NB(C6F5)3 (6) and PhH2NB(C6F5)3 (7) led to deprotonation and formation of imidazolium amido-borate salts [ItBuH][H2NB(C6F5)3] (8), [ItBuH][PhHNB(C6F5)3] (9) and [ItBuH][Ph2NB(C6F5)3] (10). Similar reactions of the amine-borane adducts EtNH2B(C6F5)3 (11) tBuNH2B(C6F5)3 (12) and Et2NHB(C6F5)3 (13) gave the amidoboranes EtHNB(C6F5)2 (14) tBuHNB(C6F5)2 (15) and Et2NB(C6F5)2 (16) respectively, with liberation of C6F5H and an equivalent of unreacted carbene. Mechanistically these reactions are thought to proceed through transient imidazolium salts similar to (8)-(10). In addition, the combination of carbene (3) and the cation [CPh3]+ in frustrated Lewis pair chemistry has been probed. Reaction of this combination at room temperature results in the immediate formation of [C3H2N2tBu2(C6H5)CPh2][B(C6F5)4] (17) stemming from carbene attack at a para-carbon of one of the phenyl rings of trityl. Addition of carbene to the benzyl amine adduct of [CPh3][B(C6F5)4] results in the formation of [ItBuH][B(C6F5)4] (18) and the secondary amine Ph3CNHCH2Ph (19), thus providing the first example of an all carbon-based frustrated Lewis pair. Crystallographic data for (2), (4), (9) and (13) are reported.

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 score0.006

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 communication0.0000.001
Open science0.0000.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

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 head0.012
GPT teacher head0.227
Teacher spread0.215 · 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

Citations109
Published2009
Admission routes1
Has abstractyes

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Same venueDalton TransactionsSame topicOrganoboron and organosilicon chemistryFrench-language works237,207