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Record W1975026852 · doi:10.1002/ejic.200700217

Steric and Electronic Effects in the Dimerization of Wanzlick Carbenes: The Alkyl Effect

2007· article· en· W1975026852 on OpenAlexafffund
Michael Denk, Azardokht Hezarkhani

Bibliographic record

VenueEuropean Journal of Inorganic Chemistry · 2007
Typearticle
Languageen
FieldChemistry
TopicN-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Canadian institutionsUniversity of Guelph
FundersNatural Sciences and Engineering Research Council of Canada
KeywordsSteric effectsChemistryAlkylIsopropylElectronic effectSubstituentMedicinal chemistryStereochemistryOrganic chemistry

Abstract

fetched live from OpenAlex

Abstract The steric and electronic influence of N ‐alkyl substituents on the dimerization energies Δ G ° of Wanzlick carbenes (imidazolidin‐2‐ylidenes) was investigated experimentally and through DFT methods for a series of non‐symmetrically substituted Wanzlick carbenes. A series of 3‐alkyl‐1‐ tert ‐butylimidazolidin‐2‐ylidenes with decreasing steric demand of the alkyl substituent (isopropyl, ethyl and methyl) were obtained in four steps from the commercially available N ‐alkylaminoethanol compounds. The carbenes are hydrolytically sensitive, colorless oils that can be distilled without decomposition and show no sign of dimerization to the respective enetetramines, even after prolonged heating. Calculations at the B98/6‐31G(d) level confirm that the dimerization of all three carbenes is thermodynamically unfavorable. To separate the steric and electronic stabilization of Wanzlick carbenes by N ‐alkyl substituents, the formation energies of R,H 3 mono‐alkyl enetetramines were used to derive electronic increments for the N ‐alkyl substituents. The computational data show that all alkyl substituents electronically stabilize Wanzlick carbenes vs. their dimerization products with increments ranging from 2.97 kcal mol –1 ( N ‐methyl) to as high as 6.28 kcal mol –1 ( N ‐ tert ‐butyl). For combinations of N ‐methyl, N ‐ethyl and N ‐isopropyl substituents, the increments are additive and the dimerization energies were found to be free of noticeably steric effects. Significant steric strain was found for all t Bu‐substituted carbenes with strain energies of the dimerization products ranging from 6.92 kcal mol –1 [formation of ( E )‐Me 2 t Bu 2 ‐enetetramine] to 24.23 kcal mol –1 (formation of t Bu 4 enetetramine). The tert ‐butyl substituent thus assumes a unique position by strongly stabilizing the carbenes electronically as well as sterically.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)

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)0.002
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 score0.011
Threshold uncertainty score0.865

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0020.000
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 science0.0010.000
Research integrity0.0000.001
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 head0.003
GPT teacher head0.197
Teacher spread0.195 · 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

Citations36
Published2007
Admission routes2
Has abstractyes

Explore more

Same venueEuropean Journal of Inorganic ChemistrySame topicN-Heterocyclic Carbenes in Organic and Inorganic ChemistryFrench-language works237,207