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Record W2300575345 · doi:10.14288/1.0061128

Exploring and exploiting Ruthenium-porphyrin complexes : functionalization, atropisomerism, small-molecule recognition, catalysis, and biological implications

2010· article· en· W2300575345 on OpenAlexaff
Júlio S. Rebouças

Bibliographic record

VenueOpen Collections · 2010
Typearticle
Languageen
FieldChemistry
TopicAxial and Atropisomeric Chirality Synthesis
Canadian institutionsUniversity of British Columbia
Fundersnot available
KeywordsPorphyrinSurface modificationRutheniumChemistryCatalysisAtropisomerCombinatorial chemistrySmall moleculeMolecular recognitionMoleculeNanotechnologyPhotochemistryOrganic chemistryMaterials scienceBiochemistry

Abstract

fetched live from OpenAlex

This thesis represents a contribution to advances in ruthenium-porphyrin chemistry. The synthesis of Ru(carbonyl) porphyrins via a new metallation strategy using hexakis(N,N-dimethylformamide)ruthenium(III) triflate is examined in detail, covering a broad range of porphyrins. Mechanistic insights, advantages, and limitations of the methodology are also addressed. The method is also shown to be of value in the preparation of other related Ru macrocyclic complexes, such as those of tetradentate Schiff-bases. The direct β-functionalization of Ru(carbonyl) porphyrins is explored, as a convenient alternative for the Ru-metallation of β-functionalized free-bases. Specifically, protocols for β-octachlorination, β-octabromination, and β-mononitration are discussed. Electrochemical studies on Ru(carbonyl) porphyrins are explored as probes for investigating some structural aspects of these complexes. It is proposed that Ru complexation hinders distortion of the porphyrin ring from a planar configuration, and examination of literature crystallographic data is used to rationalize such a "Ru effect". The effect has direct consequences in hampering aryl-ring rotation in meso-tetraarylporphyrins, and this is exploited to yield the first examples of atropisomerism in non-ortho-substituted porphyrins containing non-bulky meta-substituents. Ruthenium porphyrins are used as models for studying several aspects of heme-proteins that contain S-donor ligands proximal to the heme moiety. The coordination capability of the Ru(porphyrin) moiety is explored for preparation of adducts with thiols, organic disulfides, and trisulfides. The reactions between Ru porphyrins and H₂S are also discussed. The steric and electronic effects involved in small-molecule recognition by simple metalloporphyrins using Ru porphyrins and thiols as probes are examined thoroughly. The model proposed to describe thiol coordination is also extended to another coordination system, that with primary amines, and represents a successful, general attempt to depict quantitatively the non-bonding interactions between axial ligands and the porphyrin plane. The implications of the findings within the thiol--Ru-porphyrin systems to the evolution of heme-thiol(ate) proteins are contemplated, and the application of the amine--Ru-porphyrin models to examine the interactions between primary amines and heme-proteins is demonstrated. The first studies on investigation of the O₂-oxidation of thiols catalyzed by Ru porphyrins are presented, together with a tentative mechanism that accommodates generally the kinetic and spectroscopic data. The ability of Ru porphyrins to perform O₂-oxidative N-dealkylations of tertiary amines, which is a classical cytochrome P450-catalyzed reaction, is also demonstrated. Finally, a simple (phosphine-free) RuCl₃-based, H₂-hydrogenation method is shown to be useful for the preparation of mesoporphyrin dimethyl ester.

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 categoriesScience and technology studies, Insufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.538
Threshold uncertainty score0.999

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 studies0.0030.000
Scholarly communication0.0010.000
Open science0.0000.000
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 head0.124
GPT teacher head0.257
Teacher spread0.133 · 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.

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

Citations0
Published2010
Admission routes1
Has abstractyes

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