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Enregistrement W2002597248 · doi:10.1021/om060758c

Cationic and Formally Zwitterionic Rhodium(I) and Iridium(I) Derivatives of a P,N-Substituted Indene:  A Comparative Synthetic, Structural, and Catalytic Investigation

2007· article· en· W2002597248 sur OpenAlexaff
J. Cipot, Robert McDonald, Michael J. Ferguson, G. Schatte, Mark Stradiotto

Notice bibliographique

RevueOrganometallics · 2007
Typearticle
Langueen
DomaineChemistry
ThématiqueOrganometallic Complex Synthesis and Catalysis
Établissements canadiensUniversity of SaskatchewanUniversity of AlbertaDalhousie University
Organismes subventionnairesnon disponible
Mots-clésChemistryIsostructuralIridiumRhodiumIndeneYield (engineering)Cationic polymerizationMedicinal chemistryCatalysisCrystal structureStereochemistryCrystallographyOrganic chemistry

Résumé

récupéré en direct d'OpenAlex

A family of neutral, cationic, and formally zwitterionic Rh(I) and Ir(I) complexes featuring 1-P i Pr 2 -2-NMe 2 -indene ( 3a ), 3-P i Pr 2 -2-NMe 2 -indene ( 3b ), or 3-P i Pr 2 -2-NMe 2 -indenide ( 3c ) ligands have been prepared and structurally characterized. Whereas treatment of 3a with 0.5 equiv of [(COD)RhCl] 2 afforded (COD)RhCl(κ 1 - P,N- 3a ) ( 4a ) in 96% isolated yield, [(COD)M(κ 2 - P, N - 3a )] + X - ([ 5a ] + PF 6 -, M = Rh; [ 6a ] + SO 3 CF 3 -, M = Ir) complexes were obtained in 14% and 41% isolated yield from 3a and the appropriate in-situ-prepared [(COD)M(THF) 2 ] + X - precursor. The isomeric complexes [(COD)M(κ 2 - P, N - 3b )] + X - ([ 5b ] + X -, M = Rh; [ 6b ] + X -, M = Ir) were prepared using a similar protocol employing NEt 3, with isolated yields ranging from 37% to 94% depending on the identity of M and X. The zwitterionic complexes (COD)M(κ 2 - P, N - 3c ) ( 5c, M = Rh; 6c, M = Ir) were prepared in 89% and 93% isolated yield, either upon treatment of [ 5b ] + X - or [ 6b ] + X - with NaN(SiMe 3 ) 2 or via addition of 0.5 equiv of [(COD)MCl] 2 to [ 3c ]Li. The Rh(I) complexes (CO)(Cl)Rh(κ 2 - P, N - 3b ) ( 7 ) and [(CO) 2 Rh(κ 2 - P, N - 3b )] + PF 6 - ( 8 ) were prepared in 43% and 66% isolated yield. Single-crystal X-ray diffraction data were obtained for 4a ·CH 2 Cl 2, [ 5b ] + BF 4 -, 5c, [ 6b ] + SO 3 CF 3 -, [ 6b ] + PF 6 -, 6c, and 7, the analysis of which revealed an effectively isostructural relationship among the metal coordination environments in [ 5b ] + X -, [ 6b ] + X -, 5c, and 6c . Despite the structural similarities that are apparent within the cation/zwitterion pairs [ 5b ] + X - / 5c and [ 6b ] + X - / 6c, reactivity studies involving these complexes highlighted important distinctions within and between these pairs of complexes. While both the κ 2 - P, N - 3b and the COD ligands in [ 5b ] + BF 4 - were displaced upon exposure to excess PMePh 2, under similar conditions only the COD ligand in 5c underwent substitution, affording (PMePh 2 ) 2 Rh(κ 2 - P, N - 3c ) ( 9 ) in 66% isolated yield. Temperature-dependent 1 H NMR line shape changes observed for 9 were rationalized in terms of the operation of at least one dynamic process in this complex (Δ G ⧧ 298 ≈ 14 kcal/mol). Further reactivity differences were observed when [ 5b ] + PF 6 -, [ 6b ] + PF 6 -, 5c, and 6c were employed as catalysts for the hydrogenation and hydrosilylation of alkenes. While [ 6b ] + PF 6 - proved to be the most effective styrene hydrogenation catalyst in CH 2 Cl 2 or THF, similarly high conversion to ethylbenzene was achieved by use of 5c as a catalyst in benzene, a solvent in which [ 5b ] + PF 6 - and [ 6b ] + PF 6 - are not soluble. The catalytic utility of 5c and 6c was demonstrated further in hydrosilylation reactions employing triethylsilane and styrene, wherein these zwitterionic complexes were observed to outperform their cationic relatives. While nearly quantitative yields were obtained by use of either 5c (toluene or THF) or 6c (1,2-dichloroethane or THF) as a catalyst, these complexes were found to exhibit remarkably high, but divergent, selectivity for E -1-triethylsilyl-2-phenylethene ( 10b ) and 1-triethylsilyl-2-phenylethane ( 10a ), respectively. By comparison, 10a and 10b were produced in a 1.3:1 ratio in reactions employing Crabtree's catalyst ([(COD)Ir(PCy 3 )(Py)] + PF 6 -, COD = η 4 -1,5-cyclooctadiene, Cy = cyclohexyl, Py = pyridine; 1 ) under similar conditions. When catalytic activity/selectivity and solvent compatibility are considered, the results of these catalytic studies suggest that zwitterionic species such as 5c and 6c represent an effective class of catalyst complexes for the addition of E−H bonds to unsaturated substrates, whose properties are in some cases complementary to those of more traditional Rh(I) and Ir(I) [(COD)M(κ 2 - P, N )] + X - salts.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction distillée sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.

score de la tête « metaresearch » (Codex)0,000
score de la tête « metaresearch » (Gemma)0,000
Version: codex-gemma-dda1882f352aStatut de validation: machine_predicted_unvalidated
Catégories candidatesMéta-épidémiologie (sens strict)
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Expérimental (laboratoire) · Signal consensuel: Expérimental (laboratoire)
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,273
Score d'incertitude au seuil1,000

Scores Codex et Gemma par catégorie

CatégorieCodexGemma
Métarecherche0,0000,000
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0010,000
Bibliométrie0,0000,000
Études des sciences et des technologies0,0000,001
Communication savante0,0000,000
Science ouverte0,0000,000
Intégrité de la recherche0,0000,000
Charge utile insuffisante (le modèle a refusé de juger)0,0010,000

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,021
Tête enseignante GPT0,245
Écart entre enseignants0,224 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule tête enseignante, pas un consensus.

Devis d'étudeExpérimental (laboratoire)
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations50
Publié2007
Routes d'admission1
Résumé présentoui

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