Reactivity of Terminal Iron Borylenes and Bis(borylenes) with Carbodiimides: Cycloaddition, Metathesis, Insertion and C−H Activation Pathways

التفاصيل البيبلوغرافية
العنوان: Reactivity of Terminal Iron Borylenes and Bis(borylenes) with Carbodiimides: Cycloaddition, Metathesis, Insertion and C−H Activation Pathways
المؤلفون: Carsten Lenczyk, Alexander Hermann, Alexander Hofmann, Holger Braunschweig, Fabian Schorr, Merle Arrowsmith, Alexander Matler
المصدر: European Journal of Inorganic Chemistry. 2021:4619-4631
بيانات النشر: Wiley, 2021.
سنة النشر: 2021
مصطلحات موضوعية: Inorganic Chemistry, Reaction mechanism, Terminal (electronics), Chemistry, Stereochemistry, X-ray crystallography, Reactivity (chemistry), ddc:546, Metathesis, Cycloaddition
الوصف: The reactions of carbodiimides with the iron arylborylene complex [Fe=BDur(CO)\(_{3}\)(PMe\(_{3}\))] (Dur=2,3,5,6-Me\(_{4}\)C\(_{6}\)H) and the iron bis(borylene) complex [Fe{=BDur}{=BN(SiMe\(_{3}\))\(_{2}\)}(CO)\(_{3}\)] yield a wide variety of temperature-dependent products, including known FeBNC and novel FeBNB metallacycles, complexes of N-heterocyclic boracarbene and spiro-boracarbene ligands and a unique 1,3,2,4-diazadiborolyl pianostool complex, characterized by NMR spectroscopy and X-ray crystallography. The product distributions can be rationalized by considering sequences of cycloaddition, metathesis, insertion, and C−H activation pathways mainly governed by sterics.
وصف الملف: application/pdf
تدمد: 1099-0682
1434-1948
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf6f44da35dea79a3bf904997b39cd07
https://doi.org/10.1002/ejic.202100629
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....cf6f44da35dea79a3bf904997b39cd07
قاعدة البيانات: OpenAIRE