HEИндивидуална стипендия2022–2024

Cross-Bit · Bismuth Redox Catalysis for C–C Coupling Reactions

„Хоризонт Европа“ — Действия „Мария Склодовска-Кюри“

Период
2022-06-01 → 2024-05-31
Финансиране от ЕС
173 847 €
Участници
1
Схема
HORIZON-TMA-MSCA-PF-EF

Линиите свързват координатора с партньорите.

Накратко на български

Бизмутът се изследва като катализатор за създаване на нови химични връзки между въглерод и азот или въглерод и въглерод. Това помага за разработването на нови методи за изграждане на сложни молекули в лаборатории и индустрията.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Bismuth Redox Catalysis for C–C Coupling Reactions

The formation of C‒C and C‒heteroatom bonds through transition metal-catalyzed cross-coupling reactions represents the cornerstone strategy to build chemical complexity in a myriad of contexts, spanning from academic laboratories to industrial settings. These remarkable reactions generally proceed through three elementary steps—oxidative addition, transmetallation and reductive elimination—which couple two organic fragments together using transition-metal complexes as redox-active catalysts. Recently, bismuth—a main-group element—has been found to take part in this type of redox events, resulting in the formation of C–F and C–O bonds, or in H-transfer processes. However, at the outset of these investigations, the use of bismuth redox catalysis to forge the highly coveted and synthetically relevant C–C and C–N bonds remained elusive. In this project, we aimed at two main objectives: 1) The discovery and study of new fundamental organometallic steps in bismuth redox chemistry, with a focus on oxidative additions and formal reductive-elimination processes. 2) Harnessing this new redox behavior to unlock unprecedented bismuth-catalyzed cross-coupling catalytic cycles to forge new C–N and C–C bonds. Thus, we proposed the design of low-valent Bi(I/III) or Bi(I/II/III) redox platforms, cycling through key steps of classical transition metal-catalyzed couplings. We developed new types of oxidative-addition reactions, which were often found to follow unprecedented radical mechanisms. The study of these and other challenging steps, such as novel formal reductive-elimination processes from Bi(III), allowed forging new C–N and C–C bonds upon regeneration of Bi(I). Furthermore, all these processes could be aided by the introduction of photochemical steps, generating highly reactive excited-state bismuth complexes. All these findings converged in the development of novel bismuth catalyzed cross-coupling reactions that take place through a combination of radical and polar mechanisms. Besides the conceptual breakthrough derived from these discoveries, these ideas represent a proof-of-concept to implement bismuth-catalyzed cross-coupling reactions as competent, cheaper, and less toxic alternatives to traditional methods based on transition-metal catalysis.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Formation of CC bonds through transition metal-catalyzed cross-coupling represents the cornerstone strategy to build chemical complexity in a myriad of contexts, spanning from academic laboratories to industrial settings. These remarkable reactions generally proceed through three elementary steps oxidative addition, transmetallation and reductive elimination which couple two organic fragments together using transition-metal complexes as redox-active catalysts. Very recently, bismuth a main-group element has been found to take part in this type of redox events, resulting in the formation of different Cheteroatom bonds, or in H-transfer processes. However, the use of bismuth redox catalysis to forge the highly coveted and synthetically relevant CC bond remains elusive.In this project, we aim to harness this novel redox behavior of bismuth complexes to unlock the unprecedented bismuth-catalyzed CC cross-coupling full catalytic cycle between organic electrophiles and organometallic nucleophiles. For this, we propose the design of a low-valent bismuth(I/III) redox platform, which would cycle through the three key steps of a classical transition metal-mediated coupling. This will involve the study and optimization of challenging processes (such as an unprecedented CC reductive elimination at a bismuth(III) center), which will be approached through a combination of careful ligand design, experimental/theoretical mechanistic analysis, and combinatorial screenings.Besides the conceptual breakthrough derived from such discovery, this idea will be used to implement bismuth-catalyzed cross-coupling reactions as competent, cheaper, and less toxic alternatives to traditional methods based on transition-metal catalysis. Furthermore, the unique properties of bismuth as a main-group redox catalyst could potentially combine advantages of both early and late transition metals, resulting in the development of more versatile catalytic systems.

Оригинален текст от CORDIS (на английски).

Участници

  • MAX PLANCK INSTITUT FUER KOHLENFORSCHUNG · Muelheim An Der RuhrКоординаторГермания

Връзки

Данни: CORDIS, © Европейски съюз