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Mesoionic Carbenes: Exceptionally Electron-Rich Carbon-Donor Ligands in Synthesis, Catalysis, and Materials Science

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Organometallic Chemistry".

Deadline for manuscript submissions: closed (15 November 2019) | Viewed by 4134

Special Issue Editor


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Molecular Inorganic Chemistry and Catalysis, Fakultät für Chemie, Universität Bielefeld, Universitätsstr. 25, D-33615 Bielefeld, Germany
Interests: carbon-donor ligands; organometallic catalysis; open-shell (nontransition metals) molecules; molecular materials derived from stable radicals/π-conjugated systems; small molecule activation and functionalization; low-valent main-group chemistry; main-group catalysis; computational calculations; multireference methods
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Special Issue Information

Dear Colleagues,

Ligands have the ability to control the electronic and structural properties of metal complexes and, therefore, to regulate the way they react. Consequently, major advances in molecular science in general are directly related to the emergence of new types of innovative ligands. 1,3-Imidazole derived N-heterocyclic carbenes (NHCs) (A) are a prominent example and ranked as very versatile carbon-donor ligands in organometallic chemistry and catalysis. NHCs typically bind to metals at the C2-carbon atom and are generally regarded as normal or classical NHCs. The strong σ-donor ability of NHCs leads to the formation of a rather robust M‒C(NHC) bond, giving rise to very stable metal complexes. In addition, it also enhances the reactivity of metal complexes by making the metal atom more electron rich. NHCs have also been utilized in main-group chemistry and numerous molecules with fascinating structures and intriguing bonding situations have been stabilized by the use of NHCs. This is clearly because of the strong σ-donor strength, as well as auspicious steric features of NHCs. Over the past few years, a relatively new type of carbenes (B), in which the carbene carbon atom is located at the unusual C4-position, has received significant attention, as they are even stronger σ-donors than their classical (C2) analogs A. Similarly, 1,2,3-triazole derived C4-carbenes (D) have also been shown as very powerful ligands in catalysis and organometallic chemistry. These so-called abnormal-NHCs (aNHCs) are also referred to as mesoionic carbenes (MICs), as no neutral Lewis form without the introduction of formal charges can be written for B and D.

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While D are stronger σ-donors than classical NHCs A and C, aNHCs (or MICs) B are exceptional. Whether described as aNHCs or MICs, these C4 carbenes B and D have already been recognized as very powerful ligands in synthesis and catalysis. Moreover, the scope of MICs is continuously expanding with the availability of their efficient synthetic methods. In addition, the possibility of incorporating new functionalities in MICs offers unique opportunities for controlling/modifying the stability, reactivity, and other properties of derived complexes.

The central aim of this Special Issue is to compile the original cutting-edge research in MIC chemistry that encompasses the structural and electronic investigations of unique molecular entities, catalysis, small molecular activation, organic synthesis, theoretical analysis, and molecular materials, among others.

Prof. Dr. Rajendra S. Ghadwal
Guest Editor

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Keywords

  • Carbene
  • Mesoionic carbenes (MICs)
  • Abnormal carbenes (aNHCs)
  • C4-/C5-carbenes
  • Anionic dicarbenes
  • Di- and multi-topic carbenes
  • Heteroatom functionalized carbenes
  • Electronic and steric properties
  • Stabilization of reactive main-group species
  • Transition metal complexes
  • Main-group compounds
  • Computational study
  • Bond activation and functionalization
  • Small molecule activation
  • Organic synthesis
  • Structure-reactivity correlations
  • Catalysis
  • Mechanistic insight

Published Papers (1 paper)

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Research

18 pages, 4108 KiB  
Article
Possible Synthetic Approaches for Heterobimetallic Complexes by Using nNHC/tzNHC Heteroditopic Carbene Ligands
by Andrea Longhi, Marco Baron, Marzio Rancan, Gregorio Bottaro, Lidia Armelao, Paolo Sgarbossa and Cristina Tubaro
Molecules 2019, 24(12), 2305; https://doi.org/10.3390/molecules24122305 - 21 Jun 2019
Cited by 8 | Viewed by 3222
Abstract
The synthesis of heterobimetallic complexes remains a synthetic challenge in the field of organometallic chemistry. A possible approach in this regard might be the use of a bidentate heteroditopic bis(carbene) ligand that combines an imidazol-2-ylidene (nNHC) with a 1,2,3-triazol-5-ylidene (tz [...] Read more.
The synthesis of heterobimetallic complexes remains a synthetic challenge in the field of organometallic chemistry. A possible approach in this regard might be the use of a bidentate heteroditopic bis(carbene) ligand that combines an imidazol-2-ylidene (nNHC) with a 1,2,3-triazol-5-ylidene (tzNHC) connected by an organic spacer. The optimized strategy to heterobimetallic complexes with this type of ligand involves a 3-step procedure: (i) Coordination of the nNHC, functionalized with a 1,2,3-triazole ring, to a metal center; (ii) formation of the triazolium ring by alkylation of the triazole N-3; (iii) deprotonation of the tzNHC precursor and coordination of the second metal center. Following this procedure, a novel Au(I)-Ag(I) dinuclear complex was isolated and its properties were compared to the analogous homobimetallic Ag(I)-Ag(I) and Au(I)-Au(I) complexes. The study was completed by the determination of the molecular structures of some synthetic intermediates. Full article
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