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Open AccessJournal ArticleDOI

Synthesis, stability, and (de)hydrogenation catalysis by normal and abnormal alkene- and picolyl-tethered NHC ruthenium complexes

TLDR
A series of p-cymene and cyclopentadienyl Ru(II)-aNHC complexes were synthesized from 2-methylimidazolium salts with either an N-bound alkenyl (1, 3) or picolyl tether (6, 7) as mentioned in this paper.
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This article is published in Organometallics.The article was published on 2019-06-21 and is currently open access. It has received 20 citations till now. The article focuses on the topics: Cyclopentadienyl complex & Ruthenium.

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Recent advances on N-heterocyclic carbene transition metal complexes for dehydrogenative catalysis using alcohols

TL;DR: A brief overview of recent advances on NHC-TM complexes for dehydrogenative catalysis using alcohols can be found in this article, where N-heterocyclic carbenes (NHCs) are green and versatile ligands for the development of transition metal catalysts.
Journal ArticleDOI

Abnormal N-Heterocyclic Carbene Palladium Complexes for the Copolymerization of Ethylene and Polar Monomers

TL;DR: Palladium complexes bearing abnormal imidazo[1,5-a]pyridine (aImPy)-based N-heterocyclic carbene ligands were developed for the homopolymerization of olefins and the copolymerisation of OLEFins as discussed by the authors.
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Electronically tuneable orthometalated Ru<sup>II</sup>–NHC complexes as efficient catalysts for C–C and C–N bond formations <i>via</i> borrowing hydrogen strategy

TL;DR: A series of simple and electronically tuneable cyclometalated Ru II -NHC complexes have been explored as efficient catalysts for various C-C/N bond forming reactions via a BH methodology as mentioned in this paper .
Journal ArticleDOI

Electronically Tuneable Orthometalated RuII-NHC Complexes as Efficient Catalysts for the C-C and C-N Bond Formations via Borrowing Hydrogen Strategy

TL;DR: In this paper, the catalytic activities of a series of simple and electronically tuneable cyclometalated RuII-NHC complexes (2a-d) were explored in various C-C/N bond formations following the borrowing hydrogen process.
References
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Journal ArticleDOI

Electronic Structure Trends in N‐Heterocyclic Carbenes (NHCs) with Varying Number of Nitrogen Atoms and NHC ? Transition‐Metal Bond Properties

TL;DR: The singlet-triplet energy gap was used as a measure of the stability of the N-heterocyclic carbene (NHC) towards dimerisation and natural population analysis provided insight into the variation of the pπ population and the natural charge at Ccarbene with NHC structure.
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Carbon-based two electron σ-donor ligands beyond classical N-heterocyclic carbenes

TL;DR: Recent advances in NHC chemistry of compounds featuring the aforementioned ligands, which are exclusively derived by the functionalization of NHCs, 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene (IPr) in particular are summarized.
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Coordination chemistry of ditopic carbanionic N-heterocyclic carbenes

TL;DR: A comprehensive review of the chemistry of carbanionic carbenes can be found in this paper, with a particular focus on their isolation as alkali-metal salts and their subsequent reactivity.
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Exploring the Scope of Pyridyl- and Picolyl-Functionalized 1,2,3-Triazol-5-ylidenes in Bidentate Coordination to Ruthenium(II) Cymene Chloride Complexes

TL;DR: In this paper, N-heterocyclic carbene precursors for bidentate coordination to ruthenium(II) through the CNHC and Npyridyl donors were investigated.
Journal ArticleDOI

Current advances on ruthenium(II) N-heterocyclic carbenes in hydrogenation reactions

TL;DR: In this paper, a brief overview of advances on ruthenium(II) N-heterocyclic carbene complexes (NHCs) applied for hydrogenation reactions undertaken during the last five years is provided.
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Q1. What contributions have the authors mentioned in the paper "Synthesis, stability, and (de)hydrogenation catalysis by normal and abnormal alkene- and picolyl-tethered nhc ruthenium complexes" ?

In this paper, a series of p-cymene and cyclopentadienyl Ru ( II ) -aNHC derivatives have been synthesized from 2methylimidazolium salts with either an N-bound alkenyl ( 1, 3 ) or picolyl tether ( 6, 7 ).