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Rare‐Earth‐ and Uranium‐Mesoionic Carbenes: A New Class of f‐Block Carbene Complex Derived from an N‐Heterocyclic Olefin
Neutral mesoionic carbenes (MICs) have emerged as an important class of carbene, however they are found in the free form or ligated to only a few d‐block ions. Unprecedented f‐block MIC complexes [M(N′′)(3){CN(Me)C(Me)N(Me)CH}] (M=U, Y, La, Nd; N′′=N(SiMe(3))(2)) are reported. These complexes were p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601227/ https://www.ncbi.nlm.nih.gov/pubmed/28719735 http://dx.doi.org/10.1002/anie.201706546 |
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author | Seed, John A. Gregson, Matthew Tuna, Floriana Chilton, Nicholas F. Wooles, Ashley J. McInnes, Eric J. L. Liddle, Stephen T. |
author_facet | Seed, John A. Gregson, Matthew Tuna, Floriana Chilton, Nicholas F. Wooles, Ashley J. McInnes, Eric J. L. Liddle, Stephen T. |
author_sort | Seed, John A. |
collection | PubMed |
description | Neutral mesoionic carbenes (MICs) have emerged as an important class of carbene, however they are found in the free form or ligated to only a few d‐block ions. Unprecedented f‐block MIC complexes [M(N′′)(3){CN(Me)C(Me)N(Me)CH}] (M=U, Y, La, Nd; N′′=N(SiMe(3))(2)) are reported. These complexes were prepared by a formal 1,4‐proton migration reaction when the metal triamides [M(N′′)(3)] were treated with the N‐heterocyclic olefin H(2)C=C(NMeCH)(2), which constitutes a new, general way to prepare MIC complexes. Quantum chemical calculations on the 5f(3) uranium(III) complex suggest the presence of a U=C donor‐acceptor bond, composed of a MIC→U σ‐component and a U(5f)→MIC(2p) π‐back‐bond, but for the d(0)f(0) Y and La and 4f(3) Nd congeners only MIC→M σ‐bonding is found. Considering the generally negligible π‐acidity of MICs, this is surprising and highlights that greater consideration should possibly be given to recognizing MICs as potential π‐acid ligands when coordinated to strongly reducing metals. |
format | Online Article Text |
id | pubmed-5601227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56012272017-10-03 Rare‐Earth‐ and Uranium‐Mesoionic Carbenes: A New Class of f‐Block Carbene Complex Derived from an N‐Heterocyclic Olefin Seed, John A. Gregson, Matthew Tuna, Floriana Chilton, Nicholas F. Wooles, Ashley J. McInnes, Eric J. L. Liddle, Stephen T. Angew Chem Int Ed Engl Communications Neutral mesoionic carbenes (MICs) have emerged as an important class of carbene, however they are found in the free form or ligated to only a few d‐block ions. Unprecedented f‐block MIC complexes [M(N′′)(3){CN(Me)C(Me)N(Me)CH}] (M=U, Y, La, Nd; N′′=N(SiMe(3))(2)) are reported. These complexes were prepared by a formal 1,4‐proton migration reaction when the metal triamides [M(N′′)(3)] were treated with the N‐heterocyclic olefin H(2)C=C(NMeCH)(2), which constitutes a new, general way to prepare MIC complexes. Quantum chemical calculations on the 5f(3) uranium(III) complex suggest the presence of a U=C donor‐acceptor bond, composed of a MIC→U σ‐component and a U(5f)→MIC(2p) π‐back‐bond, but for the d(0)f(0) Y and La and 4f(3) Nd congeners only MIC→M σ‐bonding is found. Considering the generally negligible π‐acidity of MICs, this is surprising and highlights that greater consideration should possibly be given to recognizing MICs as potential π‐acid ligands when coordinated to strongly reducing metals. John Wiley and Sons Inc. 2017-08-09 2017-09-11 /pmc/articles/PMC5601227/ /pubmed/28719735 http://dx.doi.org/10.1002/anie.201706546 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Seed, John A. Gregson, Matthew Tuna, Floriana Chilton, Nicholas F. Wooles, Ashley J. McInnes, Eric J. L. Liddle, Stephen T. Rare‐Earth‐ and Uranium‐Mesoionic Carbenes: A New Class of f‐Block Carbene Complex Derived from an N‐Heterocyclic Olefin |
title | Rare‐Earth‐ and Uranium‐Mesoionic Carbenes: A New Class of f‐Block Carbene Complex Derived from an N‐Heterocyclic Olefin |
title_full | Rare‐Earth‐ and Uranium‐Mesoionic Carbenes: A New Class of f‐Block Carbene Complex Derived from an N‐Heterocyclic Olefin |
title_fullStr | Rare‐Earth‐ and Uranium‐Mesoionic Carbenes: A New Class of f‐Block Carbene Complex Derived from an N‐Heterocyclic Olefin |
title_full_unstemmed | Rare‐Earth‐ and Uranium‐Mesoionic Carbenes: A New Class of f‐Block Carbene Complex Derived from an N‐Heterocyclic Olefin |
title_short | Rare‐Earth‐ and Uranium‐Mesoionic Carbenes: A New Class of f‐Block Carbene Complex Derived from an N‐Heterocyclic Olefin |
title_sort | rare‐earth‐ and uranium‐mesoionic carbenes: a new class of f‐block carbene complex derived from an n‐heterocyclic olefin |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601227/ https://www.ncbi.nlm.nih.gov/pubmed/28719735 http://dx.doi.org/10.1002/anie.201706546 |
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