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Unexpected ortho C–H bond activation in coordinated 7,8-benzoquinoline: synthesis and characterisation of heteroleptic Ir(iii)-7,8-benzoquinoline complexes
Two iridium(iii) complexes were isolated via the reaction of pyridine-2-aldoxime (Hpyrald) with 7,8-benzoquinoline (benzq)-derived iridium starting material, namely [(benzq)(2)Ir(μ-Cl)(2)Ir(benzq)(2)] (1). Among the two complexes, [Ir(III)(benzq)(2)(pyrald)] (2) and [Ir(III)(benzq-κN,κC(10))(benzq-κ...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697031/ https://www.ncbi.nlm.nih.gov/pubmed/35423828 http://dx.doi.org/10.1039/d1ra00860a |
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author | Pradhan, Kahnu Charan Kisan, Hemanta K. Pal, Satyanarayan |
author_facet | Pradhan, Kahnu Charan Kisan, Hemanta K. Pal, Satyanarayan |
author_sort | Pradhan, Kahnu Charan |
collection | PubMed |
description | Two iridium(iii) complexes were isolated via the reaction of pyridine-2-aldoxime (Hpyrald) with 7,8-benzoquinoline (benzq)-derived iridium starting material, namely [(benzq)(2)Ir(μ-Cl)(2)Ir(benzq)(2)] (1). Among the two complexes, [Ir(III)(benzq)(2)(pyrald)] (2) and [Ir(III)(benzq-κN,κC(10))(benzq-κC(2))(Hpyrald)(Cl)] (3), the later displayed unusual ortho C–H bond activation in one of the coordinated 7,8-benzoquinoline rings. The complex (2) presented a usual structure as expected. |
format | Online Article Text |
id | pubmed-8697031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86970312022-04-13 Unexpected ortho C–H bond activation in coordinated 7,8-benzoquinoline: synthesis and characterisation of heteroleptic Ir(iii)-7,8-benzoquinoline complexes Pradhan, Kahnu Charan Kisan, Hemanta K. Pal, Satyanarayan RSC Adv Chemistry Two iridium(iii) complexes were isolated via the reaction of pyridine-2-aldoxime (Hpyrald) with 7,8-benzoquinoline (benzq)-derived iridium starting material, namely [(benzq)(2)Ir(μ-Cl)(2)Ir(benzq)(2)] (1). Among the two complexes, [Ir(III)(benzq)(2)(pyrald)] (2) and [Ir(III)(benzq-κN,κC(10))(benzq-κC(2))(Hpyrald)(Cl)] (3), the later displayed unusual ortho C–H bond activation in one of the coordinated 7,8-benzoquinoline rings. The complex (2) presented a usual structure as expected. The Royal Society of Chemistry 2021-03-30 /pmc/articles/PMC8697031/ /pubmed/35423828 http://dx.doi.org/10.1039/d1ra00860a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Pradhan, Kahnu Charan Kisan, Hemanta K. Pal, Satyanarayan Unexpected ortho C–H bond activation in coordinated 7,8-benzoquinoline: synthesis and characterisation of heteroleptic Ir(iii)-7,8-benzoquinoline complexes |
title | Unexpected ortho C–H bond activation in coordinated 7,8-benzoquinoline: synthesis and characterisation of heteroleptic Ir(iii)-7,8-benzoquinoline complexes |
title_full | Unexpected ortho C–H bond activation in coordinated 7,8-benzoquinoline: synthesis and characterisation of heteroleptic Ir(iii)-7,8-benzoquinoline complexes |
title_fullStr | Unexpected ortho C–H bond activation in coordinated 7,8-benzoquinoline: synthesis and characterisation of heteroleptic Ir(iii)-7,8-benzoquinoline complexes |
title_full_unstemmed | Unexpected ortho C–H bond activation in coordinated 7,8-benzoquinoline: synthesis and characterisation of heteroleptic Ir(iii)-7,8-benzoquinoline complexes |
title_short | Unexpected ortho C–H bond activation in coordinated 7,8-benzoquinoline: synthesis and characterisation of heteroleptic Ir(iii)-7,8-benzoquinoline complexes |
title_sort | unexpected ortho c–h bond activation in coordinated 7,8-benzoquinoline: synthesis and characterisation of heteroleptic ir(iii)-7,8-benzoquinoline complexes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697031/ https://www.ncbi.nlm.nih.gov/pubmed/35423828 http://dx.doi.org/10.1039/d1ra00860a |
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