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m-Carborane as a Novel Core for Periphery-Decorated Macromolecules
Closom-C(2)B(10)H(12) can perform as a novel core of globular periphery-decorated macromolecules. To do this, a new class of di and tetrabranched m-carborane derivatives has been synthesized by a judicious choice of the synthetic procedure, starting with 9,10-I(2)-1,7-closo-C(2)B(10)H(10). The 2a-NP...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356233/ https://www.ncbi.nlm.nih.gov/pubmed/32570849 http://dx.doi.org/10.3390/molecules25122814 |
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author | Bennour, Ines Teixidor, Francesc Kelemen, Zsolt Viñas, Clara |
author_facet | Bennour, Ines Teixidor, Francesc Kelemen, Zsolt Viñas, Clara |
author_sort | Bennour, Ines |
collection | PubMed |
description | Closom-C(2)B(10)H(12) can perform as a novel core of globular periphery-decorated macromolecules. To do this, a new class of di and tetrabranched m-carborane derivatives has been synthesized by a judicious choice of the synthetic procedure, starting with 9,10-I(2)-1,7-closo-C(2)B(10)H(10). The 2a-NPA (sum of the natural charges of the two bonded atoms) value for a bond, which is defined as the sum of the NPA charges of the two bonded atoms, matches the order of electrophilic reaction at the different cluster bonds of the icosahedral o-and m- carboranes that lead to the formation of B-I bonds. As for m-carborane, most of the 2a-NPA values of B-H vertexes are positive, and their functionalization is more challenging. The synthesis and full characterization of dibranched 9,10-R(2)-1,7-closo-carborane (R = CH(2)CHCH(2), HO(CH(2))(3), Cl(CH(2))(3), TsO(CH(2))(3), C(6)H(5)COO(CH(2))(3), C(6)H(5)COO(CH(2))(3), N(3)(CH(2))(3), CH(3)CHCH, and C(6)H(5)C(2)N(3)(CH(2))(3)) compounds as well as the tetrabranched 9,10-R(2)-1,7-R(2)-closo-C(2)B(10)H(8) (R = CH(2)CHCH(2), HO(CH(2))(3)) are presented. The X-ray diffraction of 9,10-(HO(CH(2))(3))(2)-1,7-closo-C(2)B(10)H(10) and 9,10-(CH(3)CHCH)(2)-1,7-closo-C(2)B(10)H(10), as well as their Hirshfeld surface analysis and decomposed fingerprint plots, are described. These new reported tetrabranched m-carborane derivatives provide a sort of novel core for the synthesis of 3D radially grown periphery-decorated macromolecules that are different to the 2D radially grown core of the tetrabranched o-carborane framework. |
format | Online Article Text |
id | pubmed-7356233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73562332020-07-31 m-Carborane as a Novel Core for Periphery-Decorated Macromolecules Bennour, Ines Teixidor, Francesc Kelemen, Zsolt Viñas, Clara Molecules Article Closom-C(2)B(10)H(12) can perform as a novel core of globular periphery-decorated macromolecules. To do this, a new class of di and tetrabranched m-carborane derivatives has been synthesized by a judicious choice of the synthetic procedure, starting with 9,10-I(2)-1,7-closo-C(2)B(10)H(10). The 2a-NPA (sum of the natural charges of the two bonded atoms) value for a bond, which is defined as the sum of the NPA charges of the two bonded atoms, matches the order of electrophilic reaction at the different cluster bonds of the icosahedral o-and m- carboranes that lead to the formation of B-I bonds. As for m-carborane, most of the 2a-NPA values of B-H vertexes are positive, and their functionalization is more challenging. The synthesis and full characterization of dibranched 9,10-R(2)-1,7-closo-carborane (R = CH(2)CHCH(2), HO(CH(2))(3), Cl(CH(2))(3), TsO(CH(2))(3), C(6)H(5)COO(CH(2))(3), C(6)H(5)COO(CH(2))(3), N(3)(CH(2))(3), CH(3)CHCH, and C(6)H(5)C(2)N(3)(CH(2))(3)) compounds as well as the tetrabranched 9,10-R(2)-1,7-R(2)-closo-C(2)B(10)H(8) (R = CH(2)CHCH(2), HO(CH(2))(3)) are presented. The X-ray diffraction of 9,10-(HO(CH(2))(3))(2)-1,7-closo-C(2)B(10)H(10) and 9,10-(CH(3)CHCH)(2)-1,7-closo-C(2)B(10)H(10), as well as their Hirshfeld surface analysis and decomposed fingerprint plots, are described. These new reported tetrabranched m-carborane derivatives provide a sort of novel core for the synthesis of 3D radially grown periphery-decorated macromolecules that are different to the 2D radially grown core of the tetrabranched o-carborane framework. MDPI 2020-06-18 /pmc/articles/PMC7356233/ /pubmed/32570849 http://dx.doi.org/10.3390/molecules25122814 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bennour, Ines Teixidor, Francesc Kelemen, Zsolt Viñas, Clara m-Carborane as a Novel Core for Periphery-Decorated Macromolecules |
title | m-Carborane as a Novel Core for Periphery-Decorated Macromolecules |
title_full | m-Carborane as a Novel Core for Periphery-Decorated Macromolecules |
title_fullStr | m-Carborane as a Novel Core for Periphery-Decorated Macromolecules |
title_full_unstemmed | m-Carborane as a Novel Core for Periphery-Decorated Macromolecules |
title_short | m-Carborane as a Novel Core for Periphery-Decorated Macromolecules |
title_sort | m-carborane as a novel core for periphery-decorated macromolecules |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356233/ https://www.ncbi.nlm.nih.gov/pubmed/32570849 http://dx.doi.org/10.3390/molecules25122814 |
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