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Synthesis and Structural Characterization of Amidine, Amide, Urea and Isocyanate Derivatives of the Amino-closo-dodecaborate Anion [B(12)H(11)NH(3)](−)
The synthesis and structural characterization of new derivatives of [B(12)H(12)](2−) is of fundamental interest and is expected to allow for extended applications. Herein we report on the synthesis of a series of amidine, amide, urea and isocyanate derivatives based on the amino-closo-dodecaborate a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321512/ https://www.ncbi.nlm.nih.gov/pubmed/30501105 http://dx.doi.org/10.3390/molecules23123137 |
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author | Zhang, Yuanbin Sun, Yuji Wang, Tao Liu, Jiyong Spingler, Bernhard Duttwyler, Simon |
author_facet | Zhang, Yuanbin Sun, Yuji Wang, Tao Liu, Jiyong Spingler, Bernhard Duttwyler, Simon |
author_sort | Zhang, Yuanbin |
collection | PubMed |
description | The synthesis and structural characterization of new derivatives of [B(12)H(12)](2−) is of fundamental interest and is expected to allow for extended applications. Herein we report on the synthesis of a series of amidine, amide, urea and isocyanate derivatives based on the amino-closo-dodecaborate anion [B(12)H(11)NH(3)](−). Their structures have been confirmed by spectroscopic methods, and nine crystal structures are presented. |
format | Online Article Text |
id | pubmed-6321512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63215122019-01-14 Synthesis and Structural Characterization of Amidine, Amide, Urea and Isocyanate Derivatives of the Amino-closo-dodecaborate Anion [B(12)H(11)NH(3)](−) Zhang, Yuanbin Sun, Yuji Wang, Tao Liu, Jiyong Spingler, Bernhard Duttwyler, Simon Molecules Article The synthesis and structural characterization of new derivatives of [B(12)H(12)](2−) is of fundamental interest and is expected to allow for extended applications. Herein we report on the synthesis of a series of amidine, amide, urea and isocyanate derivatives based on the amino-closo-dodecaborate anion [B(12)H(11)NH(3)](−). Their structures have been confirmed by spectroscopic methods, and nine crystal structures are presented. MDPI 2018-11-29 /pmc/articles/PMC6321512/ /pubmed/30501105 http://dx.doi.org/10.3390/molecules23123137 Text en © 2018 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 Zhang, Yuanbin Sun, Yuji Wang, Tao Liu, Jiyong Spingler, Bernhard Duttwyler, Simon Synthesis and Structural Characterization of Amidine, Amide, Urea and Isocyanate Derivatives of the Amino-closo-dodecaborate Anion [B(12)H(11)NH(3)](−) |
title | Synthesis and Structural Characterization of Amidine, Amide, Urea and Isocyanate Derivatives of the Amino-closo-dodecaborate Anion [B(12)H(11)NH(3)](−) |
title_full | Synthesis and Structural Characterization of Amidine, Amide, Urea and Isocyanate Derivatives of the Amino-closo-dodecaborate Anion [B(12)H(11)NH(3)](−) |
title_fullStr | Synthesis and Structural Characterization of Amidine, Amide, Urea and Isocyanate Derivatives of the Amino-closo-dodecaborate Anion [B(12)H(11)NH(3)](−) |
title_full_unstemmed | Synthesis and Structural Characterization of Amidine, Amide, Urea and Isocyanate Derivatives of the Amino-closo-dodecaborate Anion [B(12)H(11)NH(3)](−) |
title_short | Synthesis and Structural Characterization of Amidine, Amide, Urea and Isocyanate Derivatives of the Amino-closo-dodecaborate Anion [B(12)H(11)NH(3)](−) |
title_sort | synthesis and structural characterization of amidine, amide, urea and isocyanate derivatives of the amino-closo-dodecaborate anion [b(12)h(11)nh(3)](−) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321512/ https://www.ncbi.nlm.nih.gov/pubmed/30501105 http://dx.doi.org/10.3390/molecules23123137 |
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