Isolation of a bis(oxazol-2-ylidene)-phenylborylene adduct and its reactivity as a boron-centered nucleophile

An isolable phenylborylene species supported by two oxazol-2-ylidene ligands was synthesized and structurally characterized. Computational studies revealed the presence of lone-pair electrons on the boron atom in this molecule; therefore, there are eight electrons around the three-coordinate boron c...

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Main Authors: Vidović, Dragoslav, Kong, Ling Bing, Li, Yongxin, Ganguly, Rakesh, Kinjo, Rei
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2014
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Online Access:https://hdl.handle.net/10356/105355
http://hdl.handle.net/10220/20493
http://dx.doi.org/10.1002/anie.201405201
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1053552019-12-06T21:49:49Z Isolation of a bis(oxazol-2-ylidene)-phenylborylene adduct and its reactivity as a boron-centered nucleophile Vidović, Dragoslav Kong, Ling Bing Li, Yongxin Ganguly, Rakesh Kinjo, Rei School of Physical and Mathematical Sciences DRNTU::Science::Chemistry An isolable phenylborylene species supported by two oxazol-2-ylidene ligands was synthesized and structurally characterized. Computational studies revealed the presence of lone-pair electrons on the boron atom in this molecule; therefore, there are eight electrons around the three-coordinate boron center. The nucleophilic property was confirmed by the reactions with trifluoromethanesulfonic acid and [(thf)Cr(CO)5], which gave the corresponding conjugate acid and a chromium–borylene complex, respectively. 2014-09-10T07:09:38Z 2019-12-06T21:49:49Z 2014-09-10T07:09:38Z 2019-12-06T21:49:49Z 2014 2014 Journal Article Kong, L., Li, Y., Ganguly, R., Vidovic, D., & Kinjo, R. (2014). Isolation of a Bis(oxazol-2-ylidene)-Phenylborylene Adduct and its Reactivity as a Boron-Centered Nucleophile. Angewandte Chemie International Edition, 53(35), 9280-9283. 1433-7851 https://hdl.handle.net/10356/105355 http://hdl.handle.net/10220/20493 http://dx.doi.org/10.1002/anie.201405201 en Angewandte Chemie international edition © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic DRNTU::Science::Chemistry
spellingShingle DRNTU::Science::Chemistry
Vidović, Dragoslav
Kong, Ling Bing
Li, Yongxin
Ganguly, Rakesh
Kinjo, Rei
Isolation of a bis(oxazol-2-ylidene)-phenylborylene adduct and its reactivity as a boron-centered nucleophile
description An isolable phenylborylene species supported by two oxazol-2-ylidene ligands was synthesized and structurally characterized. Computational studies revealed the presence of lone-pair electrons on the boron atom in this molecule; therefore, there are eight electrons around the three-coordinate boron center. The nucleophilic property was confirmed by the reactions with trifluoromethanesulfonic acid and [(thf)Cr(CO)5], which gave the corresponding conjugate acid and a chromium–borylene complex, respectively.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Vidović, Dragoslav
Kong, Ling Bing
Li, Yongxin
Ganguly, Rakesh
Kinjo, Rei
format Article
author Vidović, Dragoslav
Kong, Ling Bing
Li, Yongxin
Ganguly, Rakesh
Kinjo, Rei
author_sort Vidović, Dragoslav
title Isolation of a bis(oxazol-2-ylidene)-phenylborylene adduct and its reactivity as a boron-centered nucleophile
title_short Isolation of a bis(oxazol-2-ylidene)-phenylborylene adduct and its reactivity as a boron-centered nucleophile
title_full Isolation of a bis(oxazol-2-ylidene)-phenylborylene adduct and its reactivity as a boron-centered nucleophile
title_fullStr Isolation of a bis(oxazol-2-ylidene)-phenylborylene adduct and its reactivity as a boron-centered nucleophile
title_full_unstemmed Isolation of a bis(oxazol-2-ylidene)-phenylborylene adduct and its reactivity as a boron-centered nucleophile
title_sort isolation of a bis(oxazol-2-ylidene)-phenylborylene adduct and its reactivity as a boron-centered nucleophile
publishDate 2014
url https://hdl.handle.net/10356/105355
http://hdl.handle.net/10220/20493
http://dx.doi.org/10.1002/anie.201405201
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