The University of Southampton
University of Southampton Institutional Repository

Synthesis and X-ray characterization of the organotriboroxinate salts [Me3NCH2CH2OH][Ph4B3O3] and [NEt3H][Ph3B3O3(OH)], and the X-ray structure of the triarylboroxine, (4-MeOC6H4)(3)B3O3

Synthesis and X-ray characterization of the organotriboroxinate salts [Me3NCH2CH2OH][Ph4B3O3] and [NEt3H][Ph3B3O3(OH)], and the X-ray structure of the triarylboroxine, (4-MeOC6H4)(3)B3O3
Synthesis and X-ray characterization of the organotriboroxinate salts [Me3NCH2CH2OH][Ph4B3O3] and [NEt3H][Ph3B3O3(OH)], and the X-ray structure of the triarylboroxine, (4-MeOC6H4)(3)B3O3
The synthesis and characterization of the organotriboroxinate salts [Me3NCH2CH2OH][B3O4Ph4] (1) and [NEt3H][B3O3Ph3(OH)] (3) are reported. Compound 3 contains the first example of a hybrid inorganic/organic triboroxinate anion. Compounds I and 3 have been structurally characterized by single-crystal X-ray diffraction studies, which reveal H-bond ion-pair interactions between anions and cations in both 1 and 3, and additional anion-anion H-bond interactions in 3. Compound 3 exists as a dimer in the solid-state. A single crystal X-ray diffraction study of the triarylboroxine, (4-MeOC6H4)(3)B3O3, is also reported.
boroxinate anions, boroxines, x-ray structures molecular-structure, amine adducts, crystal-structures, ring
0277-5387
1011-1016
Beckett, Michael A.
5b021ef6-fa5c-4f6d-9998-3313558f0dc1
Coles, Simon J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Fischer, Lars
9842cd0b-8b60-468b-9020-3480535803bd
Stiefvater-Thomas, Ben M.
584d9d51-bc15-41e5-8f91-55b3208c390e
Varma, K. Sukuma
efe16deb-8a97-40a0-b59a-adc924f9775f
Beckett, Michael A.
5b021ef6-fa5c-4f6d-9998-3313558f0dc1
Coles, Simon J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Fischer, Lars
9842cd0b-8b60-468b-9020-3480535803bd
Stiefvater-Thomas, Ben M.
584d9d51-bc15-41e5-8f91-55b3208c390e
Varma, K. Sukuma
efe16deb-8a97-40a0-b59a-adc924f9775f

Beckett, Michael A., Coles, Simon J., Light, Mark E., Fischer, Lars, Stiefvater-Thomas, Ben M. and Varma, K. Sukuma (2006) Synthesis and X-ray characterization of the organotriboroxinate salts [Me3NCH2CH2OH][Ph4B3O3] and [NEt3H][Ph3B3O3(OH)], and the X-ray structure of the triarylboroxine, (4-MeOC6H4)(3)B3O3. Polyhedron, 25 (4), 1011-1016. (doi:10.1016/j.poly.2005.11.032).

Record type: Article

Abstract

The synthesis and characterization of the organotriboroxinate salts [Me3NCH2CH2OH][B3O4Ph4] (1) and [NEt3H][B3O3Ph3(OH)] (3) are reported. Compound 3 contains the first example of a hybrid inorganic/organic triboroxinate anion. Compounds I and 3 have been structurally characterized by single-crystal X-ray diffraction studies, which reveal H-bond ion-pair interactions between anions and cations in both 1 and 3, and additional anion-anion H-bond interactions in 3. Compound 3 exists as a dimer in the solid-state. A single crystal X-ray diffraction study of the triarylboroxine, (4-MeOC6H4)(3)B3O3, is also reported.

This record has no associated files available for download.

More information

Published date: 2006
Keywords: boroxinate anions, boroxines, x-ray structures molecular-structure, amine adducts, crystal-structures, ring

Identifiers

Local EPrints ID: 44378
URI: http://eprints.soton.ac.uk/id/eprint/44378
ISSN: 0277-5387
PURE UUID: 43c5916e-055d-45bd-bf95-6cd4e1cd39fd
ORCID for Simon J. Coles: ORCID iD orcid.org/0000-0001-8414-9272
ORCID for Mark E. Light: ORCID iD orcid.org/0000-0002-0585-0843

Catalogue record

Date deposited: 01 Mar 2007
Last modified: 16 Mar 2024 03:05

Export record

Altmetrics

Contributors

Author: Michael A. Beckett
Author: Simon J. Coles ORCID iD
Author: Mark E. Light ORCID iD
Author: Lars Fischer
Author: Ben M. Stiefvater-Thomas
Author: K. Sukuma Varma

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×