The University of Southampton
University of Southampton Institutional Repository

Synthesis and XRD study of an C2-linked bis(quaternary ammonium) pentaborate: [Me3NCH2CH2NMe3][B5O6(OH)4]2

Synthesis and XRD study of an C2-linked bis(quaternary ammonium) pentaborate: [Me3NCH2CH2NMe3][B5O6(OH)4]2
Synthesis and XRD study of an C2-linked bis(quaternary ammonium) pentaborate: [Me3NCH2CH2NMe3][B5O6(OH)4]2

The synthesis and characterization of a C2 (ethane) linked bis(trimethylammonium) pentaborate salt, [Me3NCH2CH2NMe3][B5O6(OH)4]2 (1), is reported. Compound 1 has been characterized by 1H, 11B, and 13C NMR Spectroscopy, IR spectroscopy, thermal (TGA/DSC) analysis, and single-crystal X-ray diffraction. There are two independent crystallographic pentaborate(1-) anions in the solid-state structure and these link by H-bonds at β-sites into a centrosymmetric tetrameric chain. These chains are crossed-linked by R22(8) H-bond motifs to α-sites of neighboring pentaborate tetrameric units. The [Me3NCH2CH2NMe3]2+ cations are located between these tetrameric pentaborate(1-) units.

1,2-bis(trimethylammonium)ethane, Oxidoborate, pentaborate(1-), polyborate, X-ray structure
1042-6507
Beckett, Michael A.
5b021ef6-fa5c-4f6d-9998-3313558f0dc1
Coles, Simon J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Horton, Peter N.
154c8930-bfc3-495b-ad4a-8a278d5da3a5
Rixon, Thomas A.
f5d9498d-b8cc-43b4-9b32-99253e1263db
Beckett, Michael A.
5b021ef6-fa5c-4f6d-9998-3313558f0dc1
Coles, Simon J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Horton, Peter N.
154c8930-bfc3-495b-ad4a-8a278d5da3a5
Rixon, Thomas A.
f5d9498d-b8cc-43b4-9b32-99253e1263db

Beckett, Michael A., Coles, Simon J., Horton, Peter N. and Rixon, Thomas A. (2019) Synthesis and XRD study of an C2-linked bis(quaternary ammonium) pentaborate: [Me3NCH2CH2NMe3][B5O6(OH)4]2. Phosphorus, Sulfur and Silicon and the Related Elements. (doi:10.1080/10426507.2019.1631308).

Record type: Article

Abstract

The synthesis and characterization of a C2 (ethane) linked bis(trimethylammonium) pentaborate salt, [Me3NCH2CH2NMe3][B5O6(OH)4]2 (1), is reported. Compound 1 has been characterized by 1H, 11B, and 13C NMR Spectroscopy, IR spectroscopy, thermal (TGA/DSC) analysis, and single-crystal X-ray diffraction. There are two independent crystallographic pentaborate(1-) anions in the solid-state structure and these link by H-bonds at β-sites into a centrosymmetric tetrameric chain. These chains are crossed-linked by R22(8) H-bond motifs to α-sites of neighboring pentaborate tetrameric units. The [Me3NCH2CH2NMe3]2+ cations are located between these tetrameric pentaborate(1-) units.

Text
RIXON Revised manuscript - Accepted Manuscript
Download (541kB)

More information

Accepted/In Press date: 9 June 2019
e-pub ahead of print date: 20 June 2019
Keywords: 1,2-bis(trimethylammonium)ethane, Oxidoborate, pentaborate(1-), polyborate, X-ray structure

Identifiers

Local EPrints ID: 433025
URI: http://eprints.soton.ac.uk/id/eprint/433025
ISSN: 1042-6507
PURE UUID: 7476effc-d140-4a06-bd87-4a51b79d50be
ORCID for Simon J. Coles: ORCID iD orcid.org/0000-0001-8414-9272
ORCID for Peter N. Horton: ORCID iD orcid.org/0000-0001-8886-2016

Catalogue record

Date deposited: 06 Aug 2019 16:30
Last modified: 16 Mar 2024 08:01

Export record

Altmetrics

Contributors

Author: Michael A. Beckett
Author: Simon J. Coles ORCID iD
Author: Peter N. Horton ORCID iD
Author: Thomas A. Rixon

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.

×