The University of Southampton
University of Southampton Institutional Repository

Coordination polymers and polygons using di-pyridyl-thiadiazole spacers and substituted phosphorodithioato NiII complexes: potential and limitations for inorganic crystal engineering

Coordination polymers and polygons using di-pyridyl-thiadiazole spacers and substituted phosphorodithioato NiII complexes: potential and limitations for inorganic crystal engineering
Coordination polymers and polygons using di-pyridyl-thiadiazole spacers and substituted phosphorodithioato NiII complexes: potential and limitations for inorganic crystal engineering
Coordinatively unsaturated P-substituted dithiophosphonato, dithiophosphato, and dithiophosphito complexes {[Ni?(MeO)2PS2)2] (1), [Ni((EtO)2PS2)2] (2), [Ni(MeOdtp)2] (3), and [Ni((Ph)2PS2)2] (4)} were reacted with the bis-functional ligands 3,5-di-(4-pyridyl)-1,2,4-thiadiazole (L1) and 3,5-di-(3-pyridyl)-1,2,4-thiadiazole (L2) to give the coordination polymers (1–4·L1)?, (3·L2)?, and (4·L2·2C7H8)? and the discrete dimers (1–2·L2)2, all characterised by single crystal X-ray diffraction. A comparison of the structures shows that L1 can be exploited for the predictable assembly of undulating chains independent of the nature of the NiII complex, while L2 allows for the existence of different supramolecular constructs ensuing from different ligand conformations deriving from the rotation of the pyridyl rings.
1466-8033
5620-5629
Aragoni, M. Carla
3e73ed7a-2cf7-4f5e-9359-61d6e34a6cd5
Arca, Massimiliano
f90b59f6-4dfb-471d-912e-3515e6507165
Coles, Simon
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Crespo Alonso, Miriam
14268c27-dd92-499a-9573-e553b6b2aac3
Coles, Susanne
9cd8719f-45b0-422e-a294-9b08ab79709b
Davies, Robert P.
37552576-6a8d-4dbc-af70-12870f40a048
Hursthouse, Mike
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Isaia, Francesco
11f997fe-81a3-4298-bbdc-15e5f2bf18cc
Lai, Romina
ff52746f-5c38-4caf-94ff-eea3cb93123b
Lippolis, Vito
d9833a14-4aab-4827-a2ba-be818871dcf5
Aragoni, M. Carla
3e73ed7a-2cf7-4f5e-9359-61d6e34a6cd5
Arca, Massimiliano
f90b59f6-4dfb-471d-912e-3515e6507165
Coles, Simon
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Crespo Alonso, Miriam
14268c27-dd92-499a-9573-e553b6b2aac3
Coles, Susanne
9cd8719f-45b0-422e-a294-9b08ab79709b
Davies, Robert P.
37552576-6a8d-4dbc-af70-12870f40a048
Hursthouse, Mike
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Isaia, Francesco
11f997fe-81a3-4298-bbdc-15e5f2bf18cc
Lai, Romina
ff52746f-5c38-4caf-94ff-eea3cb93123b
Lippolis, Vito
d9833a14-4aab-4827-a2ba-be818871dcf5

Aragoni, M. Carla, Arca, Massimiliano, Coles, Simon, Crespo Alonso, Miriam, Coles, Susanne, Davies, Robert P., Hursthouse, Mike, Isaia, Francesco, Lai, Romina and Lippolis, Vito (2016) Coordination polymers and polygons using di-pyridyl-thiadiazole spacers and substituted phosphorodithioato NiII complexes: potential and limitations for inorganic crystal engineering. CrystEngComm, 18 (30), 5620-5629. (doi:10.1039/c6ce00991c).

Record type: Article

Abstract

Coordinatively unsaturated P-substituted dithiophosphonato, dithiophosphato, and dithiophosphito complexes {[Ni?(MeO)2PS2)2] (1), [Ni((EtO)2PS2)2] (2), [Ni(MeOdtp)2] (3), and [Ni((Ph)2PS2)2] (4)} were reacted with the bis-functional ligands 3,5-di-(4-pyridyl)-1,2,4-thiadiazole (L1) and 3,5-di-(3-pyridyl)-1,2,4-thiadiazole (L2) to give the coordination polymers (1–4·L1)?, (3·L2)?, and (4·L2·2C7H8)? and the discrete dimers (1–2·L2)2, all characterised by single crystal X-ray diffraction. A comparison of the structures shows that L1 can be exploited for the predictable assembly of undulating chains independent of the nature of the NiII complex, while L2 allows for the existence of different supramolecular constructs ensuing from different ligand conformations deriving from the rotation of the pyridyl rings.

Text
c6ce00991c.pdf - Version of Record
Available under License Creative Commons Attribution.
Download (5MB)

More information

Accepted/In Press date: 6 June 2016
e-pub ahead of print date: 6 June 2016
Published date: 14 August 2016
Organisations: Characterisation and Analytics, Organic Chemistry: SCF

Identifiers

Local EPrints ID: 402131
URI: http://eprints.soton.ac.uk/id/eprint/402131
ISSN: 1466-8033
PURE UUID: 3eba06b6-9e75-4e16-8b56-101c19d247f3
ORCID for Simon Coles: ORCID iD orcid.org/0000-0001-8414-9272

Catalogue record

Date deposited: 01 Nov 2016 16:52
Last modified: 16 Mar 2024 03:05

Export record

Altmetrics

Contributors

Author: M. Carla Aragoni
Author: Massimiliano Arca
Author: Simon Coles ORCID iD
Author: Miriam Crespo Alonso
Author: Susanne Coles
Author: Robert P. Davies
Author: Mike Hursthouse
Author: Francesco Isaia
Author: Romina Lai
Author: Vito Lippolis

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.

×