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Enantiotropic conformational polymorphism in 2,2,4,4-bis-(2?,2?-dimethylpropane-1?,3?-dioxy)-6,6-dichlorocyclotriphosphazene

Enantiotropic conformational polymorphism in 2,2,4,4-bis-(2?,2?-dimethylpropane-1?,3?-dioxy)-6,6-dichlorocyclotriphosphazene
Enantiotropic conformational polymorphism in 2,2,4,4-bis-(2?,2?-dimethylpropane-1?,3?-dioxy)-6,6-dichlorocyclotriphosphazene
Conformational polymorphism has previously been observed in 2,2-dichloro-4,4:6,6-bis(2,2'-dimethlypropane-1,3-dioxy)-cyclotriphosphazene and the crystal structures of two forms were reported. In that study the melting points of both forms (alpha and beta) were reported as 211-212 degrees C and no investigation was made on the stability of, or the thermodynamic relationships between the polymorphs. In the present work the two forms were characterized by various analytical techniques, such as single-crystal X-ray diffraction, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), thermomicroscopy (TM) and variable temperature single crystal and powder X-ray diffraction. Thermal analysis suggests that the polymorphs are enantiotropically related and it is found that the solid-solid transformation of the beta to alpha form may start with defects of alpha form inside the beta form followed by a nucleation and growth type mechanism involving at least three main molecular centred events; conformational change, rotation and tilting.
1466-8033
4102-4109
Hacıvelioğlu, Ferda
4ec6cd47-a17b-42dd-80f9-ac865966ba73
Montis, Riccardo
11e15e46-6671-4ed0-9457-db82828bcdc7
Davies, David B.
675b90e6-0c3c-468b-9996-326220517cc6
Kılıç, Adem
565a42ec-2d18-4142-8b37-bb74b244b2f5
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Coles, Simon J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Hacıvelioğlu, Ferda
4ec6cd47-a17b-42dd-80f9-ac865966ba73
Montis, Riccardo
11e15e46-6671-4ed0-9457-db82828bcdc7
Davies, David B.
675b90e6-0c3c-468b-9996-326220517cc6
Kılıç, Adem
565a42ec-2d18-4142-8b37-bb74b244b2f5
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Coles, Simon J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8

Hacıvelioğlu, Ferda, Montis, Riccardo, Davies, David B., Kılıç, Adem, Hursthouse, Michael B. and Coles, Simon J. (2011) Enantiotropic conformational polymorphism in 2,2,4,4-bis-(2?,2?-dimethylpropane-1?,3?-dioxy)-6,6-dichlorocyclotriphosphazene. CrystEngComm, 13 (12), 4102-4109. (doi:10.1039/c1ce05163f).

Record type: Article

Abstract

Conformational polymorphism has previously been observed in 2,2-dichloro-4,4:6,6-bis(2,2'-dimethlypropane-1,3-dioxy)-cyclotriphosphazene and the crystal structures of two forms were reported. In that study the melting points of both forms (alpha and beta) were reported as 211-212 degrees C and no investigation was made on the stability of, or the thermodynamic relationships between the polymorphs. In the present work the two forms were characterized by various analytical techniques, such as single-crystal X-ray diffraction, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), thermomicroscopy (TM) and variable temperature single crystal and powder X-ray diffraction. Thermal analysis suggests that the polymorphs are enantiotropically related and it is found that the solid-solid transformation of the beta to alpha form may start with defects of alpha form inside the beta form followed by a nucleation and growth type mechanism involving at least three main molecular centred events; conformational change, rotation and tilting.

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More information

Published date: 2011
Organisations: Organic Chemistry: Synthesis, Catalysis and Flow

Identifiers

Local EPrints ID: 346129
URI: http://eprints.soton.ac.uk/id/eprint/346129
ISSN: 1466-8033
PURE UUID: 7ae63fcb-d1a4-4879-a2ab-f89fbbd67150
ORCID for Simon J. Coles: ORCID iD orcid.org/0000-0001-8414-9272

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Date deposited: 20 Dec 2012 15:46
Last modified: 15 Mar 2024 03:01

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Contributors

Author: Ferda Hacıvelioğlu
Author: Riccardo Montis
Author: David B. Davies
Author: Adem Kılıç
Author: Simon J. Coles ORCID iD

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