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Charge-transfer adducts of N-methylthiazolidine-2-thione with IBr and I-2: An example of polymorphism featuring interpenetrating three-dimensional subcomponent assemblies and halogen center dot center dot center dot pi center dot center dot center dot halogen weak interactions

Charge-transfer adducts of N-methylthiazolidine-2-thione with IBr and I-2: An example of polymorphism featuring interpenetrating three-dimensional subcomponent assemblies and halogen center dot center dot center dot pi center dot center dot center dot halogen weak interactions
Charge-transfer adducts of N-methylthiazolidine-2-thione with IBr and I-2: An example of polymorphism featuring interpenetrating three-dimensional subcomponent assemblies and halogen center dot center dot center dot pi center dot center dot center dot halogen weak interactions
Two polymorphic forms of the 1:1 charge-transfer adduct between N-methylthiazolidine-2-thione and IBr have been isolated: their structural analyses by a recently reported procedure for comparison of multiple crystal forms of the same molecular structure reveal some interesting geometrical 3D similarity relationships that can be interpreted in terms of different sets of halogen ······halogen weak interactions. The 1:1 charge-transfer adduct with I2 has also been isolated and structurally characterized and proven to be isostructural with one of the two polymorphic forms of the IBr adduct.
spectroscopy, differential scanning calorimetry, polymorphism, parameters, crystallization, hydrochloride, powder diffraction, forms, crystal, phase, local-anesthetic drugs
1528-7483
1284-1290
Aragoni, M.C.
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Arca, M.
d852c450-c522-47cb-a577-9babf59dd503
Demartin, F.
ee16d0d0-16df-4214-aa39-b5d8b043f737
Devillanova, F.A.
20c07fe4-3b8e-46f4-a241-60ae5189efee
Gelbrich, T.
42309d69-eaf1-4bb7-ba2e-db61f338e370
Garau, A.
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Hursthouse, M.B.
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Isaia, F.
01929115-e3d5-4af1-b79b-439cfa32fd27
Lippolis, V.
6890f6ab-6860-4752-9639-5bdfeef0e90d
Aragoni, M.C.
aec09914-2339-4bd2-aa6f-3c80c0febe9a
Arca, M.
d852c450-c522-47cb-a577-9babf59dd503
Demartin, F.
ee16d0d0-16df-4214-aa39-b5d8b043f737
Devillanova, F.A.
20c07fe4-3b8e-46f4-a241-60ae5189efee
Gelbrich, T.
42309d69-eaf1-4bb7-ba2e-db61f338e370
Garau, A.
5f40709b-2bc5-4d2d-9311-57813e34080d
Hursthouse, M.B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Isaia, F.
01929115-e3d5-4af1-b79b-439cfa32fd27
Lippolis, V.
6890f6ab-6860-4752-9639-5bdfeef0e90d

Aragoni, M.C., Arca, M., Demartin, F., Devillanova, F.A., Gelbrich, T., Garau, A., Hursthouse, M.B., Isaia, F. and Lippolis, V. (2007) Charge-transfer adducts of N-methylthiazolidine-2-thione with IBr and I-2: An example of polymorphism featuring interpenetrating three-dimensional subcomponent assemblies and halogen center dot center dot center dot pi center dot center dot center dot halogen weak interactions. Crystal Growth & Design, 7 (7), 1284-1290. (doi:10.1021/cg0606545).

Record type: Article

Abstract

Two polymorphic forms of the 1:1 charge-transfer adduct between N-methylthiazolidine-2-thione and IBr have been isolated: their structural analyses by a recently reported procedure for comparison of multiple crystal forms of the same molecular structure reveal some interesting geometrical 3D similarity relationships that can be interpreted in terms of different sets of halogen ······halogen weak interactions. The 1:1 charge-transfer adduct with I2 has also been isolated and structurally characterized and proven to be isostructural with one of the two polymorphic forms of the IBr adduct.

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Published date: 2007
Keywords: spectroscopy, differential scanning calorimetry, polymorphism, parameters, crystallization, hydrochloride, powder diffraction, forms, crystal, phase, local-anesthetic drugs

Identifiers

Local EPrints ID: 54234
URI: http://eprints.soton.ac.uk/id/eprint/54234
ISSN: 1528-7483
PURE UUID: dadf7650-f2e9-40c5-9a1e-899d27bbf53a

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Date deposited: 31 Jul 2008
Last modified: 15 Mar 2024 10:45

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Contributors

Author: M.C. Aragoni
Author: M. Arca
Author: F. Demartin
Author: F.A. Devillanova
Author: T. Gelbrich
Author: A. Garau
Author: M.B. Hursthouse
Author: F. Isaia
Author: V. Lippolis

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