Low temperature polymorphism in 3-amino-1-propanol
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Publication Date: | 2003 |
Other Authors: | , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | https://hdl.handle.net/10316/5164 https://doi.org/10.1016/S0022-2860(03)00049-8 |
Summary: | 3-Amino-1-propanol (3AP) was investigated by differential scanning calorimetry, and low temperature powder X-ray diffraction and Raman spectroscopy. Within the range of temperatures studied (-150-25 °C), 3AP was found to be able to crystallize in two monotropic polymorphs. Fast cooling rates produce an amorphous state that, on heating, crystallizes into the metastable polymorph. At higher temperatures, this metastable crystalline phase converts into the stable crystal. Using intermediate cooling rates, 3AP crystallizes as the metastable polymorph, the solid[right triple arrow]solid transition leading to conversion of this form into the stable polymorph occurring during the subsequent heating. Slower cooling rates enable formation of the stable crystal on cooling. The two crystalline polymorphs were structurally characterized by powder X-ray diffraction and Raman spectroscopy. It was concluded that different conformations are assumed by the individual molecules of 3AP in the two crystalline varieties, with the molecules assuming the all-trans configuration in the metastable crystalline state and having the heavy atom backbone trans but the NH2 and OH groups gauche in the stable crystal. |
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Low temperature polymorphism in 3-amino-1-propanol3-Amino-1-propanolX-ray diffraction and Raman spectroscopyDifferential Scanning Calorimetry3-Amino-1-propanol (3AP) was investigated by differential scanning calorimetry, and low temperature powder X-ray diffraction and Raman spectroscopy. Within the range of temperatures studied (-150-25 °C), 3AP was found to be able to crystallize in two monotropic polymorphs. Fast cooling rates produce an amorphous state that, on heating, crystallizes into the metastable polymorph. At higher temperatures, this metastable crystalline phase converts into the stable crystal. Using intermediate cooling rates, 3AP crystallizes as the metastable polymorph, the solid[right triple arrow]solid transition leading to conversion of this form into the stable polymorph occurring during the subsequent heating. Slower cooling rates enable formation of the stable crystal on cooling. The two crystalline polymorphs were structurally characterized by powder X-ray diffraction and Raman spectroscopy. It was concluded that different conformations are assumed by the individual molecules of 3AP in the two crystalline varieties, with the molecules assuming the all-trans configuration in the metastable crystalline state and having the heavy atom backbone trans but the NH2 and OH groups gauche in the stable crystal.http://www.sciencedirect.com/science/article/B6TGS-481FSJV-2/1/6d44932042d3990f18c7e3cb071cddf82003info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttps://hdl.handle.net/10316/5164https://hdl.handle.net/10316/5164https://doi.org/10.1016/S0022-2860(03)00049-8engJournal of Molecular Structure. 649:1-2 (2003) 143-153Cacela, C.Baudot, A.Duarte, M. L.Matos-Beja, A. M.Silva, M. RamosPaixão, J. A.Fausto, R.info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2023-11-24T09:38:33Zoai:estudogeral.uc.pt:10316/5164Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T05:24:07.551699Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Low temperature polymorphism in 3-amino-1-propanol |
title |
Low temperature polymorphism in 3-amino-1-propanol |
spellingShingle |
Low temperature polymorphism in 3-amino-1-propanol Cacela, C. 3-Amino-1-propanol X-ray diffraction and Raman spectroscopy Differential Scanning Calorimetry |
title_short |
Low temperature polymorphism in 3-amino-1-propanol |
title_full |
Low temperature polymorphism in 3-amino-1-propanol |
title_fullStr |
Low temperature polymorphism in 3-amino-1-propanol |
title_full_unstemmed |
Low temperature polymorphism in 3-amino-1-propanol |
title_sort |
Low temperature polymorphism in 3-amino-1-propanol |
author |
Cacela, C. |
author_facet |
Cacela, C. Baudot, A. Duarte, M. L. Matos-Beja, A. M. Silva, M. Ramos Paixão, J. A. Fausto, R. |
author_role |
author |
author2 |
Baudot, A. Duarte, M. L. Matos-Beja, A. M. Silva, M. Ramos Paixão, J. A. Fausto, R. |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Cacela, C. Baudot, A. Duarte, M. L. Matos-Beja, A. M. Silva, M. Ramos Paixão, J. A. Fausto, R. |
dc.subject.por.fl_str_mv |
3-Amino-1-propanol X-ray diffraction and Raman spectroscopy Differential Scanning Calorimetry |
topic |
3-Amino-1-propanol X-ray diffraction and Raman spectroscopy Differential Scanning Calorimetry |
description |
3-Amino-1-propanol (3AP) was investigated by differential scanning calorimetry, and low temperature powder X-ray diffraction and Raman spectroscopy. Within the range of temperatures studied (-150-25 °C), 3AP was found to be able to crystallize in two monotropic polymorphs. Fast cooling rates produce an amorphous state that, on heating, crystallizes into the metastable polymorph. At higher temperatures, this metastable crystalline phase converts into the stable crystal. Using intermediate cooling rates, 3AP crystallizes as the metastable polymorph, the solid[right triple arrow]solid transition leading to conversion of this form into the stable polymorph occurring during the subsequent heating. Slower cooling rates enable formation of the stable crystal on cooling. The two crystalline polymorphs were structurally characterized by powder X-ray diffraction and Raman spectroscopy. It was concluded that different conformations are assumed by the individual molecules of 3AP in the two crystalline varieties, with the molecules assuming the all-trans configuration in the metastable crystalline state and having the heavy atom backbone trans but the NH2 and OH groups gauche in the stable crystal. |
publishDate |
2003 |
dc.date.none.fl_str_mv |
2003 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/10316/5164 https://hdl.handle.net/10316/5164 https://doi.org/10.1016/S0022-2860(03)00049-8 |
url |
https://hdl.handle.net/10316/5164 https://doi.org/10.1016/S0022-2860(03)00049-8 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Molecular Structure. 649:1-2 (2003) 143-153 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
aplication/PDF |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
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