Structural and vibrational characterization of methyl glycolate in the low temperature crystalline and glassy states

Detalhes bibliográficos
Autor(a) principal: Jarmelo, Susana
Data de Publicação: 2000
Outros Autores: Maria, Teresa M. R., Leitão, Maria Luísa P., Fausto, Rui
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/10719
https://doi.org/10.1039/a909291i
Resumo: The low temperature phases of methyl glycolate (MGly) were identified and characterized structurally by differential scanning calorimetry, infrared and Raman spectroscopies and molecular modeling. Within the temperature range 13–273 K, MGly may exist in three solid phases. A crystalline phase (I) can be formed from the liquid upon slow cooling [Tonset=222–227 K] or from the low temperature glassy state resulting from fast deposition of the vapour onto a cold substrate at 13 K and subsequent warming. A mixture of the glassy state and crystalline phase (I) is obtained by cooling the liquid at higher cooling rates (vcooling?10 K min–1). Upon heating this mixture, devitrification occurs at ca. 175 K, the cold liquid then formed giving rise to a second crystalline variety (II) at Tonset=198–207 K. In the glassy state, individual MGly molecules may assume the two conformational states previously observed for this compound isolated in an argon matrix and in the liquid phase [S. Jarmelo and R. Fausto, J. Mol. Struct., 1999, 509, 183]. On the contrary, the crystalline phase I was found to exhibit conformational selectivity—in this phase, all individual molecules assume a conformation analogous to the most stable conformer found for the isolated molecule and in the liquid (the syn-syn s-cis conformer, where the H–O–C–C, O–C–CO and OC–O–C dihedrals are ca. 0°). In agreement with the spectroscopic results, a molecular modeling analysis reveals that, in this phase, two non-equivalent molecules exhibiting an intramolecular OH···O hydrogen bond exist, which are connected by a relatively strong intermolecular OH···O hydrogen bond. Crystalline state II could not be characterized in detail structurally, but the thermodynamic studies seem to indicate that it corresponds to a metastable crystalline form having a more relaxed structure and a slightly higher energy than crystalline state I. The observed temperature of fusion for the two observed crystalline forms are: I, 264 K and II, 260 K.
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spelling Structural and vibrational characterization of methyl glycolate in the low temperature crystalline and glassy statesThe low temperature phases of methyl glycolate (MGly) were identified and characterized structurally by differential scanning calorimetry, infrared and Raman spectroscopies and molecular modeling. Within the temperature range 13–273 K, MGly may exist in three solid phases. A crystalline phase (I) can be formed from the liquid upon slow cooling [Tonset=222–227 K] or from the low temperature glassy state resulting from fast deposition of the vapour onto a cold substrate at 13 K and subsequent warming. A mixture of the glassy state and crystalline phase (I) is obtained by cooling the liquid at higher cooling rates (vcooling?10 K min–1). Upon heating this mixture, devitrification occurs at ca. 175 K, the cold liquid then formed giving rise to a second crystalline variety (II) at Tonset=198–207 K. In the glassy state, individual MGly molecules may assume the two conformational states previously observed for this compound isolated in an argon matrix and in the liquid phase [S. Jarmelo and R. Fausto, J. Mol. Struct., 1999, 509, 183]. On the contrary, the crystalline phase I was found to exhibit conformational selectivity—in this phase, all individual molecules assume a conformation analogous to the most stable conformer found for the isolated molecule and in the liquid (the syn-syn s-cis conformer, where the H–O–C–C, O–C–CO and OC–O–C dihedrals are ca. 0°). In agreement with the spectroscopic results, a molecular modeling analysis reveals that, in this phase, two non-equivalent molecules exhibiting an intramolecular OH···O hydrogen bond exist, which are connected by a relatively strong intermolecular OH···O hydrogen bond. Crystalline state II could not be characterized in detail structurally, but the thermodynamic studies seem to indicate that it corresponds to a metastable crystalline form having a more relaxed structure and a slightly higher energy than crystalline state I. The observed temperature of fusion for the two observed crystalline forms are: I, 264 K and II, 260 K.FEDER, programa PRAXIS XXI (QUI/2/2.1/412/94)Royal Society of Chemistry2000info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/10719http://hdl.handle.net/10316/10719https://doi.org/10.1039/a909291iengPhysical Chemistry Chemical Physics. 2 (2000) 1155-11631463-9076Jarmelo, SusanaMaria, Teresa M. R.Leitão, Maria Luísa P.Fausto, Ruiinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-09-17T08:37:45Zoai:estudogeral.uc.pt:10316/10719Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:36.136617Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Structural and vibrational characterization of methyl glycolate in the low temperature crystalline and glassy states
title Structural and vibrational characterization of methyl glycolate in the low temperature crystalline and glassy states
spellingShingle Structural and vibrational characterization of methyl glycolate in the low temperature crystalline and glassy states
Jarmelo, Susana
title_short Structural and vibrational characterization of methyl glycolate in the low temperature crystalline and glassy states
title_full Structural and vibrational characterization of methyl glycolate in the low temperature crystalline and glassy states
title_fullStr Structural and vibrational characterization of methyl glycolate in the low temperature crystalline and glassy states
title_full_unstemmed Structural and vibrational characterization of methyl glycolate in the low temperature crystalline and glassy states
title_sort Structural and vibrational characterization of methyl glycolate in the low temperature crystalline and glassy states
author Jarmelo, Susana
author_facet Jarmelo, Susana
Maria, Teresa M. R.
Leitão, Maria Luísa P.
Fausto, Rui
author_role author
author2 Maria, Teresa M. R.
Leitão, Maria Luísa P.
Fausto, Rui
author2_role author
author
author
dc.contributor.author.fl_str_mv Jarmelo, Susana
Maria, Teresa M. R.
Leitão, Maria Luísa P.
Fausto, Rui
description The low temperature phases of methyl glycolate (MGly) were identified and characterized structurally by differential scanning calorimetry, infrared and Raman spectroscopies and molecular modeling. Within the temperature range 13–273 K, MGly may exist in three solid phases. A crystalline phase (I) can be formed from the liquid upon slow cooling [Tonset=222–227 K] or from the low temperature glassy state resulting from fast deposition of the vapour onto a cold substrate at 13 K and subsequent warming. A mixture of the glassy state and crystalline phase (I) is obtained by cooling the liquid at higher cooling rates (vcooling?10 K min–1). Upon heating this mixture, devitrification occurs at ca. 175 K, the cold liquid then formed giving rise to a second crystalline variety (II) at Tonset=198–207 K. In the glassy state, individual MGly molecules may assume the two conformational states previously observed for this compound isolated in an argon matrix and in the liquid phase [S. Jarmelo and R. Fausto, J. Mol. Struct., 1999, 509, 183]. On the contrary, the crystalline phase I was found to exhibit conformational selectivity—in this phase, all individual molecules assume a conformation analogous to the most stable conformer found for the isolated molecule and in the liquid (the syn-syn s-cis conformer, where the H–O–C–C, O–C–CO and OC–O–C dihedrals are ca. 0°). In agreement with the spectroscopic results, a molecular modeling analysis reveals that, in this phase, two non-equivalent molecules exhibiting an intramolecular OH···O hydrogen bond exist, which are connected by a relatively strong intermolecular OH···O hydrogen bond. Crystalline state II could not be characterized in detail structurally, but the thermodynamic studies seem to indicate that it corresponds to a metastable crystalline form having a more relaxed structure and a slightly higher energy than crystalline state I. The observed temperature of fusion for the two observed crystalline forms are: I, 264 K and II, 260 K.
publishDate 2000
dc.date.none.fl_str_mv 2000
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/10719
http://hdl.handle.net/10316/10719
https://doi.org/10.1039/a909291i
url http://hdl.handle.net/10316/10719
https://doi.org/10.1039/a909291i
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Physical Chemistry Chemical Physics. 2 (2000) 1155-1163
1463-9076
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dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
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