Structure and Morphology of Poly(diethyl trimethylene-1,1-dicarboxylate) Crystals

Poly(diethyl trimethylene-1,1-dicarboxylate) oligomers with an average degree of polymerization (DP) of 20 and a polydispersity of 1.13 have been isothermally crystallized at 30 °C from benzene and also crystallized from the melt (T m = 176 °C). The crystals were investigated using electron microsco...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Macromolecules 2002-08, Vol.35 (18), p.6975-6984
Hauptverfasser: Sikorski, Pawel, Atkins, Edward D. T, Kagumba, Lawino C, Penelle, Jacques
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 6984
container_issue 18
container_start_page 6975
container_title Macromolecules
container_volume 35
creator Sikorski, Pawel
Atkins, Edward D. T
Kagumba, Lawino C
Penelle, Jacques
description Poly(diethyl trimethylene-1,1-dicarboxylate) oligomers with an average degree of polymerization (DP) of 20 and a polydispersity of 1.13 have been isothermally crystallized at 30 °C from benzene and also crystallized from the melt (T m = 176 °C). The crystals were investigated using electron microscopy (imaging and diffraction), X-ray diffraction, and computational modeling. The diffraction signals index on an orthorhombic unit cell with parameters a = 1.554 ± 0.002 nm, b = 1.136 ± 0.002 nm, and c (chain axis) = 0.585 ± 0.002 nm. A space group of P212121 is assigned on the basis of systematic absences of h00, 0k0, and 00l for odd h, k, and l respectively; thus, two antiparallel chain segments pass through the basal ab plane of the unit cell. The calculated density of 1.20 g·cm-3 is commensurate with the measured value of 1.17 ± 0.03 g·cm-3. The repetitive −CH2−CH2−CX2− backbone conformation, where the side groups X are ethyl esters (−COOC2H5), has the torsional angle sequence GT ḠGT Ḡ with the trans bonds at the dimethylene C−CH2−CH2−C sites. This conformation generates a 2-fold helix with a pitch that matches the measured crystallographic c-value of 0.585 nm. Ellipsoidal-shaped, lamellar-like crystals, with lateral dimensions on the micron scale but only 7.23 nm thick, are obtained by isothermal crystallization from benzene at 30 °C. Electron and X-ray diffraction data show that the molecular axes are orthogonal to the lamellar surface and that the crystal thickness matches a DP of 20. Thus, a degree of selective crystallization of molecular length occurs in these solution-grown crystals at fixed temperature. Under appropriate conditions, the crystals also stack to generate a one-dimensional lattice. This feature does not occur in the melt-crystallized fibers; in this case, the lamellar-like character is suppressed as the polydisperse molecules interpenetrate to form a crystal with a greater coherence length in the c-direction but, of course, with chain-end defects.
doi_str_mv 10.1021/ma020486z
format Article
fullrecord <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_ma020486z</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>a734671408</sourcerecordid><originalsourceid>FETCH-LOGICAL-a325t-7ea0422af1cdfc6ec168b231db4cbed10f253295556fa32975eb0d0712058973</originalsourceid><addsrcrecordid>eNptkF9LwzAUxYMoOKcPfoO-CA6M3iRN0z7K0ClsOlnfQ5qmrrNrRpLB6qe3OpkvPp0L93fO_YPQJYFbApTcrRVQiNPk8wgNCKeAecr4MRoA0BhnNBOn6Mz7FQAhPGYD9LYIbqvD1plItWU0s26ztI197yJbRXPbdNdlbcKya6Lg6vVPZVqDyQ3BZa2VK-yua1Qwo2jsOh9U48_RSdWLufjVIcofH_LxE56-Tp7H91OsGOUBC6MgplRVRJeVTowmSVpQRsoi1oUpCVSUM5pxzpOqd2SCmwJKEIQCTzPBhmi0j9XOeu9MJTf9gsp1koD8foU8vKJnr_bsRnmtmsqpVtf-z8BSASLJeg7vudoHszv0lfuQiWCCy3y-kHwyA5a_5HLyl6u0lyu7dW1_8D_zvwDkHHmZ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Structure and Morphology of Poly(diethyl trimethylene-1,1-dicarboxylate) Crystals</title><source>ACS Publications</source><creator>Sikorski, Pawel ; Atkins, Edward D. T ; Kagumba, Lawino C ; Penelle, Jacques</creator><creatorcontrib>Sikorski, Pawel ; Atkins, Edward D. T ; Kagumba, Lawino C ; Penelle, Jacques</creatorcontrib><description>Poly(diethyl trimethylene-1,1-dicarboxylate) oligomers with an average degree of polymerization (DP) of 20 and a polydispersity of 1.13 have been isothermally crystallized at 30 °C from benzene and also crystallized from the melt (T m = 176 °C). The crystals were investigated using electron microscopy (imaging and diffraction), X-ray diffraction, and computational modeling. The diffraction signals index on an orthorhombic unit cell with parameters a = 1.554 ± 0.002 nm, b = 1.136 ± 0.002 nm, and c (chain axis) = 0.585 ± 0.002 nm. A space group of P212121 is assigned on the basis of systematic absences of h00, 0k0, and 00l for odd h, k, and l respectively; thus, two antiparallel chain segments pass through the basal ab plane of the unit cell. The calculated density of 1.20 g·cm-3 is commensurate with the measured value of 1.17 ± 0.03 g·cm-3. The repetitive −CH2−CH2−CX2− backbone conformation, where the side groups X are ethyl esters (−COOC2H5), has the torsional angle sequence GT ḠGT Ḡ with the trans bonds at the dimethylene C−CH2−CH2−C sites. This conformation generates a 2-fold helix with a pitch that matches the measured crystallographic c-value of 0.585 nm. Ellipsoidal-shaped, lamellar-like crystals, with lateral dimensions on the micron scale but only 7.23 nm thick, are obtained by isothermal crystallization from benzene at 30 °C. Electron and X-ray diffraction data show that the molecular axes are orthogonal to the lamellar surface and that the crystal thickness matches a DP of 20. Thus, a degree of selective crystallization of molecular length occurs in these solution-grown crystals at fixed temperature. Under appropriate conditions, the crystals also stack to generate a one-dimensional lattice. This feature does not occur in the melt-crystallized fibers; in this case, the lamellar-like character is suppressed as the polydisperse molecules interpenetrate to form a crystal with a greater coherence length in the c-direction but, of course, with chain-end defects.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma020486z</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Properties and characterization ; Structure, morphology and analysis</subject><ispartof>Macromolecules, 2002-08, Vol.35 (18), p.6975-6984</ispartof><rights>Copyright © 2002 American Chemical Society</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a325t-7ea0422af1cdfc6ec168b231db4cbed10f253295556fa32975eb0d0712058973</citedby><cites>FETCH-LOGICAL-a325t-7ea0422af1cdfc6ec168b231db4cbed10f253295556fa32975eb0d0712058973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ma020486z$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma020486z$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=13870769$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Sikorski, Pawel</creatorcontrib><creatorcontrib>Atkins, Edward D. T</creatorcontrib><creatorcontrib>Kagumba, Lawino C</creatorcontrib><creatorcontrib>Penelle, Jacques</creatorcontrib><title>Structure and Morphology of Poly(diethyl trimethylene-1,1-dicarboxylate) Crystals</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>Poly(diethyl trimethylene-1,1-dicarboxylate) oligomers with an average degree of polymerization (DP) of 20 and a polydispersity of 1.13 have been isothermally crystallized at 30 °C from benzene and also crystallized from the melt (T m = 176 °C). The crystals were investigated using electron microscopy (imaging and diffraction), X-ray diffraction, and computational modeling. The diffraction signals index on an orthorhombic unit cell with parameters a = 1.554 ± 0.002 nm, b = 1.136 ± 0.002 nm, and c (chain axis) = 0.585 ± 0.002 nm. A space group of P212121 is assigned on the basis of systematic absences of h00, 0k0, and 00l for odd h, k, and l respectively; thus, two antiparallel chain segments pass through the basal ab plane of the unit cell. The calculated density of 1.20 g·cm-3 is commensurate with the measured value of 1.17 ± 0.03 g·cm-3. The repetitive −CH2−CH2−CX2− backbone conformation, where the side groups X are ethyl esters (−COOC2H5), has the torsional angle sequence GT ḠGT Ḡ with the trans bonds at the dimethylene C−CH2−CH2−C sites. This conformation generates a 2-fold helix with a pitch that matches the measured crystallographic c-value of 0.585 nm. Ellipsoidal-shaped, lamellar-like crystals, with lateral dimensions on the micron scale but only 7.23 nm thick, are obtained by isothermal crystallization from benzene at 30 °C. Electron and X-ray diffraction data show that the molecular axes are orthogonal to the lamellar surface and that the crystal thickness matches a DP of 20. Thus, a degree of selective crystallization of molecular length occurs in these solution-grown crystals at fixed temperature. Under appropriate conditions, the crystals also stack to generate a one-dimensional lattice. This feature does not occur in the melt-crystallized fibers; in this case, the lamellar-like character is suppressed as the polydisperse molecules interpenetrate to form a crystal with a greater coherence length in the c-direction but, of course, with chain-end defects.</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Properties and characterization</subject><subject>Structure, morphology and analysis</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNptkF9LwzAUxYMoOKcPfoO-CA6M3iRN0z7K0ClsOlnfQ5qmrrNrRpLB6qe3OpkvPp0L93fO_YPQJYFbApTcrRVQiNPk8wgNCKeAecr4MRoA0BhnNBOn6Mz7FQAhPGYD9LYIbqvD1plItWU0s26ztI197yJbRXPbdNdlbcKya6Lg6vVPZVqDyQ3BZa2VK-yua1Qwo2jsOh9U48_RSdWLufjVIcofH_LxE56-Tp7H91OsGOUBC6MgplRVRJeVTowmSVpQRsoi1oUpCVSUM5pxzpOqd2SCmwJKEIQCTzPBhmi0j9XOeu9MJTf9gsp1koD8foU8vKJnr_bsRnmtmsqpVtf-z8BSASLJeg7vudoHszv0lfuQiWCCy3y-kHwyA5a_5HLyl6u0lyu7dW1_8D_zvwDkHHmZ</recordid><startdate>20020827</startdate><enddate>20020827</enddate><creator>Sikorski, Pawel</creator><creator>Atkins, Edward D. T</creator><creator>Kagumba, Lawino C</creator><creator>Penelle, Jacques</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20020827</creationdate><title>Structure and Morphology of Poly(diethyl trimethylene-1,1-dicarboxylate) Crystals</title><author>Sikorski, Pawel ; Atkins, Edward D. T ; Kagumba, Lawino C ; Penelle, Jacques</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a325t-7ea0422af1cdfc6ec168b231db4cbed10f253295556fa32975eb0d0712058973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Properties and characterization</topic><topic>Structure, morphology and analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sikorski, Pawel</creatorcontrib><creatorcontrib>Atkins, Edward D. T</creatorcontrib><creatorcontrib>Kagumba, Lawino C</creatorcontrib><creatorcontrib>Penelle, Jacques</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sikorski, Pawel</au><au>Atkins, Edward D. T</au><au>Kagumba, Lawino C</au><au>Penelle, Jacques</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure and Morphology of Poly(diethyl trimethylene-1,1-dicarboxylate) Crystals</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2002-08-27</date><risdate>2002</risdate><volume>35</volume><issue>18</issue><spage>6975</spage><epage>6984</epage><pages>6975-6984</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>Poly(diethyl trimethylene-1,1-dicarboxylate) oligomers with an average degree of polymerization (DP) of 20 and a polydispersity of 1.13 have been isothermally crystallized at 30 °C from benzene and also crystallized from the melt (T m = 176 °C). The crystals were investigated using electron microscopy (imaging and diffraction), X-ray diffraction, and computational modeling. The diffraction signals index on an orthorhombic unit cell with parameters a = 1.554 ± 0.002 nm, b = 1.136 ± 0.002 nm, and c (chain axis) = 0.585 ± 0.002 nm. A space group of P212121 is assigned on the basis of systematic absences of h00, 0k0, and 00l for odd h, k, and l respectively; thus, two antiparallel chain segments pass through the basal ab plane of the unit cell. The calculated density of 1.20 g·cm-3 is commensurate with the measured value of 1.17 ± 0.03 g·cm-3. The repetitive −CH2−CH2−CX2− backbone conformation, where the side groups X are ethyl esters (−COOC2H5), has the torsional angle sequence GT ḠGT Ḡ with the trans bonds at the dimethylene C−CH2−CH2−C sites. This conformation generates a 2-fold helix with a pitch that matches the measured crystallographic c-value of 0.585 nm. Ellipsoidal-shaped, lamellar-like crystals, with lateral dimensions on the micron scale but only 7.23 nm thick, are obtained by isothermal crystallization from benzene at 30 °C. Electron and X-ray diffraction data show that the molecular axes are orthogonal to the lamellar surface and that the crystal thickness matches a DP of 20. Thus, a degree of selective crystallization of molecular length occurs in these solution-grown crystals at fixed temperature. Under appropriate conditions, the crystals also stack to generate a one-dimensional lattice. This feature does not occur in the melt-crystallized fibers; in this case, the lamellar-like character is suppressed as the polydisperse molecules interpenetrate to form a crystal with a greater coherence length in the c-direction but, of course, with chain-end defects.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma020486z</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0024-9297
ispartof Macromolecules, 2002-08, Vol.35 (18), p.6975-6984
issn 0024-9297
1520-5835
language eng
recordid cdi_crossref_primary_10_1021_ma020486z
source ACS Publications
subjects Applied sciences
Exact sciences and technology
Organic polymers
Physicochemistry of polymers
Properties and characterization
Structure, morphology and analysis
title Structure and Morphology of Poly(diethyl trimethylene-1,1-dicarboxylate) Crystals
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T12%3A46%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Structure%20and%20Morphology%20of%20Poly(diethyl%20trimethylene-1,1-dicarboxylate)%20Crystals&rft.jtitle=Macromolecules&rft.au=Sikorski,%20Pawel&rft.date=2002-08-27&rft.volume=35&rft.issue=18&rft.spage=6975&rft.epage=6984&rft.pages=6975-6984&rft.issn=0024-9297&rft.eissn=1520-5835&rft.coden=MAMOBX&rft_id=info:doi/10.1021/ma020486z&rft_dat=%3Cacs_cross%3Ea734671408%3C/acs_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true