Structural similarity and similarity in thermal properties of the polymorphs: melting and crystallization from the melt of tolbutamide and chlorpropamide
The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The asymmetry in thermal transformations was revealed for both substances. Under heating, all tolbutamide/chlorpropamide polymorphs transform into hi...
Saved in:
Published in: | Journal of thermal analysis and calorimetry Vol. 142; no. 2; pp. 841 - 848 |
---|---|
Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Cham
Springer International Publishing
01-10-2020
Springer Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Abstract | The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The asymmetry in thermal transformations was revealed for both substances. Under heating, all tolbutamide/chlorpropamide polymorphs transform into high-temperature I
H
/ε polymorph, which melts at 128 °C. The crystal structures of the high-temperature polymorphs, I
H
and ε, are very similar to each other in the unit cell parameters and in the arrangement of z-shaped infinite hydrogen-bonded ribbons. Under cooling, other polymorph crystallizes from the melt, V for tolbutamide and β for chlorpropamide, thus making easy the obtaining of these metastable polymorphs. The polymorphs of tolbutamide and chlorpropamide crystallized from their melts turned out to be also very similar to each other in their structures (space group, unit cell parameters, arrangement of π-shaped infinite hydrogen-bonded ribbons). Solid–solid transformation V ⇒ II in tolbutamide was detected both in samples stored under room conditions and those melted in capillaries, thus providing new easy way for II tolbutamide crystallization. In generalizing our results, one can expect that if evident similarity is found among the polymorphs of similar molecules in their crystal structure, the similarity in their thermal properties can be also found, and vice versa. |
---|---|
AbstractList | The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The asymmetry in thermal transformations was revealed for both substances. Under heating, all tolbutamide/chlorpropamide polymorphs transform into high-temperature I
H
/ε polymorph, which melts at 128 °C. The crystal structures of the high-temperature polymorphs, I
H
and ε, are very similar to each other in the unit cell parameters and in the arrangement of z-shaped infinite hydrogen-bonded ribbons. Under cooling, other polymorph crystallizes from the melt, V for tolbutamide and β for chlorpropamide, thus making easy the obtaining of these metastable polymorphs. The polymorphs of tolbutamide and chlorpropamide crystallized from their melts turned out to be also very similar to each other in their structures (space group, unit cell parameters, arrangement of π-shaped infinite hydrogen-bonded ribbons). Solid–solid transformation V ⇒ II in tolbutamide was detected both in samples stored under room conditions and those melted in capillaries, thus providing new easy way for II tolbutamide crystallization. In generalizing our results, one can expect that if evident similarity is found among the polymorphs of similar molecules in their crystal structure, the similarity in their thermal properties can be also found, and vice versa. The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The asymmetry in thermal transformations was revealed for both substances. Under heating, all tolbutamide/chlorpropamide polymorphs transform into high-temperature I.sup.H/[epsilon] polymorph, which melts at 128 °C. The crystal structures of the high-temperature polymorphs, I.sup.H and [epsilon], are very similar to each other in the unit cell parameters and in the arrangement of z-shaped infinite hydrogen-bonded ribbons. Under cooling, other polymorph crystallizes from the melt, V for tolbutamide and [beta] for chlorpropamide, thus making easy the obtaining of these metastable polymorphs. The polymorphs of tolbutamide and chlorpropamide crystallized from their melts turned out to be also very similar to each other in their structures (space group, unit cell parameters, arrangement of [pi]-shaped infinite hydrogen-bonded ribbons). Solid-solid transformation V â II in tolbutamide was detected both in samples stored under room conditions and those melted in capillaries, thus providing new easy way for II tolbutamide crystallization. In generalizing our results, one can expect that if evident similarity is found among the polymorphs of similar molecules in their crystal structure, the similarity in their thermal properties can be also found, and vice versa. The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The asymmetry in thermal transformations was revealed for both substances. Under heating, all tolbutamide/chlorpropamide polymorphs transform into high-temperature IH/ε polymorph, which melts at 128 °C. The crystal structures of the high-temperature polymorphs, IH and ε, are very similar to each other in the unit cell parameters and in the arrangement of z-shaped infinite hydrogen-bonded ribbons. Under cooling, other polymorph crystallizes from the melt, V for tolbutamide and β for chlorpropamide, thus making easy the obtaining of these metastable polymorphs. The polymorphs of tolbutamide and chlorpropamide crystallized from their melts turned out to be also very similar to each other in their structures (space group, unit cell parameters, arrangement of π-shaped infinite hydrogen-bonded ribbons). Solid–solid transformation V ⇒ II in tolbutamide was detected both in samples stored under room conditions and those melted in capillaries, thus providing new easy way for II tolbutamide crystallization. In generalizing our results, one can expect that if evident similarity is found among the polymorphs of similar molecules in their crystal structure, the similarity in their thermal properties can be also found, and vice versa. |
Audience | Academic |
Author | Drebushchak, T. N. Drebushchak, V. A. |
Author_xml | – sequence: 1 givenname: T. N. orcidid: 0000-0001-7589-6938 surname: Drebushchak fullname: Drebushchak, T. N. email: tanya@xray.nsu.ru organization: Institute of Solid State Chemistry and Mechanochemistry, SB RAS, Novosibirsk State University – sequence: 2 givenname: V. A. orcidid: 0000-0002-2106-6194 surname: Drebushchak fullname: Drebushchak, V. A. organization: Novosibirsk State University, V.S. Sobolev Institute of Geology and Mineralogy, SB RAS |
BookMark | eNp9kktr3DAQgE1JoXn9gZ4MPfXgdCRZttVbCH0EAoWkOQutLO0q6OFKMnTzT_pvq7UL6UIpOmg0fN8MkuasOvHBq6p6i-AKAfQfEgLWkwYwNMDanjbtq-oU0WFoMMPdSYlJiTtE4U11ltITADAG6LT69ZDjLPMcha2TccaKaPK-Fn78-2h8nXcqugJNMUwqZqNSHfQhW0_B7l2I0y59rJ2y2fjt4su4T1lYa55FNsHXOga3CAdokYPdzFk4M6pV2NlSptRfUhfVay1sUpd_9vPq8fOn7zdfm7tvX25vru8aSTHJTSfRAIJotKFaspa1eEAUw7BBUjApVDsi2WHSK40llWKUSrPyGCAYHXUvFDmv3q11S-cfs0qZP4U5-tKS47YnpVrXdS_UVljFjdchRyGdSZJfd4Rh6IHRQl39gyprVM7I8mXalPyR8P5IKExWP_NWzCnx24f7YxavrIwhpag0n6JxIu45An6YAr5OAS9TwJcp4G2RyCqlAvutii-3-4_1G2GcuZA |
CitedBy_id | crossref_primary_10_1021_acs_molpharmaceut_2c00434 crossref_primary_10_1107_S2052520622000889 crossref_primary_10_1016_j_ijpharm_2022_122057 crossref_primary_10_1021_acs_cgd_2c01065 crossref_primary_10_1039_D3CC04725C |
Cites_doi | 10.1007/s10973-016-5954-0 10.1107/S0021889807067908 10.1107/S2052519213018861 10.1107/S0108768111004290 10.1039/C7CE02221B 10.1080/0889311X.2016.1251909 10.1007/s10973-019-08031-z 10.1002/jps.22061 10.1039/C6CE00764C 10.1039/c3ra41559g 10.1016/j.addr.2016.12.001 10.1007/s10973-017-6928-6 10.1007/s10973-018-7637-5 10.1016/j.xphs.2016.03.021 10.1007/s10973-018-7553-8 10.1007/s10973-017-6091-0 10.1002/ceat.200500397 10.1007/s10973-007-8822-0 10.1007/s10973-004-0586-1 10.1107/S0108270108034550 10.1515/zpch-1897-2233 10.1039/C0CE00073F 10.1039/C1CE05189J 10.1107/S1600536806035628 10.1107/S010876810903290X 10.1021/cr400249d 10.1007/s10973-018-7142-x |
ContentType | Journal Article |
Copyright | Akadémiai Kiadó, Budapest, Hungary 2020 COPYRIGHT 2020 Springer Akadémiai Kiadó, Budapest, Hungary 2020. |
Copyright_xml | – notice: Akadémiai Kiadó, Budapest, Hungary 2020 – notice: COPYRIGHT 2020 Springer – notice: Akadémiai Kiadó, Budapest, Hungary 2020. |
DBID | AAYXX CITATION ISR |
DOI | 10.1007/s10973-020-09475-4 |
DatabaseName | CrossRef Science in Context |
DatabaseTitle | CrossRef |
DatabaseTitleList | |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
EISSN | 1588-2926 |
EndPage | 848 |
ExternalDocumentID | A639207095 10_1007_s10973_020_09475_4 |
GrantInformation_xml | – fundername: Ministry of Education and Science of the Russian Federation grantid: АААА-А17-117030310274-5; 0330-2016-0004 funderid: http://dx.doi.org/10.13039/501100003443 |
GroupedDBID | -4Y -58 -5G -BR -EM -Y2 -~C .86 .VR 06C 06D 0R~ 0VY 1N0 2.D 203 29L 2J2 2JN 2JY 2KG 2KM 2LR 2P1 2VQ 2~H 30V 4.4 406 408 409 40D 40E 53G 5GY 5QI 5VS 67Z 6NX 8TC 8UJ 95- 95. 95~ 96X AAAVM AABHQ AABYN AAFGU AAGCJ AAHNG AAIAL AAIKT AANZL AARHV AARTL AATNV AATVU AAUCO AAUYE AAWCG AAYFA AAYIU AAYQN AAYTO ABBBX ABBXA ABDBF ABDZT ABECU ABFGW ABFTV ABHLI ABHQN ABJOX ABKAS ABKCH ABKTR ABMNI ABMQK ABNWP ABPTK ABQBU ABSXP ABTEG ABTHY ABTKH ABTMW ABULA ABWNU ABXPI ACBMV ACBRV ACBXY ACBYP ACGFS ACHSB ACHXU ACIGE ACIPQ ACIWK ACKNC ACMDZ ACMLO ACOKC ACOMO ACSNA ACTTH ACVWB ACWMK ADHIR ADINQ ADKNI ADKPE ADMDM ADOXG ADPHR ADRFC ADTPH ADURQ ADYFF ADZKW AEBTG AEEQQ AEFIE AEGAL AEGNC AEJHL AEJRE AEKMD AENEX AEOHA AEPYU AESKC AETLH AEVLU AEXYK AFEXP AFGCZ AFLOW AFNRJ AFQWF AFWTZ AFZKB AGAYW AGDGC AGGDS AGJBK AGMZJ AGQMX AGWIL AGWZB AGYKE AHAVH AHBYD AHKAY AHSBF AHYZX AI. AIAKS AIIXL AILAN AIMYW AITGF AJBLW AJDOV AJGSW AJRNO AJZVZ AKQUC ALMA_UNASSIGNED_HOLDINGS ALWAN AMKLP AMXSW AMYLF AOCGG ARMRJ AXYYD AYJHY AZFZN B-. B0M BA0 BDATZ BGNMA CAG COF CS3 CSCUP DDRTE DL5 DNIVK DPUIP DU5 EAD EAP EBLON EBS EIOEI EJD EMK EPL ESBYG ESX F5P FEDTE FERAY FFXSO FIGPU FINBP FNLPD FRRFC FSGXE FWDCC G-Y G-Z GGCAI GGRSB GJIRD GNWQR GQ6 GQ7 GQ8 GXS HF~ HG5 HG6 HMJXF HQYDN HRMNR HVGLF HZ~ I-F IAO IHE IJ- IKXTQ ISR ITC ITM IWAJR IXC IXE IZIGR IZQ I~X I~Z J-C J0Z JBSCW JCJTX JZLTJ KDC KOV LAK LLZTM M4Y MA- MET MKB N2Q N9A NB0 NDZJH NPVJJ NQJWS NU0 O9- O93 O9G O9I O9J OAM OVD P19 P9N PF0 PT4 PT5 QOK QOR QOS R89 R9I RKA RNI RNS ROL RPX RSV RZC RZE RZK S16 S1Z S26 S27 S28 S3B SAP SCG SCLPG SCM SDH SHX SISQX SJYHP SNE SNPRN SNX SOHCF SOJ SPISZ SQXTU SRMVM SSLCW STPWE SZN T13 T16 TEORI TSG TSK TSV TUC TUS U2A UG4 UNUBA UOJIU UTJUX UZXMN VC2 VFIZW VH1 W23 W48 W4F WJK WK8 YLTOR Z45 Z5O Z7R Z7S Z7U Z7V Z7W Z7X Z7Y Z7Z Z81 Z83 Z85 Z86 Z87 Z88 Z8M Z8N Z8O Z8P Z8Q Z8R Z8T Z8W Z91 Z92 ZE2 ZMTXR ~02 ~8M AACDK AAEOY AAJBT AASML AAYXX AAYZH ABAKF ACAOD ACDTI ACZOJ AEFQL AEMSY AFBBN AGJZZ AGQEE AGRTI AIGIU CITATION H13 |
ID | FETCH-LOGICAL-c523t-6c180a3f1b5fc94942815208b1ca9cae4d1c6237ef2c5cadcef91380a95df7ae3 |
IEDL.DBID | AEJHL |
ISSN | 1388-6150 |
IngestDate | Tue Nov 19 04:54:08 EST 2024 Tue Nov 19 20:38:25 EST 2024 Tue Nov 12 23:16:26 EST 2024 Thu Aug 01 19:36:58 EDT 2024 Thu Nov 21 21:32:53 EST 2024 Sat Dec 16 12:02:38 EST 2023 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Keywords | Chlorpropamide X-ray diffraction DSC Tolbutamide Polymorphism |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c523t-6c180a3f1b5fc94942815208b1ca9cae4d1c6237ef2c5cadcef91380a95df7ae3 |
ORCID | 0000-0001-7589-6938 0000-0002-2106-6194 |
PQID | 2473815666 |
PQPubID | 2043843 |
PageCount | 8 |
ParticipantIDs | proquest_journals_2473815666 gale_infotracmisc_A639207095 gale_infotracacademiconefile_A639207095 gale_incontextgauss_ISR_A639207095 crossref_primary_10_1007_s10973_020_09475_4 springer_journals_10_1007_s10973_020_09475_4 |
PublicationCentury | 2000 |
PublicationDate | 2020-10-01 |
PublicationDateYYYYMMDD | 2020-10-01 |
PublicationDate_xml | – month: 10 year: 2020 text: 2020-10-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | Cham |
PublicationPlace_xml | – name: Cham – name: Dordrecht |
PublicationSubtitle | An International Forum for Thermal Studies |
PublicationTitle | Journal of thermal analysis and calorimetry |
PublicationTitleAbbrev | J Therm Anal Calorim |
PublicationYear | 2020 |
Publisher | Springer International Publishing Springer Springer Nature B.V |
Publisher_xml | – name: Springer International Publishing – name: Springer – name: Springer Nature B.V |
References | BrogJPChanezCLCrochetAFrommKMPolymorphism, what it is and how to identify it: a systematic reviewRSC Adv2013316905169311:CAS:528:DC%2BC3sXhsVShsLjI10.1039/c3ra41559g DrebushchakTNDrebushchakVAPankrushinaNABoldyrevaEVSingle-crystal to single-crystal conformational polymorphic transformation in tolbutamide at 313 K. Relation to other polymorphic transformations in tolbutamide and chlorpropamideCrystEngComm201618573657431:CAS:528:DC%2BC28XpvVamsLY%3D10.1039/C6CE00764C MacraeCFBrunoIJChisholmJAEdgingtonPRMcCabePPidcockERodriguez-MongeLTaylorRvan de StreekJWoodPAMercury CSD 2.0—new features for the visualization and investigation of crystal structuresJ Appl Cryst2008414664701:CAS:528:DC%2BD1cXjt1Gmtb0%3D10.1107/S0021889807067908 DrebushchakVAMcGregorLRychkovDACooling rate “window” in the crystallization of metacetamol form IIJ Therm Anal Calorim2017127180718141:CAS:528:DC%2BC28XhvFegtrzJ10.1007/s10973-016-5954-0 DrebushchakTNChesalovYABoldyrevaEVA conformational polymorphic transition in the high-temperature epsilon-form of chlorpropamide on cooling: a new ε′-formActa Cryst B2009657707811:CAS:528:DC%2BD1MXhsVaksr%2FI10.1107/S010876810903290X BrittainHGPolymorphism in pharmaceutical solids1999New YorkMarcel Dekker Inc. ZhaoYZhengZBLiSThermodynamic relationship between flupirtine maleate polymorphsJ Therm Anal Calorim2018134205720631:CAS:528:DC%2BC1cXhs1ClsLfI10.1007/s10973-018-7637-5 SvärdMValaviMKhamarDKuhsMRasmusonÅCThermodynamic stability analysis of tolbutamide polymorphs and solubility in organic solventsJ Pharm Sci2016105190119061:CAS:528:DC%2BC28XhtF2mtrnL10.1016/j.xphs.2016.03.02127238487 Roque-FloresRLdo Rosário MatosJSimultaneous measurements of X-ray diffraction–differential scanning calorimetry. The investigation of the phase transition of ganciclovir and characterization of its polymorphic formsJ Therm Anal Calorim2019137134713581:CAS:528:DC%2BC1MXmtF2gt78%3D10.1007/s10973-019-08031-z DrebushchakVACalibration coefficient of a heat-flow DSC; Part II. Optimal calibration procedureJ Therm Anal Calorim2005792132181:CAS:528:DC%2BD2MXhs1ahtbs%3D10.1007/s10973-004-0586-1 DrebushchakVADrebushchakTNChukanovNVBoldyrevaEVTransitions among five polymorphs of chlorpropamide near the melting pointJ Therm Anal Calorim2008933433511:CAS:528:DC%2BD1cXosl2mu7s%3D10.1007/s10973-007-8822-0 DetrichÁDömötörKJKatonaMTMarkovitsILángJVPolymorphic forms of bisoprolol fumarateJ Therm Anal Calorim2019135304330551:CAS:528:DC%2BC1cXhtlKmt7vP10.1007/s10973-018-7553-8 KarpinskiPHPolymorphism of active pharmaceutical ingredientsChem Eng Technol2006292332371:CAS:528:DC%2BD28Xhs1alsb0%3D10.1002/ceat.200500397 OstwaldWStudien über die Bildung und Umwandlung fester KörperZ Phys Chem1897222893301:CAS:528:DyaD28Xpt1elsw%3D%3D10.1515/zpch-1897-2233 PriceSLWhy don’t we find more polymorphs?Acta Cryst B2013693133281:CAS:528:DC%2BC3sXhtFChsr3N10.1107/S2052519213018861 Cruz-CabezaAJBernsteinJConformational polymorphismChem Rev2014114217021911:CAS:528:DC%2BC3sXhvFCrsLvP10.1021/cr400249d24350653 BernsteinJPolymorphism in molecular crystals2002OxfordClarendon Press ThirunahariSAitipamulaSChowPSTanRBHConformational polymorphism of tolbutamide: a structural, spectroscopic, and thermodynamic characterization of Burger’s forms I–IVJ Pharm Sci201099297529901:CAS:528:DC%2BC3cXlsVSkurg%3D10.1002/jps.2206120091821 BouvartNPalixRMArkhipovSGTumanovIAMichalchukAALBoldyrevaEVPolymorphism of chlorpropamide on liquid-assisted mechanical treatment: choice of liquid and type of mechanical treatment matterCrystEngComm201820179718031:CAS:528:DC%2BC1cXisFKqs7k%3D10.1039/C7CE02221B NathNKNangiaANovel form V of tolbutamide and a high Z′ crystal structure of form IIICrystEngComm20111347511:CAS:528:DC%2BC3MXisFyrug%3D%3D10.1039/C0CE00073F DrebushchakTNDrebushchakVABoldyrevaEVSolid-state transformations in the β-form of chlorpropamide on cooling to 100 KActa Cryst B2011671631761:CAS:528:DC%2BC3MXjt1yqurs%3D10.1107/S0108768111004290 NeglurRHostenEAucampMLiebenbergWGrooffDWater and the relationship to the crystal structure stability of azithromycin. Thermal investigations of solvatomorphism, amorphism and polymorphismJ Therm Anal Calorim20181323733841:CAS:528:DC%2BC1cXjs1Clsg%3D%3D10.1007/s10973-017-6928-6 DrebushchakTNOgienkoAABoldyrevaEV‘Hedvall effect’ in cryogrinding of molecular crystals. A case study of a polymorphic transition in chlorpropamideCrystEngComm201113440544101:CAS:528:DC%2BC3MXotV2itrk%3D10.1039/C1CE05189J BombiczPThe way from isostructurality to polymorphism. Where are the borders? The role of supramolecular interactions and crystal symmetriesCrystallogr Rev20172311815110.1080/0889311X.2016.1251909 WinXPOW. Stoe & Cie GmbH. Darmstadt: Germany; 2011. HigashiKUedaKMoribeKRecent progress of structural study of polymorphic pharmaceutical drugsAdv Drug Deliv Rev201711771851:CAS:528:DC%2BC28XitVyru7fP10.1016/j.addr.2016.12.00127940141 OsieckaNJuszyńska-GałązkaEGalewskiZJaworska-GołąbTDeptuchAMassalska-ArodźMInsight into polymorphism of the ethosuximide (ETX)J Therm Anal Calorim20181339619671:CAS:528:DC%2BC1cXktFOntr0%3D10.1007/s10973-018-7142-x DrebushchakTNChukanovNVBoldyrevaEVA new polymorph of chlorpropamide: 4-chloro-N-(propylaminocarbonyl) benzenesulfonamideActa Cryst E200662o4393o43951:CAS:528:DC%2BD28XhtVeht7jM10.1107/S1600536806035628 de SouzaCMdos SantosJAdo NascimentoALJúniorJVJúniorFJde Lima NetoSAde SouzaFSMacêdoROThermal analysis study of solid dispersions hydrochlorothiazideJ Therm Anal Calorim20181316816891:CAS:528:DC%2BC2sXhvFagtLg%3D10.1007/s10973-017-6091-0 DrebushchakTNChukanovNVBoldyrevaEVTwo polymorphs of chlorpropamide: the δ-form and the high-temperature ε-formActa Cryst C200864o623o6251:CAS:528:DC%2BD1cXhsVKhtL%2FJ10.1107/S0108270108034550 TN Drebushchak (9475_CR27) 2011; 13 VA Drebushchak (9475_CR11) 2008; 93 S Thirunahari (9475_CR10) 2010; 99 Y Zhao (9475_CR20) 2018; 134 N Bouvart (9475_CR24) 2018; 20 9475_CR22 VA Drebushchak (9475_CR30) 2017; 127 TN Drebushchak (9475_CR9) 2016; 18 RL Roque-Flores (9475_CR19) 2019; 137 TN Drebushchak (9475_CR26) 2009; 65 (9475_CR1) 1999 CF Macrae (9475_CR23) 2008; 41 J Bernstein (9475_CR2) 2002 K Higashi (9475_CR7) 2017; 117 P Bombicz (9475_CR6) 2017; 23 W Ostwald (9475_CR29) 1897; 22 TN Drebushchak (9475_CR14) 2011; 67 Á Detrich (9475_CR16) 2019; 135 NK Nath (9475_CR13) 2011; 13 PH Karpinski (9475_CR8) 2006; 29 R Neglur (9475_CR17) 2018; 132 VA Drebushchak (9475_CR21) 2005; 79 M Svärd (9475_CR12) 2016; 105 CM de Souza (9475_CR15) 2018; 131 N Osiecka (9475_CR18) 2018; 133 JP Brog (9475_CR3) 2013; 3 TN Drebushchak (9475_CR25) 2008; 64 AJ Cruz-Cabeza (9475_CR5) 2014; 114 SL Price (9475_CR4) 2013; 69 TN Drebushchak (9475_CR28) 2006; 62 |
References_xml | – volume: 127 start-page: 1807 year: 2017 ident: 9475_CR30 publication-title: J Therm Anal Calorim doi: 10.1007/s10973-016-5954-0 contributor: fullname: VA Drebushchak – volume: 41 start-page: 466 year: 2008 ident: 9475_CR23 publication-title: J Appl Cryst doi: 10.1107/S0021889807067908 contributor: fullname: CF Macrae – volume: 69 start-page: 313 year: 2013 ident: 9475_CR4 publication-title: Acta Cryst B doi: 10.1107/S2052519213018861 contributor: fullname: SL Price – volume: 67 start-page: 163 year: 2011 ident: 9475_CR14 publication-title: Acta Cryst B doi: 10.1107/S0108768111004290 contributor: fullname: TN Drebushchak – volume: 20 start-page: 1797 year: 2018 ident: 9475_CR24 publication-title: CrystEngComm doi: 10.1039/C7CE02221B contributor: fullname: N Bouvart – volume: 23 start-page: 118 year: 2017 ident: 9475_CR6 publication-title: Crystallogr Rev doi: 10.1080/0889311X.2016.1251909 contributor: fullname: P Bombicz – volume: 137 start-page: 1347 year: 2019 ident: 9475_CR19 publication-title: J Therm Anal Calorim doi: 10.1007/s10973-019-08031-z contributor: fullname: RL Roque-Flores – volume: 99 start-page: 2975 year: 2010 ident: 9475_CR10 publication-title: J Pharm Sci doi: 10.1002/jps.22061 contributor: fullname: S Thirunahari – volume: 18 start-page: 5736 year: 2016 ident: 9475_CR9 publication-title: CrystEngComm doi: 10.1039/C6CE00764C contributor: fullname: TN Drebushchak – volume: 3 start-page: 16905 year: 2013 ident: 9475_CR3 publication-title: RSC Adv doi: 10.1039/c3ra41559g contributor: fullname: JP Brog – volume-title: Polymorphism in pharmaceutical solids year: 1999 ident: 9475_CR1 – volume: 117 start-page: 71 year: 2017 ident: 9475_CR7 publication-title: Adv Drug Deliv Rev doi: 10.1016/j.addr.2016.12.001 contributor: fullname: K Higashi – volume: 132 start-page: 373 year: 2018 ident: 9475_CR17 publication-title: J Therm Anal Calorim doi: 10.1007/s10973-017-6928-6 contributor: fullname: R Neglur – volume: 134 start-page: 2057 year: 2018 ident: 9475_CR20 publication-title: J Therm Anal Calorim doi: 10.1007/s10973-018-7637-5 contributor: fullname: Y Zhao – volume: 105 start-page: 1901 year: 2016 ident: 9475_CR12 publication-title: J Pharm Sci doi: 10.1016/j.xphs.2016.03.021 contributor: fullname: M Svärd – volume: 135 start-page: 3043 year: 2019 ident: 9475_CR16 publication-title: J Therm Anal Calorim doi: 10.1007/s10973-018-7553-8 contributor: fullname: Á Detrich – volume: 131 start-page: 681 year: 2018 ident: 9475_CR15 publication-title: J Therm Anal Calorim doi: 10.1007/s10973-017-6091-0 contributor: fullname: CM de Souza – volume: 29 start-page: 233 year: 2006 ident: 9475_CR8 publication-title: Chem Eng Technol doi: 10.1002/ceat.200500397 contributor: fullname: PH Karpinski – volume: 93 start-page: 343 year: 2008 ident: 9475_CR11 publication-title: J Therm Anal Calorim doi: 10.1007/s10973-007-8822-0 contributor: fullname: VA Drebushchak – volume: 79 start-page: 213 year: 2005 ident: 9475_CR21 publication-title: J Therm Anal Calorim doi: 10.1007/s10973-004-0586-1 contributor: fullname: VA Drebushchak – volume: 64 start-page: o623 year: 2008 ident: 9475_CR25 publication-title: Acta Cryst C doi: 10.1107/S0108270108034550 contributor: fullname: TN Drebushchak – ident: 9475_CR22 – volume: 22 start-page: 289 year: 1897 ident: 9475_CR29 publication-title: Z Phys Chem doi: 10.1515/zpch-1897-2233 contributor: fullname: W Ostwald – volume: 13 start-page: 47 year: 2011 ident: 9475_CR13 publication-title: CrystEngComm doi: 10.1039/C0CE00073F contributor: fullname: NK Nath – volume: 13 start-page: 4405 year: 2011 ident: 9475_CR27 publication-title: CrystEngComm doi: 10.1039/C1CE05189J contributor: fullname: TN Drebushchak – volume: 62 start-page: o4393 year: 2006 ident: 9475_CR28 publication-title: Acta Cryst E doi: 10.1107/S1600536806035628 contributor: fullname: TN Drebushchak – volume: 65 start-page: 770 year: 2009 ident: 9475_CR26 publication-title: Acta Cryst B doi: 10.1107/S010876810903290X contributor: fullname: TN Drebushchak – volume-title: Polymorphism in molecular crystals year: 2002 ident: 9475_CR2 contributor: fullname: J Bernstein – volume: 114 start-page: 2170 year: 2014 ident: 9475_CR5 publication-title: Chem Rev doi: 10.1021/cr400249d contributor: fullname: AJ Cruz-Cabeza – volume: 133 start-page: 961 year: 2018 ident: 9475_CR18 publication-title: J Therm Anal Calorim doi: 10.1007/s10973-018-7142-x contributor: fullname: N Osiecka |
SSID | ssj0009901 |
Score | 2.3570492 |
Snippet | The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The... |
SourceID | proquest gale crossref springer |
SourceType | Aggregation Database Publisher |
StartPage | 841 |
SubjectTerms | Analysis Analytical Chemistry Capillaries Chemistry Chemistry and Materials Science Chlorpropamide Crystal structure Crystallization Crystals Diffraction High temperature Hydrogen Hydrogen bonding Inorganic Chemistry Measurement Science and Instrumentation Melts (crystal growth) Molecular structure Parameters Physical Chemistry Polymer Sciences Polymorphism Similarity Structure Thermal properties Thermal transformations Thermodynamic properties Tolbutamide Unit cell X ray powder diffraction X-rays |
Title | Structural similarity and similarity in thermal properties of the polymorphs: melting and crystallization from the melt of tolbutamide and chlorpropamide |
URI | https://link.springer.com/article/10.1007/s10973-020-09475-4 https://www.proquest.com/docview/2473815666 |
Volume | 142 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LbxMxELZoe4ALb9RAqSyExAGM1vs2t6hNFRDiQEBqT9as14ao-4iyyaE_hX_LjLNLmgIHuOxq7bE18syOZ2zPZ8Ze5tYUSaoyYWRkRSzBCbAWhIykhdDkqQopd3g6yz6d56cTgsmJfi1dNJdvhx1Jb6iv5bqpjLYcA4ERSZaIeI8d4NyToHIfjCcfph-3WLsq2MRZqASEd97nyvy5l5356KZV_m171M86Z_f-i9_77G7vZPLxRisesFu2echunwx3uz1iP2YeNpYgN3g3r-cY3qI3zqEpr3_OG07uYY1EC1qzXxL4Km8dlfJFW13VLUqpe8drW9Hpad_eLK_Q4ayqPr-TU_6Kb0BEvnFbFesV1PPSbhp8r7Ab7N8XPWZfzyZfTqaiv6RBGIxhVyI1Mg8gcrJInFGxwnAGXYIgL6QBZcDGpTToYmXWhSYxUBrrFEomAJWULgMbPWH7TdvYQ8bLEKIyMYV0JohtAEVuCzBWYvCf4TMdsdeDqPRig8Wht6jLNNwah1v74dbxiL0gaWoCuWjoFM03WHedfj_7rMfoloVo61QyYq96IteulmCgT0pAhggXa4fyaIcSBWZ2qwel0b0V6HQYZxGh8aTI-ptBS7bVf-f96b-RP2N3QlI0f8bwiO2jCtnnbK8r18f9v0Hv84uL05_FoQ6E |
link.rule.ids | 315,782,786,27933,27934,41073,42142,48344,48347,49649,49652,52153 |
linkProvider | Springer Nature |
linkToHtml | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LbxMxELZoeigX3ohAAQshcQBL632bW9SHUlF6IEVqT5Z31oZI-4iyyaE_hX_LjLOrNDwOcFlp7Rlr5Jm1Z9Yznxl7m1soklRlAmRkRSyNE8ZaI2QkrQkhT1VItcPTWXZxlR-fEExOPNTC-Gz34UjSr9S3it1URmeOgcCQJEtEvMf2Ce08HLH9ydX19fEWbFcFm0ALrYAAz_timT-PsrMh_bos_3Y-6red0_v_J_ADdq93M_lkYxcP2R3bPGIHR8Ptbo_Zj5kHjiXQDd7N6zkGuOiPc9OUt1_nDScHsUaiBf21XxL8Km8dtfJFW93ULeqp-8hrW1H-tOeH5Q26nFXVV3hyqmDxDETkmduqWK9MPS_thuF7hcPg-L7pCft6enJ5NBX9NQ0CMIpdiRRkHpjIySJxoGKFAQ06BUFeSDAKjI1LCehkZdaFkIApwTqFqgmMSkqXGRs9ZaOmbewzxsvQRGUChXQQxDYwRW4LA1Zi-J_hMx2z94Ou9GKDxqG3uMs03RqnW_vp1vGYvSF1aoK5aCiP5ptZd50-m33RE3TMQlztVDJm73oi166WBkxfloACETLWDuXhDiUqDHa7B6vR_TrQ6TDOIsLjSVH0D4OVbLv_LvvzfyN_zQ6ml5_P9fnZxacX7G5IRuczDg_ZCM3JvmR7Xbl-1X8oPwHKLREE |
linkToPdf | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LbxMxELZoKkEvvBEpBSyExAGsrvdtblHb0AhUIVIkbpbXD4i0jyibHPpT-LfMeHdJw-OAuKy09ow18sx6Z-yZz4S8zK0uklRkTPPIspgrx5S1ivGIWxXqPBUh1g6fz7OLL_npGcLk_Kzi99nuw5FkV9OAKE31-nhp3PG1wjeR4fljwCA8yRIW75F93BaLR2R_Mrt8N90C74qgC7rAIhD8vC-c-fMoOz-nX5fo385K_S9oeuf_hb9LbvfuJ5109nKP3LD1fXLrZLj17QH5PveAsgjGQdtFtYDAF_x0qmpz_XVRU3QcKyBa4m7-CmFZaeOwlS6b8qpqQH_tW1rZEvOqPb9eXYErWpZ95SfFyhbPgESeuSmLzVpVC2M7hm8lDAPj-6aH5PP07PLknPXXNzAN0e2apZrngYocLxKnRSwg0AFnIcgLrpXQysaGa3C-MutCnWhltHUC1BQokRiXKRs9IqO6qe1jQk2oIpPogjsdxDZQRW4LpS23RZjBMx2T14Pe5LJD6ZBbPGacbgnTLf10y3hMXqBqJcJf1Jhf81Vt2lbO5p_kBBy2EFZBkYzJq57INeuV0qovVwCBEDFrh_JohxIUpne7BwuS_frQyjDOIsTpSUH0N4PFbLv_Lvvhv5E_Jzc_nk7lh9nF-yfkIESb84mIR2QE1mSfkr3WbJ7138wPPmYZmw |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Structural+similarity+and+similarity+in+thermal+properties+of+the+polymorphs%3A+melting+and+crystallization+from+the+melt+of+tolbutamide+and+chlorpropamide&rft.jtitle=Journal+of+thermal+analysis+and+calorimetry&rft.au=Drebushchak%2C+T.+N.&rft.au=Drebushchak%2C+V.+A.&rft.date=2020-10-01&rft.pub=Springer+International+Publishing&rft.issn=1388-6150&rft.eissn=1588-2926&rft.volume=142&rft.issue=2&rft.spage=841&rft.epage=848&rft_id=info:doi/10.1007%2Fs10973-020-09475-4&rft.externalDocID=10_1007_s10973_020_09475_4 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1388-6150&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1388-6150&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1388-6150&client=summon |