Effect of functional group position in co-formers and solvent on cocrystal polymorphism/stoichiomorphism: a case study
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Published in | Journal of molecular liquids Vol. 388; p. 122741 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
15.10.2023
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Online Access | Get full text |
ISSN | 0167-7322 |
DOI | 10.1016/j.molliq.2023.122741 |
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ArticleNumber | 122741 |
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Author | Qi, Luguang Ye, Yang Bai, Yunhe Xiao, Yuntian Xuanyuan, Shutian Li, Chang Xie, Chuang Hao, Hongxun |
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Cites_doi | 10.1002/anie.201106391 10.1021/acs.cgd.1c00009 10.1021/acs.cgd.0c01352 10.1039/c2ce25299f 10.1016/j.molstruc.2019.127176 10.1021/cg901270x 10.1002/anie.201501638 10.1016/j.ijpharm.2012.04.027 10.1016/0263-7855(96)00018-5 10.1039/C9CE00031C 10.1002/jcc.22885 10.1002/anie.202103516 10.1039/C9CE00124G 10.1039/c3ce42008f 10.1039/c2ce26801a 10.1016/j.compbiolchem.2018.11.014 10.15171/apb.2016.062 10.1021/acs.cgd.8b00114 10.1021/j100161a070 10.1016/j.ijpharm.2020.119694 10.1021/cg2013232 10.1016/j.ces.2020.116082 10.1021/acs.cgd.1c01190 10.1002/jps.24345 10.1016/j.dyepig.2022.110947 10.1107/S2052252519012363 10.1021/cg5005243 10.1039/C6CE02227H 10.1021/cg401179s 10.1021/acs.cgd.7b01206 10.3390/molecules26144185 10.1039/C0NJ00569J 10.1039/D0CE00498G 10.1039/C4CE00472H |
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References | 10.1016/j.molliq.2023.122741_b0115 Limwikrant (10.1016/j.molliq.2023.122741_b0090) 2012; 431 Eddleston (10.1016/j.molliq.2023.122741_b0045) 2013; 13 Halasz (10.1016/j.molliq.2023.122741_b0085) 2011; 35 Yan (10.1016/j.molliq.2023.122741_b0025) 2011; 50 Ahuja (10.1016/j.molliq.2023.122741_b0185) 2019; 21 Aitipamula (10.1016/j.molliq.2023.122741_b0010) 2014; 16 Vener (10.1016/j.molliq.2023.122741_b0150) 2014; 14 Cheng (10.1016/j.molliq.2023.122741_b0155) 2021; 21 Ahuja (10.1016/j.molliq.2023.122741_b0190) 2020; 22 Gadade (10.1016/j.molliq.2023.122741_b0070) 2016; 6 Wang (10.1016/j.molliq.2023.122741_b0135) 2019; 6 Hasa (10.1016/j.molliq.2023.122741_b0065) 2015; 54 Desiraju (10.1016/j.molliq.2023.122741_b0005) 1989 Grossjohann (10.1016/j.molliq.2023.122741_b0050) 2015; 104 Chen (10.1016/j.molliq.2023.122741_b0015) 2018; 18 Xie (10.1016/j.molliq.2023.122741_b0165) 2010; 10 Prasana (10.1016/j.molliq.2023.122741_b0130) 2019; 78 Yu (10.1016/j.molliq.2023.122741_b0055) 2021; 229 Croker (10.1016/j.molliq.2023.122741_b0100) 2013; 15 Humphrey (10.1016/j.molliq.2023.122741_b0125) 1996; 14 Zhang (10.1016/j.molliq.2023.122741_b0030) 2023; 209 Kavitha (10.1016/j.molliq.2023.122741_b0105) 2020; 1202 10.1016/j.molliq.2023.122741_b0145 Diniz (10.1016/j.molliq.2023.122741_b0140) 2020; 587 Zhang (10.1016/j.molliq.2023.122741_b0180) 2012; 14 Diez (10.1016/j.molliq.2023.122741_b0060) 2018; 18 Lu (10.1016/j.molliq.2023.122741_b0120) 2012; 33 Ueto (10.1016/j.molliq.2023.122741_b0075) 2012; 12 Nanubolu (10.1016/j.molliq.2023.122741_b0080) 2017; 19 Stainton (10.1016/j.molliq.2023.122741_b0035) 2022; 22 Wu (10.1016/j.molliq.2023.122741_b0170) 2019; 21 Rappe (10.1016/j.molliq.2023.122741_b0160) 1991; 95 Fischer (10.1016/j.molliq.2023.122741_b0095) 2014; 16 Murray (10.1016/j.molliq.2023.122741_b0175) 2011; 1 Wu (10.1016/j.molliq.2023.122741_b0020) 2021; 21 Nugrahani (10.1016/j.molliq.2023.122741_b0040) 2021; 26 Jain (10.1016/j.molliq.2023.122741_b0110) 2021; 60 |
References_xml | – volume: 50 start-page: 12483 year: 2011 ident: 10.1016/j.molliq.2023.122741_b0025 article-title: A Cocrystal Strategy to Tune the Luminescent Properties of Stilbene-Type Organic Solid-State Materials publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.201106391 – volume: 21 start-page: 2371 year: 2021 ident: 10.1016/j.molliq.2023.122741_b0020 article-title: New Salts and Cocrystals of Pymetrozine with Improvements on Solubility and Humidity Stability: Experimental and Theoretical Study publication-title: Cryst. Growth Des. doi: 10.1021/acs.cgd.1c00009 – volume: 21 start-page: 1993 year: 2021 ident: 10.1016/j.molliq.2023.122741_b0155 article-title: Toward Understanding the Growth of Cefradine in Aqueous Solution publication-title: Cryst. Growth Des. doi: 10.1021/acs.cgd.0c01352 – volume: 14 start-page: 4644 year: 2012 ident: 10.1016/j.molliq.2023.122741_b0180 article-title: The theophylline–oxalic acid co-crystal system: solid phases, thermodynamics and crystallisation publication-title: CrystEngComm. doi: 10.1039/c2ce25299f – volume: 1202 year: 2020 ident: 10.1016/j.molliq.2023.122741_b0105 article-title: An analysis of structural, spectroscopic signatures, reactivity and anti-bacterial study of synthetized 4-chloro-3-sulfamoylbenzoic acid publication-title: J. Mol. Struct. doi: 10.1016/j.molstruc.2019.127176 – volume: 10 start-page: 3363 year: 2010 ident: 10.1016/j.molliq.2023.122741_b0165 article-title: Direct Precipitation of Micron-Size Salbutamol Sulfate: New Insights into the Action of Surfactants and Polymeric Additives publication-title: Cryst. Growth Des. doi: 10.1021/cg901270x – volume: 54 start-page: 7371 year: 2015 ident: 10.1016/j.molliq.2023.122741_b0065 article-title: Cocrystal Formation through Mechanochemistry: from Neat and Liquid-Assisted Grinding to Polymer-Assisted Grinding publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.201501638 – volume: 431 start-page: 237 year: 2012 ident: 10.1016/j.molliq.2023.122741_b0090 article-title: Formation mechanism of a new carbamazepine/malonic acid cocrystal polymorph publication-title: Int. J. Pharm. doi: 10.1016/j.ijpharm.2012.04.027 – volume: 14 start-page: 33 year: 1996 ident: 10.1016/j.molliq.2023.122741_b0125 article-title: VMD: Visual molecular dynamics publication-title: J. Mol. Graph. doi: 10.1016/0263-7855(96)00018-5 – volume: 21 start-page: 3209 year: 2019 ident: 10.1016/j.molliq.2023.122741_b0170 article-title: Molecular interaction transfer among solvents and solutes modulates the formation of linezolid crystals publication-title: CrystEngComm. doi: 10.1039/C9CE00031C – volume: 33 start-page: 580 year: 2012 ident: 10.1016/j.molliq.2023.122741_b0120 article-title: Multiwfn: A multifunctional wavefunction analyzer publication-title: J. Comput. Chem. doi: 10.1002/jcc.22885 – ident: 10.1016/j.molliq.2023.122741_b0115 – volume: 60 start-page: 12841 year: 2021 ident: 10.1016/j.molliq.2023.122741_b0110 article-title: Synthetic Approaches to Halogen Bonded Ternary Cocrystals publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.202103516 – volume: 21 start-page: 2863 year: 2019 ident: 10.1016/j.molliq.2023.122741_b0185 article-title: Investigation of solid–liquid phase diagrams of the sulfamethazine–salicylic acid co-crystal publication-title: CrystEngComm. doi: 10.1039/C9CE00124G – volume: 16 start-page: 3451 year: 2014 ident: 10.1016/j.molliq.2023.122741_b0010 article-title: Polymorphism in cocrystals: a review and assessment of its significance publication-title: CrystEngComm. doi: 10.1039/c3ce42008f – volume: 15 start-page: 2044 year: 2013 ident: 10.1016/j.molliq.2023.122741_b0100 article-title: Solution mediated phase transformations between co-crystals publication-title: CrystEngComm. doi: 10.1039/c2ce26801a – volume: 78 start-page: 9 year: 2019 ident: 10.1016/j.molliq.2023.122741_b0130 article-title: Molecular docking studies, charge transfer excitation and wave function analyses (ESP, ELF, LOL) on valacyclovir : A potential antiviral drug publication-title: Comput. Biol. Chem. doi: 10.1016/j.compbiolchem.2018.11.014 – volume: 6 start-page: 479 year: 2016 ident: 10.1016/j.molliq.2023.122741_b0070 article-title: Pharmaceutical Cocrystals: Regulatory and Strategic Aspects, Design and Development, Adv publication-title: Pharm Bull. doi: 10.15171/apb.2016.062 – ident: 10.1016/j.molliq.2023.122741_b0145 – volume: 1 start-page: 153 year: 2011 ident: 10.1016/j.molliq.2023.122741_b0175 article-title: The electrostatic potential: an overview, WIREs Computational Molecular publication-title: Science. – year: 1989 ident: 10.1016/j.molliq.2023.122741_b0005 article-title: Crystal engineering: the design of organic solids publication-title: Materials Science Monographs – volume: 18 start-page: 3263 year: 2018 ident: 10.1016/j.molliq.2023.122741_b0060 article-title: Crystallization at Solvent Interfaces Enables Access to a Variety of Cocrystal Polymorphs and Hydrates publication-title: Cryst. Growth Des. doi: 10.1021/acs.cgd.8b00114 – volume: 95 start-page: 3358 year: 1991 ident: 10.1016/j.molliq.2023.122741_b0160 article-title: Charge equilibration for molecular dynamics simulations publication-title: J. Phys. Chem. doi: 10.1021/j100161a070 – volume: 587 year: 2020 ident: 10.1016/j.molliq.2023.122741_b0140 article-title: Enhancing the solubility and permeability of the diuretic drug furosemide via multicomponent crystal forms publication-title: Int. J. Pharm. doi: 10.1016/j.ijpharm.2020.119694 – volume: 12 start-page: 485 year: 2012 ident: 10.1016/j.molliq.2023.122741_b0075 article-title: Polymorphs and a Hydrate of Furosemide-Nicotinamide 1:1 Cocrystal publication-title: Cryst. Growth Des. doi: 10.1021/cg2013232 – volume: 229 year: 2021 ident: 10.1016/j.molliq.2023.122741_b0055 article-title: Cocrystallization of urea and succinic acid in “Nano-Crystallizer” publication-title: Chem. Eng. Sci. doi: 10.1016/j.ces.2020.116082 – volume: 22 start-page: 1665 year: 2022 ident: 10.1016/j.molliq.2023.122741_b0035 article-title: Chameleon Behavior of a New Salt of 3-(Aminocarbonyl) Pyridinium Malonate and Implications for Polymorphism on the Salt/Cocrystal Continuum publication-title: Cryst. Growth Des. doi: 10.1021/acs.cgd.1c01190 – volume: 104 start-page: 1385 year: 2015 ident: 10.1016/j.molliq.2023.122741_b0050 article-title: Polymorphism in Sulfadimidine/4-Aminosalicylic Acid Cocrystals: Solid-State Characterization and Physicochemical Properties publication-title: J. Pharm. Sci. doi: 10.1002/jps.24345 – volume: 209 year: 2023 ident: 10.1016/j.molliq.2023.122741_b0030 article-title: Efficient single benzene AIE system: Optical waveguide and invisible ink publication-title: Dyes and Pigments. doi: 10.1016/j.dyepig.2022.110947 – volume: 6 start-page: 1064 year: 2019 ident: 10.1016/j.molliq.2023.122741_b0135 article-title: Consistency and variability of cocrystals containing positional isomers: the self-assembly evolution mechanism of supramolecular synthons of cresol-piperazine publication-title: IUCrJ. doi: 10.1107/S2052252519012363 – volume: 14 start-page: 4997 year: 2014 ident: 10.1016/j.molliq.2023.122741_b0150 article-title: Evaluation of the Lattice Energy of the Two-Component Molecular Crystals Using Solid-State Density Functional Theory publication-title: Cryst. Growth Des. doi: 10.1021/cg5005243 – volume: 19 start-page: 355 year: 2017 ident: 10.1016/j.molliq.2023.122741_b0080 article-title: Designing a new cocrystal of olanzapine drug and observation of concomitant polymorphism in a ternary cocrystal system publication-title: CrystEngComm. doi: 10.1039/C6CE02227H – volume: 13 start-page: 4599 year: 2013 ident: 10.1016/j.molliq.2023.122741_b0045 article-title: Cocrystallization by Freeze-Drying: Preparation of Novel Multicomponent Crystal Forms publication-title: Cryst. Growth Des. doi: 10.1021/cg401179s – volume: 18 start-page: 1358 year: 2018 ident: 10.1016/j.molliq.2023.122741_b0015 article-title: Cocrystals Mitigate Negative Effects of High pH on Solubility and Dissolution of a Basic Drug publication-title: Cryst. Growth Des. doi: 10.1021/acs.cgd.7b01206 – volume: 26 start-page: 4185 year: 2021 ident: 10.1016/j.molliq.2023.122741_b0040 article-title: Challenges and Progress in Nonsteroidal Anti-Inflammatory Drugs Co-Crystal Development publication-title: Molecules. doi: 10.3390/molecules26144185 – volume: 35 start-page: 24 year: 2011 ident: 10.1016/j.molliq.2023.122741_b0085 article-title: The cocrystal of 4-oxopimelic acid and 4,4′-bipyridine: polymorphism and solid-state transformations publication-title: New J. Chem. doi: 10.1039/C0NJ00569J – volume: 22 start-page: 3463 year: 2020 ident: 10.1016/j.molliq.2023.122741_b0190 article-title: Solution and calorimetric thermodynamic study of a new 1: 1 sulfamethazine–3-methylsalicylic acid co-crystal publication-title: CrystEngComm. doi: 10.1039/D0CE00498G – volume: 16 start-page: 8272 year: 2014 ident: 10.1016/j.molliq.2023.122741_b0095 article-title: Evaluation of the formation pathways of cocrystal polymorphs in liquid-assisted syntheses publication-title: CrystEngComm. doi: 10.1039/C4CE00472H |
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