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Journal articles on the topic 'Solvatomorphisme'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

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1

Brittain, Harry G. "Polymorphism Solvatomorphism 2008." Journal of Pharmaceutical Sciences 99, no. 9 (2010): 3648–64. http://dx.doi.org/10.1002/jps.21966.

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2

Grell, Toni, Mauro Barbero, Franco Pattarino, Giovanni Battista Giovenzana, and Valentina Colombo. "Solvatomorphism of Moxidectin." Molecules 26, no. 16 (2021): 4869. http://dx.doi.org/10.3390/molecules26164869.

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The solvatomorphism of the anthelmintic drug moxidectin is investigated, and a new solvatomorph with nitromethane is reported. Moreover, the hitherto unknown crystal structures of the solvatomorphs with ethanol and 2-propanol are reported and discussed. The thermal characterization of these solvatomorphs through variable-temperature powder X-ray diffraction analysis (VT-PXRD) is also described, providing new insights into the crystallochemistry of this active pharmaceutical ingredient.

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3

Macedi, Eleonora, Alessandra Meli, Francesco De Riccardis, et al. "Molecular recognition and solvatomorphism of a cyclic peptoid: formation of a stable 1D porous framework." CrystEngComm 19, no. 32 (2017): 4704–8. http://dx.doi.org/10.1039/c7ce01077j.

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4

Brittain, Harry G. "Polymorphism and Solvatomorphism 2005." Journal of Pharmaceutical Sciences 96, no. 4 (2007): 705–28. http://dx.doi.org/10.1002/jps.20772.

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5

Brittain, Harry G. "Polymorphism and Solvatomorphism 2006." Journal of Pharmaceutical Sciences 97, no. 9 (2008): 3611–36. http://dx.doi.org/10.1002/jps.21274.

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6

Brittain, Harry G. "Polymorphism and Solvatomorphism 2007." Journal of Pharmaceutical Sciences 98, no. 5 (2009): 1617–42. http://dx.doi.org/10.1002/jps.21518.

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7

Brittain, Harry G. "Polymorphism and Solvatomorphism 2009." Journal of Pharmaceutical Sciences 100, no. 4 (2011): 1260–79. http://dx.doi.org/10.1002/jps.22386.

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8

Brittain, Harry G. "Polymorphism and Solvatomorphism 2010." Journal of Pharmaceutical Sciences 101, no. 2 (2012): 464–84. http://dx.doi.org/10.1002/jps.22788.

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9

Pike, Sarah J., Andrew D. Bond, and Christopher A. Hunter. "Solvatomorphism of Reichardt's dye." CrystEngComm 20, no. 21 (2018): 2912–15. http://dx.doi.org/10.1039/c8ce00480c.

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10

Bloch, Witold M., Ravichandar Babarao, and Matthew L. Schneider. "On/off porosity switching and post-assembly modifications of Cu4L4 metal–organic polyhedra." Chemical Science 11, no. 14 (2020): 3664–71. http://dx.doi.org/10.1039/d0sc00070a.

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The crystal packing and porosity of Cu<sub>4</sub>L<sub>4</sub> metal–organic polyhedra can be controlled by exploiting their rich solvatomorphism, structural non-rigidity and amenability to covalent post-assembly modifications.

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11

Perlovich, German L., Svetlana V. Blokhina, Nikolay G. Manin, Tatyana V. Volkova, and Valery V. Tkachev. "Polymorphism and solvatomorphism of bicalutamide." Journal of Thermal Analysis and Calorimetry 111, no. 1 (2012): 655–62. http://dx.doi.org/10.1007/s10973-012-2540-y.

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12

Krishnaswamy, Shobhana, Soumyakanta Prusty, Daniel Chartrand, Garry S. Hanan, and Dillip K. Chand. "Conformational Solvatomorphism in a [2]Catenane." Crystal Growth & Design 20, no. 9 (2020): 5820–33. http://dx.doi.org/10.1021/acs.cgd.0c00421.

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13

Wang, Xiaoying, Ningbo Gong, Shiying Yang, Guanhua Du, and Yang Lu. "Studies on Solvatomorphism of Betulinic Acid." Journal of Pharmaceutical Sciences 103, no. 9 (2014): 2696–703. http://dx.doi.org/10.1002/jps.23853.

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14

du Plessis, Marike, and Leonard J. Barbour. "Supramolecular isomerism and solvatomorphism in a novel coordination compound." Dalton Trans. 41, no. 14 (2012): 3895–98. http://dx.doi.org/10.1039/c1dt11564b.

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15

Gutierrez, Julio, Rodney Eisenberg, Gabrielle Herrensmith, Thomas Tobin, Tonglei Li, and Sihui Long. "Solvatomorphism in (E)-2-(2,6-dichloro-4-hydroxybenzylidene)hydrazinecarboximidamide." Acta Crystallographica Section C Crystal Structure Communications 67, no. 8 (2011): o310—o314. http://dx.doi.org/10.1107/s0108270111023845.

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16

Iwata, Kentaro, Masatoshi Karashima, and Yukihiro Ikeda. "Cocrystallization Enhanced TAK-441 Aqueous Solubility and Suppressed High Solvatomorphism." Crystal Growth & Design 16, no. 8 (2016): 4599–606. http://dx.doi.org/10.1021/acs.cgd.6b00691.

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17

Petruševski, Gjorgji, Marina Kajdžanoska, Sonja Ugarkovic, et al. "Solvatomorphism of codeine phosphate sesquihydrate—Vibrational spectroscopy and thermoanalytical characterization." Vibrational Spectroscopy 63 (November 2012): 460–68. http://dx.doi.org/10.1016/j.vibspec.2012.09.010.

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18

DELGADO, G., M. GUILLEN, and A. J. MORA. "4-METHYL HYPPURIC ACID: A CASE OF POLYMORPHISM AND SOLVATOMORPHISM." Periódico Tchê Química 16, no. 32 (2019): 812–19. http://dx.doi.org/10.52571/ptq.v16.n32.2019.830_periodico32_pgs_812_819.pdf.

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Polymorphism is known as the ability of a solid material to exist in more than one form or crystal structure, with important applications in the preparation of active pharmaceutical ingredients. Characterization of different polymorphs of the specific metabolite of 4-xylene can contribute to the chemical and pharmaceutical industry. Polymorphism is of particular importance in industrial processes, where different physical properties of polymorphic forms can substantially alter the viability and quality of a manufactured product. This is particularly so for the design and production of drugs in

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19

Wang, Wenjing, Kongzhao Su, El-Sayed M. El-Sayed, Miao Yang, and Daqiang Yuan. "Solvatomorphism Influence of Porous Organic Cage on C2H2/CO2 Separation." ACS Applied Materials & Interfaces 13, no. 20 (2021): 24042–50. http://dx.doi.org/10.1021/acsami.1c04573.

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20

Xing, Cheng, Guo shun Zhang, Ning bo Gong, Guan hua Du, and Yang Lu. "New crystal forms and amorphous phase of sophoricoside: X-ray structures and characterization." Royal Society Open Science 6, no. 1 (2019): 181905. http://dx.doi.org/10.1098/rsos.181905.

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Sophoricoside, which is an isoflavone glycoside found in many plant species, has recently attracted attention because of its anti-fertility activity. One solvent-free form, two solvatomorphs and an amorphous phase of sophoricoside are reported for the first time. X-ray diffractometry, differential scanning calorimetry, thermal gravimetric analysis and Fourier-transform infrared spectroscopy were used to characterize the different forms. The results show that factors such as crystal symmetry, intermolecular arrangement, conformational flexibility, hydrogen-bonding interactions and solvent incor

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21

Kumar Dey, Sandeep, and Gopal Das. "A selective fluoride encapsulated neutral tripodal receptor capsule: solvatochromism and solvatomorphism." Chemical Communications 47, no. 17 (2011): 4983. http://dx.doi.org/10.1039/c0cc05430e.

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22

Kamiński, Daniel M., Anna A. Hoser, Mariusz Gagoś, et al. "Solvatomorphism of 2-(4-Fluorophenylamino)-5-(2,4-dihydroxybenzeno)-1,3,4-thiadiazole Chloride." Crystal Growth & Design 10, no. 8 (2010): 3480–88. http://dx.doi.org/10.1021/cg1003319.

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23

Pan, Bochen, Zhanzhong Wang, Yichun Shen, Liangxiao Wei, Hongyuan Wei, and Leping Dang. "Solvatomorphism and phase transformation of CL-20: probing properties and investigating mechanisms." CrystEngComm 22, no. 20 (2020): 3451–62. http://dx.doi.org/10.1039/d0ce00059k.

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24

Lemmer, Helanie, Nicole Stieger, Wilna Liebenberg, and Mino R. Caira. "Solvatomorphism of the Antibacterial Dapsone: X-ray Structures and Thermal Desolvation Kinetics." Crystal Growth & Design 12, no. 3 (2012): 1683–92. http://dx.doi.org/10.1021/cg300019f.

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25

Djemel, Abdelhak, Olaf Stefanczyk, Mathieu Marchivie, et al. "Solvatomorphism-Induced 45 K Hysteresis Width in a Spin-Crossover Mononuclear Compound." Chemistry - A European Journal 24, no. 55 (2018): 14760–67. http://dx.doi.org/10.1002/chem.201802572.

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26

Boonprab, Theerapoom, Phimphaka Harding, Keith S. Murray, et al. "Solvatomorphism and anion effects in predominantly low spin iron(iii) Schiff base complexes." Dalton Transactions 47, no. 35 (2018): 12449–58. http://dx.doi.org/10.1039/c8dt02016g.

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27

Sirirak, Jitnapa, David J. Harding, Phimphaka Harding, Lujia Liu, and Shane G. Telfer. "Solvatomorphism and Electronic Communication in FeIII N,N-Bis(salicylidene)-1,3-propanediamine Dimers." Australian Journal of Chemistry 68, no. 5 (2015): 766. http://dx.doi.org/10.1071/ch14441.

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The reaction of H2salpn (H2salpn = N,N′-bis(salicylidene)-1,3-propanediamine) with Fe(ClO4)3 in a ratio of 1 : 1 and 3 : 2, leads to dark red crystals of the solvatomorphs [(salpn)Fe(μ2-salpn)Fe(salpn)]·0.5MeOH (1) and [(salpn)Fe(μ2-salpn)Fe(salpn)]·MeOH (2), respectively. X-Ray crystallographic studies reveal a slightly distorted octahedral geometry and meridional configuration of the N and O donor atoms with one of the salpn ligands acting as a bridge between the two FeIII atoms to create a dimer. The Fe–N/O bond distances for both dimers indicate that the Fe centres are high spin. Supramole

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28

Wei, Wei, Guo Wang, Ying Zhang, Feilong Jiang, Mingyan Wu, and Maochun Hong. "A Versatile Tripodal Host with Cylindrical Conformation: Solvatomorphism, Inclusion Behavior, and Separation of Guests." Chemistry - A European Journal 17, no. 7 (2011): 2189–98. http://dx.doi.org/10.1002/chem.201002246.

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29

Guan, Shengyang, David C. Mayer, Christian Jandl, Sebastian J. Weishäupl, Angela Casini, and Alexander Pöthig. "Investigation of Solvatomorphism and Its Photophysical Implications for Archetypal Trinuclear Au3(1-Methylimidazolate)3." Molecules 26, no. 15 (2021): 4404. http://dx.doi.org/10.3390/molecules26154404.

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A new solvatomorph of [Au3(1-Methylimidazolate)3] (Au3(MeIm)3)—the simplest congener of imidazolate-based Au(I) cyclic trinuclear complexes (CTCs)—has been identified and structurally characterized. Single-crystal X-ray diffraction revealed a dichloromethane solvate exhibiting remarkably short intermolecular Au⋯Au distances (3.2190(7) Å). This goes along with a dimer formation in the solid state, which is not observed in a previously reported solvent-free crystal structure. Hirshfeld analysis, in combination with density functional theory (DFT) calculations, indicates that the dimerization is

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30

Shevchenko, Anna, David Din Belle, Saara Tiittanen, et al. "Coupling Polymorphism/Solvatomorphism and Physical Stability Evaluation with Early Salt Synthesis Optimization of an Investigational Drug." Organic Process Research & Development 15, no. 3 (2011): 666–72. http://dx.doi.org/10.1021/op200026f.

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31

Rat, S., K. Ridier, L. Vendier, G. Molnár, L. Salmon, and A. Bousseksou. "Solvatomorphism and structural-spin crossover property relationship in bis[hydrotris(1,2,4-triazol-1-yl)borate]iron(ii)." CrystEngComm 19, no. 24 (2017): 3271–80. http://dx.doi.org/10.1039/c7ce00741h.

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32

Dey, Dhananjay, and Deepak Chopra. "Solvatomorphism in (Z)-4-fluoro-N′-(3-fluorophenyl)benzimidamide: the role of intermolecular O–H⋯F interaction." CrystEngComm 18, no. 42 (2016): 8291–300. http://dx.doi.org/10.1039/c6ce01668e.

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33

Cibian, Mihaela, and Garry S. Hanan. "Geometry and Spin Change at the Heart of a Cobalt(II) Complex: A Special Case of Solvatomorphism." Chemistry - A European Journal 21, no. 26 (2015): 9474–81. http://dx.doi.org/10.1002/chem.201500852.

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34

Chen, Yong, Wei Lu, and Chi-Ming Che. "Luminescent Pincer-Type Cyclometalated Platinum(II) Complexes with Auxiliary Isocyanide Ligands: Phase-Transfer Preparation, Solvatomorphism, and Self-Aggregation." Organometallics 32, no. 1 (2012): 350–53. http://dx.doi.org/10.1021/om300965b.

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35

Castañeda, Raúl, Victor N. Khrustalev, Alexandr Fonari, Jean-Luc Bredas, Yulia A. Getmanenko, and Tatiana V. Timofeeva. "Mixed-stack architecture and solvatomorphism of trimeric perfluoro-ortho-phenylene mercury complexes with dithieno[3,2-b:2′,3′-d]thiophene." Journal of Molecular Structure 1100 (November 2015): 506–12. http://dx.doi.org/10.1016/j.molstruc.2015.07.053.

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36

Chopra, Deepak, and Tayur N. Guru Row. "Solvatomorphism in 3-Fluorobenzoylaminophenyl 3-Fluorobenzoate: A Subtle Interplay of Strong Hydrogen Bonds and Weak Intermolecular Interactions Involving Disordered Fluorine." Crystal Growth & Design 6, no. 6 (2006): 1267–70. http://dx.doi.org/10.1021/cg060082o.

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37

Stöger, Berthold, Paul Kautny, Daniel Lumpi, Erich Zobetz, and Johannes Fröhlich. "Solvatomorphism of 9,9′-[1,3,4-thiadiazole-2,5-diylbis(2,3-thiophendiyl-4,1-phenylene)]bis[9H-carbazole]: isostructurality, modularity and order–disorder theory." Acta Crystallographica Section B Structural Science 68, no. 6 (2012): 667–76. http://dx.doi.org/10.1107/s0108768112039651.

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During a systematic investigation of the crystallization behaviour of 9,9′-[1,3,4-thiadiazole-2,5-diylbis(2,3-thiophendiyl-4,1-phenylene)]bis[9H-carbazole] (I), six single crystalline solvates were obtained and characterized by X-ray diffraction at 100 K. The structure of the hemi-2-butanone (MEK) solvate contains two crystallographically independent molecules of (I) related by pseudo-inversion symmetry. The structure is polytypic and composed of non-polar (I) layers and polar solvent layers. It can be described according to an extended order–disorder (OD) theory with relaxed vicinity conditio

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38

Cleetus, Annie, Gulshan Rani, G. B. Dharma Rao, and Deepak Chopra. "Crystal structures of the anhydrous and two solvated forms of methyl 4-(4-fluorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate." Acta Crystallographica Section C Structural Chemistry 76, no. 8 (2020): 786–94. http://dx.doi.org/10.1107/s2053229620009560.

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Methyl 4-(4-fluorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate, (I), was found to exhibit solvatomorphism. The compound was prepared using a classic Biginelli reaction under mild conditions, without using catalysts and in a solvent-free environment. Single crystals of two solvatomorphs and one anhydrous form of (I) were obtained through various crystallization methods. The anhydrous form, C13H13FN2O3, was found to crystallize in the monoclinic space group C2/c. It showed one molecule in the asymmetric unit. The solvatomorph with included carbon tetrachloride, C13H13FN2O3·0

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39

Germán-Acacio, Juan Manuel, Hugo Juárez Garrido, Reyna Reyes Martinez, and David Morales-Morales. "Solvatomorphism: the inclusion of unexpected guests. An interesting case of study of different solvates in the tecton [Pd(1,10-phen)(2,3,5,6-S-C6F4H)2]." Acta Crystallographica Section A Foundations and Advances 73, a1 (2017): a351. http://dx.doi.org/10.1107/s010876731709657x.

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40

Jurić, Marijana, Berislav Perić, Nevenka Brničević, et al. "Supramolecular motifs and solvatomorphism within the compounds [M(bpy)3]2[NbO(C2O4)3]Cl·nH2O (M = Fe2+, Co2+, Ni2+, Cu2+and Zn2+; n = 11, 12). Syntheses, structures and magnetic properties." Dalton Trans., no. 6 (2008): 742–54. http://dx.doi.org/10.1039/b707937k.

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