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Journal articles on the topic 'Inclusion compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Hollingsworth, Mark D. "Inclusion compounds." Current Opinion in Solid State and Materials Science 1, no. 4 (1996): 514–21. http://dx.doi.org/10.1016/s1359-0286(96)80067-2.

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2

Dash, Simanchal. "Inclusion Complexes of Some Substituted 4-Thiazolidinones with Activating and Deactivating Group." Asian Journal of Chemistry 32, no. 1 (2019): 133–36. http://dx.doi.org/10.14233/ajchem.2020.22335.

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Some substituted 4-thiazolidinones have been prepared by taking 2-hydrazinobenzothiazole as a staring material. Polar solvent water makes less solubility of these compounds. Hence inclusions of compounds are prepared by taking suitable ratio of compound and β-cyclodextrin. The purpose of this work is to synthesize more soluble and more bioaccesible compounds. The synthesized compounds and their inclusions are known from the study of their thermodynamic properties and spectral characteristics (UV, IR and NMR). Pharmaceutical activity of the compounds and inclusion can be performed by using the

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3

Huang, Lei, and Alan E. Tonelli. "Polymer Inclusion Compounds." Journal of Macromolecular Science, Part C: Polymer Reviews 38, no. 4 (1998): 781–837. http://dx.doi.org/10.1080/15583729808546037.

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4

Harata, K. "Cyclodextrin inclusion compounds." Acta Crystallographica Section A Foundations of Crystallography 43, a1 (1987): C65. http://dx.doi.org/10.1107/s0108767387083764.

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5

Bishop, Roger, Donald C. Craig, Ian G. Dance, Marcia L. Scudder, and Alison T. Ung. "Helical tubulate inclusion compounds." Supramolecular Chemistry 2, no. 2-3 (1993): 123–31. http://dx.doi.org/10.1080/10610279308038306.

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6

HOLLINGSWORTH, M. D. "ChemInform Abstract: Inclusion Compounds." ChemInform 28, no. 9 (2010): no. http://dx.doi.org/10.1002/chin.199709238.

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7

Saenger, W. "Inclusion compounds – an overview." Acta Crystallographica Section A Foundations of Crystallography 43, a1 (1987): C64. http://dx.doi.org/10.1107/s0108767387083788.

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8

Gee, Michael A., Robert F. Frindt, Per Joensen, and S. Roy Morrison. "Inclusion compounds of MoS2." Materials Research Bulletin 21, no. 5 (1986): 543–49. http://dx.doi.org/10.1016/0025-5408(86)90108-x.

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9

Gurarslan, Alper, Jialong Shen, Yavuz Caydamli, and Alan E. Tonelli. "Pyriproxyfen cyclodextrin inclusion compounds." Journal of Inclusion Phenomena and Macrocyclic Chemistry 82, no. 3-4 (2015): 489–96. http://dx.doi.org/10.1007/s10847-015-0526-7.

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10

Bratu, I., Irina Kacso, Gh Borodi, Daniela E. Constantinescu та Felicia Dragan. "Inclusion compound of Fosinopril withβ-cyclodextrin". Spectroscopy 23, № 1 (2009): 51–58. http://dx.doi.org/10.1155/2009/275398.

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Solid state interactions of bioactive substance (4-cyclohexyl-1-[2-[(2-methyl-1-propanoyloxy-propoxy)-(4-phenylbutyl)phosphoryl]acetyl]-pyrrolidine-2-carboxylic acid, called Fosinopril), withβ-cyclodextrin (β-CD), the so-called inclusion compounds of a bioactive (cardiovascular) drug is obtained by different preparation methods: kneading, co-precipitation and freeze-drying. The so obtained compounds were investigated by FTIR spectroscopy, X-ray diffraction method, and differential scanning calorimetric measurements (DSC) to evidence their formation. X-ray diffraction patterns show that the inc

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11

Botta, C., R. Treviganti, G. Bongiovanni, A. Mura, and R. Tubino. "Photoluminescence of oligothiophene inclusion compounds." Synthetic Metals 101, no. 1-3 (1999): 565–68. http://dx.doi.org/10.1016/s0379-6779(98)00322-1.

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12

Lavy, Tali, Yana Sheynin, Moshe Kapon, and Menahem Kaftory. "Inclusion compounds of 2,5-diphenylhydroquinone." Acta Crystallographica Section C Crystal Structure Communications 60, no. 1 (2003): o50—o53. http://dx.doi.org/10.1107/s0108270103022716.

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13

Kubik, Stefan, Olaf Höller, Andreas Steinert, Martin Tolksdorf, and Günter Wulff. "Inclusion compounds of derivatized amyloses." Macromolecular Symposia 99, no. 1 (1995): 93–102. http://dx.doi.org/10.1002/masy.19950990111.

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14

Lavy, T., and M. Kaftory. "Photochemical reactions in inclusion compounds." Acta Crystallographica Section A Foundations of Crystallography 61, a1 (2005): c111. http://dx.doi.org/10.1107/s0108767305095334.

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15

le Roex, T., and L. Nassimbeni. "Gas storage by inclusion compounds." Acta Crystallographica Section A Foundations of Crystallography 62, a1 (2006): s225. http://dx.doi.org/10.1107/s010876730609550x.

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16

Williams, D. J. "Inclusion compounds. Vol. 2. Structural aspects of inclusion compounds formed by organic host lattices." Endeavour 10, no. 1 (1986): 53. http://dx.doi.org/10.1016/0160-9327(86)90069-4.

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17

Donnelly, Mary-Ellen, Craig Bull, Athina Frantzana, Stefan Klotz, and John Loveday. "Hydrogen-rich Inclusion Compounds at High-pressure." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C754. http://dx.doi.org/10.1107/s2053273314092456.

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Molecular hydrogen (H2) has been proposed as an alternative fuel source for vehicles. Though H2has many benefits, such as clean combustion and the highest known energy density by mass, there are issues in how to store it in a safe and cost effective way. One solution is to store hydrogen in a chemical compound, and gas clathrates (crystalline inclusion compounds) have shown promising results. Pressure provides a powerful means to tune the properties of such compounds and its effects on potential hydrogen storage materials are widely explored. We have recently developed a hydrogen-compatible ga

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18

Davies, J. Eric D., and Vivienne A. Knott. "Clathrate and inclusion compounds. Part 10 [1]. Solid state 13C NMR studies of inclusion compounds." Journal of Molecular Structure 174 (May 1988): 229–34. http://dx.doi.org/10.1016/0022-2860(88)80162-5.

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19

HIROTSU, Ken, and Taiichi HIGUCHI. "Structure of macrocyclic cyclophane inclusion compounds." Nihon Kessho Gakkaishi 28, no. 4 (1986): 261–72. http://dx.doi.org/10.5940/jcrsj.28.261.

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20

Kuhnert-Brandstätter, Maria, and A. Burger. "Phase diagrams of urea inclusion compounds." Journal of thermal analysis 50, no. 4 (1997): 559–67. http://dx.doi.org/10.1007/bf01979028.

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21

Aky�z, Sevim, and �akil Erk. "Sixth international seminar on inclusion compounds." Journal of Inclusion Phenomena and Molecular Recognition in Chemistry 26, no. 1-3 (1996): v. http://dx.doi.org/10.1007/bf01029922.

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22

Loi, M. A., A. Mura, G. Bongiovanni, C. Botta, G. Di Silvestro, and R. Tubino. "Energy transfer in oligothiophene inclusion compounds." Synthetic Metals 121, no. 1-3 (2001): 1299–300. http://dx.doi.org/10.1016/s0379-6779(00)01252-2.

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23

Taverner, B. C., and D. C. Levendis. "Disorder in thiourea/selenourea inclusion compounds." Acta Crystallographica Section A Foundations of Crystallography 49, s1 (1993): c177. http://dx.doi.org/10.1107/s0108767378094921.

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24

Botta, C., R. Bosisio, G. Bongiovanni, A. Mura, and R. Tubino. "Optical properties of oligothiophene inclusion compounds." Synthetic Metals 84, no. 1-3 (1997): 535–36. http://dx.doi.org/10.1016/s0379-6779(97)80849-1.

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25

Nassimbeni, Luigi R. "Structure–reactivity relations of inclusion compounds." CrystEngComm 5, no. 35 (2003): 200–203. http://dx.doi.org/10.1039/b304873j.

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26

Kaftory, M., F. Toda, K. Tanaka, and M. Yagi. "Selective Reactions in Crystalline Inclusion Compounds." Molecular Crystals and Liquid Crystals Incorporating Nonlinear Optics 186, no. 1 (1990): 167–76. http://dx.doi.org/10.1080/00268949008037207.

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27

Barbour, L. "Structure–property relationships of inclusion compounds." Acta Crystallographica Section A Foundations of Crystallography 67, a1 (2011): C10—C11. http://dx.doi.org/10.1107/s010876731109979x.

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28

Boysen, Hans. "The crystallography of aperiodic inclusion compounds." Ferroelectrics 250, no. 1 (2001): 7–12. http://dx.doi.org/10.1080/00150190108225021.

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29

Ramon, G., L. R. Nassimbeni, and E. Weber. "Inclusion compounds from a Diol Host." Acta Crystallographica Section A Foundations of Crystallography 62, a1 (2006): s77. http://dx.doi.org/10.1107/s0108767306098461.

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30

Su, H., and L. R. Nassimbeni. "Controlled host:guest ratio in inclusion compounds." Acta Crystallographica Section A Foundations of Crystallography 56, s1 (2000): s312. http://dx.doi.org/10.1107/s0108767300026623.

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31

Nassimbeni, L. R. "Structure-reactivity relationships of inclusion compounds." Acta Crystallographica Section A Foundations of Crystallography 58, s1 (2002): c190. http://dx.doi.org/10.1107/s0108767302092619.

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32

Aky�z, Sevim, and �akil Erk. "PrefaceSixth International Seminar on Inclusion Compounds." Journal of Inclusion Phenomena and Molecular Recognition in Chemistry 24, no. 1-2 (1996): v. http://dx.doi.org/10.1007/bf01053422.

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33

Siling, S. A., N. N. Godovikov, I. I. Ponomarev, et al. "Inclusion compounds of hexazocyclanes with water." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 6 (1985): 1254–58. http://dx.doi.org/10.1007/bf00956094.

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34

Ramon, Gaëlle, Luigi R. Nassimbeni, and Jana H. Taljaard. "Guest Controlled Packing in Inclusion Compounds." Journal of Chemical Crystallography 42, no. 10 (2012): 1014–21. http://dx.doi.org/10.1007/s10870-012-0350-5.

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35

Sopkov�, Anna. "Fourth international seminar on inclusion compounds." Journal of Inclusion Phenomena and Molecular Recognition in Chemistry 14, no. 1 (1992): 1–3. http://dx.doi.org/10.1007/bf01041360.

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36

Guarino, A. "Photophysics of host—guest inclusion compounds." Journal of Photochemistry 35, no. 1 (1986): 1–11. http://dx.doi.org/10.1016/0047-2670(86)87112-x.

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37

Williams, D. J. "Inclusion compounds. Vol. 1. Structural aspects of inclusion compounds formed by organic and organometallic host lattices." Endeavour 10, no. 1 (1986): 53. http://dx.doi.org/10.1016/0160-9327(86)90068-2.

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38

Rusa, Cristian C., Constantin Luca, and Alan E. Tonelli. "Polymer−Cyclodextrin Inclusion Compounds: Toward New Aspects of Their Inclusion Mechanism." Macromolecules 34, no. 5 (2001): 1318–22. http://dx.doi.org/10.1021/ma001868c.

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39

Cardoso, T., C. I. C. Galhano, M. F. Ferreira Marques та A. Moreira da Silva. "Thymoquinoneβ-Cyclodextrin Nanoparticles System: A Preliminary Study". Spectroscopy: An International Journal 27 (2012): 329–36. http://dx.doi.org/10.1155/2012/902486.

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Thymoquinone is a natural product, the main constituent ofNigella sativaseeds, which exhibits anti-inflammatory and anticancer activities. Among several existing molecules capable of forming an inclusion compound structure, cyclodextrins are applied in the pharmaceutical industry either to increase solubility of hydrophobic molecules or to protect molecules from inactivation or degradation.β-Cyclodextrin is currently the most common cyclodextrin in pharmaceutical formulations and probably the best studied in humans. In order to study the properties of inclusion compounds based on cyclodextrins

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40

Bogdanov, Anita, Valeria Endrész, Szabolcs Urbán, et al. "Application of DNA Chip Scanning Technology for Automatic Detection of Chlamydia trachomatis and Chlamydia pneumoniae Inclusions." Antimicrobial Agents and Chemotherapy 58, no. 1 (2013): 405–13. http://dx.doi.org/10.1128/aac.01400-13.

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ABSTRACTChlamydiae are obligate intracellular bacteria that propagate in the inclusion, a specific niche inside the host cell. The standard method for counting chlamydiae is immunofluorescent staining and manual counting of chlamydial inclusions. High- or medium-throughput estimation of the reduction in chlamydial inclusions should be the basis of testing antichlamydial compounds and other drugs that positively or negatively influence chlamydial growth, yet low-throughput manual counting is the common approach. To overcome the time-consuming and subjective manual counting, we developed an auto

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41

Bourne, Susan A., Katherine L. Gifford^Nash, and Fumio Toda. "Dimethyl acetamide inclusion compounds with multipedal hosts." Journal of Molecular Structure 474, no. 1-3 (1999): 223–33. http://dx.doi.org/10.1016/s0022-2860(98)00575-4.

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42

Fogagnolo, Marco, Giancarlo Fantin, and Olga Bortolini. "Inclusion Compounds of Dehydrocholic Acid with Solvents." International Journal of Molecular Sciences 8, no. 7 (2007): 662–69. http://dx.doi.org/10.3390/i8070662.

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43

Segre, Ulderico, Marina Brustolon, Louis Claude Brunel, and Anna Lisa Maniero. "High-field EPR of irradiated inclusion compounds." Chemical Physics Letters 308, no. 5-6 (1999): 408–12. http://dx.doi.org/10.1016/s0009-2614(99)00629-6.

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44

Le Bas, G., S. A. Mason, and J. Doucet. "Order–disorder phenomena in cyclodextrin inclusion compounds." Acta Crystallographica Section A Foundations of Crystallography 52, a1 (1996): C421. http://dx.doi.org/10.1107/s0108767396082670.

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45

Nassimbeni, L. R. "Inclusion compounds: relating structure to thermal stability." Acta Crystallographica Section A Foundations of Crystallography 52, a1 (1996): C417. http://dx.doi.org/10.1107/s0108767396082840.

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46

Bongiovanni, G., C. Botta, G. Di Silvestro, M. A. Loi, A. Mura, and R. Tubino. "Energy transfer in nanostructured oligothiophene inclusion compounds." Chemical Physics Letters 345, no. 5-6 (2001): 386–94. http://dx.doi.org/10.1016/s0009-2614(01)00898-3.

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47

Rahman, A. Noman M. M., Roger Bishop, Donald C. Craig, Christopher E. Marjo, and Marcia L. Scudder. "Staircase Inclusion Compounds Formed by Tetrahalodiquinoline Hosts." Crystal Growth & Design 2, no. 5 (2002): 421–26. http://dx.doi.org/10.1021/cg020017o.

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48

Khaldoyanidi, K. A. "Phase diagrams with nonstoichiometric intermediate inclusion compounds." Russian Journal of Inorganic Chemistry 61, no. 1 (2016): 115–18. http://dx.doi.org/10.1134/s0036023616010113.

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49

Rusa, Cristian C., Justin Fox, and Alan E. Tonelli. "Competitive Formation of Polymer−Cyclodextrin Inclusion Compounds." Macromolecules 36, no. 8 (2003): 2742–47. http://dx.doi.org/10.1021/ma021755o.

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50

Harris, Kenneth D. M., and John M. Thomas. "Probing the Properties of Urea Inclusion Compounds." Molecular Crystals and Liquid Crystals Incorporating Nonlinear Optics 186, no. 1 (1990): 177–84. http://dx.doi.org/10.1080/00268949008037208.

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