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Статті в журналах з теми "Host-Guest inclusion complex"
Tanaka, Koichi, Naoki Daikawa, and Shigeru Ohba. "Novel Bisurea Host Compounds." Journal of Chemical Research 2002, no. 11 (November 2002): 579–81. http://dx.doi.org/10.3184/030823402103170853.
Повний текст джерелаLi, Chun-Rong, Hua-Ming Feng, Jin-Yi Zhao, Zhu Li, Bing Bian, Tie-Hong Meng, Xian-Yun Hu, Heng Wang, and Xin Xiao. "Supramolecular Interaction Between Cucurbit[8]uril and the Quinolone Antibiotic Ofloxacin." Australian Journal of Chemistry 72, no. 12 (2019): 983. http://dx.doi.org/10.1071/ch19341.
Повний текст джерелаWagner, Brian D., Shannon J. Fitzpatrick, Monica A. Gill, Andrew I. MacRae, and Natasa Stojanovic. "A fluorescent host-guest complex of cucurbituril in solution: a molecular Jack O'Lantern." Canadian Journal of Chemistry 79, no. 7 (July 1, 2001): 1101–4. http://dx.doi.org/10.1139/v01-094.
Повний текст джерелаTahir, M. Nazir, Yihong Cao, Abdelkrim Azzouz та René Roy. "Host-guest chemistry of the sulfasalazine-β-cyclodextrin inclusion complex". Tetrahedron 85 (квітень 2021): 132052. http://dx.doi.org/10.1016/j.tet.2021.132052.
Повний текст джерелаD’Aria, Federica, Carla Serri, Marcella Niccoli, Laura Mayol, Vincenzo Quagliariello, Rosario Vincenzo Iaffaioli, Marco Biondi та Concetta Giancola. "Host–guest inclusion complex of quercetin and hydroxypropyl-β-cyclodextrin". Journal of Thermal Analysis and Calorimetry 130, № 1 (16 лютого 2017): 451–56. http://dx.doi.org/10.1007/s10973-017-6135-5.
Повний текст джерелаAramoto, Hikaru, Motofumi Osaki, Subaru Konishi, Chiharu Ueda, Yuichiro Kobayashi, Yoshinori Takashima, Akira Harada, and Hiroyasu Yamaguchi. "Redox-responsive supramolecular polymeric networks having double-threaded inclusion complexes." Chemical Science 11, no. 17 (2020): 4322–31. http://dx.doi.org/10.1039/c9sc05589d.
Повний текст джерелаAlrawashdeh, Lubna, Khaleel I. Assaf, Walhan Alshaer, Fadwa Odeh, and Suhair A. Bani-Atta. "Preparation, characterization, and biological activity study of thymoquinone-cucurbit[7]uril inclusion complex." RSC Advances 12, no. 4 (2022): 1982–88. http://dx.doi.org/10.1039/d1ra08460g.
Повний текст джерелаWilson, Lee D., and Ronald E. Verrall. "A 1H NMR study of cyclodextrin - hydrocarbon surfactant inclusion complexes in aqueous solutions." Canadian Journal of Chemistry 76, no. 1 (January 1, 1998): 25–34. http://dx.doi.org/10.1139/v97-208.
Повний текст джерелаZhou, Jiong, Bin Hua, Li Shao, Hao Feng, and Guocan Yu. "Host–guest interaction enhanced aggregation-induced emission and its application in cell imaging." Chemical Communications 52, no. 33 (2016): 5749–52. http://dx.doi.org/10.1039/c6cc01860b.
Повний текст джерелаRahaman, Habibur, Niloy Roy, Aditi Roy, Samapika Ray та Mahendra Nath Roy. "Exploring Existence of Host-Guest Inclusion Complex of β-Cyclodextrin of a Biologically Active Compound with the Manifestation of Diverse Interactions". Emerging Science Journal 2, № 5 (4 листопада 2018): 251. http://dx.doi.org/10.28991/esj-2018-01149.
Повний текст джерелаДисертації з теми "Host-Guest inclusion complex"
Roy, Aditi. "Study to explore molecular inclusion complexes of cyclic hosts with vital guests in various environments." Thesis, University of North Bengal, 2018. http://ir.nbu.ac.in/handle/123456789/2633.
Повний текст джерелаDaver, Henrik. "Quantum Chemical Modeling of Phosphoesterase Mimics and Chemistry in Confined Spaces." Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-148259.
Повний текст джерелаAt the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 5: Manuscript.
Bezuidenhout, Charl Xavier. "Polar ordering of guest molecules in host-guest inclusion complexes." Thesis, Stellenbosch : Stellenbosch University, 2011. http://hdl.handle.net/10019.1/18107.
Повний текст джерелаENGLISH ABSTRACT: 2,7-dimethylocta-3,5-diyne-2,7-diol forms inclusion complexes with various guests molecules, where the guest molecules are polar-ordered. A Cambridge Structural Database (CSD) search revealed ten inclusion complexes where the guest molecules were polar-ordered. Using Density Functional Theory (DFT) computational methods (in the absence of the host), we evaluated the intra-channel and lateral guest-guest interactions between the guest molecules. Two polar-ordered inclusion complexes ((1,4,7-cyclohexane-1,2,4,5,7,8-hexaoxonane)·CHCl3 and (2,4,6-(endolongifolyl)-1,3,5-trioxane)·CDCl3) were singled out in the CSD search for further studies along with 2,7-dimethylocta-3,5-diyne-2,7-diol. Synthesis of any 1,2,4,5,7,8-hexaoxonane and 1,3,5-trioxane derivatives was attempted to establish whether the polar-ordering ability extends into the family of compounds. We managed to produce three new polar-ordered inclusion complexes with 2,7-dimethylocta-3,5-diyne-2,7-diol (ClC(CH3)3, BrC(CH3)3 and IC(CH3)3), thus extending the series to six guest polar-ordered systems. We were only able to synthesise 1,4,7-cyclohexane-1,2,4,5,7,8-hexaoxonane and produce the CHCl3 inclusion complex and one new polar-ordered inclusion complex (CHBr3). Three 1,3,5-trioxanes was synthesised (the cyclohexyl, cyclohex-3-en-1-yl and cyclopentyl derivatives), which did not include any solvents. However, these 1,3,5-trioxanes also form polar-ordered crystals. These compounds and inclusion complexes were analysed by means of single crystal X-ray diffraction to determine their crystal structures. All the crystal structures could be solved and refined to adequate accuracy (except for 2,4,6-tri(cyclopentyl)-1,3,5-trioxane) with no disorder of the guest molecules (where applicable) and their polar-ordering property investigated. Due to their vast molecular differences, these compounds were studied separately by means of visual crystal structure analysis and computational modelling techniques (Density functional theory, molecular mechanics, molecular dynamics and molecular quench dynamics).
AFRIKAANSE OPSOMMING: 2,7-dimetielokta-3,5-diyn-2,7-diol vorm insluitingskomplekse met verskeie molekules as gaste, waar die gas-molekules polêr georden is. 'n Cambridge Struktuur Databasis (CSD) soektog lewer tien insluitings komplekse waarvan die gas-molekules polêr georden is. Deur gebruik te maak van Digtheidsfunksionele teorie (DFT) berekeninge (in die afwesigheid van die gasheer) het ons die inter-kanaal en wedersydse gas-gas interaksies tussen die gas molekules geëvalueer. Twee polêr geordende insluitingskomplekse ((1,4,7-sikloheksaan-1,2,4,5,7,8-heksaoksonaan)·CHCl3 en (2,4,6-(endolongifolyl)-1,3,5-trioksaan)·CDCl3) is uitgesonder uit die CSD soektog vir verdere studies saam met 2,7-dimetielokta-3,5-diyn-2,7-diol. Aanslag was gemaak om enige 1,2,4,5,7,8-heksaoksonaan en 1,3,5-trioksaan derivate te sintetiseer en vas te stel of die polêre ordensvermoë oor die familie van verbindings strek. Ons het daarin geslaag om drie nuwe polêr geordende insluitingskomplekse op te lewer met 2,7-dimetielokta-3,5-diyn-2,7-diol (Cl(CH3)3, BrC(CH3)3 en I(CH3)3), en sodoende die reeks uitgebrei na ses gaste wat polêr geordende insluitingskomplekse vorm. Net 1,4,7-sikloheksaan-1,2,4,5,7,8-heksaoksonaan kon gesintetiseer word en dit lewer twee polêr geordende insluitingskomplekse (CHCl3 en CHBr3 (nuut)). Drie 1,3,5-trioksane is gesintetiseer (die sikloheksiel, sikloheks-3-een-1-iel en siklopentiel derivate) en het nie enige oplosmiddels (gaste) ingesluit nie. Nietemin vorm hiedie 1,3,5-trioksane ook polêr geordende kristalle. Hierdie verbindings en insluitingskomplekse is geanaliseer deur middel van enkelkristal X-straal diffraksie om hul kristalstrukture te bepaal. Alle kristalstrukture was opgelos en verwerk tot voldoende akkuraatheid (behalwe vir 2,4,6-tri(siklopentiel)-1,3,5-trioxane) met geen wanorde in die gas molekuul posisies nie (waar van toepassing) en hul polêre ordensvermoë is ondersoek. As gevolg van groot verskille in hul molekulêre strukture, is hierdie verbindings afsonderlik bestudeer deur middel van molekulêre modellerings metodes (Digtheidsfunksionele teorie, molekulêre meganika, molekulêre dinamika en molekulêre stakings dinamika).
Kundu, Mitali. "Exploration of inclusion complexes between host and guest molecules and solvation effect of some vital molecules in various environments." Thesis, University of North Bengal, 2017. http://ir.nbu.ac.in/handle/123456789/2689.
Повний текст джерелаO'Brien, Mark. "Spectroscopic Studies of Inclusion Host-Guest Complexes Between Cyclophane Corrals and Polcyclic Aromatic Hydrocarbons." TopSCHOLAR®, 2005. http://digitalcommons.wku.edu/theses/470.
Повний текст джерелаMondal, Jaygopal. "Solvation consequences of different aqueous media on some biologically active compounds: a physico-chemical study." Thesis, University of North Bengal, 2021. http://ir.nbu.ac.in/handle/123456789/4751.
Повний текст джерелаBarman, Siti. "Investigation on solvation behaviour and host guest inclusion complexes of some significant molecules with diverse cyclic compounds." Thesis, University of North Bengal, 2017. http://ir.nbu.ac.in/handle/123456789/2588.
Повний текст джерелаGroom, Jazerie J. "Evaluation of Apparent Formation Constants of Host-Guest Inclusion Complexes of Solutes with Soluble Calixarenes Using High Performance Liquid Chromatography." Youngstown State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1389273191.
Повний текст джерелаSaha, Binoy Chandra. "Host guest inclusion complexes and thermodynamic properties of some imperative molecules with the manifestation of diverse interections by physiochemical investigation." Thesis, University of North Bengal, 2020. http://ir.nbu.ac.in/handle/123456789/3966.
Повний текст джерелаRahaman, Habibur. "Diverse Interactions of Some Significant Compounds Prevailing in Different Solvent Systems with the Manifestation of Solvation Consequence by Physicochemical Investigations." Thesis, University of North Bengal, 2019. http://ir.nbu.ac.in/handle/123456789/2814.
Повний текст джерелаЧастини книг з теми "Host-Guest inclusion complex"
Wagner, Brian D. "Host–Guest Inclusion Complexes." In Supramolecular Chemistry in Corrosion and Biofouling Protection, 17–40. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003169130-3.
Повний текст джерелаCheetham, A. K., and B. K. Peterson. "Computer Simulations of Host-Guest Complexes." In Inclusion Phenomena and Molecular Recognition, 277–87. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-0603-0_29.
Повний текст джерелаToda, Fumio. "Reaction control of guest compounds in host-guest inclusion complexes." In Topics in Current Chemistry, 211–38. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/3-540-19338-3_5.
Повний текст джерелаWagner, Brian D. "Fluorescence Studies of the Hydrogen Bonding of Excited-State Molecules within Supramolecular Host-Guest Inclusion Complexes." In Hydrogen Bonding and Transfer in the Excited State, 175–91. Chichester, UK: John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470669143.ch8.
Повний текст джерелаGonzález-Gaitano, G., T. Sanz, R. Gabarró, J. A. Rodríguez-Cheda, M. C. Sáez, and G. Tardajos. "Molar Partial Properties in Host-Guest Systems: Application to the Inclusion Complexes between β- Cyclodextrin and Sodium Alkanoates." In Proceedings of the Ninth International Symposium on Cyclodextrins, 667–70. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4681-4_158.
Повний текст джерелаVitale, Rosa Maria, and Pietro Amodeo. "Self-Inclusion Complexes of Monofunctionalized Beta-Cyclodextrins as Host–Guest Interaction Model Systems and Simple and Sensitive Testbeds for Implicit Solvation Methods." In Computational Electrostatics for Biological Applications, 271–96. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-12211-3_14.
Повний текст джерелаEbmeyer, Frank, and Fritz Vogtle. "New hosts for the molecular recognition and encapsulation of guest compounds." In Inclusion Compounds, 263–82. Oxford University PressOxford, 1991. http://dx.doi.org/10.1093/oso/9780198552925.003.0006.
Повний текст джерелаHarata, Kazuaki. "Recent advances in the X-ray analysis of cyclodextrin complexes." In Inclusion Compounds, 311–44. Oxford University PressOxford, 1991. http://dx.doi.org/10.1093/oso/9780198552932.003.0009.
Повний текст джерелаIwamoto, Toschitake. "Inclusion compounds of multi-dimensional cyanometal complex hosts." In Inclusion Compounds, 177–212. Oxford University PressOxford, 1991. http://dx.doi.org/10.1093/oso/9780198552932.003.0006.
Повний текст джерелаAndreetti, Giovanni D., Franco Ugozzoli, Rocco Ungaro,, and Andrea Pochini. "Inclusion of ions and neutral molecules in calixarenes." In Inclusion Compounds, 64–125. Oxford University PressOxford, 1991. http://dx.doi.org/10.1093/oso/9780198552925.003.0003.
Повний текст джерелаТези доповідей конференцій з теми "Host-Guest inclusion complex"
Hu, Shenshui, Cuiling Xu, Lingzi Meng, Yongbin He, and Dafu Cui. "Electrochemical oxygen sensor based on host-guest inclusion complex of calixarene and methyl viologen." In International Conference on Sensors and Control Techniques (ICSC2000), edited by Desheng Jiang and Anbo Wang. SPIE, 2000. http://dx.doi.org/10.1117/12.385597.
Повний текст джерелаVázquez Tato, José, Víctor Soto Tellini, Aida Ramos, Juan Trillo Novo, Francisco Meijide, and Jorge Carrazana G. "Can Guest Hydrophobicity Guide the Entrance into the Host in the Formation of an Inclusion Complex?" In The 8th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2004. http://dx.doi.org/10.3390/ecsoc-8-01996.
Повний текст джерелаKaneko, Takuma, Hirokazu Takahashi, Kenryo Ohminami, Takehisa Konishi, Masaki Ueda, Shin-ichi Nagamatsu та Takashi Fujikawa. "Host-Guest Interaction in α-Cyclodextrin Inclusion Complexes". У X-RAY ABSORPTION FINE STRUCTURE - XAFS13: 13th International Conference. AIP, 2007. http://dx.doi.org/10.1063/1.2644519.
Повний текст джерела