Статті в журналах з теми "Host - guest inclusion complexes"
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Mejuto, Juan C., and Jesus Simal-Gandara. "Host–Guest Complexes." International Journal of Molecular Sciences 23, no. 24 (December 12, 2022): 15730. http://dx.doi.org/10.3390/ijms232415730.
Повний текст джерелаMalinska, Maura. "Insights into molecular recognition from the crystal structures of p-tert-butylcalix[6]arene complexed with different solvents." IUCrJ 9, no. 1 (November 16, 2021): 55–64. http://dx.doi.org/10.1107/s2052252521010678.
Повний текст джерелаToda, Fumio. "Crystalline inclusion complexes as media of molecular recognitions and selective reactions." Pure and Applied Chemistry 73, no. 7 (July 1, 2001): 1137–45. http://dx.doi.org/10.1351/pac200173071137.
Повний текст джерелаKadu, Rahul, Vineeta Pillai, Amrit V. та Vinay K. Singh. "Synthesis and spectral characterization of bimetallic metallomacrocyclic structures [MII2-μ2-bis-{(κ2S,S-S2CN(R)C6H4)2O}] (M = Ni/Zn/Cd): density functional theory and host–guest reactivity studies". RSC Advances 5, № 129 (2015): 106688–99. http://dx.doi.org/10.1039/c5ra22175g.
Повний текст джерелаHettiarachchi, D. Saroja N., and Donal H. Macartney. "Cucurbit[7]uril host-guest complexes with cationic bis(4,5-dihydro-1H-imidazol-2-yl) guests in aqueous solution." Canadian Journal of Chemistry 84, no. 6 (June 1, 2006): 905–14. http://dx.doi.org/10.1139/v06-099.
Повний текст джерелаZhang, Meng, Nicolas Levaray, Josée R. Daniel, Karen C. Waldron, and X. X. Zhu. "Cholic acid dimers as invertible amphiphilic pockets: synthesis, molecular modeling, and inclusion studies." Canadian Journal of Chemistry 95, no. 7 (July 2017): 792–98. http://dx.doi.org/10.1139/cjc-2016-0621.
Повний текст джерелаSuwinska, Kinga. "Intermolecular interactions in inclusion complexes." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C673. http://dx.doi.org/10.1107/s2053273314093267.
Повний текст джерелаGómez-González, Borja, Luis García-Río, Nuno Basílio, Juan C. Mejuto, and Jesus Simal-Gandara. "Molecular Recognition by Pillar[5]arenes: Evidence for Simultaneous Electrostatic and Hydrophobic Interactions." Pharmaceutics 14, no. 1 (December 28, 2021): 60. http://dx.doi.org/10.3390/pharmaceutics14010060.
Повний текст джерелаLiu, Yu, Chang-Cheng You, Takehiko Wada та Yoshihisa Inoue. "Effect of Host Substituent upon Inclusion Complexation of Aliphatic Alcohols with Organoseleno β-Cyclodextrins". Journal of Chemical Research 2000, № 2 (лютий 2000): 90–92. http://dx.doi.org/10.3184/030823400103166490.
Повний текст джерелаFu, T. Y., J. R. Scheffer, and J. Trotter. "Structures and Photochemistry of Inclusion Compounds of 9,10-Dihydro-9,10-ethenoanthracene-11,12-bis(diphenylmethanol)." Acta Crystallographica Section B Structural Science 53, no. 2 (April 1, 1997): 300–305. http://dx.doi.org/10.1107/s0108768196013614.
Повний текст джерелаDutta, Ashutosh, Niloy Roy, Koyeli Das, Debadrita Roy, Raja Ghosh, and Mahendra Nath Roy. "Synthesis and Characterization of Host Guest Inclusion Complexes of Cyclodextrin Molecules with Theophylline by Diverse Methodologies." Emerging Science Journal 4, no. 1 (February 1, 2020): 52–72. http://dx.doi.org/10.28991/esj-2020-01210.
Повний текст джерелаRusso, Marco, and Paolo Lo Meo. "Binding abilities of a chiral calix[4]resorcinarene: a polarimetric investigation on a complex case of study." Beilstein Journal of Organic Chemistry 13 (December 15, 2017): 2698–709. http://dx.doi.org/10.3762/bjoc.13.268.
Повний текст джерелаGiastas, Petros, Konstantina Yannakopoulou та Irene M. Mavridis. "Molecular structures of the inclusion complexes β-cyclodextrin–1,2-bis(4-aminophenyl)ethane and β-cyclodextrin–4,4′-diaminobiphenyl; packing of dimeric β-cyclodextrin inclusion complexes". Acta Crystallographica Section B Structural Science 59, № 2 (26 березня 2003): 287–99. http://dx.doi.org/10.1107/s010876810300257x.
Повний текст джерелаBarman, Biraj Kumar, Kanak Roy, and Mahendra Nath Roy. "Probing Inclusion Complexes of Pentoxifylline and Pralidoxim inside Cyclic Oligosaccharides by Physicochemical Methodologies." Zeitschrift für Physikalische Chemie 233, no. 8 (August 27, 2019): 1109–27. http://dx.doi.org/10.1515/zpch-2017-1020.
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 джерелаBoland, Patricia G., Sara J. Accardi, Carrie A. Snow, and Brian D. Wagner. "Investigations of the supramolecular host properties of a fluorescent bistren cage compound." Canadian Journal of Chemistry 87, no. 2 (February 2009): 448–52. http://dx.doi.org/10.1139/v08-179.
Повний текст джерелаRodríguez, Silvio D., and Delia L. Bernik. "Host–Guest Molecular Interactions in Vanillin/Amylose Inclusion Complexes." Applied Spectroscopy 67, no. 8 (August 2013): 884–91. http://dx.doi.org/10.1366/12-06981.
Повний текст джерелаIyengar, Suman, та Michael C. Biewer. "Observation of photochromic γ-cyclodextrin host–guest inclusion complexes". Chemical Communications, № 13 (31 травня 2002): 1398–99. http://dx.doi.org/10.1039/b204322j.
Повний текст джерелаIyengar, Suman, and Michael C. Biewer. "Solid-State Interactions in Photochromic Host−Guest Inclusion Complexes†." Crystal Growth & Design 5, no. 6 (November 2005): 2043–45. http://dx.doi.org/10.1021/cg050313b.
Повний текст джерелаRoy, Mahendra Nath, Deepak Ekka, Subhadeep Saha та Milan Chandra Roy. "Host–guest inclusion complexes of α and β-cyclodextrins with α-amino acids". RSC Adv. 4, № 80 (2014): 42383–90. http://dx.doi.org/10.1039/c4ra07877b.
Повний текст джерелаNutho, Bodee, Nadtanet Nunthaboot, Peter Wolschann, Nawee Kungwan, and Thanyada Rungrotmongkol. "Metadynamics supports molecular dynamics simulation-based binding affinities of eucalyptol and beta-cyclodextrin inclusion complexes." RSC Advances 7, no. 80 (2017): 50899–911. http://dx.doi.org/10.1039/c7ra09387j.
Повний текст джерелаWarttmann, Inge, and Günter Häfelinger. "Ab initio MO Optimizations of Osmiumtetracarbonyldihydride and Metallacyclophanes with two Osmium Atoms and their Molecular Complexes with Different Guests." Zeitschrift für Naturforschung B 53, no. 10 (October 1, 1998): 1223–35. http://dx.doi.org/10.1515/znb-1998-1020.
Повний текст джерелаSaha, Subhadeep, Tanusree Ray, Saptarshi Basak, and Mahendra Nath Roy. "NMR, surface tension and conductivity studies to determine the inclusion mechanism: thermodynamics of host–guest inclusion complexes of natural amino acids in aqueous cyclodextrins." New Journal of Chemistry 40, no. 1 (2016): 651–61. http://dx.doi.org/10.1039/c5nj02179k.
Повний текст джерелаAssaf, Khaleel I., Husam Abed alfattah, Ala'a F. Eftaiha, Sanaa K. Bardaweel, Mohammad A. Alnajjar, Fatima A. Alsoubani, Abdussalam K. Qaroush, Musa I. El-Barghouthi, and Werner M. Nau. "Encapsulation of ionic liquids inside cucurbiturils." Organic & Biomolecular Chemistry 18, no. 11 (2020): 2120–28. http://dx.doi.org/10.1039/d0ob00001a.
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 джерелаChen, Ning, and Ya Bin Li. "Study on the Inclusion Behavior of Cucurbit [n] uril with Phenylalanine." Advanced Materials Research 197-198 (February 2011): 1153–56. http://dx.doi.org/10.4028/www.scientific.net/amr.197-198.1153.
Повний текст джерелаPrabodh, Amrutha, Stephan Sinn, Laura Grimm, Zsombor Miskolczy, Mónika Megyesi, László Biczók, Stefan Bräse, and Frank Biedermann. "Teaching indicators to unravel the kinetic features of host–guest inclusion complexes." Chemical Communications 56, no. 82 (2020): 12327–30. http://dx.doi.org/10.1039/d0cc03715j.
Повний текст джерелаPan, Fangfang, Mohadeseh Dashti, Michael R. Reynolds, Kari Rissanen, John F. Trant, and Ngong Kodiah Beyeh. "Halogen bonding and host–guest chemistry between N-alkylammonium resorcinarene halides, diiodoperfluorobutane and neutral guests." Beilstein Journal of Organic Chemistry 15 (April 18, 2019): 947–54. http://dx.doi.org/10.3762/bjoc.15.91.
Повний текст джерелаHunt, Lee E., Susan A. Bourne, and Mino R. Caira. "Inclusion of Hydroxycinnamic Acids in Methylated Cyclodextrins: Host-Guest Interactions and Effects on Guest Thermal Stability." Biomolecules 11, no. 1 (December 31, 2020): 45. http://dx.doi.org/10.3390/biom11010045.
Повний текст джерелаCetina, Mario, and Kari Rissanen. "From Self-inclusion and Host-guest Complexes to Channel Structures." Croatica Chemica Acta 85, no. 3 (2012): 319–25. http://dx.doi.org/10.5562/cca2058.
Повний текст джерелаSaenger, W., and T. Steiner. "Cyclodextrin Inclusion Complexes: Host–Guest Interactions and Hydrogen-Bonding Networks." Acta Crystallographica Section A Foundations of Crystallography 54, no. 6 (November 1, 1998): 798–805. http://dx.doi.org/10.1107/s0108767398010733.
Повний текст джерелаFabbiani, F. P. A., G. Buth, R. Granero García, F. J. Lahoz, C. Paulmann, and S. Saouane. "Host–guest interactions in cyclodextrin inclusion complexes at extreme conditions." Acta Crystallographica Section A Foundations of Crystallography 68, a1 (August 7, 2012): s115. http://dx.doi.org/10.1107/s0108767312097772.
Повний текст джерелаWang, Jin, and Xuetong Zhang. "Binary Crystallized Supramolecular Aerogels Derived from Host–Guest Inclusion Complexes." ACS Nano 9, no. 11 (November 2, 2015): 11389–97. http://dx.doi.org/10.1021/acsnano.5b05281.
Повний текст джерелаZhang, Jinyu, Dan Xu, Wenjing Qian, Jingyue Zhu, and Feng Yan. "Host–guest inclusion complexes derived heteroatom-doped porous carbon materials." Carbon 105 (August 2016): 183–90. http://dx.doi.org/10.1016/j.carbon.2016.04.034.
Повний текст джерелаTirapegui, Cristian, Francisco Jara, Juan Guerrero, and Marcos Caroli Rezende. "Host–guest interactions in cyclodextrin inclusion complexes with solvatochromic dyes." Journal of Physical Organic Chemistry 19, no. 11 (November 2006): 786–92. http://dx.doi.org/10.1002/poc.1080.
Повний текст джерелаMosinger, Jiří, Viktor Kliment, Jan Sejbal, Pavel Kubát, and Kamil Lang. "Host-guest complexes of anionic porphyrin sensitizers with cyclodextrins." Journal of Porphyrins and Phthalocyanines 06, no. 08 (August 2002): 514–26. http://dx.doi.org/10.1142/s1088424602000646.
Повний текст джерелаRoy, Mahendra Nath, Subhadeep Saha, Siti Barman, and Deepak Ekka. "Host–guest inclusion complexes of RNA nucleosides inside aqueous cyclodextrins explored by physicochemical and spectroscopic methods." RSC Advances 6, no. 11 (2016): 8881–91. http://dx.doi.org/10.1039/c5ra24102b.
Повний текст джерелаLee, Jae-ung, Sung-Sik Lee, Sungyul Lee, and Han Bin Oh. "Noncovalent Complexes of Cyclodextrin with Small Organic Molecules: Applications and Insights into Host–Guest Interactions in the Gas Phase and Condensed Phase." Molecules 25, no. 18 (September 4, 2020): 4048. http://dx.doi.org/10.3390/molecules25184048.
Повний текст джерелаChen, Shunwei, Zhe Han, Dongju Zhang, and Jinhua Zhan. "Theoretical study of the inclusion complexation of TCDD with cucurbit[n]urils." RSC Adv. 4, no. 94 (2014): 52415–22. http://dx.doi.org/10.1039/c4ra06011c.
Повний текст джерелаStasyuk, Anton J., Olga A. Stasyuk, Miquel Solà, and Alexander A. Voityuk. "Photoinduced electron transfer in nanotube⊃C70 inclusion complexes: phenine vs. nanographene nanotubes." Chemical Communications 56, no. 83 (2020): 12624–27. http://dx.doi.org/10.1039/d0cc04261g.
Повний текст джерелаLitim, Abdelkarim, Youghourta Belhocine, Tahar Benlecheb, Monira Galal Ghoniem, Zoubir Kabouche, Fatima Adam Mohamed Ali, Babiker Yagoub Abdulkhair, Mahamadou Seydou, and Seyfeddine Rahali. "DFT-D4 Insight into the Inclusion of Amphetamine and Methamphetamine in Cucurbit[7]uril: Energetic, Structural and Biosensing Properties." Molecules 26, no. 24 (December 10, 2021): 7479. http://dx.doi.org/10.3390/molecules26247479.
Повний текст джерелаCheng, Si-Yuan, Yun-Xia Qu, Zhu Tao, Kai-Zhi Zhou, Lian-Tong Wei, Cong Wang, Wei-Wei Zhao, Dao-Fa Jiang, and Pei-Hua Ma. "The Host–Guest Properties Observed Between the Viologens and Cyclopentanocucurbit[6]uril." Australian Journal of Chemistry 73, no. 7 (2020): 601. http://dx.doi.org/10.1071/ch19400.
Повний текст джерелаDračínský, Martin, Carina Santos Hurtado, Eric Masson, and Jiří Kaleta. "Stuffed pumpkins: mechanochemical synthesis of host–guest complexes with cucurbit[7]uril." Chemical Communications 57, no. 17 (2021): 2132–35. http://dx.doi.org/10.1039/d1cc00240f.
Повний текст джерелаHerbstein, F. H. "Conformational Isomerism of the Host as a Factor in Molecular Recognition in Host–Guest Inclusion Complexes: Example of Tris(5-acetyl-3-thienyl)methane." Acta Crystallographica Section B Structural Science 53, no. 1 (February 1, 1997): 168–75. http://dx.doi.org/10.1107/s0108768196010907.
Повний текст джерелаKawase, Takeshi, and Masaji Oda. "Complexation of carbon nanorings with fullerenes." Pure and Applied Chemistry 78, no. 4 (January 1, 2006): 831–39. http://dx.doi.org/10.1351/pac200678040831.
Повний текст джерелаFerino-Pérez, Anthuan, Juan José Gamboa-Carballo, Ronald Ranguin, Joëlle Levalois-Grützmacher, Yves Bercion, Sarra Gaspard, Ramón Alain Miranda-Quintana, Melvin Arias та Ulises J. Jáuregui-Haza. "Evaluation of the molecular inclusion process of β-hexachlorocyclohexane in cyclodextrins". RSC Advances 9, № 47 (2019): 27484–99. http://dx.doi.org/10.1039/c9ra04431k.
Повний текст джерелаOno, Toshikazu, and Yoshio Hisaeda. "Vapochromism of Organic Crystals Based on Macrocyclic Compounds and Inclusion Complexes." Symmetry 12, no. 11 (November 19, 2020): 1903. http://dx.doi.org/10.3390/sym12111903.
Повний текст джерелаMagalhães, Clara I. R., Ana C. Gomes, André D. Lopes, Isabel S. Gonçalves, Martyn Pillinger, Eunyoung Jin, Ikjin Kim, et al. "Ferrocene and ferrocenium inclusion compounds with cucurbiturils: a study of metal atom dynamics probed by Mössbauer spectroscopy." Physical Chemistry Chemical Physics 19, no. 32 (2017): 21548–55. http://dx.doi.org/10.1039/c7cp04416j.
Повний текст джерелаTriamchaisri, Nat, Pisanu Toochinda, and Luckhana Lawtrakul. "Structural Investigation of Beta-Cyclodextrin Complexes with Cannabidiol and Delta-9-Tetrahydrocannabinol in 1:1 and 2:1 Host-Guest Stoichiometry: Molecular Docking and Density Functional Calculations." International Journal of Molecular Sciences 24, no. 2 (January 12, 2023): 1525. http://dx.doi.org/10.3390/ijms24021525.
Повний текст джерелаCaira, Mino, Susan Bourne та Buntubonke Mzondo. "Cyclodextrin inclusion complexes of the antioxidant α-lipoic acid". Acta Crystallographica Section A Foundations and Advances 70, a1 (5 серпня 2014): C992. http://dx.doi.org/10.1107/s205327331409007x.
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