Статті в журналах з теми "Guest inclusion complexes"
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Malinska, 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 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 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 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 джерелаMejuto, 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 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 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 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 джерелаKadokawa, Jun-ichi. "Synthesis of Amylosic Supramolecular Materials by Glucan Phosphorylase-Catalyzed Enzymatic Polymerization According to the Vine-Twining Approach." Synlett 31, no. 07 (January 30, 2020): 648–56. http://dx.doi.org/10.1055/s-0039-1690804.
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 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 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 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 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 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 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 джерелаLavorgna, Margherita, Martina Dragone, Chiara Russo, Gianluca D’Abrosca, Roberta Nugnes, Elena Orlo, Maria della Valle та ін. "Characterization of Complexes between Imidacloprid and β-Cyclodextrin: Evaluation of the Toxic Activity in Algae and Rotifers". Molecules 28, № 7 (29 березня 2023): 3049. http://dx.doi.org/10.3390/molecules28073049.
Повний текст джерелаKadokawa, Jun-ichi. "Fabrication of Nanostructured Supramolecules through Helical Inclusion of Amylose toward Hydrophobic Polyester Guests, Biomimetically through Vine-Twining Polymerization Process." Biomimetics 8, no. 7 (November 1, 2023): 516. http://dx.doi.org/10.3390/biomimetics8070516.
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 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 джерелаSardaru, Monica-Cornelia, Oana Carp, Elena-Laura Ursu, Anda-Mihaela Craciun, Corneliu Cojocaru, Mihaela Silion, Vladyslava Kovalska, Ionel Mangalagiu, Ramona Danac, and Alexandru Rotaru. "Cyclodextrin Encapsulated pH Sensitive Dyes as Fluorescent Cellular Probes: Self-Aggregation and In Vitro Assessments." Molecules 25, no. 19 (September 24, 2020): 4397. http://dx.doi.org/10.3390/molecules25194397.
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 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 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 джерелаRizzi, Vito, Sergio Matera, Paola Semeraro, Paola Fini, and Pinalysa Cosma. "Interactions between 4-thiothymidine and water-soluble cyclodextrins: Evidence for supramolecular structures in aqueous solutions." Beilstein Journal of Organic Chemistry 12 (March 21, 2016): 549–63. http://dx.doi.org/10.3762/bjoc.12.54.
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 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 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 джерелаMohamed, Mohamed H., Lee D. Wilson, John V. Headley, and Kerry M. Peru. "A spectral displacement study of cyclodextrin/naphthenic acids inclusion complexes." Canadian Journal of Chemistry 87, no. 12 (December 2009): 1747–56. http://dx.doi.org/10.1139/v09-140.
Повний текст джерелаChai, Xiang Hua, Ruo Hui Lin, Ke Gang Wu та Shu Ri Li. "Characterization of β-Cyclodextrin-Thymol Inclusion Complexes". Advanced Materials Research 233-235 (травень 2011): 1766–73. http://dx.doi.org/10.4028/www.scientific.net/amr.233-235.1766.
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 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 джерелаTan, Libo, and Lingyan Kong. "Starch-guest inclusion complexes: Formation, structure, and enzymatic digestion." Critical Reviews in Food Science and Nutrition 60, no. 5 (January 7, 2019): 780–90. http://dx.doi.org/10.1080/10408398.2018.1550739.
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 джерелаWang, Hai Ming, та Gerhard Wenz. "Topochemical control of the photodimerization of aromatic compounds by γ-cyclodextrin thioethers in aqueous solution". Beilstein Journal of Organic Chemistry 9 (12 вересня 2013): 1858–66. http://dx.doi.org/10.3762/bjoc.9.217.
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 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 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 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 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 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 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 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 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 джерелаChen, Lu, and Yanbin Huang. "The guest polymer effect on the dissolution of drug–polymer crystalline inclusion complexes." RSC Advances 11, no. 22 (2021): 13091–96. http://dx.doi.org/10.1039/d1ra01926k.
Повний текст джерелаKühne, Irina A., Kane Esien, Laurence C. Gavin, Helge Müller-Bunz, Solveig Felton, and Grace G. Morgan. "Modulation of Mn3+ Spin State by Guest Molecule Inclusion." Molecules 25, no. 23 (November 28, 2020): 5603. http://dx.doi.org/10.3390/molecules25235603.
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 джерелаBacchi, A., G. Cantoni, D. Crocco, M. Granelli, P. Pagano, and P. Pelagatti. "Hydrogen-bond networks in polymorphs and solvates of metallorganic complexes containing ruthenium and aminoamide ligands." CrystEngComm 16, no. 6 (2014): 1001–9. http://dx.doi.org/10.1039/c3ce41920g.
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