Статті в журналах з теми "Host-Guest moleculars"
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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 джерелаChen, Kaifei, Seyed Hesam Mousavi, Ranjeet Singh, Randall Q. Snurr, Gang Li, and Paul A. Webley. "Gating effect for gas adsorption in microporous materials—mechanisms and applications." Chemical Society Reviews 51, no. 3 (2022): 1139–66. http://dx.doi.org/10.1039/d1cs00822f.
Повний текст джерелаLebedinskiy, Konstantin, Ivan Barvík, Zdeněk Tošner, Ivana Císařová, Jindřich Jindřich, and Radim Hrdina. "Spatial arrangements of cyclodextrin host–guest complexes in solution studied by 13C NMR and molecular modelling." Beilstein Journal of Organic Chemistry 20 (February 20, 2024): 331–35. http://dx.doi.org/10.3762/bjoc.20.33.
Повний текст джерелаElemans, Johannes A. A. W., Roeland J. M. Nolte, and Alan E. Rowan. "Hierarchical self-assembly of a host-guest porphyrin array." Journal of Porphyrins and Phthalocyanines 07, no. 04 (April 2003): 249–54. http://dx.doi.org/10.1142/s1088424603000331.
Повний текст джерелаLiang, Guodong, Jacky W. Y. Lam, Wei Qin, Jie Li, Ni Xie, and Ben Zhong Tang. "Molecular luminogens based on restriction of intramolecular motions through host–guest inclusion for cell imaging." Chem. Commun. 50, no. 14 (2014): 1725–27. http://dx.doi.org/10.1039/c3cc48625g.
Повний текст джерелаSuzuki, Akira, Yuya Miyake, Ryoga Shibata, and Kazuyuki Takai. "Spin and charge interactions between nanographene host and ferrocene." Beilstein Journal of Organic Chemistry 20 (May 2, 2024): 1011–19. http://dx.doi.org/10.3762/bjoc.20.89.
Повний текст джерелаSun, Zhaoxi, Qiaole He, Zhihao Gong, Payam Kalhor, Zhe Huai, and Zhirong Liu. "A General Picture of Cucurbit[8]uril Host–Guest Binding: Recalibrating Bonded Interactions." Molecules 28, no. 7 (March 31, 2023): 3124. http://dx.doi.org/10.3390/molecules28073124.
Повний текст джерелаYoshida, Hiroaki, Ken Kikuta, and Toshiyuki Kida. "Fabrication of supramolecular cyclodextrin–fullerene nonwovens by electrospinning." Beilstein Journal of Organic Chemistry 15 (January 9, 2019): 89–95. http://dx.doi.org/10.3762/bjoc.15.10.
Повний текст джерелаArchana Sumohan Pillai, Sivaraj Ramasamy, Varnitha Manikandan, Aleyamma Alexander та Israel V.M.V. Enoch. "Anticancer Activity of the Host-Guest Complex of Camptothecin with β-Cyclodextrin-Folate Conjugate. Encapsulation and Efficacy". International Journal of Research in Pharmaceutical Sciences 11, SPL4 (21 грудня 2020): 1286–91. http://dx.doi.org/10.26452/ijrps.v11ispl4.4294.
Повний текст джерелаWen, Huimin, Wengang Li, Jiewei Chen, Gen He, Longhua Li, Mark A. Olson, Andrew C. H. Sue, J. Fraser Stoddart, and Xuefeng Guo. "Complex formation dynamics in a single-molecule electronic device." Science Advances 2, no. 11 (November 2016): e1601113. http://dx.doi.org/10.1126/sciadv.1601113.
Повний текст джерелаMarjo, CE, R. Bishop, DC Craig, and ML Scudder. "A Tetrachloro Guest in a Molecular Box." Australian Journal of Chemistry 49, no. 3 (1996): 337. http://dx.doi.org/10.1071/ch9960337.
Повний текст джерелаSerillon, Dylan, Carles Bo, and Xavier Barril. "Testing automatic methods to predict free binding energy of host–guest complexes in SAMPL7 challenge." Journal of Computer-Aided Molecular Design 35, no. 2 (January 19, 2021): 209–22. http://dx.doi.org/10.1007/s10822-020-00370-6.
Повний текст джерелаWard, M. D., and A. M. Pivovar. "Organic host–guest molecular assemblies." Current Opinion in Solid State and Materials Science 4, no. 6 (December 1999): 581–86. http://dx.doi.org/10.1016/s1359-0286(00)00013-9.
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 джерелаChan, Alan Kwun-Wa, Wai Han Lam, Yuya Tanaka, Keith Man-Chung Wong, and Vivian Wing-Wah Yam. "Multiaddressable molecular rectangles with reversible host–guest interactions: Modulation of pH-controlled guest release and capture." Proceedings of the National Academy of Sciences 112, no. 3 (January 7, 2015): 690–95. http://dx.doi.org/10.1073/pnas.1423709112.
Повний текст джерелаItoh, H., B. Chazallon, H. Schober, K. Kawamura, and W. F. Kuhs. "Inelastic neutron scattering and molecular dynamics studies on low-frequency modes of clathrate hydrates." Canadian Journal of Physics 81, no. 1-2 (January 1, 2003): 493–501. http://dx.doi.org/10.1139/p03-034.
Повний текст джерелаZhou, Mingming, Caichao Ye та Dong Xiang. "Theoretical Studies on the Role of Guest in α-CL-20/Guest Crystals". Molecules 27, № 10 (19 травня 2022): 3266. http://dx.doi.org/10.3390/molecules27103266.
Повний текст джерелаSinawang, Garry, Motofumi Osaki, Yoshinori Takashima, Hiroyasu Yamaguchi, and Akira Harada. "Supramolecular self-healing materials from non-covalent cross-linking host–guest interactions." Chemical Communications 56, no. 32 (2020): 4381–95. http://dx.doi.org/10.1039/d0cc00672f.
Повний текст джерелаMartín Carmona, María Antonia. "Natural and synthetic cavitands: challenges in chemistry and pharmaceutical technology." Anales de la Real Academia Nacional de Farmacia 87, no. 87(04) (2021): 381–94. http://dx.doi.org/10.53519/analesranf.2021.87.04.02.
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 джерелаGoubitz, Kees, Pavla Čapková, Klára Melánová, Wim Molleman, and Henk Schenk. "Structure determination of two intercalated compounds VOPO4·(CH2)4O and VOPO4·OH—(CH2)2—O—(CH2)2—OH; synchrotron powder diffraction and molecular modelling." Acta Crystallographica Section B Structural Science 57, no. 2 (April 1, 2001): 178–83. http://dx.doi.org/10.1107/s0108768100015603.
Повний текст джерелаNagatomo, Nao, Hisashi Oishi, Yutaka Kuwahara, Makoto Takafuji, Reiko Oda, Taisuke Hamada, and Hirotaka Ihara. "Enantioselective Self-Assembled Nanofibrillar Network with Glutamide-Based Organogelator." Nanomaterials 11, no. 6 (May 23, 2021): 1376. http://dx.doi.org/10.3390/nano11061376.
Повний текст джерелаBruns. "Exploring and Exploiting the Symmetry-Breaking Effect of Cyclodextrins in Mechanomolecules." Symmetry 11, no. 10 (October 5, 2019): 1249. http://dx.doi.org/10.3390/sym11101249.
Повний текст джерелаEikeland, Espen, Solveig Madsen, Jacob Overgaard, Mark Spackman, and Bo Iversen. "Exploring Host-Guest Interactions: a Single Crystal High-Pressure study." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C756. http://dx.doi.org/10.1107/s2053273314092432.
Повний текст джерелаRissanen, Kari. "Crystallography of encapsulated molecules." Chemical Society Reviews 46, no. 9 (2017): 2638–48. http://dx.doi.org/10.1039/c7cs00090a.
Повний текст джерелаAhn, Yun-Ho, Byeonggwan Lee, and Kyuchul Shin. "Structural Identification of Binary Tetrahydrofuran + O2 and 3-Hydroxytetrahydrofuran + O2 Clathrate Hydrates by Rietveld Analysis with Direct Space Method." Crystals 8, no. 8 (August 18, 2018): 328. http://dx.doi.org/10.3390/cryst8080328.
Повний текст джерелаCheng, Peiming, Lixuan Cai, Danni Yan, Lipeng Zhou, and Qingfu Sun. "Molecular Cage Promoted Aerobic Oxidation or Photo-Induced Rearrangement of Spiroepoxy Naphthalenone." Catalysts 11, no. 4 (April 9, 2021): 484. http://dx.doi.org/10.3390/catal11040484.
Повний текст джерелаTanaka, Koichi, Takaichi Hiratsuka, Yuko Kojima, and Yasuko T. Osano. "Synthesis, Structure and Chiral Inclusion Crystallisation of Tetrakis(4-Ethynylphenyl)Ethylene Derivatives." Journal of Chemical Research 2002, no. 5 (May 2002): 209–12. http://dx.doi.org/10.3184/030823402103171889.
Повний текст джерелаShao, Li, Bin Hua, Jie Yang, and Guocan Yu. "Construction of a photo-responsive supra-amphiphile based on a tetracationic cyclobis(paraquat-p-phenylene) and an azobenzene-containing guest in water." Chemical Communications 52, no. 39 (2016): 6573–76. http://dx.doi.org/10.1039/c6cc02434c.
Повний текст джерелаHayashida, Osamu, Yudai Tanaka, and Takaaki Miyazaki. "Synthesis and Guest-Binding Properties of pH/Reduction Dual-Responsive Cyclophane Dimer." Molecules 26, no. 11 (May 22, 2021): 3097. http://dx.doi.org/10.3390/molecules26113097.
Повний текст джерелаThomas, Sajesh, Rebecca Fuller, Alexandre Sobolev, Philip Schauer, Simon Grabowsky, George Koutsantonis, and Mark Spackman. "Supramolecular Stark Effect in Host-Guest Complexes via Charge Density Analysis." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C674. http://dx.doi.org/10.1107/s2053273314093255.
Повний текст джерелаBhaskar Reddy, Manda, Myadaraboina Shailaja, Alla Manjula, Joseph Richard Premkumar, Garikapati Narahari Sastry, Katukuri Sirisha, and Akella Venkata Subrahmanya Sarma. "Design and synthesis of Tröger's base ditopic receptors: host–guest interactions, a combined theoretical and experimental study." Organic & Biomolecular Chemistry 13, no. 4 (2015): 1141–49. http://dx.doi.org/10.1039/c4ob02266a.
Повний текст джерелаLEE, WONBAE, JUN CHUN, YOON KYUNG CHANG, YOUNG KWAN LIM, CHEON-GYU CHO та HAIWON LEE. "IMMOBILIZATION AND CHARACTERIZATION OF AN ARTIFICIALLY ASSEMBLED TRI-STRAND β-SHEET STRUCTURE ON A RIGID Au(111) SURFACE". International Journal of Nanoscience 05, № 06 (грудень 2006): 803–8. http://dx.doi.org/10.1142/s0219581x06005182.
Повний текст джерелаBock, Hans, Norbert Nagel, and Christian Näther. "Wechselwirkungen in Molekülkristallen, 147 [1, 2]. Isostrukturelle Wirt/Gast-Einschluß-Verbindungen von N,N'-Ditosyl- p-phenylendiamin mit Aceton, Cyclopentanon, Cyclopent-2-en-l-on, 1,3-Dioxolan, Tetrahydrofuran und 2,5-Dihydrofuran / Interactions in Molecular Crystals, 147 [1, 2], Isostructural Host/Guest-Inclusion Compounds of N,N'-Ditosyl-p-phenylenediamine with Acetone, Cyclopentanone, Cyclopent-2-ene-l-one, 1,3-Dioxolane, Tetrahydrofurane, and 2,5-D ihydrofurane." Zeitschrift für Naturforschung B 53, no. 12 (December 1, 1998): 1401–12. http://dx.doi.org/10.1515/znb-1998-1202.
Повний текст джерелаDanylyuk, Oksana, Karolina Kedra-Krolik, Marta Worzakowska, Joanna Osypiuk-Tomasik, and Vladimir Fedin. "Phase transformations in cucurbituril host-guest complexes." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C646. http://dx.doi.org/10.1107/s205327331409353x.
Повний текст джерелаZyryanov, Grigory V., Dmitry S. Kopchuk, Igor S. Kovalev, Sougata Santra, Adinath Majee, and Brindaban C. Ranu. "Pillararenes as Promising Carriers for Drug Delivery." International Journal of Molecular Sciences 24, no. 6 (March 8, 2023): 5167. http://dx.doi.org/10.3390/ijms24065167.
Повний текст джерелаKärger, Jörg, Dieter Freude, and Jürgen Haase. "Diffusion in Nanoporous Materials: Novel Insights by Combining MAS and PFG NMR." Processes 6, no. 9 (September 1, 2018): 147. http://dx.doi.org/10.3390/pr6090147.
Повний текст джерелаSnelgrove, Matthew P., and Michaele J. Hardie. "Coordination polymers with embedded recognition sites: lessons from cyclotriveratrylene-type ligands." CrystEngComm 23, no. 23 (2021): 4087–102. http://dx.doi.org/10.1039/d1ce00471a.
Повний текст джерелаKalchenko, Olga, Sergiy Cherenok, Sergiy Suikov, and Vitaly Kalchenko Vitaly Kalchenko. "Study of Calixarene Complexation with Biologically Active." French-Ukrainian Journal of Chemistry 5, no. 2 (2017): 49–55. http://dx.doi.org/10.17721/fujcv5i2p49-55.
Повний текст джерелаKhan, Sadaf Bashir, and Shern-Long Lee. "Supramolecular Chemistry: Host–Guest Molecular Complexes." Molecules 26, no. 13 (June 30, 2021): 3995. http://dx.doi.org/10.3390/molecules26133995.
Повний текст джерелаYoshida, Jun, Shuhei Tamura, Hidetaka Yuge, and Go Watanabe. "Left- and right-circularly polarized light-sensing based on colored and mechano-responsive chiral nematic liquid crystals." Soft Matter 14, no. 1 (2018): 27–30. http://dx.doi.org/10.1039/c7sm01975k.
Повний текст джерелаSheng, Xinru, Errui Li, and Feihe Huang. "Construction of pillar[4]arene[1]quinone–1,10-dibromodecane pseudorotaxanes in solution and in the solid state." Beilstein Journal of Organic Chemistry 16 (December 2, 2020): 2954–59. http://dx.doi.org/10.3762/bjoc.16.245.
Повний текст джерелаChong, Samantha, Tom Hasell, Jamie Culshaw, Marc Little, Marc Schmidtmann, Daniel Holden, Linjiang Chen, Kim Jelfs, and Andrew Cooper. "Exploiting weak supramolecular interactions to assemble organic cage materials." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C632. http://dx.doi.org/10.1107/s205327331409367x.
Повний текст джерелаKircheva, Nikoleta, Vladislava Petkova, Stefan Dobrev, Valya Nikolova, Silvia Angelova, and Todor Dudev. "N-Methyl- and N-Phenylpiperazine Functionalized Styryl Dyes Inside Cucurbiturils: Theoretical Assessment of the Factors Governing the Host–Guest Recognition." Molecules 28, no. 24 (December 16, 2023): 8130. http://dx.doi.org/10.3390/molecules28248130.
Повний текст джерелаSouza, Barbara E., and Jin-Chong Tan. "Mechanochemical approaches towards the in situ confinement of 5-FU anti-cancer drug within MIL-100 (Fe) metal–organic framework." CrystEngComm 22, no. 27 (2020): 4526–30. http://dx.doi.org/10.1039/d0ce00638f.
Повний текст джерелаLing, Xing Yi, David N. Reinhoudt, and Jurriaan Huskens. "From supramolecular chemistry to nanotechnology: Assembly of 3D nanostructures." Pure and Applied Chemistry 81, no. 12 (November 3, 2009): 2225–33. http://dx.doi.org/10.1351/pac-con-09-07-04.
Повний текст джерелаFacey, Glenn A., and Ilia Korobkov. "Investigation of the disorder of dibromo- and dichloromethane in their tri-ortho-thymotide clathrates using X-ray diffraction and solid-state 2H NMR spectroscopy." Canadian Journal of Chemistry 89, no. 7 (July 2011): 854–62. http://dx.doi.org/10.1139/v10-178.
Повний текст джерелаWu, Jinyang, Xuan Sun, Xianghui Li, Xiaowei Li, Wen Feng, and Lihua Yuan. "Multi-Responsive Molecular Encapsulation and Release Based on Hydrogen-Bonded Azo-Macrocycle." Molecules 28, no. 11 (May 30, 2023): 4437. http://dx.doi.org/10.3390/molecules28114437.
Повний текст джерелаMustafa, Siti Fatimah Zaharah, Hasmerya Maarof, Mohammed Abu Naser, Hassan H. Abdallah, Ahmad Irfan, and Rashid Ahmed. "Behavioral pattern exploration of single guest, hexadecane-1,16-diol and hexadecane in urea inclusion compounds via molecular dynamics simulation." Journal of Theoretical and Computational Chemistry 15, no. 06 (September 2016): 1650047. http://dx.doi.org/10.1142/s0219633616500474.
Повний текст джерелаMujahid, Adnan, Adeel Afzal, and Franz L. Dickert. "Transitioning from Supramolecular Chemistry to Molecularly Imprinted Polymers in Chemical Sensing." Sensors 23, no. 17 (August 27, 2023): 7457. http://dx.doi.org/10.3390/s23177457.
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