Статті в журналах з теми "Cavitandi"
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Shi, Qixun, Matthew P. Mower, Donna G. Blackmond, and Julius Rebek. "Water-soluble cavitands promote hydrolyses of long-chain diesters." Proceedings of the National Academy of Sciences 113, no. 33 (August 1, 2016): 9199–203. http://dx.doi.org/10.1073/pnas.1610006113.
Повний текст джерелаTurunen, Lotta, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, and Kari Rissanen. "Halogen-bonded solvates of tetrahaloethynyl cavitands." CrystEngComm 19, no. 35 (2017): 5223–29. http://dx.doi.org/10.1039/c7ce01118k.
Повний текст джерелаBrekalo, Deliz, Kane, Friščić, and Holman. "Exploring the Scope of Macrocyclic “Shoe-last” Templates in the Mechanochemical Synthesis of RHO Topology Zeolitic Imidazolate Frameworks (ZIFs)." Molecules 25, no. 3 (February 1, 2020): 633. http://dx.doi.org/10.3390/molecules25030633.
Повний текст джерелаPedrini, Alessandro, Federico Bertani, and Enrico Dalcanale. "Fluorinated Tetraphosphonate Cavitands." Molecules 23, no. 10 (October 17, 2018): 2670. http://dx.doi.org/10.3390/molecules23102670.
Повний текст джерелаTurunen, L., N. K. Beyeh, F. Pan, A. Valkonen, and K. Rissanen. "Tetraiodoethynyl resorcinarene cavitands as multivalent halogen bond donors." Chem. Commun. 50, no. 100 (2014): 15920–23. http://dx.doi.org/10.1039/c4cc07771g.
Повний текст джерелаDalcanale, E., M. Torelli, I. Domenichelli, A. Pedrini, F. Guagnini, R. Pinalli, F. Terenziani, F. Artoni, and R. Brighenti. "pH-Driven Conformational Switching of Quinoxaline Cavitands in Polymer Matrices." Synlett 29, no. 19 (July 24, 2018): 2503–8. http://dx.doi.org/10.1055/s-0037-1610219.
Повний текст джерелаPinalli, Roberta, та Chiara Massera. "Nitrosonium complexation by the tetraphosphonate cavitand 5,11,17,23-tetramethyl-6,10:12,16:18,22:24,4-tetrakis(phenylphosphonato-κ2O,O)resorcin(4)arene". Acta Crystallographica Section E Crystallographic Communications 73, № 12 (3 листопада 2017): 1801–5. http://dx.doi.org/10.1107/s2056989017015857.
Повний текст джерелаRahman, Faiz-Ur, Yong-sheng Li, Ioannis D. Petsalakis, Giannoula Theodorakopoulos, Julius Rebek, and Yang Yu. "Recognition with metallo cavitands." Proceedings of the National Academy of Sciences 116, no. 36 (August 19, 2019): 17648–53. http://dx.doi.org/10.1073/pnas.1909154116.
Повний текст джерелаBiavardi, Elisa, and Chiara Massera. "Crystal structure of a host–guest complex between mephedrone hydrochloride and a tetraphosphonate cavitand." Acta Crystallographica Section E Crystallographic Communications 75, no. 2 (January 29, 2019): 277–83. http://dx.doi.org/10.1107/s2056989019001464.
Повний текст джерелаPedrini, Alessandro. "Host–guest supramolecular interactions between a resorcinarene-based cavitand bearing a –COOH moiety and acetic acid." Acta Crystallographica Section E Crystallographic Communications 75, no. 3 (February 22, 2019): 397–401. http://dx.doi.org/10.1107/s2056989019002512.
Повний текст джерелаHaino, Takeharu, Ryo Sekiya, Kentaro Harada, and Natsumi Nitta. "Resorcinarene-Based Supramolecular Capsules: Supramolecular Functions and Applications." Synlett 33, no. 06 (October 27, 2021): 518–30. http://dx.doi.org/10.1055/a-1679-8141.
Повний текст джерелаSantonocito, Rossella, Nunzio Tuccitto, Andrea Pappalardo, and Giuseppe Trusso Sfrazzetto. "Smartphone-Based Dopamine Detection by Fluorescent Supramolecular Sensor." Molecules 27, no. 21 (November 3, 2022): 7503. http://dx.doi.org/10.3390/molecules27217503.
Повний текст джерелаNaumann, Christoph, Esteban Román, Carlos Peinador, Tong Ren, Brian O. Patrick, Angel E. Kaifer, and John C. Sherman. "Expanding Cavitand Chemistry: The Preparation and Characterization of [n]Cavitands withn≥4." Chemistry 7, no. 8 (April 17, 2001): 1637–45. http://dx.doi.org/10.1002/1521-3765(20010417)7:8<1637::aid-chem16370>3.0.co;2-x.
Повний текст джерелаHamada, Fumio, Shigeki Ito, Miyuki Narita, and Norio Nashirozawa. "Selective chloromethylation of cavitand at the upper rim and induced fit type complexation with metal cations by new cavitands: Aza-crown-modified cavitands." Tetrahedron Letters 40, no. 8 (February 1999): 1527–30. http://dx.doi.org/10.1016/s0040-4039(98)02702-6.
Повний текст джерелаBoerrigter, Harold, Willem Verboom, Gerrit J. van Hummel, Sybolt Harkema, and David N. Reinhoudt. "Selective functionalization of resorcinarene cavitands; Single crystal X-ray structure of a distally functionalized cavitand." Tetrahedron Letters 37, no. 29 (July 1996): 5167–70. http://dx.doi.org/10.1016/0040-4039(96)01027-1.
Повний текст джерелаWishard, Anthony, and Bruce C. Gibb. "Dynamic light scattering studies of the effects of salts on the diffusivity of cationic and anionic cavitands." Beilstein Journal of Organic Chemistry 14 (August 23, 2018): 2212–19. http://dx.doi.org/10.3762/bjoc.14.195.
Повний текст джерелаLagauzere, Muriel, and Jean Pierre Franc. "La nouvelle veine d'essais du tunnel hydrodynamique du LEGI." La Houille Blanche, no. 4 (August 2018): 73–76. http://dx.doi.org/10.1051/lhb/2018044.
Повний текст джерелаKobayashi, Mutsumi, Mei Takatsuka, Ryo Sekiya, and Takeharu Haino. "Molecular recognition of upper rim functionalized cavitand and its unique dimeric capsule in the solid state." Organic & Biomolecular Chemistry 13, no. 6 (2015): 1647–53. http://dx.doi.org/10.1039/c4ob02251c.
Повний текст джерелаJanosi, Tibor Zoltan, Jouko Korppi-Tommola, Zsolt Csok, Laszlo Kollar, Pasi Myllyperkio, and Janos Erostyak. "Anthracene Fluorescence Quenching by a Tetrakis (Ketocarboxamide) Cavitand." Journal of Spectroscopy 2014 (2014): 1–8. http://dx.doi.org/10.1155/2014/708739.
Повний текст джерелаWan, Yun-Hui, Yu-Jie Zhu, Julius Rebek, and Yang Yu. "Recognition of Hydrophilic Cyclic Compounds by a Water-Soluble Cavitand." Molecules 26, no. 7 (March 30, 2021): 1922. http://dx.doi.org/10.3390/molecules26071922.
Повний текст джерелаTucci, Fabio C., Dmitry M. Rudkevich, and Julius Rebek. "Deeper Cavitands." Journal of Organic Chemistry 64, no. 12 (June 1999): 4555–59. http://dx.doi.org/10.1021/jo990209z.
Повний текст джерелаRudkevich, Dmitry M., and Julius Rebek, Jr. "Deepening Cavitands." European Journal of Organic Chemistry 1999, no. 9 (September 1999): 1991–2005. http://dx.doi.org/10.1002/(sici)1099-0690(199909)1999:9<1991::aid-ejoc1991>3.0.co;2-5.
Повний текст джерелаStarnes, Stephen D., Dmitry M. Rudkevich, and Julius Rebek. "Cavitand−Porphyrins." Journal of the American Chemical Society 123, no. 20 (May 2001): 4659–69. http://dx.doi.org/10.1021/ja010038r.
Повний текст джерелаDumoulin, Fabienne, Derya Topkaya, Songül Yaşar, Vefa Ahsen, and Ümit İşci. "Covalent or supramolecular combinations of resorcinarenes and porphyrinoids." Journal of Porphyrins and Phthalocyanines 20, no. 05 (May 2016): 571–81. http://dx.doi.org/10.1142/s108842461630010x.
Повний текст джерелаHavlík, Martin, Václav Parchaňský, Petr Bouř, Vladimír Král, and Bohumil Dolensky. "Bridged bis-Tröger’s base molecular tweezers as new cavitand family." Collection of Czechoslovak Chemical Communications 74, no. 7-8 (2009): 1091–99. http://dx.doi.org/10.1135/cccc2009036.
Повний текст джерелаBrancatelli, Giovanna, Enrico Dalcanale, Roberta Pinalli, and Silvano Geremia. "Probing the Structural Determinants of Amino Acid Recognition: X-Ray Studies of Crystalline Ditopic Host-Guest Complexes of the Positively Charged Amino Acids, Arg, Lys, and His with a Cavitand Molecule." Molecules 23, no. 12 (December 19, 2018): 3368. http://dx.doi.org/10.3390/molecules23123368.
Повний текст джерелаMosca, Simone, Dariush Ajami та Julius Rebek. "Recognition and sequestration of ω-fatty acids by a cavitand receptor". Proceedings of the National Academy of Sciences 112, № 36 (24 серпня 2015): 11181–86. http://dx.doi.org/10.1073/pnas.1515233112.
Повний текст джерелаSumby, Christopher J., Julie Fisher, Timothy J. Prior, and Michaele J. Hardie. "Tris(pyridylmethylamino)cyclotriguaiacylene Cavitands: An Investigation of the Solution and Solid-State Behaviour of Metallo-Supramolecular Cages and Cavitand-Based Coordination Polymers." Chemistry - A European Journal 12, no. 11 (April 3, 2006): 2945–59. http://dx.doi.org/10.1002/chem.200501542.
Повний текст джерелаKiss, László, Zoltán Nagymihály, Péter Szabó, László Kollár, and Sándor Kunsági-Máté. "Anodic Polymerization of Phenylphenols in Methyl Isobutyl Ketone and Mesityl Oxide: Incorporation of a Cavitand into the Layers Formed for Sensing Phenols in Organic Media." Molecules 27, no. 17 (August 23, 2022): 5366. http://dx.doi.org/10.3390/molecules27175366.
Повний текст джерелаSliwa, Wanda, and Jerzy Peszke. "Chemistry of Cavitands." Mini-Reviews in Organic Chemistry 4, no. 2 (May 1, 2007): 125–42. http://dx.doi.org/10.2174/157019307780599306.
Повний текст джерелаRudkevich, Dmitry M., Göran Hilmersson, and Julius Rebek. "Self-Folding Cavitands." Journal of the American Chemical Society 120, no. 47 (December 1998): 12216–25. http://dx.doi.org/10.1021/ja982970g.
Повний текст джерелаRenslo, Adam R., Dmitry M. Rudkevich, and Julius Rebek. "Self-Complementary Cavitands." Journal of the American Chemical Society 121, no. 32 (August 1999): 7459–60. http://dx.doi.org/10.1021/ja991537j.
Повний текст джерелаOgoshi, T., Y. Nakamoto, S. Kanai, S. Fujinami, and T. Yamagishi. "Pillar-Shaped Cavitands." Synfacts 2008, no. 7 (July 2008): 0709. http://dx.doi.org/10.1055/s-2008-1077809.
Повний текст джерелаMann, Enrique, and Julius Rebek. "Deepened chiral cavitands." Tetrahedron 64, no. 36 (September 2008): 8484–87. http://dx.doi.org/10.1016/j.tet.2008.05.136.
Повний текст джерелаSorrell, Thomas N., and Joseph L. Richards. "Selectively Difunctionalized Cavitands." Synlett 1992, no. 02 (1992): 155–56. http://dx.doi.org/10.1055/s-1992-21300.
Повний текст джерелаFar, Adel Rafai, Alexander Shivanyuk, and Julius Rebek. "Water-Stabilized Cavitands." Journal of the American Chemical Society 124, no. 12 (March 2002): 2854–55. http://dx.doi.org/10.1021/ja012453p.
Повний текст джерелаIrwin, Jacob L., David J. Sinclair, Alison J. Edwards, and Michael S. Sherburn. "Chiral Conjoined Cavitands." Australian Journal of Chemistry 57, no. 4 (2004): 339. http://dx.doi.org/10.1071/ch03299.
Повний текст джерелаVerboom, Willem. "ChemInform Abstract: Cavitands." ChemInform 33, no. 16 (May 22, 2010): no. http://dx.doi.org/10.1002/chin.200216260.
Повний текст джерелаKiss, László, Zoltán Nagymihály, László Kollár, and Sándor Kunsági-Máté. "Voltammetric and Fluorimetric Studies of Dibenzoylmethane on Glassy Carbon Electrodes and Its Interaction with Tetrakis (3,5-Dicarboxyphenoxy) Cavitand Derivative." Molecules 28, no. 1 (December 26, 2022): 185. http://dx.doi.org/10.3390/molecules28010185.
Повний текст джерелаPinalli, Roberta, Jakub W. Trzciński, Enrico Dalcanale, and Chiara Massera. "A new, deep quinoxaline-based cavitand receptor for the complexation of benzene." Acta Crystallographica Section E Crystallographic Communications 75, no. 2 (January 4, 2019): 103–8. http://dx.doi.org/10.1107/s2056989018017784.
Повний текст джерелаLin, Jing-Xiang, Yu-Xi Chen, Dan Zhao, Yu Chen, Xiu-Qiang Lu, Jian Lü, and Rong Cao. "Controlled nitrite anion encapsulation and release in the molecular cavity of decamethylcucurbit[5]uril: solution and solid state studies." Inorganic Chemistry Frontiers 6, no. 1 (2019): 303–8. http://dx.doi.org/10.1039/c8qi01168k.
Повний текст джерелаIhm, Chaesang, and Kyungsoo Paek. "Hetero dimer from tetrakisammonium cavitand and tetratopic crown ether cavitand." Tetrahedron Letters 48, no. 18 (April 2007): 3263–66. http://dx.doi.org/10.1016/j.tetlet.2007.03.005.
Повний текст джерелаYu, Yang, Yong-Sheng Li, and Julius Rebek. "Binding of alkyl halides in water-soluble cavitands with urea rims." New Journal of Chemistry 42, no. 12 (2018): 9945–48. http://dx.doi.org/10.1039/c8nj01567h.
Повний текст джерелаNissink, J. Willem M., Harold Boerrigter, Willem Verboom, David N. Reinhoudt, and John H. van der Maas. "An infrared study of host–guest association in solution by substituted resorcinarene cavitands. Part I. Structural aspects of halide complexation by a tetraurea cavitand." Journal of the Chemical Society, Perkin Transactions 2, no. 11 (1998): 2541–46. http://dx.doi.org/10.1039/a802783h.
Повний текст джерелаGavette, Jesse V., Kang-Da Zhang, Dariush Ajami, and Julius Rebek. "Folded alkyl chains in water-soluble capsules and cavitands." Org. Biomol. Chem. 12, no. 34 (2014): 6561–63. http://dx.doi.org/10.1039/c4ob01032a.
Повний текст джерелаLiang, Rongzu, Dongdong Bu, Xiaoshi Su, Xin Wei, Edvinas Orentas, Julius Rebek, and Qixun Shi. "Organic pollutants in water-soluble cavitands and capsules: contortions of molecules in nanospace." Organic Chemistry Frontiers 9, no. 7 (2022): 1890–96. http://dx.doi.org/10.1039/d2qo00139j.
Повний текст джерелаKobayashi, Kenji, and Masamichi Yamanaka. "Self-assembled capsules based on tetrafunctionalized calix[4]resorcinarene cavitands." Chemical Society Reviews 44, no. 2 (2015): 449–66. http://dx.doi.org/10.1039/c4cs00153b.
Повний текст джерелаMurray, James, Kimoon Kim, Tomoki Ogoshi, Wei Yao, and Bruce C. Gibb. "The aqueous supramolecular chemistry of cucurbit[n]urils, pillar[n]arenes and deep-cavity cavitands." Chemical Society Reviews 46, no. 9 (2017): 2479–96. http://dx.doi.org/10.1039/c7cs00095b.
Повний текст джерелаZhang, Kang-Da, Dariush Ajami, Jesse V. Gavette, and Julius Rebek. "Complexation of alkyl groups and ghrelin in a deep, water-soluble cavitand." Chem. Commun. 50, no. 38 (2014): 4895–97. http://dx.doi.org/10.1039/c4cc01643b.
Повний текст джерелаGrajda, M., M. J. Lewińska, and A. Szumna. "The templation effect as a driving force for the self-assembly of hydrogen-bonded peptidic capsules in competitive media." Organic & Biomolecular Chemistry 15, no. 40 (2017): 8513–17. http://dx.doi.org/10.1039/c7ob01925d.
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