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Journal articles on the topic 'Ditope receptors'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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1

Rahimizadeh, Mohammad, E. Rezaei Seresht, Mehdi Bakavoli, and Mehdi Pordel. "Glycoluril-derived crown clips as new ditopic receptors." Canadian Journal of Chemistry 85, no. 11 (November 1, 2007): 964–68. http://dx.doi.org/10.1139/v07-115.

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Several new ditopic receptors have been synthesized from 4,4′-bis(methoxyphenyl)glycoluril (1). The first receptor site is a cleft composed of two fused 2-imidazolone rings, which are flanked by two aromatic side walls, and the second site is a crown ether moiety.Key words: receptors, crown compounds, glycoluril, molecular clips.

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2

Kirkovits, Gregory J., James A. Shriver, Philip A. Gale, and Jonathan L. Sessler. "ChemInform Abstract: Synthetic Ditopic Receptors." ChemInform 33, no. 37 (May 20, 2010): no. http://dx.doi.org/10.1002/chin.200237275.

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3

SUTHERLAND, I. O. "ChemInform Abstract: Synthetic Ditopic Receptors." ChemInform 24, no. 1 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199301298.

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4

Lacy, Stephen M., Dmitry M. Rudkevich, Willem Verboom, and David N. Reinhoudt. "Neutral ditopic receptors for adenosine monophosphate." Tetrahedron Letters 35, no. 32 (August 1994): 5953–56. http://dx.doi.org/10.1016/s0040-4039(00)78228-1.

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5

Ilioudis, Christos A., and Jonathan W. Steed. "Polyaza metacyclophanes as ditopic anion receptors." Organic & Biomolecular Chemistry 3, no. 16 (2005): 2935. http://dx.doi.org/10.1039/b506828b.

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6

Schmuck, Carsten, Daniel Rupprecht, Matthias Junkers, and Thomas Schrader. "Artificial Ditopic Arg-Gly-Asp (RGD) Receptors." Chemistry - A European Journal 13, no. 24 (August 17, 2007): 6864–73. http://dx.doi.org/10.1002/chem.200601821.

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7

Bartsch, Richard A., Lyle W. Spruce, David W. Purkiss, Mi-Ja Goo, and Bronislaw P. Czech. "New ditopic receptors for alkylammonium ion complexation." Journal of Inclusion Phenomena and Molecular Recognition in Chemistry 15, no. 2 (1993): 181–93. http://dx.doi.org/10.1007/bf00710227.

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8

Fedorova, O. A., Y. V. Fedorov, E. N. Andrjukhina, S. P. Gromov, and M. V. Alfimov. "Cation-dependent photochromic properties of novel ditopic receptors." Pure and Applied Chemistry 75, no. 8 (January 1, 2003): 1077–84. http://dx.doi.org/10.1351/pac200375081077.

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Novel crown-containing 2-styrylbenzothiazoles were prepared to obtain optical ditopic receptors that can bind alkaline-earth metal cations by a crown ether fragment and could serve as host for the heavy metal cations and proton owing to the presence of the heterocyclic part. Photochemical transformations of the ditopic receptors depend on the type of metal cations present in solution. They include trans–cis-isomerization, [2+2]-cycloaddition, and electrocyclic reaction.

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9

Francesconi, Oscar, Cristina Nativi, Gabriele Gabrielli, Matteo Gentili, Marco Palchetti, Beatrice Bonora, and Stefano Roelens. "Pyrrolic Tripodal Receptors for the Molecular Recognition of Carbohydrates: Ditopic Receptors for Dimannosides." Chemistry - A European Journal 19, no. 35 (July 9, 2013): 11742–52. http://dx.doi.org/10.1002/chem.201204298.

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10

Bourguignon, Jean, Ulf Bremberg, Georges Dupas, Kristina Hallman, Lars Hagberg, Laurent Hortala, Vincent Levacher, et al. "Chiral ditopic receptors. Application to palladium-catalyzed allylic alkylation." Tetrahedron 59, no. 48 (November 2003): 9583–89. http://dx.doi.org/10.1016/j.tet.2003.10.005.

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11

Marsh, Andrew, Nathaniel W. Alcock, William Errington, and Rajeeve Sagar. "Synthesis and characterisation of new ditopic receptors for guanosine." Tetrahedron 59, no. 29 (July 2003): 5595–601. http://dx.doi.org/10.1016/s0040-4020(03)00708-7.

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12

Stephan, Holger, Karsten Gloe, Petra Schiessl, and Franz P. Schmidtchen. "Lipophilic ditopic guanidinium receptors: selective extractants for tetrahedral oxoanions." Supramolecular Chemistry 5, no. 4 (September 1995): 273–80. http://dx.doi.org/10.1080/10610279508233954.

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13

Dey, Swapan, Dibyendu Sain, Ashish Kumar, and Chanda Kumari. "A series of ditopic receptors for succinic acid binding." RSC Adv. 4, no. 93 (2014): 51486–95. http://dx.doi.org/10.1039/c4ra07537d.

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Three ditopic-abiotic receptors (R1, R2 and R3) have been designed and synthesised. The receptors have been applied for the recognition of dicarboxylic acids viz. malonic, succinic, glutaric and adipic acids. Among them, succinic acid shows the highest binding efficiency to all receptors. Recognition of succinic acid is very important due to its various adverse effects on human health upon prolonged exposure.

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14

Jagleniec, Damian, Krzysztof Ziach, Kajetan Dąbrowa, and Jan Romański. "The Effect of Substitution Pattern on Binding Ability in Regioisomeric Ion Pair Receptors Based on an Aminobenzoic Platform." Molecules 24, no. 16 (August 18, 2019): 2990. http://dx.doi.org/10.3390/molecules24162990.

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A series of ditopic ion pair receptors equipped with 4-nitrophenylurea and 1-aza-18-crown-6-ether linked by ortho-(1), meta-(2), and para-(3) substituted benzoic acid were readily synthesized in three steps from commercially available materials. The binding properties of these regioisomeric receptors were determined using UV-vis and 1H NMR spectroscopy in MeCN and in the solid state by single-crystal X-ray diffraction crystallography. The solution studies revealed that, apart from carboxylates, all the anions tested formed stronger complexes in the presence of sodium cations. Receptors 2 and 3 were found to interact with ion pairs with remarkably higher affinity than ortho-substituted 1. 1H NMR titration experiments showed that both urea NH protons interacted with anions with comparable strength in the case of receptors 2 and 3, but only one of the NHs was effective in anion binding in the case of receptor 1. X-ray analysis of the crystal structure of receptor 1 and 1·NaPF6 complex showed that binding was hampered due to the formation of an intramolecular hydrogen bond. Analysis of the crystal structures of 2·NaBr and 3·NaBr complexes revealed that proper mutual orientation of binding domains was responsible for the improved binding of the sodium salts.

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15

Abdi Bellau, Mohamed, Olga Bortolini, Giancarlo Fantin, Marco Fogagnolo, Daniele Ragno, Ignacio Delso, and Pedro Merino. "Native Quercetin as a Chloride Receptor in an Organic Solvent." Molecules 23, no. 12 (December 19, 2018): 3366. http://dx.doi.org/10.3390/molecules23123366.

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The binding properties of quercetin toward chloride anions were investigated by means of 1H-NMR, 13C-NMR, and electrospray ionization mass spectrometry (ESI-MS) measurements, as well as computational calculations. The results indicate that quercetin behaves primarily as a ditopic receptor with the binding site of the B ring that exhibits stronger chloride affinity compared to the A ring. However, these sites are stronger receptors than those of catechol and resorcinol because of their conjugation with the carbonyl group located on the C ring. The 1:1 and 1:2 complexation of this flavonoid with Cl− was also supported by ESI mass spectrometry.

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16

Kryatova, Olga P., Alexander G. Kolchinski, and Elena V. Rybak-Akimova. "Metal-containing ditopic receptors for molecular recognition of diammonium cations." Tetrahedron 59, no. 2 (January 2003): 231–39. http://dx.doi.org/10.1016/s0040-4020(02)01482-5.

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17

Costero, Ana M., Gemma M. Rodríguez-Muñiz, Salvador Gil, Sergio Peransi, and Pablo Gaviña. "Solid–liquid extraction of ω-amino acids using ditopic receptors." Tetrahedron 64, no. 1 (January 2008): 110–16. http://dx.doi.org/10.1016/j.tet.2007.10.066.

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18

Cafeo, Grazia, Andrzej Kaledkowski, Franz H. Kohnke, and Angela Messina. "Strapped Calix[]furan[]pyrroles, Novel Examples of Ditopic Molecular Receptors." Supramolecular Chemistry 18, no. 3 (May 1, 2006): 273–79. http://dx.doi.org/10.1080/10610270500484811.

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19

Six, Natacha, Stéphane Menuel, Hervé Bricout, Frédéric Hapiot, and Eric Monflier. "Ditopic Cyclodextrin-Based Receptors: New Perspectives in Aqueous Organometallic Catalysis." Advanced Synthesis & Catalysis 352, no. 9 (June 8, 2010): 1467–75. http://dx.doi.org/10.1002/adsc.201000027.

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20

Goswami, Shyamaprosad, Rinku Chakrabarty, Swapan Dey, and Hoong-Kun Fun. "Steric inhibition of hydrogen bonding in molecular recognition of dicarboxylic acids: di-topic receptors containing a nitro group designed to behave like monotopic receptors." RSC Adv. 4, no. 91 (2014): 49663–71. http://dx.doi.org/10.1039/c4ra06994c.

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21

Carreira-Barral, Israel, Marta Mato-Iglesias, Andrés de Blas, Carlos Platas-Iglesias, Peter A. Tasker, and David Esteban-Gómez. "Ditopic receptors containing urea groups for solvent extraction of Cu(ii) salts." Dalton Transactions 46, no. 10 (2017): 3192–206. http://dx.doi.org/10.1039/c7dt00093f.

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22

La Monica, Laura, and Donato Monti. "Flexible dizinc diporphyrin systems as selective receptors for ditopic amine ligands." Journal of Porphyrins and Phthalocyanines 06, no. 01 (January 2002): 58–65. http://dx.doi.org/10.1142/s1088424602000099.

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Zinc (II) diporphyrin systems, characterised by the presence of flexible oligooxaethylene spacers of different lengths, have been synthesised and the binding properties toward a series of aliphatic and aromatic diamine derivatives characterised by different structural and coordination properties, investigated. The results obtained, compared to that for a rigid diporphyrin cleft, point out that the observed degree of selectivity is dependent both on the length of the spacer and on the nature of the nitrogen ligands.

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23

Stetson, Christopher M., Shiro Nishikawa, David W. Purkiss, N. Kent Dalley, and Richard A. Bartsch. "Synthesis and evaluation of new ditopic cyclophane receptors for benzoic acid." Journal of Physical Organic Chemistry 18, no. 11 (November 2005): 1107–15. http://dx.doi.org/10.1002/poc.981.

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24

Isabel Burguete, M., Santiago V. Luis, Juan F. Miravet, Lorena Payá, Manuel Querol, Enrique García-España, and Conxa Soriano. "An efficient preparation of ditopic receptors based on polyaza[n]paracyclophanes." Chemical Communications, no. 17 (1998): 1823–24. http://dx.doi.org/10.1039/a803790f.

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25

Załubiniak, Dominika, Maciej Zakrzewski, and Piotr Piątek. "Highly effective ion-pair receptors based on 2,2-bis(aminomethyl)-propionic acid." Dalton Transactions 45, no. 39 (2016): 15557–64. http://dx.doi.org/10.1039/c6dt02833k.

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Working in concert cation and anion binding domains of ditopic receptors based on 2,2-bis-(aminomethyl)-propionic acid allow for highly effective complexation of sodium salts of chloride, bromide and nitrate.

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26

Kim, Dong-Wan, Jung-Hwan Kim, Jae-Young Hwang, Myong-Yong Choi, and Jae-Sang Kim. "Beryllium(II) Recognition by Allosteric Effects in 1,2-Ethylenedioxybenzene Based Ditopic Receptors." Bulletin of the Korean Chemical Society 32, no. 8 (August 20, 2011): 2643–47. http://dx.doi.org/10.5012/bkcs.2011.32.8.2643.

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27

Cametti, Massimo, Maija Nissinen, Antonella Dalla Cort, Luigi Mandolini, and Kari Rissanen. "Uranyl-salophen based ditopic receptors for the recognition of quaternary ammonium halides." Chemical Communications, no. 19 (2003): 2420. http://dx.doi.org/10.1039/b307849c.

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28

Yamato, Takehiko, Shofiur Rahman, Zeng Xi, Fumika Kitajima, and Jeong Tae Gil. "Ditopic receptors of hexaamide derivatives derived from hexahomotrioxacalix[3]arene triacetic acid." Canadian Journal of Chemistry 84, no. 1 (January 1, 2006): 58–64. http://dx.doi.org/10.1139/v05-260.

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The lower rim functionalized hexahomotrioxacalix[3]arene hexaamide 7 having an amino acid moiety with cone conformation was synthesized from triol 1 by a stepwise reaction. The different extractability for alkali metal ions, transition metal ions, and alkylammonium ions from water into dichloromethane was discussed. Owing to the strong intramolecular hydrogen bond between the neighboring NH and CO groups in hexaamide 7, its affinity to metal cations was weakened. Hexaamide 7 shows a single selectivity to n-BuNH3+. The anion complexation of hexaamide 7 was also studied by 1H NMR titration experiments. Hexaamide 7 binds halides through the intermolecular hydrogen bond among the NH hydrogens of the amide in a 1:1 fashion in CDCl3. Thus, hexaamide 7 serves as a heteroditopic receptor that can complex with halides (Cl, Br) and n-BuNH3+ at the same time. The association constants calculated from the chemical shift changes of the amide protons are Ka = 536 ± 32 (mol/L)1 for Cl and Ka = 230 ± 17 (mol/L)1 for Br.Key words: hexahomotrioxacalix[3]arenes, ionophores, molecular recognition, ammonium ion, ditopic receptor.

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29

Arens, Verena, Christina Dietz, Dieter Schollmeyer, and Klaus Jurkschat. "Intramolecularly Coordinated Bis(crown ether)-Substituted Organotin Halides as Ditopic Salt Receptors." Organometallics 32, no. 9 (April 23, 2013): 2775–86. http://dx.doi.org/10.1021/om400216z.

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30

Domarco, Olaya, Iago Neira, Tamara Rama, Arturo Blanco-Gómez, Marcos D. García, Carlos Peinador, and José M. Quintela. "Synthesis of non-symmetric viologen-containing ditopic ligands and their Pd(ii)/Pt(ii)-directed self-assembly." Organic & Biomolecular Chemistry 15, no. 17 (2017): 3594–602. http://dx.doi.org/10.1039/c7ob00161d.

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31

Tagne Kuate, Alain C., Ljuba Iovkova, Wolf Hiller, Markus Schürmann, and Klaus Jurkschat. "Organotin-Substituted [13]-Crown-4 Ethers: Ditopic Receptors for Lithium and Cesium Halides†." Organometallics 29, no. 21 (November 8, 2010): 5456–71. http://dx.doi.org/10.1021/om100409v.

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32

Wong, Wallace W. H., David Curiel, Andrew R. Cowley, and Paul D. Beer. "Dinuclear zinc(ii) dithiocarbamate macrocycles: ditopic receptors for a variety of guest molecules." Dalton Transactions, no. 2 (2005): 359. http://dx.doi.org/10.1039/b415935g.

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33

BURGUETE, M. I., E. GARCIA-ESPANA, S. V. LUIS, J. F. MIRAVET, L. PAYA, M. QUEROL, and C. SORIANO. "ChemInform Abstract: A Efficient Preparation of Ditopic Receptors Based on Polyaza[n]paracyclophanes." ChemInform 29, no. 50 (June 18, 2010): no. http://dx.doi.org/10.1002/chin.199850188.

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34

Bhaskar 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.

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The host–guest interaction between flexible ditopic receptors and bisammonium ion has been investigated experimentally and computationally. The conformation folding of guest bisammonium ion molecules leads to the oscillation of the host–guest interaction.

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35

Mäkelä, T., and K. Rissanen. "Ion pair complexes and anion binding in the solution of a ditopic receptor." Dalton Transactions 45, no. 15 (2016): 6481–90. http://dx.doi.org/10.1039/c6dt00414h.

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36

Sun, Nana, Xin Xiao, Chenxi Liu, Chao Chen, and Jianzhuang Jiang. "An unprecedented porphyrin-pillar[5]arene hybrid ditopic receptor." RSC Advances 5, no. 54 (2015): 43218–24. http://dx.doi.org/10.1039/c5ra05913e.

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A porphyrin-pillar[5]arene hybrid host compound with a ditopic receptor nature was synthesized for the first time, which combines a neutral 1,4-bis(imidazol-1-yl)butane guest by means of its two active centers to form a stable supramolecular complex.

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37

Mäkelä, Toni, Miia-Elina Minkkinen, and Kari Rissanen. "Ion Pair Binding in the Solid-State with Ditopic Crown Ether Uranyl Salophen Receptors." Inorganic Chemistry 55, no. 3 (January 20, 2016): 1339–46. http://dx.doi.org/10.1021/acs.inorgchem.5b02780.

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38

Francesconi, Oscar, Matteo Gentili, Francesco Bartoli, Andrea Bencini, Luca Conti, Claudia Giorgi, and Stefano Roelens. "Phosphate binding by a novel Zn(ii) complex featuring a trans-1,2-diaminocyclohexane ligand. Effective anion recognition in water." Organic & Biomolecular Chemistry 13, no. 6 (2015): 1860–68. http://dx.doi.org/10.1039/c4ob02321h.

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Excellent affinities and selectivities toward triphosphates are achieved through an adaptive ditopic receptor featuring a metal ion and a macrocyclic polyammonium cation binding sites, concertedly bridging phosphate anions.

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39

Ajamaa, Fettah, Anne-Marie Albrecht-Gary, Juan Luis Delgado de la Cruz, Mourad Elhabiri, Jean-François Nierengarten, Nathalie Solladié, Ali Trabolsi, and Maxence Urbani. "A macrocyclic supramolecular complex obtained from a fullerene ligand bearing two pyridine substituents and a bis-Zn(II)-porphyrin receptor." Journal of Porphyrins and Phthalocyanines 10, no. 12 (December 2006): 1337–45. http://dx.doi.org/10.1142/s1088424606000715.

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A fullerene derivative bearing two pyridine subunits has been designed to allow assembly with a bis- Zn (II)-phorphyrin receptor with two equivalent Zn binding sites separated by about 20 Å. Owing to the complementarity between the bis- Zn (II)-porphyrin receptor and a fullerene ligand bearing two pyridine substituents, the substrate can be clicked on the ditopic receptor, thus leading to a stable non-covalent macrocyclic 1:1 complex.

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40

Yen, Yao-Pin, Chia-Lan Chen, Tung-Ming Fu, Chen-Yu Wu, and Chi-Yung Lin. "A Colorimetric Ditopic Receptor Modulated by Fluoride Anion and Sodium Cation Binding." Australian Journal of Chemistry 59, no. 11 (2006): 805. http://dx.doi.org/10.1071/ch06265.

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A new colorimetric ditopic receptor (1) was synthesized and characterized. Upon investigation of a series of anions, the appearance of the solution of receptor 1 with F– showed a colour change from light-yellowish to orange-red which can be detected by the naked eye. Upon subsequent addition of Na+ or Li+ to the solution, the orange-red colour was no longer observable. The remarkable colour switching (ON and OFF) is thus controlled by the anion and cation recognition.

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41

Graf, E. "Synthesis of macrocyclic ditopic receptors designed for simultaneous binding of alkaline and transition metal cations." Tetrahedron Letters 35, no. 41 (October 10, 1994): 7779–82. http://dx.doi.org/10.1016/s0040-4039(00)77370-9.

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42

Chawla, Har Mohindra, Satya Narayan Sahu, Rahul Shrivastava, and Satish Kumar. "Calix[4]arene-based ditopic receptors for simultaneous recognition of fluoride and cobalt(II) ions." Tetrahedron Letters 53, no. 17 (April 2012): 2244–47. http://dx.doi.org/10.1016/j.tetlet.2012.02.083.

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43

Furuta, Hiroyuki, Darren Magda, and Jonathan L. Sessler. "Molecular recognition via base pairing: amine-containing, cytosine-based ditopic receptors that complex guanosine monophosphate." Journal of the American Chemical Society 113, no. 3 (January 1991): 978–85. http://dx.doi.org/10.1021/ja00003a035.

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44

Kang, Kang, Jessica A. Lohrman, Sangaraiah Nagarajan, Lixi Chen, Pengchi Deng, Xin Shen, Kuirong Fu, Wen Feng, Darren W. Johnson, and Lihua Yuan. "Convergent Ditopic Receptors Enhance Anion Binding upon Alkali Metal Complexation for Catalyzing the Ritter Reaction." Organic Letters 21, no. 3 (January 14, 2019): 652–55. http://dx.doi.org/10.1021/acs.orglett.8b03778.

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45

Wong, Wallace W. H., David Curiel, Siu-Wai Lai, Michael G. B. Drew, and Paul D. Beer. "Ditopic redox-active polyferrocenyl zinc(ii) dithiocarbamate macrocyclic receptors: synthesis, coordination and electrochemical recognition properties." Dalton Transactions, no. 4 (2005): 774. http://dx.doi.org/10.1039/b416851h.

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46

Berry, Stuart N., Lei Qin, William Lewis, and Katrina A. Jolliffe. "Conformationally adaptable macrocyclic receptors for ditopic anions: analysis of chelate cooperativity in aqueous containing media." Chemical Science 11, no. 27 (2020): 7015–22. http://dx.doi.org/10.1039/d0sc02533j.

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47

Graf, Ernest, Mir Wais Hosseini, and Romain Ruppert. "Synthesis of macrocyclic ditopic receptors designed for simulataneous binding of alkaline and transition metal cations." Tetrahedron Letters 35, no. 42 (October 1994): 7779–82. http://dx.doi.org/10.1016/0040-4039(94)80116-9.

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48

Berdnikova, Daria V., Yuri V. Fedorov, and Olga A. Fedorova. "Azadithiacrown ether based ditopic receptors capable of simultaneous multi-ionic recognition of Ag+ and Hg2+." Dyes and Pigments 96, no. 1 (January 2013): 287–95. http://dx.doi.org/10.1016/j.dyepig.2012.08.017.

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49

Ziach, K., M. Karbarz, and J. Romański. "Cooperative binding and extraction of sodium nitrite by a ditopic receptor incorporated into a polymeric resin." Dalton Transactions 45, no. 29 (2016): 11639–43. http://dx.doi.org/10.1039/c6dt02235a.

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50

Moghimi, A., B. Maddah, A. Yari, M. Shamsipur, M. Boostani, M. Fall Rastegar, and A. R. Ghaderi. "Molecular recognition of amino acids with some fluorescent ditopic pyrylium- and pyridinium-based crown ether receptors." Journal of Molecular Structure 752, no. 1-3 (October 2005): 68–77. http://dx.doi.org/10.1016/j.molstruc.2005.05.043.

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