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Relevant bibliographies by topics / Resorcinareni

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Academic literature on the topic 'Resorcinareni'

Author: Grafiati

Published: 21 February 2023

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Journal articles on the topic "Resorcinareni"

1

Velásquez-Silva, Betty Astrid, Alver Castillo-Aguirre, Zuly Jenny Rivera-Monroy, and Mauricio Maldonado. "Aminomethylated Calix[4]resorcinarenes as Modifying Agents for Glycidyl Methacrylate (GMA) Rigid Copolymers Surface." Polymers 11, no. 7 (2019): 1147. http://dx.doi.org/10.3390/polym11071147.

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Functionalization of tetrapropylcalix[4]resorcinarene, tetrapentylcalix[4]resorcinarene, tetranonylcalix[4]resorcinarene, and tetra-(4-hydroxyphenyl)calix[4]resorcinarene by means of aminomethylation reactions with the amino acids β-alanine and l-proline in the presence of aqueous formaldehyde was carried out. When β-alanine was used, the reaction products were tetrabenzoxazines. The reaction with tetra-(4-hydroxyphenyl)calix[4]resorcinarene did not proceed under the experimental conditions; therefore, l-proline was used, and the corresponding tetra-Mannich base was regio- and diasteroselectiv

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Ziganshina, Albina Y., Elina E. Mansurova, Marina M. Shulaeva, Viktor V. Syakaev, Vyacheslav E. Semenov, and Igor S. Antipin. "Synthesis of 6-Methyluracilpentylviologen Resorcinarene Cavitand." Molbank 2022, no. 4 (2022): M1507. http://dx.doi.org/10.3390/m1507.

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Resorcinarenes, as macrocyclic compounds, are widely used to recognize substrates and create supramolecular assemblies. Their bowl-like form organizes functional groups at the upper and lower rims, which has a substantial impact on the molecular recognition of various substrates. As a result, resorcinarenes make good drug nanocarrier candidates. This paper presents the synthesis of a new resorcinarene cavitand functionalized along the upper rim with methyluracil and viologen fragments for its potential use in drug delivery. Methyluracils and viologens are well-known receptor-targeted compounds

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Dumoulin, 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 (2016): 571–81. http://dx.doi.org/10.1142/s108842461630010x.

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Cavitands and porphyrinoids are two major groups of molecules. If cyclodextrins are maybe the most famous type of cavitands, the properties of resorcinarenes are now well known and rise rapidly increasing attention. This mini-review aims at detailing all the combinations of resorcinarenes with porphyrinoids reported so far, evidencing the bright future of such combos. In addition, two newly synthesized porphyrins-resorcinarene hybrids are reported.

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Castillo-Aguirre and Maldonado. "Preparation of Methacrylate-based Polymers Modified with Chiral Resorcinarenes and Their Evaluation as Sorbents in Norepinephrine Microextraction." Polymers 11, no. 9 (2019): 1428. http://dx.doi.org/10.3390/polym11091428.

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Aminomethylation reactions between chiral amino compounds (S)-(-)-1-phenylethylamine and l-proline with tetranonylresorcinarene and tetra-(4-hydroxyphenyl)resorcinarene in presence of formaldehyde were studied. The reaction between l-proline and resorcinarenes generated regioselectively chiral tetra-Mannich bases, due to the molecular incorporation of the fragment of the chiral amino acid. On the other hand, tetranonylresorcinarene and (S)-(-)-1-phenylethylamine formed regio- and diasteroselectively chiral tetrabenzoxazines, both by chiral auxiliary functionalization and by the transformation

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Reynolds, Michael R., Fraser S. Pick, John J. Hayward, and John F. Trant. "A Concise Synthesis of a Methyl Ester 2-Resorcinarene: A Chair-Conformation Macrocycle." Symmetry 13, no. 4 (2021): 627. http://dx.doi.org/10.3390/sym13040627.

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Anions are important hydrogen bond acceptors in a range of biological, chemical, environmental and medical molecular recognition processes. These interactions have been exploited for the design and synthesis of ditopic resorcinarenes as the hydrogen bond strength can be tuned through the modification of the substituent at the 2-position. However, many potentially useful compounds, especially those incorporating electron-withdrawing functionalities, have not been prepared due to the challenge of their synthesis: their incorporation slows resorcinarene formation that is accessed by electrophilic

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Casas-Hinestroza, José Luis, Miguel Ángel Vela Suazo, and Mauricio Maldonado Villamil. "Experimental Comparative Study of Dynamic Behavior in Solution Phase of C-Tetra(phenyl)resorcin[4]arene and C-Tetra(phenyl)pyrogallol[4]arene." Molecules 25, no. 10 (2020): 2275. http://dx.doi.org/10.3390/molecules25102275.

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The synthesis of phenyl-resorcinarenes and pyrogallolarenes is known to produce a conformational mixture of cone and chair isomers. Depending on the synthesis conditions the composition of the conformational mixture is variable; however, the cone conformer is the greatest proportion of phenyl-resorcin[4]arenes and chair conformer of pyrogallol[4]arenes. The experimental evidence suggests that phenyl-substituted resorcinarene and pyrogallolarene exist as a dynamic boat in solution.

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Beyeh, Ngong, Arto Valkonen, Fanfang Pan, and Kari Rissanen. "Deprotonation of resorcinarenes and novel ammonium salt complexes." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C678. http://dx.doi.org/10.1107/s2053273314093218.

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The bowl shape cavity of resorcinarenes usually stabilized by four intramolecular hydrogen bonds offers an interesting array of binding modes such as C–H...π and cation...π interactions to recognize a variety of guests. The multiple hydroxyl groups can participate in a series of intermolecular hydrogen bonds with guest molecules. This unique cone conformation of resorcinarenes has led to the synthesis of many receptors with convergent arrangement of binding sites suitable for molecular recognition in many applications. Unfunctionalized resorcinarenes are known to easily form molecular complexe

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Jumina, Jumina, Dwi Siswanta, Abdul Karim Zulkarnain, et al. "Development of C-Arylcalix[4]resorcinarenes and C-Arylcalix[4]pyrogallolarenes as Antioxidant and UV-B Protector." Indonesian Journal of Chemistry 19, no. 2 (2019): 273. http://dx.doi.org/10.22146/ijc.26868.

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Indonesia is rich with essential oils such as anise and clove leave oils. In respect to explore the potential utilization of these resources, it has been conducted the transformation of p-hydroxybenzaldehyde and vanillin (4-hydroxy-3-methoxy benzaldehyde) respectively derived from anise oil and clove leaves oil to a series of C-arylcalix[4]resorcinarenes and C-arylcalix[4]pyrogallolarene macrocycles. Treatment of these aldehydes with resorcinol in the presence of HCl in absolute ethanol at reflux for 8 h afforded C-4-hydroxyphenylcalix[4]resorcinarene (3a) and C-4-hydroxy-3-methoxy phenyl-cali

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Neda, Ion, Tjark Siedentop, Alexander Vollbrecht, Holger Thönnessen, Peter G. Jones, and Reinhard Schmutzler. "A New Synthesis of Tetrakis(C-methyl)octakis(hydroxyethyl)calix[4]- resorcinarene via an Ethoxy-Tethered Trimethylsiloxy Precursor." Zeitschrift für Naturforschung B 53, no. 8 (1998): 841–48. http://dx.doi.org/10.1515/znb-1998-0811.

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Abstract The octakis(trimethylsiloxy)calix[4]resorcinarenes, 3 and 4, were synthesized by reaction of 1 and its tetrabromo derivative 2 with hexamethyldisilazane, and were found to exhibit dynamic behaviour in solution. Temperature-dependent NMR investigations confirmed the presence of at least two conformational isomers of 3 in solution. The conformation of 3 in the solid state was determined by an X-ray crystal structure analysis; the calixarene displays a boat conformation. The introduction of the ethoxy group as a spacer into the molecule of 1 was effected via its reaction with ethyl bromo

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Pedro-Hernández, Luis Daniel, and Marcos Martínez-García. "Synthesis of Open-Resorcinarene Dendrimers with L-serine (Ibuprofen) Derivatives." Current Organic Chemistry 26, no. 1 (2022): 71–80. http://dx.doi.org/10.2174/1385272825666211130164548.

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: A new class of dendrimers with open-resorcinarenes has been synthesized in good yields (77-85%). The open-resorcinarenes showed a high capacity for functionalization, having eight hydroxyl groups. The Williamson reaction with N,N-bis(2-azidoethyl)-2-bromo acetamide did not show any steric effect, obtaining sixteen azide terminal groups, which gave us the possibility to obtain a high molecular weight dendrimer via the azide-alkyne click reaction with prop-2-yn-1-yl-(ibuprofen)L-serinate derivatives to obtain the triazole ring spacers and the L-serinate(ibuprofen) derivatives as terminal group

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Dissertations / Theses on the topic "Resorcinareni"

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Vernetti, Samantha Sizemore. "Two New Resorcinarenes: A Pyridine & Acetic Acid Ligand for Metal Coordination and a Deep-Cavity Nitroquinoxaline Resorcinarene." Diss., CLICK HERE for online access, 2006. http://contentdm.lib.byu.edu/ETD/image/etd1279.pdf.

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STEFANELLI, MANUELA. "Novel receptor systems based on porphyrins and related macrocycles." Doctoral thesis, Università degli Studi di Roma "Tor Vergata", 2009. http://hdl.handle.net/2108/934.

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Il lavoro di questa tesi di dottorato riguarda essenzialmente la preparazione di recettori molecolari basati su porfirinoidi e lo studio dei sistemi supramolecolari a cui tali composti possono dar luogo in soluzione. La versatilità di sintesi e di funzionalizzazione delle porfirine, infatti, ha da sempre suscitato un grande interesse che, negli ultimi decenni, è stato rivolto non soltanto allo studio della loro reattività e delle loro proprietà chimiche e fisiche, ma anche alla preparazione e caratterizzazione di composti analoghi. L’intensa attività di ricerca su tali composti ne ha permes

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Hünig, Hagen. "Darstellung und Charakterisierung neuartiger C-Arylcalix(4)resorcinarene." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2001. http://nbn-resolving.de/urn:nbn:de:swb:14-994682363390-44859.

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In der vorliegenden Arbeit wird die Darstellung und Charakterisierung von aromatisch substituierten Calix(4)resorcinarenen behandelt. Im zweiten Kapitel werden die Grundlagen und Besonderheiten bei Calix(4)resorcinarenen angesprochen. Ein Überblick über die wichtigsten Verbindungen dieser Gruppe von Makrocyclen wird gegeben. Im Kapitel 3 werden wesentliche Methoden zur vollständigen O-Alkylierung bei Calix(4)resorcinaren genannt. Außerdem werden Methoden zur partiellen O-Alkylierung von C-Arylcalix(4)resorcinarenen vorgestellt. Das Kapitel 4 stellt die Methoden zur Strukturaufklärung mittels 2

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Hünig, Hagen. "Darstellung und Charakterisierung neuartiger C-Arylcalix(4)resorcinarene." Doctoral thesis, Technische Universität Dresden, 2000. https://tud.qucosa.de/id/qucosa%3A24757.

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In der vorliegenden Arbeit wird die Darstellung und Charakterisierung von aromatisch substituierten Calix(4)resorcinarenen behandelt. Im zweiten Kapitel werden die Grundlagen und Besonderheiten bei Calix(4)resorcinarenen angesprochen. Ein Überblick über die wichtigsten Verbindungen dieser Gruppe von Makrocyclen wird gegeben. Im Kapitel 3 werden wesentliche Methoden zur vollständigen O-Alkylierung bei Calix(4)resorcinaren genannt. Außerdem werden Methoden zur partiellen O-Alkylierung von C-Arylcalix(4)resorcinarenen vorgestellt. Das Kapitel 4 stellt die Methoden zur Strukturaufklärung mittels 2

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Hong, Wei. "The chemistry of propargyl calix(4)resorcinarene." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ32484.pdf.

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Hünig, Hagen. "Darstellung und Charakterisierung neuartiger C-Arylcalix[4]resorcinarene." [S.l. : s.n.], 2001. http://www.bsz-bw.de/cgi-bin/xvms.cgi?SWB9275691.

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Pettersen, Jade Kristin. "Preparation and properties of self-assembled resorcinarene monolayers." Thesis, Curtin University, 2010. http://hdl.handle.net/20.500.11937/933.

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Several resorcinarene and calixarene based receptors were synthesised with the overarching aim of developing selective hydrocarbon sensors for application in the petroleum exploration industry.Thioacetyl resorcinarenes functionalised at the upper rim with methoxy, propoxy and benzyloxy groups were synthesised, along with a methylene bridged cavitand. Similar hydroxy and methoxy resorcinarenes functionalised at the lower rim with decylsulfide groups were prepared, along with a p-tert-butylcalix[4]arene thiol derivative.The receptors were allowed to self-assemble on gold substrates, and the resu

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Kleinhans, Dewald Johannes. "Studies in the selective synthesis of bidentate resorcinarene ligands." Thesis, Stellenbosch : University of Stellenbosch, 2010. http://hdl.handle.net/10019.1/4194.

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Thesis (MSc (Chemistry and Polymer Science))--University of Stellenbosch, 2010.<br>ENGLISH ABSTRACT: Resorcinarenes are macrocyclic products formed from the condensation of aldehydes (aliphatic or aromatic) and resorcinol and have been used in a wide range of applications since their first synthesis. Applications include: HPLC stationary phases for the separation of pyrimidine bases, racemic drugs and isomers, the selective extractions of lanthanides and actinides, as molecular receptors, catalysis, NMR chiral shift agents, GC separations and as starting materials for the synthesis of macr

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Boxhall, Jonathan Yates. "Synthetic routes towards chiral calix[4]resorcinarenes." Thesis, Loughborough University, 2003. https://dspace.lboro.ac.uk/2134/33906.

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This thesis is divided into three chapters. Chapter 1 contains a brief overview of the literature reports in the area of calix[4]resorcinarene chemistry. The many methods available for the preparation and use of these macrocycles, their functionalisation on both the upper and lower rims and the use of Mannich reaction protocols for the introduction of chirality into these symmetrical molecules are discussed. Chapter 2 describes new methodology for the formation of a range of chiral calix[4]resorcinarenes, most notably the formation of tetra alkyloxy calix[4]resorcinarenes as racemic mixtures,

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Chan, Yohan. "Some aspects of the chemistry of resorcinarenes." Thesis, Loughborough University, 2006. https://dspace.lboro.ac.uk/2134/34718.

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This thesis has been divided in three sections. The first chapter contains a review of resorcinarene chemistry. The second chapter contains the results and the discussion and the experimental details are provided in the third chapter. The first part of chapter two contains the results and discussion related to the synthesis of benzoxazines derived from resorcin[6]arene and resorcin[4]arene and the diastereoselectivity observed in the syntheses. The second part of chapter two describes the synthesis of inherently chiral resorcinarenes using non-chiral 3-alkyloxyphenols, the synthesis of benzoxa

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Books on the topic "Resorcinareni"

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Calixarenes and Resorcinarenes: Synthesis, Properties and Applications. Wiley & Sons, Limited, John, 2009.

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Book chapters on the topic "Resorcinareni"

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Wierzbicki, Michał, Hanna Jędrzejewska, and Agnieszka Szumna. "Chiral Calixarenes and Resorcinarenes." In Calixarenes and Beyond. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31867-7_2.

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Tulli, Ludovico, and Patrick Shahgaldian. "Calixarenes and Resorcinarenes at Interfaces." In Calixarenes and Beyond. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31867-7_37.

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Schneider, H. J., and U. Schneider. "The Host-Guest Chemistry of Resorcinarenes [1]." In Calixarenes 50th Anniversary: Commemorative Issue. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0267-4_5.

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Botta, Maurizio, Maria Cristina De Rosa, Federico Corelli, Antonello Santini, and Andrea Tafi. "New C-Alkylcalix[4]Resorcinarenes: A Computational Study." In Fifth International Conference on the Spectroscopy of Biological Molecules. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1934-4_2.

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Arduini, A., A. Casnati, E. Dalcanale, A. Pochini, F. Ugozzoli, and R. Ungaro. "Calixarenes and Resorcinarenes in Molecular Recognition and Supramolecular Devices." In Supramolecular Science: Where It Is and Where It Is Going. Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4554-1_5.

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Nicod, L., E. Gaubert, H. Barnier, and M. Lemaire. "Synthesis of Water Soluble Resorcinarenes Application in Nanofiltration-Complexation." In Molecular Recognition and Inclusion. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4_76.

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Botta, M., M. Coppetti, P. Ricciardi, F. Corelli, and A. Tafi. "Artificial receptors: molecular modelling studies of calix[4]resorcinarene-capped porphyrins." In Spectroscopy of Biological Molecules: New Directions. Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4479-7_81.

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Tan, Daniel A., and Mauro Mocerino. "Calix[4]arenes and Resorcinarenes Bridged at the Wider Rim." In Calixarenes and Beyond. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31867-7_10.

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Brzózka, Zbigniew, Ewa Liszewska, Marek Pietraszkiewicz, and Rafał Gąsiorowski. "Calix[4]Resorcinarene Derivatives as Ionophores for Cations Studied in Polymeric (PVC) Membrane." In Molecular Recognition and Inclusion. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4_36.

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Beyeh, Ngong Kodiah, and Kari Rissanen. "N-Alkyl Ammonium Resorcinarene Salts: A Versatile Family of Calixarene-Related Host Molecules." In Calixarenes and Beyond. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31867-7_11.

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Conference papers on the topic "Resorcinareni"

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Kvasnica, Miroslav, and Byron W. Purse. "Synthesis of new resorcinarene-based molecular clips." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201391418945.

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Oh, Tae-Hwan, Ramakrishnan Ganesan, Je-Moon Yoon, and Jin-Baek Kim. "Negative nanomolecular resists based on Calix[4]resorcinarene." In SPIE 31st International Symposium on Advanced Lithography, edited by Qinghuang Lin. SPIE, 2006. http://dx.doi.org/10.1117/12.660111.

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Okuyama, Kenichi. "Molecular resists based on calix[4]resorcinarene derivatives for EB lithography." In SPIE Advanced Lithography, edited by Clifford L. Henderson. SPIE, 2009. http://dx.doi.org/10.1117/12.813632.

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Ariyanti, Dita, Jumina, Dyah Iswantini, Purwantiningsih, Novik Nurhidayat, and Hefni Effendi. "The synthesized sunscreen compounds: C-heptylcalix[4]resorcinarene octabenzoate and octasinnamate." In 3RD INTERNATIONAL CONFERENCE ON CHEMISTRY, CHEMICAL PROCESS AND ENGINEERING (IC3PE). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0062413.

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Handayani, Santi Nur, Heny Ekowati, Irmanto, Della Nadya Ayu Aprilia, and Silva Utami. "Synthesis of phenylcalix[4]resorcinarena sulfonate and it’s aplication as an antioxidant." In THE 14TH JOINT CONFERENCE ON CHEMISTRY 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0006139.

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Şen, Sibel, Rifat Çapan, and Gülen Türker. "Thin film properties and the detection volatile organic compounds of C-methylcalix(4)resorcinarene." In SolarPACES 2017: International Conference on Concentrating Solar Power and Chemical Energy Systems. Author(s), 2018. http://dx.doi.org/10.1063/1.5078881.

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Handayani, Santi Nur, Irmanto, and Tamimah Sufi Widianti. "Study of the adsorption kinetics of Rhodamine B onto C-2-hydroxyphenylcalix[4]resorcinarene." In VIII INTERNATIONAL ANNUAL CONFERENCE “INDUSTRIAL TECHNOLOGIES AND ENGINEERING” (ICITE 2021). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0103723.

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Busroni, Busroni, Ari Tri Wanodyo Handayani, Eka Deddy Irawan, and Chairil Anwar. "Synthesis and characterization of novel basketing of C-4-phenylocta-phenylhydrazide-calix[4]resorcinarene-PdNPs." In VIII INTERNATIONAL ANNUAL CONFERENCE “INDUSTRIAL TECHNOLOGIES AND ENGINEERING” (ICITE 2021). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0111699.

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Etika, Sri Benti, Edi Nasra, Abdul Hafids, and T. K. Sari. "Utilization of C-Cinnamal Calix[4] Resorcinarene as Adsorbent for Rhodamin B and Methanil Yellow." In International Conference on Biology, Sciences and Education (ICoBioSE 2019). Atlantis Press, 2020. http://dx.doi.org/10.2991/absr.k.200807.047.

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Paviet-Hartmann, Patricia, Jared Horkley, Joshua Pak, Eric Brown, and Terry Todd. "Resorcinarenes and Aza-crowns as New Extractants for the Separation of Technetium-99." In 2008 MRS Fall Meetin. Materials Research Society, 2008. http://dx.doi.org/10.1557/proc-1124-q10-04.

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