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Relevant bibliographies by topics / Cyclodextrins-dyes

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Academic literature on the topic 'Cyclodextrins-dyes'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Cyclodextrins-dyes"

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MOSER, JOERG G. "Porphyrins and phthalocyanines as model compounds for detoxification of tumor chemotherapeutic drugs." Journal of Porphyrins and Phthalocyanines 04, no. 01 (2000): 129–35. http://dx.doi.org/10.1002/(sici)1099-1409(200001/02)4:1<129::aid-jpp212>3.0.co;2-e.

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The fluorescence behavior of porphyrins and phthalocyanines allows one to discriminate between monomeric and associated states of the dyes. These criteria are necessary prerequisites to decide about the inclusion behaviour of the dyes in oligomeric cyclodextrins. Masking the hydrophobic portion of the dyes by cyclodextrins allows one to transport these substances as inert through the body of an animal. The story is depicted here of how to proceed from functionalized porphyrinoids to tumor therapeutic drugs.

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Malanga, Milo, Andras Darcsi, Mihaly Balint, Gabor Benkovics, Tamas Sohajda, and Szabolcs Beni. "New synthetic strategies for xanthene-dye-appended cyclodextrins." Beilstein Journal of Organic Chemistry 12 (March 17, 2016): 537–48. http://dx.doi.org/10.3762/bjoc.12.53.

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Xanthene dyes can be appended to cyclodextrins via an ester or amide bridge in order to switch the fluorescence on or off. This is made possible through the formation of nonfluorescent lactones or lactams as the fluorophore can reversibly cyclize. In this context we report a green approach for the synthesis of switchable xanthene-dye-appended cyclodextrins based on the coupling agent 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM). By using 6-monoamino-β-cyclodextrin and commercially available inexpensive dyes, we prepared rhodamine- and fluorescein-appended cyclode

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V., Jayasree, and N. Bhat S. "Host-guest complexes : spectroscopic and thermodynamic studies of cyclodextrins-dyes." Journal of Indian Chemical Society Vol. 78, October-December 2001 (2001): 533–41. https://doi.org/10.5281/zenodo.5883309.

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Department of Chemistry, North-Eastern Hill University, Shillong-793 022, India <em>Manuscript received 24 October 2000</em> The interactions between hosts <em>α</em>- and β-cyclodextrins and guests phenolphthalein, acridine, 4-(p-<em>N</em>,<em>N</em>-dimethyl-<em>N</em>-amyl)- styrylpyridinium bromide, azurene-A, azurene-B and azurene-C have been studied spectroscopically. Spectroscopic and thermodynamic parameters indicate that the interaction between the cyclodextrins and the above dyes is weak. β-Cyclodextrin forms relatively stronger complexes with the above dyes. In most

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Yoshida, Hiroko, and Mitsuhiko Hida. "Inclusion of azoniabetain dyes by cyclodextrins." Sen'i Gakkaishi 48, no. 7 (1992): 343–49. http://dx.doi.org/10.2115/fiber.48.7_343.

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Segredo-Morales, E., O. Díaz, D. Pérez, and E. González. "Analysis and future trends of cyclodextrins as adsorbents in wastewater treatment." Afinidad. Journal of Chemical Engineering Theoretical and Applied Chemistry 81, no. 604 (2025): 263–78. https://doi.org/10.55815/432096.

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Cyclodextrins, derived from starch, are introduced as promising adsorbents capable of sequestering various pollutants, including heavy metals and dyes, although their solubility in water poses challenges for their removal after use. In this paper a bibliometric analysis is conducted using the Scopus database, yielding 649 relevant documents. Analysis indicates that the use of cyclodextrins in wastewater treatment is still in the early stages of growth and maturity, with most studies focusing on their application as adsorbents for dyes and heavy metals. However, the influence of other wastewate

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Semeraro, Paola, Vito Rizzi, Paola Fini, et al. "Interaction between industrial textile dyes and cyclodextrins." Dyes and Pigments 119 (August 2015): 84–94. http://dx.doi.org/10.1016/j.dyepig.2015.03.012.

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Briant, Liza, and Alexandre Fürstenberg. "Enhancing the Brightness of Red-emitting Fluorophores in Aqueous Solution by Molecular Encapsulation." CHIMIA 79, no. 4 (2025): 259–62. https://doi.org/10.2533/chimia.2025.259.

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Fluorescence spectroscopy and microscopy in biomolecular environments are usually performed in aqueous solution and preferably using red-emitting dyes. However, water quenches their fluorescence. We explore in this contribution how host-guest interactions between red-emitting fluorophores and macrocycles such as cyclodextrins and cucurbiturils can prevent quenching by shielding the dyes from water, thereby enhancing their brightness. We successfully apply this strategy in super-resolution imaging.

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Dehabadi, Vahid Ameri, Hans-Jürgen Buschmann та Jochen Stefan Gutmann. "Spectrophotometric estimation of the accessible inclusion sites of β-cyclodextrin fixed on cotton fabrics using phenolic dyestuffs". Anal. Methods 6, № 10 (2014): 3382–87. http://dx.doi.org/10.1039/c4ay00293h.

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With the known stoichiometry of the complex formation of phenolic dyes with β-cyclodextrin, spectrophotometric study of complexation and decomplexation of these dyestuffs in cavities of cyclodextrins enables us to determine the accessible cyclodextrin sites quantitatively.

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V., Jayasree, and N. Bhat S. "Host-guest complexes : spectroscopic and thermodynamic studies of cyclodextrins-dyes." Journal of Indian Chemical Society Vol. 78, Oct-Dec 2001 (2001): 533–41. https://doi.org/10.5281/zenodo.5910047.

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Department of Chemistry, North-Eastern Hill University, Shillong-793 022, India <em>Manuscript received 24 October 2000</em> The interactions between hosts <em>α</em>- and <em>β</em>-cyclodextrins and guests phenolphthalein, acridine, 4-(<em>p-N,N</em>-dimethyi-<em>N</em>-amyl)- styrylpyridinium bmmide, azurenc-A, azurene-B and azurene-C have been studied spectroscopically. Spectroscopic and thermodynamic parameters indicate that the interaction between the cyclodcxtrins and the above dyes is weak. <em>β</em>-Cyclodextrin forms relatively stronger complexes with the above dyes.

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Shibusawa, Takao, Josuke Okamoto, Kei Abe, Kunihiko Sakata, and Yoshihiko Ito. "Inclusion of azo disperse dyes by cyclodextrins at dyeing temperature." Dyes and Pigments 36, no. 1 (1998): 79–91. http://dx.doi.org/10.1016/s0143-7208(96)00118-0.

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Dissertations / Theses on the topic "Cyclodextrins-dyes"

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Schiller, Robert Lindsay. "Kinetic and equilibrium studies of some dye-cyclodextrin inclusion complexes /." Title page, contents and abstract only, 1986. http://web4.library.adelaide.edu.au/theses/09PH/09phs334.pdf.

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West, Lee Charles. "A study of bibracchial lariat ether complexes and linked cyclodextrin dimer complexes." Title page, contents and abstract only, 2000. http://web4.library.adelaide.edu.au/theses/09PH/09phw5182.pdf.

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Includes errata attached to first leaf. Includes bibliographical references. The complexation of a range of monovalent and divalent metal ions by the bibracchial lariat ethers has been investigated. Also investigates the complexation of metal ions and the anionic azo dye Brilliant Yellow by the diazacrown linked cyclodextrin dimers.

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Park, Jong Seung. "Studies on inclusion complexes of cyclodextrin and dyes I. Synthesis and properties of dye rotaxanes, II. Formation of anisotropic supremolecules /." Available online, Georgia Institute of Technology, 2005, 2005. http://etd.gatech.edu/theses/available/etd-08262005-092849/.

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Thesis (Ph. D.)--Textile and Fiber Engineering, Georgia Institute of Technology, 2006.<br>Srinivasarao, Mohan, Committee Chair ; Bunz, Uwe, Committee Co-Chair ; Griffin, Anselm, Committee Member ; Tolbert, Laren, Committee Member ; Park, Jung, Committee Member ; Beckham, Haskell, Committee Member. Includes bibliographical references.

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Park, Jong Seung. "Studies on Inclusion Complexes of Cyclodextrin and Dyes; I.Synthesis and Properties of Dye Rotaxanes, II. Formation of Anisotropic Supremolecules." Diss., Georgia Institute of Technology, 2005. http://hdl.handle.net/1853/7482.

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Supramolecular chemistry covers intermolecular interactions where non-covalent bonds are involved, and many of them are based on host-guest interactions. Cyclodextrins (CDs) are cyclic oligosaccharides consisting of 6-, 7- or 8-glucose units, which are called alpha-, beta- or gamma-CDs, respectively. They have hydrophobic interior and hydrophilic exterior, and are widely being used as hosts for various organic molecules. The formation of CD inclusion complexes with a variety of dyes has continuously drawn our interests, since CDs are readily available and have ability to include dye molecules

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Liu, Jian. "Encapsulation of fluorescent whitening agents by cyclodextrins and their application." Thesis, University of Kent, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358719.

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Schiller, Robert Lindsay. "Kinetic and equilibrium studies of some dye-cyclodextrin inclusion complexes / Robert Lindsay Schiller." Thesis, 1986. http://hdl.handle.net/2440/20598.

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West, Lee Charles. "A study of bibracchial lariat ether complexes and linked cyclodextrin dimer complexes / by Lee Charles West." Thesis, 2000. http://hdl.handle.net/2440/19852.

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Includes errata attached to first leaf.<br>Includes bibliographical references.<br>vi, 158 leaves : ill. (some col.) ; 30 cm.<br>The complexation of a range of monovalent and divalent metal ions by the bibracchial lariat ethers has been investigated. Also investigates the complexation of metal ions and the anionic azo dye Brilliant Yellow by the diazacrown linked cyclodextrin dimers.<br>Thesis (Ph.D.)--University of Adelaide, Dept. of Chemistry, 2000

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Book chapters on the topic "Cyclodextrins-dyes"

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Shao, Y., B. Martel, M. Morcellet, M. Weltrowski, and G. Crini. "Sorption of Textile Dyes on β-Cyclodextrin-Epichlorhydrin Gels." In Proceedings of the Eighth International Symposium on Cyclodextrins. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-011-5448-2_124.

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Rémi, Edit, Éva Fenyvesi, István Rusznák, and András Víg. "The Action of Lipophilic UV Absorbers — Solubilized by Cyclodextrin — on Photofading of Aqueous Solution of Azoreactive Dyes." In Proceedings of the Eighth International Symposium on Cyclodextrins. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-011-5448-2_123.

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3

Fedorova, Olga, and Yuri Fedorov. "Cyclodextrins as Supramolecular Hosts for Dye Molecules." In Cyclodextrins - Core Concepts and New Frontiers. IntechOpen, 2023. http://dx.doi.org/10.5772/intechopen.107042.

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Cyclodextrins possess a hydrophobic cavity due to which they are suitable for inclusion of various organic dyes. The complex formation between CDs and dyes has been employed to affect the photophysical and photochemical characteristics of organic dyes such as fluorescence enhancement, charge and proton transfer, energy transfer, photochromic transformations and intramolecular excimer/exciplex formation. This fundamental approach has also potential nanotechnological application in creation of optoelectronic devices. Thus, the fluorescent hybrid nanomaterials consisting of supramolecular assembl

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