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Journal articles on the topic 'Cyclodextrins-dyes'

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1

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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2

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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3

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>&alpha;</em>- and &beta;-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. &beta;-Cyclodextrin forms relatively stronger complexes with the above dyes. In most
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4

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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5

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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6

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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7

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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8

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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9

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>&alpha;</em>- and <em>&beta;</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>&beta;</em>-Cyclodextrin forms relatively stronger complexes with the above dyes.
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10

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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11

Suzuki, Miyoko, Hidenobu Ohmori, Marton Kajtar, J�zsef Szejtli, and Maria Vikmon. "The association of inclusion complexes of cyclodextrins with azo dyes." Journal of Inclusion Phenomena and Molecular Recognition in Chemistry 18, no. 3 (1994): 255–64. http://dx.doi.org/10.1007/bf00708732.

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12

Ivanova, Bojidarka, Rositca Nikolova, Marc Lamshöft, et al. "Surface interaction and self-assembly of cyclodextrins with organic dyes." Journal of Inclusion Phenomena and Macrocyclic Chemistry 67, no. 3-4 (2009): 317–24. http://dx.doi.org/10.1007/s10847-009-9712-9.

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13

Indirapriyadharshini, V. K., P. Karunanithi, and P. Ramamurthy. "Inclusion of Resorcinol-Based Acridinedione Dyes in Cyclodextrins: Fluorescence Enhancement†." Langmuir 17, no. 13 (2001): 4056–60. http://dx.doi.org/10.1021/la0101200.

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14

Easton, Christopher J. "Cyclodextrin-based catalysts and molecular reactors." Pure and Applied Chemistry 77, no. 11 (2005): 1865–71. http://dx.doi.org/10.1351/pac200577111865.

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The naturally occurring cyclodextrins and their derivatives have been developed as miniature reaction vessels, to manipulate the outcomes of chemical transformations at the molecular level. In this manner, the rate of hydrolysis of a phosphate triester has been enhanced by almost five orders of magnitude, and the ratios of products obtained from electrophilic aromatic substitution reactions, from competing reactions to give indigoid dyes, and from nitrile oxide cycloadditions have all been changed, by factors of up to 3500 times.
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15

KATSUMATA, Chizuyo, and Kazuyoshi SEGUCHI. "Effects of Cyclodextrins on Fading of Azo Dyes with Sodium Sulfite." Journal of Japan Oil Chemists' Society 48, no. 5 (1999): 471–77. http://dx.doi.org/10.5650/jos1996.48.471.

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16

Iijima, T., та Y. Karube. "The interaction of acid azo dyes with chemically modified β-cyclodextrins". Dyes and Pigments 36, № 4 (1998): 305–11. http://dx.doi.org/10.1016/s0143-7208(97)00032-6.

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17

Buzanovskii, V. A. "Electrochemical sensors based on carbon nanotubes and their use in biomedical research.Part 2: sensors manufactured by dispersion of carbon nanotubes by means of polyethyleneimine, organic dyes, cyclodextrins, chitosan, proteins, room-temperature ionic liquids, gels, and thiols. Sensors manufactured by dispersion of carbon nanotubes by electropolymerization process. sensors manufactured by dispersion of carbon nanotubes by layer-by-layer deposition." Biomeditsinskaya Khimiya 58, no. 2 (2012): 144–59. http://dx.doi.org/10.18097/pbmc20125802144.

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Electrochemical sensors based on carbon nanotubes are widely distributed in biomedical researches. One group of these sensors contains the sensors manufactured by dispersion of carbon nanotubes on an electrode surface by means of polyethyleneimine, organic dyes, cyclodextrins, chitosan, proteins, room-temperature ionic liquids, gels, thiols, by electropolymerization process, and by layer-by-layer deposition. The development directions of such sensors are analyzed. The general information on manufacturing techniques of these sensors is submitted. The opportunities of these sensors for carrying
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18

Gribkova, Oxana L., and Alexander A. Nekrasov. "Spectroelectrochemistry of Electroactive Polymer Composite Materials." Polymers 14, no. 15 (2022): 3201. http://dx.doi.org/10.3390/polym14153201.

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In this review, we have summarized the main advantages of the method of spectroelectrochemistry as applied to recent studies on electrosynthesis and redox processes of electroactive polymer composite materials, which have found wide application in designing organic optoelectronic devices, batteries and sensors. These polymer composites include electroactive polymer complexes with large unmovable dopant anions such as polymer electrolytes, organic dyes, cyclodextrins, poly(β-hydroxyethers), as well as polymer-inorganic nanocomposites. The spectroelectrochemical methods reviewed include in situ
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19

Léonard, Estelle, and Antoine Fayeulle. "Azo-Dyes-Grafted Oligosaccharides—From Synthesis to Applications." Molecules 26, no. 11 (2021): 3063. http://dx.doi.org/10.3390/molecules26113063.

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Azobenzenes are photochromic molecules that possess a large range of applications. Their syntheses are usually simple and fast, and their purifications can be easy to perform. Oligosaccharide is also a wide family of biopolymer constituted of linear chain of saccharides. It can be extracted from biomass, as for cellulose, being the principal constituent of plant cell wall, or it can be enzymatically produced as for cyclodextrins, having properties not far from cellulose. Combining these two materials families can afford interesting applications such as controlled drug-release systems, photochr
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20

Sałdan, Anna, Małgorzata Król, Daria Śmigiel-Kamińska, Michał Woźniakiewicz, and Paweł Kościelniak. "Development of the Microemulsion Electrokinetic Capillary Chromatography Method for the Analysis of Disperse Dyes Extracted from Polyester Fibers." Molecules 27, no. 20 (2022): 6974. http://dx.doi.org/10.3390/molecules27206974.

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The study aimed to develop a method for the separation of dispersed dyes extracted from polyester fibers. Nine commercially available disperse dyes, which were used to dye three polyester fabrics, were tested. Extraction of dyes from 1 cm long threads was carried out in chlorobenzene at 100 °C for 6 h. The separation was performed using microemulsion electrokinetic capillary chromatography (MEEKC) with photodiode array detection. Microemulsion based on a borate buffer with an organic phase of n-octane and butanol and a mixture of surfactants, sodium dodecyl sulphate and sodium cholate, were us
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21

Cartwright, Steven J. "Homeopathic Potencies May Possess an Electric Field(-like) Component: Evidence from the Use of Encapsulated Solvatochromic Dyes." Homeopathy 109, no. 01 (2019): 014–22. http://dx.doi.org/10.1055/s-0039-1693985.

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Background Homeopathic potencies have been shown to interact with a range of solvatochromic dyes to produce spectroscopic changes in the visible region of the electromagnetic spectrum. Furthermore, the nature of the changes observed under different experimental conditions is beginning to limit the number of possible hypotheses that can be put forward regarding the fundamental identity of potencies. Aims and Methods The present study uses β-cyclodextrins to encapsulate solvatochromic dyes of widely varying structures. The purpose of this approach is to de-couple the primary dye–potency interact
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22

Hattori, T., S. Higuchi, and S. Tanaka. "Raman optical activity of some azo dyes induced by inclusion in cyclodextrins." Journal of Raman Spectroscopy 18, no. 3 (1987): 153–55. http://dx.doi.org/10.1002/jrs.1250180302.

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23

Hao, Rui, Yu Zhu, Xiaoyu Wang та Li Chen. "A recyclable β-cyclodextrins-based supramolecular adsorbent for removal of organic dyes". Journal of Applied Polymer Science 134, № 28 (2017): 45084. http://dx.doi.org/10.1002/app.45084.

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24

Bergmark, William R., Alan Davis, Clayton York, Ann Macintosh, and Guilford Jones. "Dramatic fluorescence effects for coumarin laser dyes coincluded with organic solvents in cyclodextrins." Journal of Physical Chemistry 94, no. 12 (1990): 5020–22. http://dx.doi.org/10.1021/j100375a047.

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25

Ghemati, Djamila, та Djamel Aliouche. "Synthesis and Characterization of Porous Materials Containing Modified Cellulose by β-Cyclodextrin for the Application in Processing Industrial Liquid Waste". Materials Science Forum 609 (січень 2009): 287–91. http://dx.doi.org/10.4028/www.scientific.net/msf.609.287.

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The cellulose made up the principal structure of many plants. The content varies according to the vegetable species, from approximately 40% in wood, to 95-99% in cotton fibers. Several ways are possible to bring an additional function to cellulose: new fibers, modification of the fibrous structure, physical or chemical treatment by a surface treatment. And due to the contribution of functions, the formerly passive cellulose becomes active. Capacity of cyclodextrins to facilitate the inclusion of hydrophobic molecules, and others chemical derivatives like the dyes, can be exploited to obtain ne
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26

Suzuki, Miyoko, Hitoshi Takai, Jozsef Szejtli, and Eva Fenyvesi. "13C-n.m.r. spectra of cyclomalto-oligosaccharides (cyclodextrins), their derivatives, and complexes with azo dyes." Carbohydrate Research 201, no. 1 (1990): 1–14. http://dx.doi.org/10.1016/0008-6215(90)84221-f.

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27

Fischer, Peter, Marc Koetse, André Laschewsky, et al. "Orientation of Nonlinear Optical Active Dyes in Electrostatically Self-Assembled Polymer Films Containing Cyclodextrins." Macromolecules 33, no. 26 (2000): 9471–73. http://dx.doi.org/10.1021/ma001041i.

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28

Bardadym, Yuliia, Serhii Kobylinskyi, Larisa Kobrina, and Serhii Riabov. "THE USE OF CYCLODEXTRINS TO INCREASE THE EFFICIENCY OF TITANIUM DIOXIDE IN THE HETEROGENEOUS CATALYSIS." Ukrainian Chemistry Journal 86, no. 7 (2020): 32–52. http://dx.doi.org/10.33609/2708-129x.86.7.2020.32-52.

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Photocatalytic oxidation is a very young direction, but in the same time it is one of the most promising, safe and effective methods of removing organic pollutants (in particular dyes and microbial pathogens) from the aquatic environment. General information on titanium dioxide, cyclodextrin and its derivatives is presented in this literature review. The results of recent studies regarding the practical application of titanium dioxide and cyclodextrins for the treatment of wastewaters and purification them from organic pollutants of various nature by the methods of heterogeneous photocatalysis
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POLITZER, I., K. CRAGO, K. AMOS, K. MITCHELL, and T. HOLLIN. "Thin-layer chromatography of laser dyes and dye analogs with cyclodextrins in the mobile phase." Talanta 39, no. 8 (1992): 953–58. http://dx.doi.org/10.1016/0039-9140(92)80277-k.

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30

Petinova, Asya, Stefan Metsov, Ivan Petkov, and Stefan Stoyanov. "Photophysical behaviours of some 2-styrylindolium dyes in aqueous solutions and in the presence of cyclodextrins." Journal of Inclusion Phenomena and Macrocyclic Chemistry 59, no. 1-2 (2007): 183–90. http://dx.doi.org/10.1007/s10847-007-9313-4.

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31

Liu, Xiaodong, Liang Yan, Wenyan Yin, et al. "A magnetic graphene hybrid functionalized with beta-cyclodextrins for fast and efficient removal of organic dyes." Journal of Materials Chemistry A 2, no. 31 (2014): 12296. http://dx.doi.org/10.1039/c4ta00753k.

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32

Rubin Pedrazzo, Alberto, Fabrizio Caldera, Marco Zanetti, Silvia Lucia Appleton, Nilesh Kumar Dahkar, and Francesco Trotta. "Mechanochemical green synthesis of hyper-crosslinked cyclodextrin polymers." Beilstein Journal of Organic Chemistry 16 (June 29, 2020): 1554–63. http://dx.doi.org/10.3762/bjoc.16.127.

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Cyclodextrin nanosponges (CD-NS) are nanostructured crosslinked polymers made up of cyclodextrins. The reactive hydroxy groups of CDs allow them to act as multifunctional monomers capable of crosslinking to bi- or multifunctional chemicals. The most common NS synthetic pathway consists in dissolving the chosen CD and an appropriate crosslinker in organic polar aprotic liquids (e.g., N,N-dimethylformamide or dimethyl sulfoxide), which affect the final result, especially for potential biomedical applications. This article describes a new, green synthetic pathway through mechanochemistry, in part
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33

Bao, Kaiyue, Anyun Zhang, Yiyao Cao, and Lei Xu. "Achievements in Preparation of Cyclodextrin–Based Porous Materials for Removal of Pollutants." Separations 11, no. 5 (2024): 143. http://dx.doi.org/10.3390/separations11050143.

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Cyclodextrin–based porous materials have been widely applied in removing various organic pollutants from water environments, due to their unique physical and chemical properties, like the size–matching effect and hydrophobic interaction. Large numbers of hydroxyl groups in its external structure give cyclodextrin a high solubility in water, but the existence of these hydroxyl groups also endows cyclodextrin with the ability to be chemically modified with various functional groups to reduce its solubility in water and, meanwhile, to develop some novel functionalized cyclodextrin–based porous ma
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34

Berberan-Santos, Mario N., Patricia Choppinet, Aleksandre Fedorov, Ludovic Jullien, and Bernard Valeur. "Multichromophoric Cyclodextrins. 8. Dynamics of Homo- and Heterotransfer of Excitation Energy in Inclusion Complexes with Fluorescent Dyes." Journal of the American Chemical Society 122, no. 48 (2000): 11876–86. http://dx.doi.org/10.1021/ja000995l.

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35

Liu, Yu, and Chang-Cheng You. "Inclusion complexation of ?-cyclodextrin and 6-O-?-�maltosyl- and 2-O-(2-hydroxypropyl)-?-cyclodextrins �with some fluorescent dyes." Journal of Physical Organic Chemistry 14, no. 1 (2000): 11–16. http://dx.doi.org/10.1002/1099-1395(200101)14:1<11::aid-poc329>3.0.co;2-7.

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36

Austin, Publishing Group. "Supramolecular Enhancement of BODIPY Singlet Oxygen Generation Using Bile Salt Micelles." Austin Journal of Analytical and Pharmaceutical Chemistry 10, no. 2 (2023): 1161. https://doi.org/10.26420/austinjanalpharmchem.2023.1161.

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Abstract Singlet Oxygen (SO) generation is the core chemical process of many medical and industrial applications. Designing efficient SO-Generating (SOG) agents is a major research focus for its utility in photodynamic therapy, wastewater treatment, material science, and organic synthesis. Photosensitization of ambient oxygen using organic dyes is an efficient approach to generating SO, though their efficiency is often severely hampered due to aggregation-induced deactivation. In this manuscript, we present the utility of bile salt micelle as supramolecular host for promoting SOG in aqueous me
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37

Alves, Daniele C. da Silva, Bronach Healy, Tian Yu, and Carmel B. Breslin. "Graphene-Based Materials Immobilized within Chitosan: Applications as Adsorbents for the Removal of Aquatic Pollutants." Materials 14, no. 13 (2021): 3655. http://dx.doi.org/10.3390/ma14133655.

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Graphene and its derivatives, especially graphene oxide (GO), are attracting considerable interest in the fabrication of new adsorbents that have the potential to remove various pollutants that have escaped into the aquatic environment. Herein, the development of GO/chitosan (GO/CS) composites as adsorbent materials is described and reviewed. This combination is interesting as the addition of graphene to chitosan enhances its mechanical properties, while the chitosan hydrogel serves as an immobilization matrix for graphene. Following a brief description of both graphene and chitosan as indepen
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Härtel, Steffen, Horst A. Diehl та Flavio Ojeda S. "Methyl-β-Cyclodextrins and Liposomes as Water-Soluble Carriers for Cholesterol Incorporation into Membranes and Its Evaluation by a Microenzymatic Fluorescence Assay and Membrane Fluidity-Sensitive Dyes". Analytical Biochemistry 258, № 2 (1998): 277–84. http://dx.doi.org/10.1006/abio.1998.2594.

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39

Murcia-Salvador, Ainoa, José A. Pellicer, María I. Fortea, et al. "Adsorption of Direct Blue 78 Using Chitosan and Cyclodextrins as Adsorbents." Polymers 11, no. 6 (2019): 1003. http://dx.doi.org/10.3390/polym11061003.

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The dyeing industry is one of the most polluting in the world. The adsorption of dyes by polymeric matrixes can be used to minimize the discharge of dyes into the environment. In the present study, chitosan-NaOH and β-cyclodextrin-epichlorohydrin polymers were used to remove the dye Direct Blue 78 from a wastewater model. To understand the adsorption behavior of Direct Blue 78 onto the polymers, adsorption rate and maximum adsorption capacity were calculated using kinetic tests and isotherm curves respectively. The kinetic data and mechanism of the adsorption process were analyzed by three mod
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40

Kircheva, Nikoleta, Stefan Dobrev, Lyubima Dasheva, Valya Nikolova, Silvia Angelova, and Todor Dudev. "Metal-Assisted Complexation of Fluorogenic Dyes by Cucurbit[7]uril and Cucurbit[8]uril: A DFT Evaluation of the Key Factors Governing the Host–Guest Recognition." Molecules 28, no. 4 (2023): 1540. http://dx.doi.org/10.3390/molecules28041540.

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With the emergence of host-guest systems, a novel branch of complexation chemistry has found wide application in industries such as food, pharmacy, medicine, environmental protection and cosmetics. Along with the extensively studied cyclodextrins and calixarenes, the innovative cucurbiturils (CB) have enjoyed increased popularity among the scientific community as they possess even better qualities as cavitands as compared to the former molecules. Moreover, their complexation abilities could further be enhanced with the assistance of metal cations, which can interestingly exert a dual effect on
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41

Urooj, Tuba, Monika Mishra, and Shivam Pandey. "Unlocking environmental solutions: a review of cyclodextrins in pollutant removal." Discover Environment 2, no. 1 (2024). http://dx.doi.org/10.1007/s44274-024-00090-w.

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AbstractCyclodextrins are cyclic oligosaccharides characterized by a hydrophobic interior and a hydrophilic outside linked by α-1,4 glycosidic bonds. Cyclodextrins are biodegradable and generally considered environmentally friendly. These are utilized in diverse applications, encompassing environmental cleanup which is enhanced through the processes of cross-linking or surface modification. These molecules have a unique structure that enables them to form inclusion complexes with various guest molecules, including organic pollutants, pesticides, dyes, pharmaceuticals, and hydrocarbons. When us
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42

Zheng, Yangyang, and Huacheng Zhang. "Boric Acid Bridged Cyclodextrins-based Polymers for Selective Adsorption of Binary Dyes." Polymer, January 2025, 128091. https://doi.org/10.1016/j.polymer.2025.128091.

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43

Khushbu and Samrat Mukhopadhyay. "Enhancing Environmental Remediation: Advancements in Chemically Crosslinked Cyclodextrin‐Based Materials for Organic and Inorganic Pollutant Removal." Advanced Sustainable Systems, October 6, 2024. http://dx.doi.org/10.1002/adsu.202400560.

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AbstractConcern over the harmful impacts of pollutants on human health and the environment has increased in recent decades due to their widespread presence in water resources. These pollutants include pesticides, poisonous textile dyes, and micropollutants. It is essential to remove these pollutants from wastewater to enhance the quality of water for industrial usage. Because of externally hydrophilic and internally hydrophobic qualities, cyclodextrin and its derivatives have shown great promise as adsorbents for the treatment of wastewater. While cyclodextrins cannot be used as adsorbents on
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44

Jiang, Jicai, Haibo Wan, Jinchang Zhang, et al. "Engineered Polymeric Microspheres with Synergistic Hydrogen‐Bonding Nanotraps and Multisite Adsorption for Ultrafast Herbicide Decontamination." Angewandte Chemie International Edition, March 11, 2025. https://doi.org/10.1002/anie.202504349.

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AbstractThe ultrafast removal of trace herbicides like paraquat (PQ) and diquat (DQ) from water is urgent yet challenging due to their highwater stability and strong‐binding properties. Here, efficient PQ and DQ removal based on hydrogen‐bonding nanotraps dominant multisite adsorption were developed. Two crosslinked polymeric microspheres, βCD‐PF and γCD‐PF, were synthesized from cyclodextrins (CDs) and hexafluorocyclotriphosphazene (HFP). The γCD‐PF microsphere with sufficient hydrogen‐bonding nanotraps on the pore surface prompts adsorption kinetics constants of PQ and DQ up to 127.09 and 19
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Jiang, Jicai, Haibo Wan, Jinchang Zhang, et al. "Engineered Polymeric Microspheres with Synergistic Hydrogen‐Bonding Nanotraps and Multisite Adsorption for Ultrafast Herbicide Decontamination." Angewandte Chemie, March 11, 2025. https://doi.org/10.1002/ange.202504349.

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Abstract:
AbstractThe ultrafast removal of trace herbicides like paraquat (PQ) and diquat (DQ) from water is urgent yet challenging due to their highwater stability and strong‐binding properties. Here, efficient PQ and DQ removal based on hydrogen‐bonding nanotraps dominant multisite adsorption were developed. Two crosslinked polymeric microspheres, βCD‐PF and γCD‐PF, were synthesized from cyclodextrins (CDs) and hexafluorocyclotriphosphazene (HFP). The γCD‐PF microsphere with sufficient hydrogen‐bonding nanotraps on the pore surface prompts adsorption kinetics constants of PQ and DQ up to 127.09 and 19
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Alcázar, Jackson J., Luis García-Río, Agustín I. Robles, et al. "Linear relationship between emission quantum yield and Stokes shift in 3-styryl aza-coumarin based dyes in the presence of cyclodextrins." Journal of Molecular Liquids, April 2023, 121790. http://dx.doi.org/10.1016/j.molliq.2023.121790.

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