Готові списки джерел за темами / Glycoconjugated dyes

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Добірка наукової літератури з теми "Glycoconjugated dyes"

Автор: Grafiati
Опубліковано: 10 березня 2023

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Статті в журналах з теми "Glycoconjugated dyes"

1

Guazzelli, Lorenzo, Giorgio Catelani, and Felicia D’Andrea. "A New Generation of Glycoconjugated Azo Dyes Based on Aminosugars." International Journal of Carbohydrate Chemistry 2015 (July 29, 2015): 1–7. http://dx.doi.org/10.1155/2015/235763.

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The third generation of glycoconjugated azo dyes (GADs) was prepared linking monoazo dyes to 6-amino-6-deoxy-d-galactose or 6′amino-6′-deoxylactose through mixed amido-ester connections. The complementary conjugation reactions were studied using the succinyl derivative of either the acetal protected aminosugar or the azo dye. Target “naturalized” GADs were obtained after acid hydrolysis of the acetal protecting groups present on the sugar moiety.
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2

Shimi, M., Vandana Sankar, M. K. Abdul Rahim, P. R. Nitha, Suresh Das, K. V. Radhakrishnan, and K. G. Raghu. "Novel glycoconjugated squaraine dyes for selective optical imaging of cancer cells." Chemical Communications 53, no. 39 (2017): 5433–36. http://dx.doi.org/10.1039/c6cc10282d.

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3

Reddington, Mark V. "New glycoconjugated cyanine dyes as fluorescent labeling reagents." Journal of the Chemical Society, Perkin Transactions 1, no. 1 (1998): 143–48. http://dx.doi.org/10.1039/a703308g.

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4

REDDINGTON, M. V. "ChemInform Abstract: New Glycoconjugated Cyanine Dyes as Fluorescent Labeling Reagents." ChemInform 29, no. 22 (June 22, 2010): no. http://dx.doi.org/10.1002/chin.199822121.

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5

Bianchini, Roberto, Giorgio Catelani, Riccardo Cecconi, Felicia D'Andrea, Lorenzo Guazzelli, Jalal Isaad, and Massimo Rolla. "Ethereal Glycoconjugated Azodyes (GADs): A New Group of Water-Soluble, Naturalised Dyes." European Journal of Organic Chemistry 2008, no. 3 (January 2008): 444–54. http://dx.doi.org/10.1002/ejoc.200700632.

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6

Calugi, Lorenzo, Marco Bonanni, Massimo Corsi, Stefano Chimichi, and Roberto Bianchini. "Suzuki and Heck Processes for the Synthesis of New Anthraquinone-Based Glycoconjugated Dyes." ChemistrySelect 3, no. 8 (February 22, 2018): 2235–39. http://dx.doi.org/10.1002/slct.201702884.

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7

Treekoon, Jongjit, Thitima Pewklang, Kantapat Chansaenpak, Jaggaiah N. Gorantla, Salila Pengthaisong, Rung-Yi Lai, James R. Ketudat-Cairns, and Anyanee Kamkaew. "Glucose conjugated aza-BODIPY for enhanced photodynamic cancer therapy." Organic & Biomolecular Chemistry 19, no. 26 (2021): 5867–75. http://dx.doi.org/10.1039/d1ob00400j.

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8

Zhang, Rui Yong, Jing Liu, Thomas R. Neu, Qian Li, Sören Bellenberg, Wolfgang Sand, and Mario Vera. "Interspecies Interactions of Metal-Oxidizing Thermo-Acidophilic Archaea Acidianus and Sulfolobus." Advanced Materials Research 1130 (November 2015): 105–8. http://dx.doi.org/10.4028/www.scientific.net/amr.1130.105.

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Анотація:
Biofilm formation of microorganisms on relevant surfaces is of great importance for biomining and acid mine drainage (AMD). Thermo-acidophilic archaea like Acidianus, Sulfolobus and Metallosphaera are of special interest due to their ability to enhance leaching rates. Visualization and investigation of microbial attachment and biofilm formation of metal-oxidizing organisms up to now has been done mostly with mesophilic or moderately thermophilic bacteria. In this study, attachment and biofilms by the crenarchaeota Sulfolobus metallicus DSM 6482T and a new isolate Acidianus sp. DSM 29099 on sulfur or pyrite were analyzed. Confocal laser scanning microscopy (CLSM) combined with fluorescent dyes specific for nucleic acids or glycoconjugates were used to monitor biofilm formation on surfaces. The data indicate that cell attachment and the subsequently formed biofilm structures were species and substrate dependent. The investigation of binary biofilms on pyrite showed that both species were heterogeneously distributed on pyrite surfaces in the form of individual cells or microcolonies. In addition, physical contact between the two species was visible, as revealed by specific lectins able to distinguish single species.
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9

Porri, Aimone, Riccardo Baroncelli, Lorenzo Guglielminetti, Sabrina Sarrocco, Lorenzo Guazzelli, Maurizio Forti, Giorgio Catelani, et al. "Fusarium oxysporum degradation and detoxification of a new textile-glycoconjugate azo dye (GAD)." Fungal Biology 115, no. 1 (January 2011): 30–37. http://dx.doi.org/10.1016/j.funbio.2010.10.001.

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10

Isaad, Jalal, and Ahmida El Achari. "A novel glycoconjugated N-acetylamino aldehyde hydrazone azo dye as chromogenic probe for cyanide detection in water." Analytica Chimica Acta 694, no. 1-2 (May 2011): 120–27. http://dx.doi.org/10.1016/j.aca.2011.03.032.

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Дисертації з теми "Glycoconjugated dyes"

1

Fogli, Silvia. "Glycoconjugated dyes: dye removal and evidence of self-assembly in solution through spectrophotometric and scattering techniques." Doctoral thesis, 2019. http://hdl.handle.net/2158/1164209.

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Анотація:
The present work focus on the characterization of five glycoconjugated dyes. These molecules are a class of compounds synthesized conjugating a unit of lactose to specifically modified disperse chromophores. The presence of lactose enhances the water solubility of these molecules, and also makes these compounds amphiphiles. The amphiphilicity allows the self-assembly of glycoconjugated dyes in solution. The behavior of these molecules in solution was studied experimentally using a variety of techniques, including UV-Visible spectroscopy, Dynamic Light Scattering (DLS) and Small Angle X-Rays Scattering (SAXS). Moreover, using a combination of SAXS and Electronic Circular Dichroism (ECD) the shape of the objects in solution could be determined. The influence on aggregates formation and behavior in solution of some parameters, such as the solvent, the interaction with surfactants and with other glycoconjugated dyes was also studied using the same techniques. A computational study of glycoconjugated dyes was performed using Force Fields. Computational tools allowed to determine the preferential conformations assumed by these molecules as monomers and dimers. Since glycoconjugated dyes have been designed for leather and textile dyeing, an additional preliminary study on the end of the life cycle for glycoconjugated dyes was carried out using two different dye removal approaches. The first approach could be intended as a possible alternative or a support for the classical methods and involved a white rot fungus, Funalia trogii, as microorganism for dye removal. This approach was tested on glycoconjugated dyes simulated effluents. The second approach was the classical one, involving activated sludge, and was carried out on glycoconjugated dyes real leather dyeing effluents.
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