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Journal articles on the topic 'Salicylaldazine'

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Author: Grafiati
Published: 10 December 2022
Last updated: 29 January 2023

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1

Liu, Lei, Bo Wu, Ping Yu, Ren-Xi Zhuo, and Shi-Wen Huang. "Sub-20 nm nontoxic aggregation-induced emission micellar fluorescent light-up probe for highly specific and sensitive mitochondrial imaging of hydrogen sulfide." Polymer Chemistry 6, no. 29 (2015): 5185–89. http://dx.doi.org/10.1039/c5py00722d.

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A salicylaldazine-based amphiphilic polymer (AIE-1) with aggregation-induced emission characteristics was utilized for the specific and sensitive detection of S2− in solution and mitochondrial imaging of H2S in HeLa cells.
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2

Zhang, Jingzhe, Zheng Zhao, Hong Shang, Qingsong Liu, and Fei Liu. "An easy-to-synthesize multi-photoresponse smart sensor for rapidly detecting Zn2+ and quantifying Fe3+ based on the enol/keto binding mode." New Journal of Chemistry 43, no. 35 (2019): 14179–89. http://dx.doi.org/10.1039/c9nj03635k.

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A readily available salicylaldazine-modified fluorene Schiff base (EASA-F) exhibits fast fluorescent OFF–ON response to Zn2+ and OFF–ON–OFF behavior to Fe3+ synchronously accompanied the diverse absorption-ratiometric and colorimetric changes.
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3

Raditoiu, Alina, Valentin Raditoiu, Florentina Monica Raduly, Georgiana Cornelia Ispas, Violeta Purcar, Adriana Nicoleta Frone, Raluca Manea, Luminita Eugenia Wagner, and Mihai Anastasescu. "Fluorescent Silica Hybrid Film-Forming Materials Based on Salicylaldazine." Coatings 10, no. 12 (December 18, 2020): 1255. http://dx.doi.org/10.3390/coatings10121255.

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Fluorescent film-forming materials were obtained by embedding salicylaldazine (SAA) in silica hybrids generated by sol–gel processes from different silane precursors in acid catalysis. Tuned local environments for the fluorophore were generated in the hosting network by modifying silica sols with organic groups through the co-condensation of tetraethylortosilicate (TEOS) and different alkoxysilanes hydrolysis products. The photophysical properties of the luminescent hybrid films were studied in direct relationship with structural, textural, and surface properties and based on interactions between SAA species and the silica hosting network. Film-forming materials were studied in order to determine differences in absorption and fluorescence emission due to the environments around the fluorophore. The variations recorded in the fluorescence emission spectra of the hybrid films were related to interactions established between the fluorophore species and their sterically hindered surroundings of the host hybrid silica, where free molecular motions are restricted. The influence of the type and amount of network modifier and of the fluorophore loading on the transparency of the films and fluorescence intensity was also investigated. The study carried out led to the elucidation of the necessary conditions for obtaining luminescent film-forming materials with high luminescence intensity and transparency useful for the design of new light concentrators.
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4

El-Sayed, Badr A., M. M. Abo-Aly, and G. M. Attia. "SYNTHESIS, VIBRATIONAL, AND ELECTRONIC STUDIES OF SALICYLALDAZINE TRANSITION METAL COMPLEXES." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 31, no. 9 (October 31, 2001): 1565–76. http://dx.doi.org/10.1081/sim-100107703.

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5

Kassim, Karimah, Muhamad Azwan Hamali, and Bohari Yamin. "A New Alternative Synthesis of Salicylaldazine via Microwave Irradiation Method." Journal of Chemistry 2019 (May 13, 2019): 1–6. http://dx.doi.org/10.1155/2019/9546373.

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Two diazine Schiff base ligands, HLa and HLb, derived from thiocarbohydrazide and salicylaldehyde derivatives were synthesized using the microwave-assisted synthesis approach. The confirmation of both ligands was elucidated through physiochemical and spectroscopy techniques as well as single X-ray crystallography diffraction. The analyses showed that the ligands synthesized were formed as azine instead of thiocarbohydrazone based on the missing thione, C=S moiety, throughout FTIR and NMR spectrascopic data. This finding was further concluded by X-ray crystal analysis. The biological properties of these ligands were screened using the disc diffusion method. The result shows that HLb shows significant inhibition towards all of the bacteria tested.
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6

Singh, B., and A. K. Srivastav. "Studies on Some Bivalent Metal Complexes of 2-Amino-benzophenone Salicylaldazine." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 26, no. 5 (May 1996): 819–30. http://dx.doi.org/10.1080/00945719608004337.

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7

Mijanuddin, Md, W. S. Sheldrick, H. Mayer-Figge, Mahammad Ali, and Nitin Chattopadhyay. "Crystal structure and feasibility of intramolecular proton transfer reaction of salicylaldazine." Journal of Molecular Structure 693, no. 1-3 (May 2004): 161–65. http://dx.doi.org/10.1016/j.molstruc.2004.02.030.

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8

AboAly, M. M., B. A. El Sayed, and A. M. Hassan. "VIBRATIONAL SPECTRA OF BENZALDAZINE AND SALICYLALDAZINE COMPLEXES WITH ZN(II) AND FE(II) IONS." Spectroscopy Letters 35, no. 3 (July 23, 2002): 337–48. http://dx.doi.org/10.1081/sl-120005670.

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9

Singh, B., and U. R. Singh. "Synthesis and Structural Characterisation of 2-Acetylthiophene Salicylaldazine Complexes of Some Bivalent Transition Metal Ions." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 22, no. 2-3 (February 1992): 247–58. http://dx.doi.org/10.1080/00945719208021386.

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10

El-Sayed, Badr A., Moustafa M. El-Desoky, Salah M. Shaaban, and Moein B. Sayed. "Electrical and spectral studies of solid organic semiconductors—I. Structural interpretation of promoted conductivity of salicylaldazine." Electrochimica Acta 35, no. 11-12 (November 1990): 1987–88. http://dx.doi.org/10.1016/0013-4686(90)87110-n.

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11

Mesbahi, Elnaz, Mojtaba Bagherzadeh, Mojtaba Amini, Ali Akbari, Arkady Ellern, and L. Keith Woo. "A novel binuclear iron(III)-salicylaldazine complex; synthesis, X-ray structure and catalytic activity in sulfide oxidation." Polyhedron 183 (June 2020): 114531. http://dx.doi.org/10.1016/j.poly.2020.114531.

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12

El-Deen, Ibrahim M. "Use of 3-(2′-formyl-1′-chlorovinyl)coumarin in the syntheses of pyrazol, salicylaldazine and pyrimidine derivatives." Chinese Journal of Chemistry 17, no. 4 (August 27, 2010): 391–97. http://dx.doi.org/10.1002/cjoc.19990170412.

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13

Zhang, Yang, Cai-Xia Wang, and Shi-Wen Huang. "Aggregation-Induced Emission (AIE) Polymeric Micelles for Imaging-Guided Photodynamic Cancer Therapy." Nanomaterials 8, no. 11 (November 7, 2018): 921. http://dx.doi.org/10.3390/nano8110921.

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Photodynamic therapy (PDT) is a noninvasive treatment for selectively killing malignant tumor cells. The photosensitizer is a necessary component of photodynamic nanomedicine. Many efforts have been made to develop new photosensitizers for efficient cancer photodynamic therapy. In this work, we report a novel nano photosensitizer, polymeric micelles (AIE-M) with aggregation induced emission characteristic, for photodynamic cancer therapy. AIE-M with sub-20 nm particle size is prepared by the self-assembly of salicylaldazine-incorporated amphiphilic polymer (AIE-1), which can produce reactive oxygen species (ROS) with light irradiation in solution. After uptake by cancer cells, AIE-M can specially sojourn in plasma membranes of cancer cells at the early stage and predominantly accumulate in the mitochondria of cancer cell at the late stage. The phototoxicity of AIE-M, resulting from the generation of intracellular ROS with light irradiation, can efficiently cause cancer cells death by apoptosis and necrosis. The advantages of AIE-M as a nano photosensitizer include the small size, highly colloidal stability in the process of preparation and storage, and high cell penetration. The ultra-low Critical Micelle Concentration (CMC) of AIE-1, negligible dark toxicity and super phototoxicity of AIE-M suggest its promising potential for image-guided PDT.
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14

Kuo, Hsiu-Ming, Yu-Te Hsu, Yi-Wen Wang, Gene-Hsiang Lee, and Chung K. Lai. "The π–π interactions enhanced in salicylaldimines and salicylaldazines." Tetrahedron 71, no. 40 (October 2015): 7729–38. http://dx.doi.org/10.1016/j.tet.2015.07.049.

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15

Silva, Artur M. S., Vera L. M. Silva, Rosa M. Claramunt, Dolores Santa María, Marta B. Ferraro, Felipe Reviriego, Ibon Alkorta, and José Elguero. "The structures of two aldazines: [1,1′-(1E ,1′E )-hydrazine-1,2-diylidenebis(methan-1-yl-1-ylidene)dinaphthalen-2-ol] (Lumogen) and 2,2′-(1E ,1′E )-hydrazine-1,2-diylidenebis(methan-1-yl-1-ylidene)diphenol (salicylaldazine) in the solid state and in solution." Magnetic Resonance in Chemistry 51, no. 9 (July 8, 2013): 530–40. http://dx.doi.org/10.1002/mrc.3983.

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16

El-Sayed, B. A., M. M. El-Desoky, S. M. Shaaban, and M. B. Sayed. "Temperature dependence of the electrical conductivity of Salicylaldazinate metal chelates." Journal of Materials Science: Materials in Electronics 3, no. 2 (June 1992): 124–26. http://dx.doi.org/10.1007/bf00695728.

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