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Relevant bibliographies by topics / Synthesis of photoactive compounds

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Journal articles

Academic literature on the topic 'Synthesis of photoactive compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Synthesis of photoactive compounds"

1

Sture, Beatrise, Mikelis Kirpluks, Sergejs Gaidukovs, and Edgars Vanags. "Synthesis of Photoactive Compounds from Tall Oil Fatty Acids." Journal of Renewable Materials 8, no. 9 (2020): 1077–89. http://dx.doi.org/10.32604/jrm.2020.09294.

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2

Kaufhold, Simon, and Kenneth Wärnmark. "Design and Synthesis of Photoactive Iron N-Heterocyclic Carbene Complexes." Catalysts 10, no. 1 (2020): 132. http://dx.doi.org/10.3390/catal10010132.

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The use of iron in photoactive metal complexes has been investigated for decades. In this respect, the charge transfer (CT) states are of particular interest, since they are usually responsible for the photofunctionality of such compounds. However, only recently breakthroughs have been made in extending CT excited state lifetimes that are notoriously short-lived in classical polypyridine iron coordination compounds. This success is in large parts owed to the use of strongly σ-donating N-heterocyclic carbene (NHC) ligands that help manipulating the photophysical and photochemical properties of

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3

Yamamoto, H., T. Sumi, N. Hamada, F. Tokunaga, T. Okamura, and N. Ueyama. "3D0900 Synthesis and characterization of the chromophore model compounds of Photoactive Yellow Protein." Seibutsu Butsuri 42, supplement2 (2002): S152. http://dx.doi.org/10.2142/biophys.42.s152_1.

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4

Collis, Gavin E., and Dieter Wege. "Approaches to Cyclopropa-Fused Quinones. The Synthesis and Photolysis of Some 4,9-Disubstituted 3,3-Dimethyl-3H-benz[f]indazoles." Australian Journal of Chemistry 56, no. 9 (2003): 903. http://dx.doi.org/10.1071/ch03060.

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Addition of 2-diazopropane to 1,4-naphthoquinone at low temperature, followed by in situ enolization and acetylation or silylation gave 3,3-dimethyl-1H-benz[f]indazol-4,9-diyl diacetate and 3,3-dimethyl-9-(t-butyl-dimethylsilyloxy)-1H-benz[f]indazol-4-ol, respectively. Functional group manipulation of the latter compound provided a number of other 4,9-disubstituted 3,3-dimethyl-3H-benz[f]indazoles. Irradiation of the diacetate led to clean extrusion of nitrogen to give the naphtho[b]cycloproparene and an alkene. Attempts to elaborate the cycloproparene into the derived cyclopropanaphthoquinone

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5

Chandrasekhar, Vadapalli, Pakkirisamy Thilagar, Alexander Steiner, and Jamie F. Bickley. "Inorganic-Cored Photoactive Assemblies: Synthesis, Structure, and Photochemical Investigations on Stannoxane-Supported Multifluorene Compounds." Chemistry - A European Journal 12, no. 34 (2006): 8847–61. http://dx.doi.org/10.1002/chem.200600556.

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6

Al-Mutabagani, Laila Ahmed, Latifah A. Alshabanah, Sobhi M. Gomha, and Hoda A. Ahmed. "Synthesis, Thermal and Optical Characterizations of New Lateral Organic Systems." Crystals 11, no. 5 (2021): 551. http://dx.doi.org/10.3390/cryst11050551.

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New laterally OCH3-substituted optical organic Schiff base/ester series, namely 4-(4-(hexyloxyphenyl)iminomethyl)-3-methoxyphenyl 4-alkoxybenzoates, were prepared and characterized with different thermal, mesomorphic, and photoactive techniques. The prepared group constitutes five homologues that differ from each other in the number of carbons in the terminal alkoxy chain (n), which varies between n = 6, 8, 10, 12, and 16 carbons. The laterally protruded methoxy group is attached to the central benzene ring that makes an angle of 120° with the molecular long axis. Molecular structures of all n

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7

Enesca, Alexandru, and Luminita Andronic. "The Influence of Photoactive Heterostructures on the Photocatalytic Removal of Dyes and Pharmaceutical Active Compounds: A Mini-Review." Nanomaterials 10, no. 9 (2020): 1766. http://dx.doi.org/10.3390/nano10091766.

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The diversification of pollutants type and concentration in wastewater has underlined the importance of finding new alternatives to traditional treatment methods. Advanced oxidation processes (AOPs), among others, are considered as promising candidate to efficiently remove organic pollutants such as dyes or pharmaceutical active compounds (PhACs). The present minireview resumes several recent achievements on the implementation and optimization of photoactive heterostructures used as photocatalysts for dyes and PhACs removal. The paper is focused on various methods of enhancing the heterostruct

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8

Wu, Si, Lei Mei, Fei-ze Li, et al. "Uranyl-Organic Coordination Compounds Incorporating Photoactive Vinylpyridine Moieties: Synthesis, Structural Characterization, and Light-Induced Fluorescence Attenuation." Inorganic Chemistry 57, no. 23 (2018): 14772–85. http://dx.doi.org/10.1021/acs.inorgchem.8b02523.

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9

Hashizume, Kazunari, Naoto Hashimoto, and Yoshihiro Miyake. "Synthesis of Positron Labeled Photoactive Compounds: 18F Labeled Aryl Azides for Positron Labeling of Biochemical Molecules." Journal of Organic Chemistry 60, no. 21 (1995): 6680–81. http://dx.doi.org/10.1021/jo00126a015.

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10

Shi, Gang, Junling Guo, Likui Wang, et al. "Photoactive PANI/TiO2/Si composite coatings with 3D bio-inspired structures." New Journal of Chemistry 41, no. 15 (2017): 6965–68. http://dx.doi.org/10.1039/c7nj00395a.

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