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Journal articles on the topic 'Synthesis of photoactive compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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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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11

Vyshnevskyi, D., V. Ovdenko, V. Pavlov, O. Mokrynskaia, and M. Davidenko. "SYNTHESIS AND OPTICAL PROPERTIES OF NEW SYMMETRIC PYRAZOL-CONTAINED HETEROCYCLES AND THE PERSPECTIVE OF DEVELOPMENT OF HOLOGRAPHIC MEDIUM BASED ON IT." Bulletin of Taras Shevchenko National University of Kyiv. Chemistry, no. 1(55) (2018): 67–70. http://dx.doi.org/10.17721/1728-2209.2018.1(55).17.

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By the interaction of a symmetric bis-aldehyde with 1-phenyl-3-methylpyrazolone-5, a new symmetrical dye capable of photoinduced isomerization was obtained. Recording media (RM) based on synthesized dye and soft polymer matrix were prepared. Intensity of absorption of RM rises with increasing of dye percentage in polymer matrix. But, Beer-Lambert law is not fulfilled. Therefore, the partial aggregation of dye molecules is present. As in the case of azo-compounds, information recording proceeds, probably, through spatial changes caused by the photoinduced E,Z double bond isomerization. Recorded

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12

Shanmugakala, R., P. Tharmaraj, C. D. Sheela, and C. Anitha. "Synthesis and Studies on S-Triazine-Based Ligand and Its Metal Complexes." International Journal of Inorganic Chemistry 2012 (December 17, 2012): 1–7. http://dx.doi.org/10.1155/2012/301086.

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Tridentate chelate complexes of ML type (where M = Cu(II), Ni(II), and Co(II)) have been synthesized from triazine-based ligand 4,6-bis(5-mercapto-1,3,4-thiadiazol-amine)2-phenylamino-1,3,5-triazine (BMTDT). Microanalytical data, magnetic susceptibility measurements, IR, 1H NMR, UV-vis, mass, and EPR spectral techniques were used to characterise the structure of chelates. The electronic absorption spectra and magnetic susceptibility measurements suggest that metal complexes show square pyramidal geometry. The electrochemical behavior of copper(II) complex is studied by cyclic voltammetry. All

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13

Brzezińska, Magdalena, Patricia García-Muñoz, Agnieszka Ruppert, and Nicolas Keller. "Photoactive ZnO Materials for Solar Light-Induced CuxO-ZnO Catalyst Preparation." Materials 11, no. 11 (2018): 2260. http://dx.doi.org/10.3390/ma11112260.

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In this work, the solar light-induced redox photoactivity of ZnO semiconductor material was used to prepare CuxO-ZnO composite catalysts at room temperature with a control of the chemical state of the copper oxide phase. Cu2(I)O-ZnO and Cu(II)O-ZnO composite catalysts were prepared by using Cu(acac)2 in tetrahydrofuran-water and Cu(NO3)2 in water as metallic precursor, respectively. Prior to the implementation of the photon-assisted synthesis method, the most efficient photoactive ZnO material was selected from among different ZnO materials prepared by the low temperature polyol and precipitat

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14

Gruzdev, Matvey, Ulyana Chervonova, Arkadiy Kolker, et al. "Dendritic Iron(III) Carbazole Complexes: Structural, Optical, and Magnetic Characteristics." Materials 14, no. 18 (2021): 5445. http://dx.doi.org/10.3390/ma14185445.

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This paper focuses on the synthesis, structural characterization, and study of the optical, magnetic, and thermal properties of novel architectures combining metal ions as magnetoactive centers and photoactive blocks formed by carbazole units. For this purpose, a series of azomethine complexes of the composition [Fe(L)2]X (L = 3,6-bis[(3′,6′-di-tert-butyl-9-carbazol)-9-carbazol]benzoyloxy-4-salicylidene-N′-ethyl-N-ethylenediamine, X = NO3−, Cl−, PF6−) were synthesized by the reaction of metal salts with Schiff bases in a mixture of solvents. The UV–Vis absorption properties were studied in dic

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15

Anitha, C., S. Sumathi, P. Tharmaraj, and C. D. Sheela. "Synthesis, Characterization, and Biological Activity of Some Transition Metal Complexes Derived from Novel Hydrazone Azo Schiff Base Ligand." International Journal of Inorganic Chemistry 2011 (January 24, 2011): 1–8. http://dx.doi.org/10.1155/2011/493942.

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A series of metal(II) complexes ML where M = VO(II), Co(II), Ni(II), Cu(II), and Zn(II) have been synthesized from azo Schiff base ligand (N′E)-N′-(5-((4-chlorophenyl)diazenyl)-2-hydroxybenzylidene)-2-hydroxybenzohydrazide and characterized on the basis of elemental analyses, electronic, IR, and 1H NMR spectra, magnetic susceptibility and also by aid of scanning electron microscopy (SEM), X-ray powder diffraction, fluorescence spectral studies, and molar conductivity measurements. Conductivity measurements reveal that the complexes are nonelectrolytes. Spectroscopy and other analytical studies

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16

Gomha, Sobhi M., Hoda A. Ahmed, Mohamed Shaban, Tariq Z. Abolibda, Muna S. Khushaim, and Khalid A. Alharbi. "Synthesis, Optical Characterizations and Solar Energy Applications of New Schiff Base Materials." Materials 14, no. 13 (2021): 3718. http://dx.doi.org/10.3390/ma14133718.

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A new set of laterally OCH3-substituted photoactive liquid crystalline analogues, 4-hexyloxy phenyl- imino-4ʹ-(3-methoxyphenyl)-4ʹ’-alkoxybenzoates, were synthesized and investigated for their mesomorphic behavior. The prepared set constitutes five analogues that differ from each other by the terminally attached compact polar group. Characterization of the synthesized derivatives is conducted using differential scanning calorimetry (DSC), polarized optical microscopy (POM), and UV-spectroscopy. Molecular structures were elucidated by elemental analyses, FT-IR and NMR spectroscopy. DSC and POM

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17

Anitha, C., C. D. Sheela, P. Tharmaraj, and V. V. Hema. "Synthesis, Spectroscopic Characterization, and Biological Activities of Metal Complexes of 4-((4-Chlorophenyl)diazenyl)-2-((p-tolylimino)methyl)phenol." Journal of Chemistry 2013 (2013): 1–12. http://dx.doi.org/10.1155/2013/724163.

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Azo Schiff base complexes of VO(II), Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) have been synthesized from 4-((4-chlorophenyl)diazenyl)-2-((p-tolylimino)methyl)phenol (CDTMP). The nature of bonding and the structural features of the complexes have been deduced from elemental analysis, molar conductance, magnetic susceptibility measurements, IR, UV-Vis,1H-NMR, EPR, mass, SEM, and fluorescence spectral studies. Spectroscopic and other analytical studies reveal square-planar geometry for copper, square-pyramidal geometry for oxovanadium, and octahedral geometry for other complexes. The EPR spectr

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18

Gravel, D., S. Gauthier, F. Brisse, et al. "Synthesis, electronic spectroscopy, and evaluation of photoconducting oligomers with pendant bichromophores. Part 1. Influence of donor–acceptor orbital overlap on aggregate emission and photoactivity." Canadian Journal of Chemistry 68, no. 6 (1990): 908–25. http://dx.doi.org/10.1139/v90-143.

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The synthesis, electronic spectroscopy, and photoactivity of two polysebacate oligomers with pendant donor–acceptor bichromophores of the alkylcarbazole–dinitrofluorene type (P1) and the alkylcarbazole–trinitrofluorenone carboxylic acid ester type (P2) are reported. The crystal structure of the basic acceptor chromophore A2 and donor-acceptor bichromophore B2 of oligomer P2 are also reported. In bichromophore B2, the amount of overlap is evaluated at 50% while the distance between the donor and the acceptor is 3.42 Å. It is shown that while no ground state intramolecular charge-transfer intera

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19

Koteja, Anna, and Jakub Matusik. "Preparation of azobenzene-intercalated kaolinite and monitoring of the photoinduced activity." Clay Minerals 54, no. 1 (2019): 57–66. http://dx.doi.org/10.1180/clm.2019.6.

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AbstractSystems consisting of layered structures and photoactive molecules have been studied extensively. The structures of resulting complexes may be controlled by UV–Vis radiation, which subsequently affects their materials properties. This study describes a synthesis route for obtaining a photoresponsive kaolinite intercalation compound. The material was prepared by co-intercalating azobenzene and benzylalkylammonium chlorides into a methoxy form of kaolinite. The resultant materials possessed large basal spacing values in the range of 45–55 Å. The UV–Vis and Fourier-transform infrared spec

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20

Ndirangu, Shem M., Yanyan Liu, Kai Xu, and Shaoxian Song. "Risk Evaluation of Pyrolyzed Biochar from Multiple Wastes." Journal of Chemistry 2019 (December 16, 2019): 1–28. http://dx.doi.org/10.1155/2019/4506314.

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This paper aims at demonstrating the significance of biochar risk evaluation and reviewing risk evaluation from the aspects of pyrolysis process, feedstock, and sources of hazards in biochar and their potential effects and the methods used in risk evaluation. Feedstock properties and the resultant biochar produced at different pyrolysis process influence their chemical, physical, and structural properties, which are vital in understanding the functionality of biochar. Biochar use has been linked to some risks in soil application such as biochar being toxic, facilitating GHGs emission, suppress

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21

Flores-Rojas, Guadalupe Gabriel, Andrea Ruiu, Mireille Vonlanthen, et al. "Synthesis and characterization of cyclen cored photoactive star compounds and their Cu(I) and Cu(II) complexes. Effect of the valence and ligand size on their molar extinction coefficient." Inorganica Chimica Acta 513 (December 2020): 119927. http://dx.doi.org/10.1016/j.ica.2020.119927.

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22

Luciani, Giuseppina, Claudio Imparato, and Giuseppe Vitiello. "Photosensitive Hybrid Nanostructured Materials: The Big Challenges for Sunlight Capture." Catalysts 10, no. 1 (2020): 103. http://dx.doi.org/10.3390/catal10010103.

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Solar radiation is becoming increasingly appreciated because of its influence on living matter and the feasibility of its application for a variety of purposes. It is an available and everlasting natural source of energy, rapidly gaining ground as a supplement and alternative to the nonrenewable energy feedstock. Actually, an increasing interest is involved in the development of efficient materials as the core of photocatalytic and photothermal processes, allowing solar energy harvesting and conversion for many technological applications, including hydrogen production, CO2 reduction, pollutant

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23

Liu, Yang, Yong-Lan Feng, and Wei-Wei Fu. "A two-dimensional zinc(II) coordination polymer based on mixed dimethyl succinate and bipyridine ligands: synthesis, structure, thermostability and luminescence properties." Acta Crystallographica Section C Structural Chemistry 72, no. 4 (2016): 308–12. http://dx.doi.org/10.1107/s2053229616003211.

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From the viewpoint of crystal engineering, the construction of crystalline polymeric materials requires a rational choice of organic bridging ligands for the self-assembly process. Multicarboxylate ligands are of particular interest due to their strong coordination activity towards metal ions, as well as their various coordination modes and versatile conformations. The structural chemistry of dicarboxylate-based coordination polymers of transition metals has been developed through the grafting of N-containing organic linkers into carboxylate-bridged transition metal networks. A new luminescent

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24

BROWNE, W. "Photochemistry of immobilized photoactive compounds." Coordination Chemistry Reviews 252, no. 23-24 (2008): 2470–79. http://dx.doi.org/10.1016/j.ccr.2008.05.009.

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25

Gulliya, Kirpal S., J. Lester Matthews, R. K. Sharma, Lauren Arnold, Tran Chanh, and Buchard Franck. "Preactivated Photoactive Compounds as Medicinal Agents." Baylor University Medical Center Proceedings 5, no. 4 (1992): 62. http://dx.doi.org/10.1080/08998280.1992.11929804.

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26

Lee, Sudarat, Eli Fahrenkrug, and Stephen Maldonado. "Synthesis of photoactive ZnSnP2 semiconductor nanowires." Journal of Materials Research 30, no. 14 (2015): 2170–78. http://dx.doi.org/10.1557/jmr.2015.195.

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27

Hudson, J. B., E. A. Graham, G. C. Chan, and G. H. N. Towers. "DIFFERENTIAL EFFECTS OF PHOTOACTIVE FURANYL COMPOUNDS ON VIRUS FUNCTIONS." Photochemistry and Photobiology 42, no. 5 (1985): 523–28. http://dx.doi.org/10.1111/j.1751-1097.1985.tb01604.x.

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28

Tyagi, Rahul, Mukesh K. Pandey, Shashwat Malhotra, et al. "Synthesis and Characterization of Photoactive Amphiphilic Polymers." Journal of Macromolecular Science, Part A 44, no. 12 (2007): 1283–87. http://dx.doi.org/10.1080/10601320701608808.

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29

Liu, Wei, Shaoping Bian, Lian Li, Lynne Samuelson, Jayant Kumar, and Sukant Tripathy. "Enzymatic Synthesis of Photoactive Poly(4-phenylazophenol)." Chemistry of Materials 12, no. 6 (2000): 1577–84. http://dx.doi.org/10.1021/cm000072p.

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30

Avó, João, Luís Cunha-Silva, João Carlos Lima, and A. Jorge Parola. "Design and Synthesis of Photoactive Ionic Liquids." Organic Letters 16, no. 10 (2014): 2582–85. http://dx.doi.org/10.1021/ol501111d.

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31

Chudov, K. A., K. S. Levchenko, V. N. Yarovenko, et al. "Synthesis of photoactive 2-aroyl-3-furylbenzofurans." Russian Chemical Bulletin 64, no. 2 (2015): 405–9. http://dx.doi.org/10.1007/s11172-015-0876-8.

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32

Herrero, J., and J. Ortega. "Electrochemical synthesis of photoactive In2Se3 thin films." Solar Energy Materials 16, no. 6 (1987): 477–85. http://dx.doi.org/10.1016/0165-1633(87)90049-9.

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33

Horiguchi, Rumiko, Yasunobu Onishi та Shuzi Hayase. "Diazo‐β‐diketone Photoactive Compounds for KrF Excimer Laser Resists". Journal of The Electrochemical Society 137, № 11 (1990): 3561–68. http://dx.doi.org/10.1149/1.2086268.

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34

Asakawa, Masumi, Peter R. Ashton, Vincenzo Balzani, et al. "Photoactive Azobenzene-Containing Supramolecular Complexes and Related Interlocked Molecular Compounds." Chemistry - A European Journal 5, no. 3 (1999): 860–75. http://dx.doi.org/10.1002/(sici)1521-3765(19990301)5:3<860::aid-chem860>3.0.co;2-k.

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35

Sasaki, Takashi, and James M. Tour. "Synthesis of a New Photoactive Nanovehicle: A Nanoworm." Organic Letters 10, no. 5 (2008): 897–900. http://dx.doi.org/10.1021/ol703027h.

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36

Fujii, Sho, Koichi Kobayashi, Noriko Nagata, Tatsuru Masuda, and Hajime Wada. "Monogalactosyldiacylglycerol Facilitates Synthesis of Photoactive Protochlorophyllide in Etioplasts." Plant Physiology 174, no. 4 (2017): 2183–98. http://dx.doi.org/10.1104/pp.17.00304.

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37

Ho, Bang-Chein, Yeh-Sen Lin, and Yu-Der Lee. "Synthesis and characteristics of organic soluble photoactive polyimides." Journal of Applied Polymer Science 53, no. 11 (1994): 1513–24. http://dx.doi.org/10.1002/app.1994.070531113.

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38

Scuderi, Viviana, Giuliana Impellizzeri, Massimo Zimbone, et al. "Rapid synthesis of photoactive hydrogenated TiO 2 nanoplumes." Applied Catalysis B: Environmental 183 (April 2016): 328–34. http://dx.doi.org/10.1016/j.apcatb.2015.10.055.

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39

Blanche, Pierre-Alexandre. "Special Issue: Photoactive Materials: Synthesis, Applications and Technology." Materials 14, no. 3 (2021): 585. http://dx.doi.org/10.3390/ma14030585.

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40

Wiggs, Robert B., Heidi B. Lobprise, James L. Matthews, and Kripal S. Gulliya. "Effects of Preactivated MC540 in the Treatment of Lymphocytic Plasmacytic Stomatitis in Feline Leukemia virus and Feline Immunodeficiency virus Positive Cats." Journal of Veterinary Dentistry 10, no. 1 (1993): 9–13. http://dx.doi.org/10.1177/089875649301000104.

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Photoactive compounds and drugs are used therapeutically as antibacterial, antiviral and antitumor agents. This report examines the use of a photoactive compound, preactivated merocyanine 540 (pMC540), in the treatment of stomatitis in two cats that are both feline immunodeficiency virus (FIV) positive. One of the cats was also feline leukemia virus (FeLV) positive. Dramatic short term improvement is reported with the dosage regimen and complications.

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41

Arooj, Q., G. J. Wilson, and F. Wang. "Shifting UV-vis absorption spectrum through rational structural modifications of zinc porphyrin photoactive compounds." RSC Advances 6, no. 19 (2016): 15345–53. http://dx.doi.org/10.1039/c5ra25214h.

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42

Glass, Sarah, Tom Rüdiger, Jan Griebel, Bernd Abel, and Agnes Schulze. "Uptake and release of photosensitizers in a hydrogel for applications in photodynamic therapy: the impact of structural parameters on intrapolymer transport dynamics." RSC Advances 8, no. 72 (2018): 41624–32. http://dx.doi.org/10.1039/c8ra08093c.

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43

Muniyandi, Kasipandi, Blassan George, Thangaraj Parimelazhagan, and Heidi Abrahamse. "Role of Photoactive Phytocompounds in Photodynamic Therapy of Cancer." Molecules 25, no. 18 (2020): 4102. http://dx.doi.org/10.3390/molecules25184102.

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Cancer is one of the greatest life-threatening diseases conventionally treated using chemo- and radio-therapy. Photodynamic therapy (PDT) is a promising approach to eradicate different types of cancers. PDT requires the administration of photosensitisers (PSs) and photoactivation using a specific wavelength of light in the presence of molecular oxygen. This photoactivation exerts an anticancer effect via apoptosis, necrosis, and autophagy of cancer cells. Recently, various natural compounds that exhibit photosensitising potentials have been identified. Photoactive substances derived from medic

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44

MIGITAKA, Sonoko, Hajime MORISHITA, Masato ITO, and Nobuaki HAYASHI. "A water-soluble photoresist using diazonium chromate as a photoactive compounds." Journal of Photopolymer Science and Technology 6, no. 1 (1993): 83–86. http://dx.doi.org/10.2494/photopolymer.6.83.

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45

Vayá, Ignacio, Virginie Lhiaubet-Vallet, M. Consuelo Jiménez, and Miguel A. Miranda. "Photoactive assemblies of organic compounds and biomolecules: drug–protein supramolecular systems." Chem. Soc. Rev. 43, no. 12 (2014): 4102–22. http://dx.doi.org/10.1039/c3cs60413f.

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46

Gao, Tai-Bao, Zhong-Ze Qu, Zhe Tang, and Deng-Ke Cao. "Cyclometalated Ir(iii) complexes incorporating a photoactive anthracene-based ligand: syntheses, crystal structures and luminescence switching by light irradiation." Dalton Transactions 46, no. 44 (2017): 15443–50. http://dx.doi.org/10.1039/c7dt02967e.

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Compound aip and its Ir(iii) complexes [Ir(dfppy)<sub>2</sub>(aip)](PF<sub>6</sub>) (1) and [Ir(ppy)<sub>2</sub>(aip)](PF<sub>6</sub>) (2) show light-irradiation-induced luminescence switching behaviors.

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47

Zhou, Yun, David M. King, Jianhua Li, Kathryn S. Barrett, Ron B. Goldfarb, and Alan W. Weimer. "Synthesis of Photoactive Magnetic Nanoparticles with Atomic Layer Deposition†." Industrial & Engineering Chemistry Research 49, no. 15 (2010): 6964–71. http://dx.doi.org/10.1021/ie901712q.

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48

Uddin, M. J., F. Cesano, F. Bonino, et al. "Photoactive TiO2 films on cellulose fibres: synthesis and characterization." Journal of Photochemistry and Photobiology A: Chemistry 189, no. 2-3 (2007): 286–94. http://dx.doi.org/10.1016/j.jphotochem.2007.02.015.

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49

Gol, Reuben, Congzhou Wang, Ram B. Gupta, and Vamsi K. Yadavalli. "Synthesis of self-suspending silica proppants using photoactive hydrogels." Journal of Petroleum Science and Engineering 157 (August 2017): 651–56. http://dx.doi.org/10.1016/j.petrol.2017.07.061.

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50

Murali, M., and A. B. Samui. "Photoactive, liquid-crystalline, hyperbranched benzylidene polyesters: Synthesis and characterization." Journal of Polymer Science Part A: Polymer Chemistry 44, no. 1 (2005): 53–61. http://dx.doi.org/10.1002/pola.21118.

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