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Journal articles on the topic 'Perylene derivatives'

Author: Grafiati

Published: 4 June 2021

Last updated: 22 February 2023

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1

Yang, X., H. J. Räder, A. Rouhanipour, and K. Müllen. "Soft Deposition of Organic Macromolecules with Fast Atom Bombardment Mass Spectrometry." European Journal of Mass Spectrometry 11, no. 3 (June 2005): 287–93. http://dx.doi.org/10.1255/ejms.762.

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In order to investigate the requirements for soft deposition of intact positively charged organic macromolecules, an homogenous series of modal compounds such as polyphenylene dendronized perylenes (PDPs), C80H52, C200H132 and C320H212 and a series of derivatives involving perylene derivative, C98H104N8O4, terrylene derivative, C78H82N6O4 and quaterrylene derivative, C140H138N10O8, were used for soft-landing experiments on a metallic or matrix coated surface using fast atom bombardment mass spectrometry. Soft-landing can be achieved at impact energies below 180 eV with no production of fragments. The deposition rate shows strong energy dependence with similar behavior of the different organic compounds. A single isotope of the molecule was selected and soft-landed at increased resolution.

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2

Gutman, Ivan, Boris Furtula, Jelena Djurdjevic, Rradmila Kovacevic, and Sonja Stankovic. "Annelated perylenes: Benzenoid molecules violating the Kekulé-structure-based cyclic conjugation models." Journal of the Serbian Chemical Society 70, no. 8-9 (2005): 1023–32. http://dx.doi.org/10.2298/jsc0509023g.

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Several currently used models for assessing the extent of cyclic conjugation in benzenoid hydrocarbons, all based on Kekul?-type structural formulas predict that there is no cyclic conjugation in the central, "empty", ring of perylene and its annelated derivatives. In this paper it is shown that in some annelated perylenes the cyclic conjugation in the "empty" ring (measured by its energy-effect) may be unexpectedly high. Therefore, in the case of these annelated perylenes, the Kekul?- structure-based models fail. The cause for such an "anomalous" behavior of annelated perylenes is discussed.

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3

Fang, Xiangdong. "BN-Embedded Perylenes." Molecules 26, no. 23 (November 25, 2021): 7148. http://dx.doi.org/10.3390/molecules26237148.

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Transition metal catalyzed coupling reaction strategy has been utilized in the synthesis of two novel BN-perylenes starting from halogenated BN-naphthalene derivatives. The molecular structures and packing modes of BN-perylenes were confirmed by NMR spectroscopy and X-ray single-crystal diffraction experiments. Their photophysical properties were further investigated using UV-vis and fluorescence spectroscopy and DFT calculations. Interestingly, the isosteric BN-insertion in perylene system resulted in stronger π-π stacking interaction both in solid and solution phases. The synthesized BN-perylenes are proved to be highly stable and thus provide a new valuable platform for novel organic materials applications which is otherwise inaccessible to date.

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4

Ling, Cheng, Miao, Zhang, Zhang, and Zhu. "Synthesis and Photocontrolled Supramolecular Self-Assembly of Azobenzene-Functionalized Perylene Bisimide Derivatives." Polymers 11, no. 7 (July 3, 2019): 1143. http://dx.doi.org/10.3390/polym11071143.

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Azobenzene (Azo) units were successfully introduced into perylene bisimide (PBI) structures in order to realize the photocontrolling of the morphology of the supramolecular assembly of PBI by a photoisomerization process. A total of three Azo-functionalized perylene bisimide derivatives (PBI1, PBI2, and PBI3) with different alkyl chain lengths were designed and synthesized by imidization of 3,4,9,10-perylene tetracarboxylic dianhydride with the corresponding amines. The structures of these compounds were characterized by proton nuclear magnetic resonance (1H NMR) and matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS). The photoisomerization behaviors of Azo units in PBIs were investigated using ultraviolet-visible (UV-VIS) absorption spectroscopy, which were obviously effected by solvents and the alkyl chain length. Furthermore, the photoisomerization of Azo units has the obviously regulatory effect on the morphology of supramolecular assembly of PBIs, especially for the medium-length alkyl chain-linked Azo-functionalized PBI derivative (PBI2). This research realized the photocontrolling of the morphology of the supramolecular assembly of PBI derivatives by photoisomerization of Azo units.

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5

Sato, Yuzuru, Akiko Ozaki, Masahiro Hosaka, Tomohisa Moriguchi, and Kazuo Shinozuka. "Synthesis and Properties of Fluorescent Biological Molecules Labeled with Novel Silylated Perylene Derivative." Key Engineering Materials 459 (December 2010): 63–66. http://dx.doi.org/10.4028/www.scientific.net/kem.459.63.

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We have synthesized novel perylene derivatives bearing a silyl function with modifiable functional groups as a feasible material for visualizing biological substances. The fluorescent perylene derivative was coupled to C-5 position of pyrimidine nucleotide and the nucleotide was subsequently incorporated to the middle position of oligoDNA using an automated DNA synthesizer. Also, the derivative was coupled with a cholesterol analog with different length of linking alkyl function. The resulting modified fluorescent oligoDNA exhibited a small change in its fluorescent signal upon hybridization with the complementary oligoDNA. While the cholesterol analogs bearing the silylated perylene exhibited marked fluorescent signal in living cells. The signal is stronger in the analog having longer linker function compared to the analog having shorter linker function. In each case, however, the signal was much prominent compared to that of dehydroergosterol (DHE), a fluorescent cholesterol analog widely used in biological study.

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6

Leowanawat, Pawaret, Agnieszka Nowak-Król, and Frank Würthner. "Tetramethoxy-bay-substituted perylene bisimides by copper-mediated cross-coupling." Organic Chemistry Frontiers 3, no. 5 (2016): 537–44. http://dx.doi.org/10.1039/c6qo00047a.

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CuBr-mediated cross-coupling of 1,6,7,12-tetrabromo-perylene-3,4,9,10-tetracarboxylic acid ester or bis(dicarboximide) with NaOMe affords the respective tetramethoxy-perylene derivatives which are excellent green and red emitters.

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7

Kitazume, Koji, Yu Chen, Mitsunari Itou, Yasuyuki Araki, Satoshi Uchida, and Osamu Ito. "Photoinduced electron-transfer processes between phthalocyanines and perylene derivatives." Journal of Porphyrins and Phthalocyanines 10, no. 10 (October 2006): 1190–96. http://dx.doi.org/10.1142/s1088424606000557.

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Photoinduced electron-transfer processes between phthalocyanines ( H2Pc and ZnPc ) as electron donors and perylene derivatives as electron acceptors have been studied using a time-resolved, nanosecond transient absorption method in benzonitrile. The observed findings show that intermolecular electron transfer takes place via the excited triplet states of ZnPc and H2Pc , as confirmed by the characteristic transient absorption bands in the near-IR region. The visible light excitation of the mixtures of H2Pc and the perylene derivatives adsorbed onto TiO2gave a relatively high photovoltaic efficiency.

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8

Jozeliūnaitė, Augustina, Romualdas Striela, Linas Labanauskas, and Edvinas Orentas. "Practical Preparation of Octa- and Tetrabromoperylene Diimides and Derivatives Thereof." Synthesis 49, no. 23 (August 2, 2017): 5176–82. http://dx.doi.org/10.1055/s-0036-1589088.

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A mild synthesis of fully brominated perylene dianhydride and diimides in one step from easily available unsubstituted precursors is presented. The partial reduction of ortho-bromo substituents with hydrazine hydrate allowed for a gram-scale synthesis of a valuable intermediate, 1,6,7,12-tetrabromoperylene diimide. Several new twisted fully core-substituted perylene diimide derivatives having sulfur, nitrogen, or oxygen substituents were synthesized using regioselective nucleophilic substitution reactions.

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9

Hemalatha, C. N., and A. M. Vijey. "3D QSAR AND DOCKING STUDY OF PERYLENE - DI IMIDES ANALOGUES AS POTENT APOPTOSIS INDUCER AND EFFICACIOUS ANTICANCER AGENT." INDIAN DRUGS 54, no. 12 (December 28, 2017): 15–27. http://dx.doi.org/10.53879/id.54.12.11012.

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The human telomeric G-Quadruplex structure is a promising target for the design of cancer drugs. The aim of this study was to investigate the anti-cancer activity of perylene derivatives by using in silico computational approach. The perylene derivatives are designed by QSAR studies using VLife MDS Software and activities for these new compounds are predicted. The best predicted activity compounds are screened by G-Quadruplex Ligand Database. Around 59 compounds are selected for docking study. Molecular docking using G-Quadruplex Ligand Database has been carried out and from the study 9 compounds showed high binding affinities for the targets. Finally, from the QSAR and docking studies, 2 compounds showed good biological activity, possessing a strong correlation coefficient, endorsing the fact that perylene derivatives are having strong affinity with the targets. With these compounds, we also observed best pKi values, which shows that they inhibit the targets and may be effective for anti-cancer therapy.

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10

Xue, CAI, QI Dong-Dong, ZHANG Yue-Xing, BIAN Yong-Zhong, and JIANG Jian-Zhuang. "Semiconductor Properties of Perylene Diimide Derivatives." Acta Physico-Chimica Sinica 26, no. 04 (2010): 1059–64. http://dx.doi.org/10.3866/pku.whxb20100421.

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11

De Boni, L., C. J. L. Constantino, L. Misoguti, R. F. Aroca, S. C. Zilio, and C. R. Mendonça. "Two-photon absorption in perylene derivatives." Chemical Physics Letters 371, no. 5-6 (April 2003): 744–49. http://dx.doi.org/10.1016/s0009-2614(03)00359-2.

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12

Dahan, Elianne, and Pudupadi R. Sundararajan. "Polymer compatibilized self-assembling perylene derivatives." European Polymer Journal 65 (April 2015): 4–14. http://dx.doi.org/10.1016/j.eurpolymj.2014.11.022.

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13

Franceschin, Marco, Antonello Alvino, Giancarlo Ortaggi, and Armandodoriano Bianco. "New hydrosoluble perylene and coronene derivatives." Tetrahedron Letters 45, no. 49 (November 2004): 9015–20. http://dx.doi.org/10.1016/j.tetlet.2004.10.040.

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14

Zhu, Lei, Ying Wang, Wenguang Wang, Xianyao Wu, and Ti Wu. "Synthesis and research of a kind of perylene imide discoid molecule." Journal of Physics: Conference Series 2226, no. 1 (March 1, 2022): 012007. http://dx.doi.org/10.1088/1742-6596/2226/1/012007.

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Abstract Discotic liquid crystal molecules are excellent organic semiconductor materials due to their high carrier mobility. Dibenzocoronene derivatives obtained by nuclear expansion with perylene diimide as a matrix are one of the discotic molecules. The key factor for the application of this type of molecule is that it can form stable and long-range ordered organic nano-scale thin films. It can be used as an efficient carrier transport channel. This paper intends to use the “channel effect” to obtain the corresponding long-range orderly ideal film. The “channeling effect” referred to in this article is to bond functional discoid molecules on the substrate firstly, than generate the corresponding self-assembled monomolecular membranes (SAMs) to form an ordered channel on the surface which strongly induces and restricts the discoid molecules that arranged in parallel and orderly with each other along the “channels” created on the surface of the SAMs. Perylene diimide derivatives are a kind of good electron transport materials, which are characterized by high carrier mobility, low processing cost, and good thermal stability. However, it has the large rigid core and the melting point is relatively high. In this paper, a monobenzocoperylene diimide derivative is designed and synthesized, which will have a strong effect on the surface of the silicon substrate, and reduce the molecular melting point by reducing the size of the perylene imide discotic molecular core expansion.

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15

Aydin, Edanur, Bilal Nisanci, Murat Acar, Arif Dastan, and Özgür Altan Bozdemir. "Synthesis and use of “clickable” bay-region tetrasubstituted perylene tetracarboxylic tetraesters and a perylene monoimide diester as energy acceptors." New Journal of Chemistry 39, no. 1 (2015): 548–54. http://dx.doi.org/10.1039/c4nj01565g.

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16

Zhu, Mingguang, Hongyu Guo, Fafu Yang, and Zusheng Wang. "Synthesis, mesomorphic and photophysical properties of novel triads and pentads of perylene liquid crystals with cholesterol units at the bay-position." RSC Advances 7, no. 8 (2017): 4320–28. http://dx.doi.org/10.1039/c6ra27003d.

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17

Fuller, C. A., and C. E. Finlayson. "Solvatochromism in perylene diimides; experiment and theory." Physical Chemistry Chemical Physics 19, no. 47 (2017): 31781–87. http://dx.doi.org/10.1039/c7cp05039a.

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18

Kang, Rui, Rong Miao, Yanyu Qi, Xingmao Chang, Congdi Shang, Li Wang, and Yu Fang. "Tuning the formation of reductive species of perylene-bisimide derivatives in DMF via aggregation matter." Chemical Communications 53, no. 72 (2017): 10018–21. http://dx.doi.org/10.1039/c7cc05645a.

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19

Madhurima, V., K. Greeshma Priyanka, K. S. N. D. Pavan, and S. Nagarajan. "Analysis of Wetting of Perylene Diimide Thin Films-on-Glass by Water." Key Engineering Materials 594-595 (December 2013): 1074–77. http://dx.doi.org/10.4028/www.scientific.net/kem.594-595.1074.

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Perylene tetracarboxylic diimide (PTCDI), derivatives have attracted the attention of the scientific community owing to their thermal stability, electron affinity-enabling n-type semiconductor behaviour and useful photophysical properties. Thin films of six new perylene tetracarboxylic diimides were fabricated on glass substrate by spin coating. The contact angles made by water on these six substrates, some with alkyl chain derivatives and the others with polar side chains, were measured using a precision contact angle goniometer. The alignment of these films on glass substrates are inferred from the contact angle data and the results are compared with those of the (self) alignment in liquid state. Derivatives with alkyl chains were seen to interact more with water, causing a lower contact angle compared to the more polar derivatives. This counter-intuitive result is interpreted in terms of molecular alignment of samples on the glass substrates.

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20

Guo, Zongxia, Kun Wang, Ping Yu, Shengyue Zhang, Kai Sun, and Zhibo Li. "Role of intrinsic hydrogen bonds in the assembly of perylene imide derivatives in solution and at the liquid–solid interface." Physical Chemistry Chemical Physics 19, no. 34 (2017): 23007–14. http://dx.doi.org/10.1039/c7cp04928e.

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21

Svetlova, Julia, Ekaterina Knizhnik, Valentin Manuvera, Vyacheslav Severov, Dmitriy Shirokov, Ekaterina Grafskaia, Pavel Bobrovsky, et al. "Nucleoside Analogs and Perylene Derivatives Modulate Phase Separation of SARS-CoV-2 N Protein and Genomic RNA In Vitro." International Journal of Molecular Sciences 23, no. 23 (December 3, 2022): 15281. http://dx.doi.org/10.3390/ijms232315281.

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The life cycle of severe acute respiratory syndrome coronavirus 2 includes several steps that are supposedly mediated by liquid–liquid phase separation (LLPS) of the viral nucleocapsid protein (N) and genomic RNA. To facilitate the rational design of LLPS-targeting therapeutics, we modeled N-RNA biomolecular condensates in vitro and analyzed their sensitivity to several small-molecule antivirals. The model condensates were obtained and visualized under physiological conditions using an optimized RNA sequence enriched with N-binding motifs. The antivirals were selected based on their presumed ability to compete with RNA for specific N sites or interfere with non-specific pi–pi/cation–pi interactions. The set of antivirals included fleximers, 5′-norcarbocyclic nucleoside analogs, and perylene-harboring nucleoside analogs as well as non-nucleoside amphiphilic and hydrophobic perylene derivatives. Most of these antivirals enhanced the formation of N-RNA condensates. Hydrophobic perylene derivatives and 5′-norcarbocyclic derivatives caused up to 50-fold and 15-fold enhancement, respectively. Molecular modeling data argue that hydrophobic compounds do not hamper specific N-RNA interactions and may promote non-specific ones. These findings shed light on the determinants of potent small-molecule modulators of viral LLPS.

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22

Tucker, Sheryl A., William E. Acree, John C. Fetzer, and Reginald H. Mitchell. "Polycyclic Aromatic Hydrocarbon Solute Probes. Part X: Evaluation of Select Hydrogenated Pyrene, Benzo[ghi]perylene, and Naphthacene Derivatives as Possible Solvent Polarity Probes." Applied Spectroscopy 47, no. 7 (July 1993): 1040–45. http://dx.doi.org/10.1366/0003702934415200.

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Fluorescence emission spectra are reported for 3,4,5-trihydrobenzo[cd]pyrene, 3,4-dihydrobenzo[ghi]perylene, 5,6,7,8,9,10-hexahydrobenzo[ghi]perylene, trans-10b,10c-dihydro-10b,10c-dimethylpyrene, trans-12b,12c-dihydro-12b,12c-dimethylbenzo[a]pyrene, and trans-14b,14c-dihydro-14b,14c-dimethylnaphtho[2,1,8-qra]naphthacene dissolved in organic nonelectrolyte solvents of varying polarity. Dihydrobenzo|ghi]perylene was found to exhibit probe character, as evidenced by a systematic variation in emission intensity ratio with solvent polarity. It has a dynamic range of 0.98 and a high fluorescence quantum yield and is thought to be noncarcinogenic. Also reported are mathematical expressions which correlate measured intensity ratios and solvent polarity probe behavior of dihydrobenzo[ghi]perylene, pyrene, benzo[ghi]perylene, coronene, and ovalene in 48 solvents of varying polarity.

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23

Berner, Nina C., Sinéad Winters, Claudia Backes, Chanyoung Yim, Kim C. Dümbgen, Izabela Kaminska, Sebastian Mackowski, Attilio A. Cafolla, Andreas Hirsch, and Georg S. Duesberg. "Understanding and optimising the packing density of perylene bisimide layers on CVD-grown graphene." Nanoscale 7, no. 39 (2015): 16337–42. http://dx.doi.org/10.1039/c5nr04772b.

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24

Huang, Yongwei, Weiguang Zhang, Haiyan Zhai, and Chunli Li. "Alkylsilane-functionalized perylenediimide derivatives with differential gas sensing properties." Journal of Materials Chemistry C 3, no. 2 (2015): 466–72. http://dx.doi.org/10.1039/c4tc02059f.

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25

Wang, Ya'nan, Chong Wang, Yuming Qi, Guokai Li, Xiaoliu Li, and Kerang Wang. "Microwave-Assisted Synthesis of Perylene Monoimide Derivatives." Chinese Journal of Organic Chemistry 41, no. 2 (2021): 702. http://dx.doi.org/10.6023/cjoc202008010.

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26

Ni, Jing Ping, and Yasukiyo Ueda. "Structures of Perylene Derivatives in Thin Film." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 316, no. 1 (May 1998): 341–46. http://dx.doi.org/10.1080/10587259808044524.

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27

van de Craats, A. M., J. M. Warman, P. Schlichting, U. Rohr, Y. Geerts, and K. Müllen. "Charge transport in mesomorphic derivatives of perylene." Synthetic Metals 102, no. 1-3 (June 1999): 1550–51. http://dx.doi.org/10.1016/s0379-6779(98)00554-2.

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28

Smieska, Louisa M., Zhong Li, David Ley, Adam B. Braunschweig, and John A. Marohn. "Trap-clearing Spectroscopy in Perylene Diimide Derivatives." Chemistry of Materials 28, no. 3 (February 2016): 813–20. http://dx.doi.org/10.1021/acs.chemmater.5b04025.

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29

Kampen, T. U., G. Salvan, A. Paraian, C. Himcinschi, A. Yu Kobitski, M. Friedrich, and D. R. T. Zahn. "Orientation of perylene derivatives on semiconductor surfaces." Applied Surface Science 212-213 (May 2003): 501–7. http://dx.doi.org/10.1016/s0169-4332(03)00390-8.

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30

Schlichting, Peter, Ulrike Rohr, and Klaus Müllen. "Easy synthesis of liquid crystalline perylene derivatives." Journal of Materials Chemistry 8, no. 12 (1998): 2651–55. http://dx.doi.org/10.1039/a804332i.

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31

Kaur, Balwinder, Nurul Quazi, Ivan Ivanov, and S. N. Bhattacharya. "Near-infrared reflective properties of perylene derivatives." Dyes and Pigments 92, no. 3 (March 2012): 1108–13. http://dx.doi.org/10.1016/j.dyepig.2011.06.011.

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32

Göltner, Christine, Dietmar Pressner, Klaus Müllen, and Hans Wolfgang Spiess. "Liquid-Crystalline Perylene Derivatives as“Discotic Pigments”." Angewandte Chemie International Edition in English 32, no. 11 (November 1993): 1660–62. http://dx.doi.org/10.1002/anie.199316601.

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33

Funahashi, Masahiro, and Akinari Sonoda. "Electron transport characteristics in nanosegregated columnar phases of perylene tetracarboxylic bisimide derivatives bearing oligosiloxane chains." Phys. Chem. Chem. Phys. 16, no. 17 (2014): 7754–63. http://dx.doi.org/10.1039/c4cp00579a.

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34

Dubey, Rajeev K., Nick Westerveld, Ernst J. R. Sudhölter, Ferdinand C. Grozema, and Wolter F. Jager. "Novel derivatives of 1,6,7,12-tetrachloroperylene-3,4,9,10-tetracarboxylic acid: synthesis, electrochemical and optical properties." Organic Chemistry Frontiers 3, no. 11 (2016): 1481–92. http://dx.doi.org/10.1039/c6qo00374e.

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35

Li, Xiangguang, Zhiwei Zheng, Wei Jiang, Wenjun Wu, Zhaohui Wang, and He Tian. "New D–A–π–A organic sensitizers for efficient dye-sensitized solar cells." Chemical Communications 51, no. 17 (2015): 3590–92. http://dx.doi.org/10.1039/c4cc08539f.

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36

Zhang, Fengxia, Xianqiang Huang, Xiaofeng Wei, Huixue Ren, Tianyi Jiang, Xuemei Li, Junsen Wu, and Yongshan Ma. "Synthesis and properties of bay unilaterally extended and mono-substituted perylene diimides." Journal of Chemical Research 44, no. 1-2 (November 14, 2019): 60–66. http://dx.doi.org/10.1177/1747519819886502.

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The synthesis of two sulfur-decorated perylene diimides, the five-membered S-heterocyclic annulated perylene diimide (1) and 1-propanethiol- N,N′-dicyclohexylperylene-3,4,9,10-tetracarboxylic diimide (2), and a novel sulfoxide-containing perylene diimide, 1-propyl sulfoxide- N,N′-dicyclohexylperylene-3,4,9,10-tetracarboxylic diimide (3), are reported. The photophysical, electrochemical, aggregation, and thermal properties of these compounds are investigated by ultraviolet visible absorption, fluorescence, cyclic voltammetric, X-ray diffraction, and thermogravimetric analysis techniques. The geometries of the compounds are optimized at the 6-31G* level of theory using density functional theory, and their potentials are correlated with molecular orbitals. The prepared perylene diimide derivatives exhibit narrow the highest occupied molecular orbitals and the lowest unoccupied molecular orbitals band gaps, and they have quite different absorptions and emissions in dichloromethane solutions, which are in agreement with the density functional theory–calculated results.

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37

Tokuo, Kokichi, Hayato Sakai, Tomo Sakanoue, Taishi Takenobu, Yasuyuki Araki, Takehiko Wada, and Taku Hasobe. "Control of the electrochemical and photophysical properties of N-substituted benzo[ghi]perylene derivatives." Materials Chemistry Frontiers 1, no. 11 (2017): 2299–308. http://dx.doi.org/10.1039/c7qm00301c.

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38

Fujimoto, Keisuke, Masaki Takahashi, Seiichiro Izawa, and Masahiro Hiramoto. "Development of Perylene-Based Non-Fullerene Acceptors through Bay-Functionalization Strategy." Materials 13, no. 9 (May 6, 2020): 2148. http://dx.doi.org/10.3390/ma13092148.

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Perylene has had a tremendous impact in the history of material research for the molecular semiconductors. Among numerous derivatives of this polyaromatic hydrocarbon, perylene diimide (PDI) represents a promising class of organic materials envisioned as non-fullerene acceptors (NFAs) for the practical organic photovoltaic (OPV) applications due to their enhanced photo- and thermal stability and remarkably high electron affinity, some of which realize band-like transport properties. The present review guides some of the representative achievements in the development of rationally designed PDI systems, highlighting synthetic methodologies based on bay-functionalization strategies for creating well-designed molecular nanostructures and structure-performance relationship of perylene-based small molecular acceptors (SMAs) for the photovoltaic outcomes.

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39

Funahashi, Masahiro, Nozomi Takeuchi, and Akinari Sonoda. "A liquid-crystalline perylene tetracarboxylic bisimide derivative bearing trisiloxan-2-yl moieties: influence on mesomorphic properties and electron transport." RSC Advances 6, no. 22 (2016): 18703–10. http://dx.doi.org/10.1039/c5ra23119a.

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Mesomorphic and electron transport properties are compared for liquid-crystalline perylene tetracarboxylic bisimide derivatives bearing linear disiloxane and trisiloxane chains, as well as trisiloxan-2-yl groups.

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40

Langhals, Heinz, and Tim Pust. "Fluorescent Nano pH Indicators Based on Supramolecular Interactions." Zeitschrift für Naturforschung B 65, no. 3 (March 1, 2010): 291–94. http://dx.doi.org/10.1515/znb-2010-0310.

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Lipophilic pH-sensitive perylene derivatives were combined with detergents in a supramolecular arrangement to obtain nanomicelles that can be applied as fluorescent pH indicators for the aqueous phase.

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41

Aksoy, Erkan, Nuriye Demi̇r, and Canan Varlikli. "White LED light production using dibromoperylene derivatives in down conversion of energy." Canadian Journal of Physics 96, no. 7 (July 2018): 734–39. http://dx.doi.org/10.1139/cjp-2017-0752.

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Perylene derivatives of N,N′-bis(2,6-diisopropylphenyl)-1,6(7)-dibromoperylene-3,4,9,10-tetracarboxylic diimide (DBrPDI) and 1,7-dibromo perylene-3,4,9,10-tetracarboxylic acid butyl ester (DBrPTE) were synthesized, and their structural and optical characterizations were explored. Both DBrPDI and DBrPTE, which were utilized as wavelength converters on a GaN/InGaN based blue LED, were singlet sensitizers and had molar absorptivity constants around 104 Lmol−1cm−1. The blue LED that was used had Commission internationale de l’eclairage (CIE) coordinates of x, y = 0.13, 0.06; power and luminous efficiencies of 2.7 lm/W and 6.6 cd/A @5 mA, respectively. Because the fluorescence quantum yield of DBrPDI was much higher than that of DBrPTE, a meaningful white light efficiency was obtained with the diimide derivative. The use of DBrPDI resulted in white light with CIE coordinates of x, y = 0.34, 0.29 and luminous efficiency of 6.35 cd/A @5 mA, respectively. Using DBrPDI in a resin matrix resulted in more than three orders of magnitude increase in the luminous efficiency value (23.0 cd/A @5 mA) while the CIE coordinates remained the same. Whenever the applied current reached 20 mA, a CRI value of Ra = 90 was obtained.

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42

Bui, Anh Thy, Clotilde Philippe, Maxime Beau, Nicolas Richy, Marie Cordier, Thierry Roisnel, Loïc Lemiègre, Olivier Mongin, Frédéric Paul, and Yann Trolez. "Synthesis, characterization and unusual near-infrared luminescence of 1,1,4,4-tetracyanobutadiene derivatives." Chemical Communications 56, no. 24 (2020): 3571–74. http://dx.doi.org/10.1039/c9cc09560h.

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Two 1,1,4,4-tetracyanobutadiene (TCBD) derivatives were prepared by reaction of tetracyanoethylene with ynamides bearing either a pyrene or a perylene unit. They display luminescence that could be detected up to 1350 nm in the solid state.

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43

Yang, Liu, Zhiwei Zheng, Yan Li, Wenjun Wu, He Tian, and Zhaohui Wang. "N-Annulated perylene-based metal-free organic sensitizers for dye-sensitized solar cells." Chemical Communications 51, no. 23 (2015): 4842–45. http://dx.doi.org/10.1039/c5cc00650c.

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A series of novel metal-free organic sensitizers based on N-annulated perylene derivatives have been conveniently synthesized, and the DSCs exhibit overall conversion efficiencies ranging from 4.90% to 8.28%.

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44

Kaur, Sandeep, Manoj Kumar, and Vandana Bhalla. "AIEE active perylene bisimide supported mercury nanoparticles for synthesis of amides via aldoximes/ketoximes rearrangement." Chemical Communications 51, no. 19 (2015): 4085–88. http://dx.doi.org/10.1039/c4cc10273h.

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AIEE active perylene bisimide derivatives 3 serve as reactors and stabilizers for the preparation of HgNPs which exhibit high catalytic efficiency in the synthesis of amides via aldoximes/ketoximes rearrangement.

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45

Torres, Érica, Rafal Bogel-Lukasik, Mário Nuno Berberan-Santos, Stefan Höfle, Alexander Colsmann, and Maria João Brites. "N,N′-Diaryl-perylene-3,9-diamine derivatives: synthesis, characterization and electroluminescence properties." RSC Advances 6, no. 109 (2016): 107180–88. http://dx.doi.org/10.1039/c6ra20126a.

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In this work, N,N′-diaryl-perylene-3,9-diamine (PDA) derivatives featuring different alkoxyl substituents at para position of the N-aryl rings were synthesized and employed as emitters in solution processed organic light emitting diodes.

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46

Wang, Wen Guang, Xu Ying Liu, Ling Liu, and Jia Ling Pu. "Design, Synthesis and Properties of Asymmetric Substituted Coronene Derivative as Discotic Liquid Crystal." Key Engineering Materials 428-429 (January 2010): 75–78. http://dx.doi.org/10.4028/www.scientific.net/kem.428-429.75.

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Asymmetric substituted coronenes as building blocks for preparation of materials used as functional molecular devices in the fields of self-organization, organic light-emitting diode, photovoltaic solar cell and field effect transistor are easily converted to potential interesting coronene’s derivatives. A novel kind of derivative of dibenzocoronene with perylene tetracarboxdiimide as discotic liquid crystal with two kinds of soft and long chains was designed and synthesized. Its structure was confirmed by 1HNMR and IR. Its UV-vis was measured. Its properties as discotic liquid crystal are investigated in progress.

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47

Johansson, Lennart B.-�. "Limiting fluorescence anisotropies of perylene and xanthene derivatives." Journal of the Chemical Society, Faraday Transactions 86, no. 12 (1990): 2103. http://dx.doi.org/10.1039/ft9908602103.

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48

Wang, Shu, Yuliang Li, Chimin Du, Zhiqiang Shi, Shengxiong Xiao, Daoben Zhu, Enqin Gao, and Shengmin Cai. "Dye sensitization of nanocrystalline TiO2 by perylene derivatives." Synthetic Metals 128, no. 3 (May 2002): 299–304. http://dx.doi.org/10.1016/s0379-6779(02)00007-3.

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49

Icil, Huriye. "Energy Transfer Studies with Perylene bis-Diimide Derivatives." Spectroscopy Letters 31, no. 4 (June 1998): 747–55. http://dx.doi.org/10.1080/00387019808007396.

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50

Sato, Kazuyuki, Kazuyuki Hino, Hiroo Takahashi, and Jin Mizuguchi. "Hydrogen gas sensor based upon perylene-imide derivatives." International Journal of Intelligent Systems Technologies and Applications 3, no. 1/2 (2007): 52. http://dx.doi.org/10.1504/ijista.2007.014126.

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