Relevant bibliographies by topics / Diimides

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Diimides'

Author: Grafiati
Published: 4 June 2021
Last updated: 27 July 2025

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Journal articles on the topic "Diimides"

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Nakano, Masahiro, Kyohei Nakano, Kazuo Takimiya, and Keisuke Tajima. "Two isomeric perylenothiophene diimides: physicochemical properties and applications in organic semiconducting devices." Journal of Materials Chemistry C 7, no. 8 (2019): 2267–75. http://dx.doi.org/10.1039/c8tc05577g.

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Two thiophene-fused perylene-3,4,9,10-tetracarboxy diimides, peryleno[2,1-b]thiophene diimide (PTIa) and peryleno[1,2-b]thiophene diimide (PTIb), were synthesized as electron-deficient building units for electronic and optoelectronic materials.
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Zou, Lin, Xiao-Ye Wang, Xiao-Xiao Zhang, et al. "Toward electron-deficient pyrene derivatives: construction of pyrene tetracarboxylic diimide containing five-membered imide rings." Chemical Communications 51, no. 63 (2015): 12585–88. http://dx.doi.org/10.1039/c5cc04860e.

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Electron-deficient pyrene-1,2,6,7-tetracarboxylic diimide (PyrDI) and pyrene-4,9-dicyano-1,2,6,7-tetracarboxylic diimide (PyrDI-CN) containing five-membered imide rings have been designed and synthesized as a new family of aromatic diimides.
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Kramer, Wolfgang H., Donya Razinoubakht, Gurjit Kaur, et al. "Awakening a Molecular Mummy: The Inter-and Intramolecular Photochemistry of Pyromellitic Diimides with Alkyl Carboxylates." Photochem 2, no. 3 (2022): 717–32. http://dx.doi.org/10.3390/photochem2030046.

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Pyromellitic acid diimides are not as chemically unreactive as conjecturable (and presupposed) from their numerous applications as electron acceptor units or electron carriers in molecular donor–acceptor dyads or triads. Similar to the corresponding phthalimides, electronically excited pyromellitic diimides oxidize alkyl carboxylates in aqueous solution via intermolecular electron transfer (PET) processes, which eventually results in radical–radical combination products, e.g., the benzylation product 6 from N,N′-dimethyl pyromellitic diimide 5. The analogous product 7 was formed with pivalic a
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Jozeliūnaitė, Augustina, Romualdas Striela, Linas Labanauskas, and Edvinas Orentas. "Practical Preparation of Octa- and Tetrabromoperylene Diimides and Derivatives Thereof." Synthesis 49, no. 23 (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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Martin, Max M., Carolin Dusold, Andreas Hirsch, and Norbert Jux. "Porphyrin-rylene-diimide-hexabenzocoronene triads." Journal of Porphyrins and Phthalocyanines 24, no. 01n03 (2020): 268–77. http://dx.doi.org/10.1142/s1088424619500810.

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Hexa-peri-hexabenzocoronenes (HBCs), substituted by two different chromophores in an ortho arrangement, were synthesized for the first time and investigated towards their photophysical properties. Rylene-diimide dyes, in particular naphthalene-diimides (NDIs) and perylene-diimides (PDIs), were attached to the HBC as the first, and porphyrins as the second chromophore. Therefore, porphyrin-NDI-HPB as well as porphyrin-PDI-HPB precursors were accessed and converted into the respective HBC derivatives applying oxidative Scholl conditions. UV-vis absorption and fluorescence emission spectroscopy s
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Zhang, Fengxia, Xianqiang Huang, Xiaofeng Wei, et al. "Synthesis and properties of bay unilaterally extended and mono-substituted perylene diimides." Journal of Chemical Research 44, no. 1-2 (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 ge
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Pirota, Valentina, Matteo Nadai, Filippo Doria, and Sara Richter. "Naphthalene Diimides as Multimodal G-Quadruplex-Selective Ligands." Molecules 24, no. 3 (2019): 426. http://dx.doi.org/10.3390/molecules24030426.

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G-quadruplexes are four-stranded nucleic acids structures that can form in guanine-rich sequences. Following the observation that G-quadruplexes are particularly abundant in genomic regions related to cancer, such as telomeres and oncogenes promoters, several G-quadruplex-binding molecules have been developed for therapeutic purposes. Among them, naphthalene diimide derivatives have reported versatility, consistent selectivity and high affinity toward the G-quadruplex structures. In this review, we present the chemical features, synthesis and peculiar optoelectronic properties (absorption, emi
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Andric, Goja, John F. Boas, Alan M. Bond, et al. "Spectroscopy of Naphthalene Diimides and Their Anion Radicals." Australian Journal of Chemistry 57, no. 10 (2004): 1011. http://dx.doi.org/10.1071/ch04130.

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Naphthalene diimides 1–4 having different N,N-disubstitution undergo single electron reduction processes either chemically or electrochemically to yield the corresponding radical anion in high yield. This study concentrates on 1, bearing pentyl side chains connected through the diimide nitrogens, and compares the results obtained against those bearing isopropyl, propargyl, and phenylalanyl side chains. Compound 1 exhibits mirror image absorption and fluorescence in the near-UV region in CH2Cl2 and dimethylformamide that is typical of monomeric N,N-dialkyl-substituted naphthalene diimides. In t
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Insuasty, Alberto, Serena Carrara, Linjing Tang, et al. "A Family of Heterocyclic Naphthalene Diimide (NDI) Analogues: Comparing Parent Isoquinoline Diimides and Phthalazine Diimides with NDI." ChemPlusChem 84, no. 10 (2019): 1638–42. http://dx.doi.org/10.1002/cplu.201900596.

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Reiß, Barbara, and Hans-Achim Wagenknecht. "Naphthalene diimides with improved solubility for visible light photoredox catalysis." Beilstein Journal of Organic Chemistry 15 (August 27, 2019): 2043–51. http://dx.doi.org/10.3762/bjoc.15.201.

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Five core-substituted naphthalene diimides bearing two dialkylamino groups were synthesized as potential visible light photoredox catalysts and characterized by methods of optical spectroscopy and electrochemistry in comparison with one unsubstituted naphthalene diimide as reference. The core-substituted naphthalene diimides differ by the alkyl groups at the imide nitrogens and at the nitrogens of the two substituents at the core in order to enhance their solubility in DMF and thereby enhance their photoredox catalytic potential. The 1-ethylpropyl group as rather short and branched alkyl subst
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Dissertations / Theses on the topic "Diimides"

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Quinn, Samuel. "Colouring naphthalene diimides." Thesis, University of Nottingham, 2018. http://eprints.nottingham.ac.uk/50038/.

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Naphthalene diimides have been explored in a wide variety of ways; They are a promising candidate for organic electronics, boasting the ability to form n-type semiconductor materials, the stability of their anions further aiding in this regard. Their electron poor aromatic core can be used in host guest chemistry to generate interlocked species. The ability to tune their electronic properties and how this could be manipulated to create photovoltaic devices is primarily focus of this thesis. A series of naphthalene diimides substituted at the core with morpholine moieties have been synthesized
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Kim, Michelle B. "The Hydrolysis of Naphthalene Diimides." Digital Archive @ GSU, 2007. http://digitalarchive.gsu.edu/chemistry_theses/7.

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The hydrolyses of naphthalene diimides (NDIs) bearing aliphatic side chains with N-methylpyrrolidinium groups placed two (1) and three (5) atoms from the central core were studied. The Ka values for the first and second hydrolyses for 1 were 2.5 ± 0.2 x 105 M-1 and 2.0 ± 0.1 x 102 M-1, respectively; for 5 they were 1.4 ± 0.1 x 105 M-1 and 44 ± 2 M-1, respectively. NDI 1 hydrolyzed 6.8 times faster than did 5. The rates for the first and second hydrolyses of 1 at 100 mM hydroxide measured by stopped-flow were 17.0 ± 0.2 s-1 and 53.0 ± 0.1 x 10-2 s-1, respectively. NMR showed both the syn and an
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Pearce, Nicholas. "Thionation of asymmetric rylene diimides." Thesis, University of Nottingham, 2016. http://eprints.nottingham.ac.uk/36228/.

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Rylene diimides have attracted much attention for use in optoelectronic devices, with excellent absorption and emission profiles, as well as a tendency to form n-type semiconductors. The absorption and emission properties of rylene diimides can be varied through functionalisation at the imide nitrogens and by substitution to the aromatic core but the effects of alterations to the imide oxygen atoms are less well understood. A series of thionated naphthalene diimides (NDIs), in which the imide oxygen atoms have been replaced with sulfur has been synthesised in a single reaction using Lawesson’s
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Llewellyn, Ben. "Synthesis and characterisation of functionalised perylene diimides." Thesis, University of Nottingham, 2016. http://eprints.nottingham.ac.uk/35539/.

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This thesis describes the synthesis of three series of perylene diimides (PDIs) by functionalisation at all four possible regions of the molecule. The synthesised compounds were then probed by optical, electrochemical and photophysical methods in order to fully elucidate their properties. Chapter 1 gives an overview of the structure, synthesis, properties and applications of PDIs and introduces the main topics investigated in this thesis. Chapter 2 describes the synthesis of two of the first examples of PDIs with an absorption maximum in the near infrared. This was achieved by functionalisatio
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Weitzel, Corey R. "Investigation into water-soluble perylene diimides for thin film formation." Thesis, Manhattan, Kan. : Kansas State University, 2008. http://hdl.handle.net/2097/778.

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Leoni, Julien Tissien. "The multifaceted roles of Perylene Diimides in Organic Solar Cells." Thesis, The University of Sydney, 2022. https://hdl.handle.net/2123/29373.

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Owing to their good photophysical properties, perylene diimides (PDI) have been shown to possess great potential in many scientific fields. Here, we demonstrate the multifaceted roles of PDIs in optoelectronic devices, such as when used in solar cells, optical cavities and even both. We use a range of perylene analogues as cathode interlayers in PTQ10:IDIC solar cells and demonstrate > 0.1V increase in Voc. With the help of time-resolved absorbance on devices and numerical drift-diffusion simulations, we show these perylene interlayers promote improved charge extraction, thereby resulting in
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Silva, Francisco de Araújo. "Estudo das propriedades eletrônicas e espectroscópicas de uma série de diimidas naftálicas com substituintes aromáticos com potencial aplicação em dispositivos de armazenamento e conversão de energia." Universidade de São Paulo, 2018. http://www.teses.usp.br/teses/disponiveis/59/59138/tde-22062018-212611/.

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As diimidas naftálicas simétricas têm sido vastamente estudadas devido suas propriedades químicas, ópticas, e eletrônicas. A possibilidade de modular suas propriedades com a substituição de grupos diversos na formação da imida, viabiliza aplicações em dispositivos eletrônicos, conversão de energia e produção de redes de coordenação metalo-orgânicas. Neste trabalho sintetizou-se uma série de 5 diimidas naftálicas (NDIs) simétricas com substituintes aromáticos. Foram analisadas as características espectroscópicas e eletrônicas com obtenção dos valores de band-gap óptico através de ensaios de vol
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Echue, Geraldine. "Novel functional materials based on perylene diimides using ionic self-assembly." Thesis, University of Bristol, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627982.

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A library of materials based on the ionic self-assembly (ISA) of a chiral perylene diimide (POI) with oppositely charged surfactants were prepared and characterised. Three classes of structurally related surfactants were used, so as to establish a set of design rules for the preparation of materials. The self-assembly behaviour of the materials in solution and the solid state was investigated; results and obtained structures were evaluated in terms of the influence of surfactant structure, solvent, concentration and non-covalent interactions. A general methodology was developed to synthesise a
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Miller, Chandra Tier. "The design, synthesis and screening of naphthalene diimides with antibacterial activity /." Digital version accessible at:, 1999. http://wwwlib.umi.com/cr/utexas/main.

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Ji, Yuyang. "GIANT MOLECULES BASED ON PERYLENE DIIMIDES: SYNTHESIS, CHARACTERIZATION AND SELF-ASSEMBLY BEHAVIORS." University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1491238979529549.

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Books on the topic "Diimides"

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Schuster, Nathaniel Joseph. Perylene-Diimide Helicenes: A New Molecular Architecture for Chiral Electronics. [publisher not identified], 2017.

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Milton, Margarita. Perylene Diimide: A Versatile Building Block for Complex Molecular Architectures and a Stable Charge Storage Material. [publisher not identified], 2018.

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Foegen, Neil. Investigations into the Optical and Electronic Properties of Perylene Diimide-Based Organic Materials as a Function of Molecular Aggregation in Solution and in Thin Films. [publisher not identified], 2021.

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4

Paul Petrus Maria de Lange. Synthesis and 1,3-dipolar reactivity of Fe(CO)3-n[subscript](CNR)n[subscript]([alpha]-diimine) complexes (n=1,3). Universiteit van Amsterdam, 1992.

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5

Williams, Benjamin Drew. Investigation of emulsion-enhanced diimide reductions. 1997.

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Lytle, Scott Allin. Diimide reductions in an emulsion based chemical system. 1996.

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Klein, René Alexander. Palladium compounds of annelated diazabiaryl derivatives and other [alpha] diimine ligands. 1996.

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8

Muller, Frederik. Reactions of dinuclear iron and ruthenium carbonyl [alpha] -diimine complexes with alkynes. 1988.

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Carbon-carbon and carbon-hydrogen coupling reactions on iron and ruthenium [alpha]-diimine complexes. Universiteit van Amsterdam, 1992.

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10

Striplin, Durwin R. Spectroscopic and magnetic investigations of Re(I)Cl(CO)₃(Ü,Üʹ-diimine) complexes and group (1B,8B) bimetallic complexes. 1994.

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Book chapters on the topic "Diimides"

1

Cua See, Kevin, and Howard E. Katz. "Naphthalenetetracarboxylic Diimides as Transparent Organic Semiconductors." In Transparent Electronics. John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470710609.ch16.

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Bhosale, Sheshanath V., Bradley E. Wilman, and Steven J. Langford. "Nanostructured Materials Based on Core-Substituted Naphthalene Diimides." In Molecules at Work. Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527645787.ch5.

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Panda, Dillip K., and Sourav Saha. "Chapter 7. Tunable Electronic Interactions between Aromatic Diimides and Anions." In Monographs in Supramolecular Chemistry. Royal Society of Chemistry, 2017. http://dx.doi.org/10.1039/9781782621386-00218.

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Maniam, Subashani, Heather F. Higginbotham, Toby D. M. Bell, and Steven J. Langford. "Chapter 8. Naphthalene Diimide-based Photovoltaics." In Monographs in Supramolecular Chemistry. Royal Society of Chemistry, 2017. http://dx.doi.org/10.1039/9781782621386-00244.

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Parshall, George W., M. D. Curtis, and R. C. Job. "Azo, Diimide, and Hydrazine Complexes of Platinum." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132432.ch6.

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Wellner, Christian, Claudia Stubinitzky, and Hans-Achim Wagenknecht. "Metal Ion- and Perylene Diimide-Mediated DNA Architectures." In DNA in Supramolecular Chemistry and Nanotechnology. John Wiley & Sons, Ltd, 2017. http://dx.doi.org/10.1002/9781118696880.ch1.3.

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Takenaka, Shigeori. "Cyclic Naphthalene Diimide Derivatives as Novel DNA Ligands." In Handbook of Chemical Biology of Nucleic Acids. Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-1313-5_31-1.

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Takenaka, Shigeori. "Cyclic Naphthalene Diimide Derivatives as Novel DNA Ligands." In Handbook of Chemical Biology of Nucleic Acids. Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-19-9776-1_31.

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Georgiev, N., H. Nichev, M. Petrov, K. Lovchinov, D. Dimova-Malinovska, and V. Bojinov. "Deposition of Perylene Diimide Derivatives for Dye-Sensitized Solar Cells." In Nanoscience Advances in CBRN Agents Detection, Information and Energy Security. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9697-2_51.

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Das, Anindita, Priya Rajdev, and Suhrit Ghosh. "Chapter 5. Naphthalene-diimide (NDI) Nanofibre, Gel and Mesoscopic Material." In Monographs in Supramolecular Chemistry. Royal Society of Chemistry, 2017. http://dx.doi.org/10.1039/9781782621386-00116.

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Conference papers on the topic "Diimides"

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Burn, Paul L. "Perylene diimide based fluorescent sensors for drug simulant detection." In Organic and Hybrid Sensors and Bioelectronics XVII, edited by Ioannis Kymissis, Emil J. List-Kratochvil, and Sahika Inal. SPIE, 2024. http://dx.doi.org/10.1117/12.3023858.

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Hsieh, Gen-Wen, Chun-Teng Chen, and He-Hua Hsu. "Transistor and Photoresponse Behaviors of Perylene Diimide Microribbon with Perovskite Nanocrystal Decoration." In 2024 31st International Workshop on Active-Matrix Flatpanel Displays and Devices (AM-FPD). IEEE, 2024. http://dx.doi.org/10.23919/am-fpd61635.2024.10615962.

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Puthilibai, G., S. Chitradevi, Geetha Chandrasekran, S. John Mary, Elakiyadevi B, and Rajamani Raja. "Synthesis, Binding Studies, and The Photophysics of Rhenium(I) Diimine Surfactant Complexes with Serum Albumins." In 2025 International Conference on Computing and Communication Technologies (ICCCT). IEEE, 2025. https://doi.org/10.1109/iccct63501.2025.11019370.

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Zuilhof, Han T., Tjeerd J. Schaafsma, and Ernst J. Sudhoelter. "Liquid crystalline perylene diimides: highly organized electron carriers." In International Symposium on Optical Science and Technology, edited by Zakya H. Kafafi. SPIE, 2001. http://dx.doi.org/10.1117/12.416943.

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Dixon, D., W. Wilson, V. Steullet, and S. Takenaka. "Studies of Naphthalene Diimides as DNA-binding Agents." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02060.

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Bell, Toby D. M., Sheryll Yap, Chintan Jani, et al. "Naphthalene diimides as tunable fluorophores suitable for single molecule applications." In Biomedical Optics (BiOS) 2007, edited by Jorg Enderlein and Zygmunt K. Gryczynski. SPIE, 2007. http://dx.doi.org/10.1117/12.701443.

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Stolte, M., S. L. Suraru, F. Würthner, et al. "Organic n-channel thin film transistors based on dichlorinated naphthalene diimides." In SPIE Photonic Devices + Applications, edited by Zhenan Bao and Iain McCulloch. SPIE, 2010. http://dx.doi.org/10.1117/12.859829.

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Tseng, Pin-Yen, Gen-Wen Hsieh, Cheng-Wei Wang, Chun-Yi Hung, and Chih-Wen Tsai. "Air-stable N-type organic microribbon transistors based on perylene diimides derivatives." In 2015 22nd International Workshop on Active-Matrix Flatpanel Displays and Devices (AM-FPD). IEEE, 2015. http://dx.doi.org/10.1109/am-fpd.2015.7173220.

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Döring, Robin Carl, Eduard Baal, Jörg Sundermeyer, and Sangam Chatterjee. "Time-resolved measurement of intramolecular photoinduced electron transfer processes in perylene diimides (Conference Presentation)." In Organic Photonic Materials and Devices XIX, edited by Christopher E. Tabor, François Kajzar, Toshikuni Kaino, and Yasuhiro Koike. SPIE, 2017. http://dx.doi.org/10.1117/12.2254325.

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Ahrens, Michael J., Michael J. Fuller, and Michael R. Wasielewski. "Aminated and cyanated perylene mono- and diimides: Liquid crystalline electron donors and acceptors for organic photonics and electronics." In Frontiers in Optics. OSA, 2003. http://dx.doi.org/10.1364/fio.2003.tuj5.

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Reports on the topic "Diimides"

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Higgins, Daniel A., Aifang Xie, and Bei Liu. Characterization of New Materials for Photovoltaic Thin Films: Aggregation Phenomena in Self-Assembled Perylene-Based Diimides. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada435695.

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