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Relevant bibliographies by topics / Perylene derivatives

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Academic literature on the topic 'Perylene derivatives'

Author: Grafiati

Published: 4 June 2021

Last updated: 22 February 2023

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Journal articles on the topic "Perylene derivatives"

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 (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 fragmen

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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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Fang, Xiangdong. "BN-Embedded Perylenes." Molecules 26, no. 23 (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-pery

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Ling, Cheng, Miao, Zhang, Zhang, and Zhu. "Synthesis and Photocontrolled Supramolecular Self-Assembly of Azobenzene-Functionalized Perylene Bisimide Derivatives." Polymers 11, no. 7 (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 deso

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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 w

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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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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 (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 effici

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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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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 (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 compou

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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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Dissertations / Theses on the topic "Perylene derivatives"

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Haddow, Sarah Louise. "Perylene derivatives and silicon nanosheets." Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/41873/.

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The work presented in this thesis explores two different topics of interest, firstly a synthetic project fabricating small building blocks for supramolecular arrays. The building blocks are a series of perylene monoimide monoahydride (PMIA) compounds, synthesised by a four step process. The PMIA compounds belong to a family of dyes called the rylenes which are known in literature for their optical properties and use in optoelectronic devices. Chapter 2 begins with the description of the synthesis and characterisation of these molecules, where Hirshfeld surface analysis is used to investigate t

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2

Engel, Egbert Konstantin. "Ultrafast exciton relaxation in quasi-one-dimensional perylene derivatives." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=97940665X.

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Engel, Egbert. "Ultrafast exciton relaxation in quasi-one-dimensional perylene derivatives." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2006. http://nbn-resolving.de/urn:nbn:de:swb:14-1143653858595-30675.

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This thesis deals with exciton relaxation processes in thin polycrystalline films and matrix-isolated molecules of the perylene derivatives PTCDA (3,4,9,10-perylenetetracarboxylic dianhydride) and MePTCDI (N,N'-dimethylperylene-3,4,9,10-dicarboximide). Using femtosecond pump-probe spectroscopy, transient absorption spectra, excitonic relaxation in the lowest excited state subsequent to excitation, and exciton-exciton interaction and annihilation at high excitation densities have been addressed. Transient absorption spectroscopy in the range 1.2eV-2.6eV has been applied to thin polycrystalline

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Engel, Egbert. "Ultrafast exciton relaxation in quasi-one-dimensional perylene derivatives." Doctoral thesis, Technische Universität Dresden, 2005. https://tud.qucosa.de/id/qucosa%3A24681.

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This thesis deals with exciton relaxation processes in thin polycrystalline films and matrix-isolated molecules of the perylene derivatives PTCDA (3,4,9,10-perylenetetracarboxylic dianhydride) and MePTCDI (N,N'-dimethylperylene-3,4,9,10-dicarboximide). Using femtosecond pump-probe spectroscopy, transient absorption spectra, excitonic relaxation in the lowest excited state subsequent to excitation, and exciton-exciton interaction and annihilation at high excitation densities have been addressed. Transient absorption spectroscopy in the range 1.2eV-2.6eV has been applied to thin polycrystalline

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Schmidt, Rüdiger. "Perylene bisimide and acene derivatives as organic semiconductors in OTFTs." kostenfrei, 2008. http://nbn-resolving.de/urn/resolver.pl?urn=nbn:de:bvb:20-opus-29314.

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Slater, Anna Grace. "The synthesis of perylene diimide derivatives for self-assembled structures." Thesis, University of Nottingham, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.546287.

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Noumissing, Sao Cherubin [Verfasser]. "Dye-sensitized solar cells based on perylene derivatives / Cherubin Noumissing Sao." Kassel : Universitätsbibliothek Kassel, 2009. http://d-nb.info/1000321401/34.

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8

Tian, Ding. "Synthesis, Characterization and Thermal Analysis of Tetrahedral and Cyano-substituted Perylene-based Derivatives." University of Akron / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=akron1407868184.

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9

Kam, Alicia Patricia. "Molecular organization and mixing in thin solid films of novel perylene tetracarboxylic dianhydride derivatives, infrared and surface enhanced Raman studies." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/NQ62324.pdf.

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Chen, Shu-Jiun, and 陳淑君. "Synthesis and Characteristics of Perylene PI derivatives." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/3hgtge.

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碩士<br>國立臺灣科技大學<br>高分子系<br>94<br>In this study, a series of perylene-3,4,9,10-tetracarboxylic acid dianhydride, (PTCDA) derivative was prepared by the reaction of bromine water、4-nitrophenol and 1,6-hexanediamine. The bromination of perylene-3,4,9,10-tetracarboxylic acid dianhydride have been synthesized, then carries on the nitrophenoxy reaction with nitrophenol to synthesize the derivative. But again carries on with two amines gathers the condensation reaction the PI derivative.The structure of derivatives were characterized by the FT-IR、UV、NMR、MASS and EA analysis.

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Book chapters on the topic "Perylene derivatives"

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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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2

Gutman, Ivan, and Slavko Radenković. "Paradise Lost—π-Electron Conjugation in Homologs and Derivatives of Perylene." In Challenges and Advances in Computational Chemistry and Physics. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-29022-5_11.

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Szarko, J., A. Neubauer, L. Socaciu-Siebert, et al. "Electron Injection Dynamics of Perylene Derivatives into ZnO and TiO2 Particle Films." In Springer Series in Chemical Physics. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-95946-5_208.

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4

Morandeira, A., A. Fürstenberg, and E. Vauthey. "Influence of solute-solvent interactions on the quenching dynamics of perylene derivatives in an electron donating solvent." In Femtochemistry and Femtobiology. Elsevier, 2004. http://dx.doi.org/10.1016/b978-044451656-5/50068-2.

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Conference papers on the topic "Perylene derivatives"

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Sasaki, Yoshihiko, Hiroyuki Takamo, and Kazuo Kasatani. "Optical nonlinearities of perylene derivatives." In Photonics Asia 2007, edited by Yiping Cui, Qihuang Gong, and Yuen-Ron Shen. SPIE, 2007. http://dx.doi.org/10.1117/12.757661.

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2

González, Miguel, Vicky Roa-Linares, and Ana Mesa-Arango. "Synthesis and Antifungal Activity of Perylene Bisimide Derivatives." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-b034.

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3

Schemme, Thomas, Katharina Ditte, Evgenij Travkin, Wei Jiang, Zhaohui Wang, and Cornelia Denz. "Perylene bisimide derivatives as innovative sensitizers for photorefractive composites." In SPIE Photonics Europe, edited by Barry P. Rand, Chihaya Adachi, and Volker van Elsbergen. SPIE, 2012. http://dx.doi.org/10.1117/12.922671.

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4

Silva, D. L., L. Misoguti, and C. R. Mendonça. "Controlling Two-Photon Excited Fluorescence in Perylene Derivatives via Femtosecond Pulses." In Frontiers in Optics. OSA, 2006. http://dx.doi.org/10.1364/fio.2006.jsua64.

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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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Zhou, Manxi, Zhimin Sun, Guangxin Chen, and Qifang Li. "Synthesis of Perylene Bisimide Derivatives and Poly(Triphenylamine-Block-Anthraquino) for Polymer Photovoltaics." In 2011 Asia-Pacific Power and Energy Engineering Conference (APPEEC). IEEE, 2011. http://dx.doi.org/10.1109/appeec.2011.5748418.

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7

Agabekov, Vladimir E., Victor A. Azarko, and Olga P. Nevdakh. "Dry resist material on base of perylene tetracarboxylic acid derivatives for laser lithography." In SPIE's 1995 Symposium on Microlithography, edited by Robert D. Allen. SPIE, 1995. http://dx.doi.org/10.1117/12.210404.

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HOFFMANN, M., T. HASCHE, K. SCHMIDT, T. W. CANZLER, V. M. AGRANOVICH, and K. LEO. "EXCITONS IN QUASI-ONE-DIMENSIONAL CRYSTALLINE PERYLENE DERIVATIVES: BAND STRUCTURE AND RELAXATION DYNAMICS." In Proceedings of 2000 International Conference. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811387_0007.

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Paez, Beynor A., Georgeta Salvan, Reinhard Scholz, Thorsten U. Kampen, and Dietrich R. T. Zahn. "Interaction of metals with perylene derivatives as a model system for contact formation in OFET structures." In Optical Science and Technology, SPIE's 48th Annual Meeting, edited by Christos D. Dimitrakopoulos. SPIE, 2003. http://dx.doi.org/10.1117/12.505905.

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Izutani, Yusuke, Keiko Kit, Toshiaki Osuga, and Seiji Tsuzuki. "Spectroscopic measurements and DFT calculations of vibrational frequencies of perylene and its derivatives in THz region." In 2009 34th International Conference on Infrared, Millimeter, and Terahertz Waves (IORMMW-THz 2009). IEEE, 2009. http://dx.doi.org/10.1109/icimw.2009.5324614.

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