Relevant bibliographies by topics / Perylene bisimide (PBI)

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Perylene bisimide (PBI)'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Perylene bisimide (PBI)"

1

Schmidt, Rüdiger, Peter Osswald, Martin Könemann, and Frank Würthner. "Synthetic Routes to Core-fluorinated Perylene Bisimide Dyes and their Properties." Zeitschrift für Naturforschung B 64, no. 6 (2009): 735–46. http://dx.doi.org/10.1515/znb-2009-0621.

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Numerous core-fluorinated perylene bisimide (PBI) dyes with various substituents at the imide positions have been synthesized by different methods. Core-difluorinated PBIs 4a-f are obtained by imidization of difluoro-substituted perylene bisanhydride 1 with appropriate primary amines or, alternatively, by nucleophilic halogen exchange reactions (Halex process) of the corresponding dibromosubstituted PBIs 2a-d,f with potassium fluoride. Core-tetrafluorinated PBIs 5a-c could also be synthesized by halogen exchange reactions of the respective tetrachlorinated PBIs 3a-c. In particular, core-fluori
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2

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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3

Xu, Xu, Yuqi Li, Zhongqiang Xiong, et al. "Preparation and model of high-performance shape-memory polyurethane with hydroxylated perylene bisimide." RSC Advances 6, no. 111 (2016): 110329–36. http://dx.doi.org/10.1039/c6ra24393b.

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He, Xu, Bing Hu, Yan Yang, et al. "Synthesis, self-aggregation and cryopreservation effects of perylene bisimide–glycopeptide conjugates." Chemical Communications 57, no. 90 (2021): 12000–12003. http://dx.doi.org/10.1039/d1cc03835d.

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Ouyang, Guanghui, David Bialas, and Frank Würthner. "Reversible fluorescence modulation through the photoisomerization of an azobenzene-bridged perylene bisimide cyclophane." Organic Chemistry Frontiers 8, no. 7 (2021): 1424–30. http://dx.doi.org/10.1039/d0qo01635g.

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An azobenzene-bridged perylene bisimide cyclophane was designed and synthesized, which showed reversible fluorescence intensity switching under light-irradiation due to cooperative adjustments of PBI–PBI and PBI–Azo interactions.
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6

Lee, Ji-Eun, Ye Ri Han, Sujin Ham, Chul-Ho Jun, and Dongho Kim. "A solution-based single-molecule study of surface-bound PBIs: solvent-mediated environmental effects on molecular flexibility." Physical Chemistry Chemical Physics 19, no. 43 (2017): 29255–62. http://dx.doi.org/10.1039/c7cp04756h.

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7

Nastasi, Francesco, Giuseppina La Ganga, Sebastiano Campagna, et al. "Multichromophoric hybrid species made of perylene bisimide derivatives and Ru(ii) and Os(ii) polypyridine subunits." Physical Chemistry Chemical Physics 19, no. 21 (2017): 14055–65. http://dx.doi.org/10.1039/c7cp01597f.

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8

Mutoh, Katsuya, Michel Sliwa, Eduard Fron, Johan Hofkens, and Jiro Abe. "Fluorescence modulation by fast photochromism of a [2.2]paracyclophane-bridged imidazole dimer possessing a perylene bisimide moiety." Journal of Materials Chemistry C 6, no. 35 (2018): 9523–31. http://dx.doi.org/10.1039/c8tc02713g.

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9

Weißenstein, Annike, and Frank Würthner. "Metal ion templated self-assembly of crown ether functionalized perylene bisimide dyes." Chemical Communications 51, no. 16 (2015): 3415–18. http://dx.doi.org/10.1039/c4cc09443c.

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10

Al-Galiby, Qusiy, Iain Grace, Hatef Sadeghi та Colin J. Lambert. "Exploiting the extended π-system of perylene bisimide for label-free single-molecule sensing". Journal of Materials Chemistry C 3, № 9 (2015): 2101–6. http://dx.doi.org/10.1039/c4tc02897j.

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We demonstrate the potential of perylene bisimide (PBI) for label-free sensing of organic molecules by investigating the change in electronic properties of five symmetric and asymmetric PBI derivatives, which share a common backbone, but are functionalised with various bay-area substituents.
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Dissertations / Theses on the topic "Perylene bisimide (PBI)"

1

Τσικριτζής, Δημήτρης. "Μελέτη διεπιφανειών οργανικών ημιαγωγών με ανόργανα υποστρώματα με εφαρμογή σε οργανικά ηλεκτρονικά". Thesis, 2014. http://hdl.handle.net/10889/8263.

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Το ερευνητικό ενδιαφέρον για τους οργανικούς ημιαγωγούς είναι συνεχώς αυξανόμενο τα τελευταία χρόνια, καθώς η αγορά των οργανικών ηλεκτρονικών είναι από τις πιο αναπτυσσόμενες. Για την καλή απόδοση των διατάξεων αυτών σημαντικός είναι ο ρόλος των διεπιφανειών. Οι οικογένειες των n-type οργανικών ημιαγωγών naphthalene bisimides και perylene bisimides έχουν δείξει καλές αποδόσεις σε οργανικά τρανζίστορ. Στην παρούσα εργασία μελετήθηκαν οι διεπιφάνειες νέων οργανικών ημιαγωγών από τις παραπάνω οι οικογένειες οργανικών πάνω σε ανόργανα υποστρώματα με φασματοσκοπίες φωτοηλεκτρονίων. Μελετήθηκε ο
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