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Academic literature on the topic 'Photo-cyclisation'
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Journal articles on the topic "Photo-cyclisation"
Shepherd, Nicholas D., Harrison S. Moore, Jonathon E. Beves, and Deanna M. D’Alessandro. "Electrochemical Switching of First-Generation Donor-Acceptor Stenhouse Adducts (DASAs): An Alternative Stimulus for Triene Cyclisation." Chemistry 3, no. 3 (July 7, 2021): 728–33. http://dx.doi.org/10.3390/chemistry3030051.
Full textBlanke, Meik, Jan Balszuweit, Marco Saccone, Christoph Wölper, David Doblas Jiménez, Markus Mezger, Jens Voskuhl, and Michael Giese. "Photo-switching and -cyclisation of hydrogen bonded liquid crystals based on resveratrol." Chemical Communications 56, no. 7 (2020): 1105–8. http://dx.doi.org/10.1039/c9cc07721a.
Full textLeitich, Johannes, Ingeborg Heise, and Kurt Schaffner. "The photo-Nazarov cyclisation of 1-cyclohexenyl-phenyl-methanone revisited." Journal of Photochemistry and Photobiology A: Chemistry 140, no. 3 (May 2001): 207–13. http://dx.doi.org/10.1016/s1010-6030(01)00417-8.
Full textYamato, Takehiko, Tatsunori Saisyo, Tohru Hironaka, and Shinpei Miyamoto. "Medium-size cyclophanes, 71. Synthesis, structures and photo-induced cyclisation of 1,2-diphenyl[2.n]metacyclophan-1-enes." Journal of Chemical Research 2006, no. 9 (September 1, 2006): 558–60. http://dx.doi.org/10.3184/030823406778521338.
Full textPaudel, Arjun, Jian-Yong Hu, and Takehiko Yamato. "Synthesis and structural properties of novel polycyclic aromatic compounds using photo-induced cyclisation of 2,7-di-tert-butyl-4-(phenylethenyl)pyrenes." Journal of Chemical Research 2008, no. 8 (August 1, 2008): 457–60. http://dx.doi.org/10.3184/030823408x338710.
Full textMaki, Yoshifumi, Kaoru Shimada, Magoichi Sako, and Kosaku Hirota. "Photo-oxidative cyclisation of 2'-hydroxychalcones leading to flavones induced by heterocycle -oxides : high efficiency of pybimido[54-]pteridine -oxide for the photochemical dehydrogenation." Tetrahedron 44, no. 11 (January 1988): 3187–94. http://dx.doi.org/10.1016/s0040-4020(01)85950-0.
Full textPashley-Johnson, Fred, Rangika Munaweera, Sheikh I. Hossain, Steven C. Gauci, Laura Delafresnaye, Hendrik Frisch, Megan L. O’Mara, Filip E. Du Prez, and Christopher Barner-Kowollik. "How molecular architecture defines quantum yields." Nature Communications 15, no. 1 (July 17, 2024). http://dx.doi.org/10.1038/s41467-024-50366-1.
Full textDissertations / Theses on the topic "Photo-cyclisation"
Lloyd, Christopher. "The Photo-initiated Bergamn Cyclisation of Z-hex-3-ene-1,5-diyne." Thesis, University of Bristol, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499954.
Full textAndrieux, Vivien. "Matériaux mous supramoléculaires électro-stimulables obtenus par auto-assemblage de viologènes." Electronic Thesis or Diss., Lyon, École normale supérieure, 2024. http://www.theses.fr/2024ENSL0038.
Full textThe aim of this thesis is to develop electron-responsive supramolecular soft-materials. The strategy for the preparation and stimulation of such materials is based on the self-assembly properties of molecular units derived from 4,4-bipyridinium salts (viologens). The thesis research work carried has been focused on the structural characterizations, the study of gelation mechanism and the stimulation (electrochemical reduction or photo-reduction) of conductive gels obtained through the self-assembly of a cholesteryl substituted viologen. A first bibliographic part will describe the principal features of supramolecular gels, the challenges related to their characterization and electric stimulation and the potential of viologen-based supramolecular gels for the development of new electron-responsive supramolecular gels. The second part of the manuscript is devoted to present the experimental work performed for the synthesis, the formulation and the characterizations that led to the design of a conductive viologen-based supramolecular gel exhibiting ideal properties for electrochemical stimulation and in situ monitoring. The stimulation of conductive viologen gels, consisting in the electrochemical reduction or photoreduction are described in a third part. This part describes in details the different strategies used to reach an efficient reduction of the viologen moieties which are entrapped in the gel supramolecular network. This work demonstrates that the studied viologen gel is one of the very first systems able to undergo reversible electrochemically induced supramolecular polymerization and de-polymerization