Literatura científica selecionada sobre o tema "Photo-cyclisation"
Crie uma referência precisa em APA, MLA, Chicago, Harvard, e outros estilos
Consulte a lista de atuais artigos, livros, teses, anais de congressos e outras fontes científicas relevantes para o tema "Photo-cyclisation".
Ao lado de cada fonte na lista de referências, há um botão "Adicionar à bibliografia". Clique e geraremos automaticamente a citação bibliográfica do trabalho escolhido no estilo de citação de que você precisa: APA, MLA, Harvard, Chicago, Vancouver, etc.
Você também pode baixar o texto completo da publicação científica em formato .pdf e ler o resumo do trabalho online se estiver presente nos metadados.
Artigos de revistas sobre o assunto "Photo-cyclisation"
Shepherd, Nicholas D., Harrison S. Moore, Jonathon E. Beves e Deanna M. D’Alessandro. "Electrochemical Switching of First-Generation Donor-Acceptor Stenhouse Adducts (DASAs): An Alternative Stimulus for Triene Cyclisation". Chemistry 3, n.º 3 (7 de julho de 2021): 728–33. http://dx.doi.org/10.3390/chemistry3030051.
Texto completo da fonteBlanke, Meik, Jan Balszuweit, Marco Saccone, Christoph Wölper, David Doblas Jiménez, Markus Mezger, Jens Voskuhl e Michael Giese. "Photo-switching and -cyclisation of hydrogen bonded liquid crystals based on resveratrol". Chemical Communications 56, n.º 7 (2020): 1105–8. http://dx.doi.org/10.1039/c9cc07721a.
Texto completo da fonteLeitich, Johannes, Ingeborg Heise e Kurt Schaffner. "The photo-Nazarov cyclisation of 1-cyclohexenyl-phenyl-methanone revisited". Journal of Photochemistry and Photobiology A: Chemistry 140, n.º 3 (maio de 2001): 207–13. http://dx.doi.org/10.1016/s1010-6030(01)00417-8.
Texto completo da fonteYamato, Takehiko, Tatsunori Saisyo, Tohru Hironaka e 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, n.º 9 (1 de setembro de 2006): 558–60. http://dx.doi.org/10.3184/030823406778521338.
Texto completo da fontePaudel, Arjun, Jian-Yong Hu e 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, n.º 8 (1 de agosto de 2008): 457–60. http://dx.doi.org/10.3184/030823408x338710.
Texto completo da fonteMaki, Yoshifumi, Kaoru Shimada, Magoichi Sako e 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, n.º 11 (janeiro de 1988): 3187–94. http://dx.doi.org/10.1016/s0040-4020(01)85950-0.
Texto completo da fontePashley-Johnson, Fred, Rangika Munaweera, Sheikh I. Hossain, Steven C. Gauci, Laura Delafresnaye, Hendrik Frisch, Megan L. O’Mara, Filip E. Du Prez e Christopher Barner-Kowollik. "How molecular architecture defines quantum yields". Nature Communications 15, n.º 1 (17 de julho de 2024). http://dx.doi.org/10.1038/s41467-024-50366-1.
Texto completo da fonteTeses / dissertações sobre o assunto "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.
Texto completo da fonteAndrieux, 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.
Texto completo da fonteThe 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