Relevant bibliographies by topics / Arene-perfluoroarene interaction

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  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Arene-perfluoroarene interaction'

Author: Grafiati
Published: 4 June 2021
Last updated: 15 February 2022

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Journal articles on the topic "Arene-perfluoroarene interaction"

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Liang, Juncong, Heng Zhang, Aiyou Hao, and Pengyao Xing. "Hierarchically Evolved Supramolecular Chirality Mediated by Arene-Perfluoroarene Interaction." ACS Applied Materials & Interfaces 13, no. 24 (June 9, 2021): 29170–78. http://dx.doi.org/10.1021/acsami.1c07720.

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Kishikawa, Keiki. "Utilization of the Perfluoroarene-Arene Interaction for Stabilization of Liquid Crystal Phases." Israel Journal of Chemistry 52, no. 10 (September 26, 2012): 800–808. http://dx.doi.org/10.1002/ijch.201200028.

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Stoll, Ion, Ralf Brodbeck, Beate Neumann, Hans-Georg Stammler, and Jochen Mattay. "Controlling the self assembly of arene functionalised 2-aminopyrimidines by arene-perfluoroarene interaction and by silver(I) complex formation." CrystEngComm 11, no. 2 (2009): 306–17. http://dx.doi.org/10.1039/b811297e.

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Kusakawa, Takumi, Shunichiro Sakai, Kyosuke Nakajima, Hidetaka Yuge, Izabela Rzeznicka, and Akiko Hori. "Synthesis, Structures and Co-Crystallizations of Perfluorophenyl Substituted β-Diketone and Triketone Compounds." Crystals 9, no. 3 (March 25, 2019): 175. http://dx.doi.org/10.3390/cryst9030175.

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Perfluorophenyl-substituted compounds, 3-hydroxy-1,3-bis(pentafluorophenyl)-2- propen-1-one (H1) and 1,5-dihydroxy-1,5-bis(pentafluorophenyl)-1,4-pentadien-3-one (H22), were prepared in 56 and 30% yields, respectively, and only the enol forms were preferentially obtained among the keto-enol tautomerism. Molecular conformations and tautomerism of the fluorine-substituted compounds were certified based on X-ray crystallographic studies and density functional calculations. The solvent dependency of the absorption spectra was only observed for the fluorinated compounds. The compounds H1 and H22 quantitatively formed co-crystals with the corresponding non-perfluorinated compounds, dibenzoylmethane (H3) and 1,5-dihydroxy-1,5-diphenyl-1,4-pentadien-3-one (H24), respectively, through the arene–perfluoroarene interaction to give the 1:1 co-crystals H1•H3 and H22•H24, which were characterized by X-ray crystallographic and elemental analysis studies.
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Lee, Ga Young, Elizabeth Hu, Arnold L. Rheingold, K. N. Houk, and Ellen M. Sletten. "Arene-Perfluoroarene Interactions in Solution." Journal of Organic Chemistry 86, no. 12 (June 2, 2021): 8425–36. http://dx.doi.org/10.1021/acs.joc.1c00921.

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Kishikawa, Keiki, Takahiro Inoue, Naoshi Hasegawa, Masahiro Takahashi, Michinari Kohri, Tatsuo Taniguchi, and Shigeo Kohmoto. "Achiral straight-rod liquid crystals indicating local biaxiality and ferroelectric switching behavior in the smectic A and nematic phases." Journal of Materials Chemistry C 3, no. 15 (2015): 3574–81. http://dx.doi.org/10.1039/c5tc00389j.

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Itoh, Takahiro, Mio Kondo, Hirotoshi Sakamoto, Kaori Wakabayashi, Mari Kanaike, Kenichiro Itami, and Shigeyuki Masaoka. "Porous frameworks constructed by non-covalent linking of substitution-inert metal complexes." Dalton Transactions 44, no. 34 (2015): 15334–42. http://dx.doi.org/10.1039/c5dt01620g.

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Flexible porous frameworks based on substitution-inert paddle-wheel Rh(ii) dimers with active sites were successfully synthesized by using multipoint arene-perfluoroarene interactions and the porous properties of the frameworks were investigated.
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Tsunoda, Mitsukimi, Martin Fleischmann, J. Stuart Jones, Nattamai Bhuvanesh, Manfred Scheer, and François P. Gabbaï. "Supramolecular aggregation of Ni(salen) with (C6F5)2Hg and [o-C6F4Hg]3." Dalton Transactions 45, no. 12 (2016): 5045–51. http://dx.doi.org/10.1039/c5dt01887k.

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Organomercurials (C6F5)2Hg and [o-C6F4Hg]3 interact with Ni(ii)-salen to form adducts held by arene-perfluoroarene and hydrogen bonding interactions, as well as interactions between Hg, the salen ligand, and Ni.
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Batsanov, Andrei S., Jonathan C. Collings, Judith A. K. Howard, Todd B. Marder, and Dmitrii F. Perepichka. "Arene–perfluoroarene interactions in crystal engineering. 5." Acta Crystallographica Section C Crystal Structure Communications 57, no. 11 (November 13, 2001): 1306–7. http://dx.doi.org/10.1107/s0108270101013075.

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Batsanov, Andrei S., Judith A. K. Howard, Todd B. Marder, and Edward G. Robins. "Arene–perfluoroarene interactions in crystal engineering. 4." Acta Crystallographica Section C Crystal Structure Communications 57, no. 11 (November 13, 2001): 1303–5. http://dx.doi.org/10.1107/s0108270101013294.

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Dissertations / Theses on the topic "Arene-perfluoroarene interaction"

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Wang, Weiran. "Synthesis of the Fluorinated Arylene Alkylene Ether and Research on Its Potential Thermotropic Behavior under Photochemical Crosslink Reaction." University of Akron / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=akron1399217687.

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Perry, Mark A. "Spectroscopic investigations of perfluoroarene: Arene interactions in solution involving hexafluorobenzene." Thesis, University of Ottawa (Canada), 2008. http://hdl.handle.net/10393/28014.

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This thesis focuses on common spectroscopic techniques to measure the photophysical consequences of perfluoroarene:arene interactions in solution. The perfluoroarene in these studies was hexafluorobenzene (C6F 6) since it structurally and electronically represents the simplest of all perfluorinated aromatic molecules. The goal of this thesis was to create a library of perfluoroarene:arene interactions and use them to influence chemical reactivity in the excited state both efficiently and predictably. The first chapter outlines the spectroscopic techniques employed, and explains the foundation of this project from solid-state applications. The remaining chapters detail perfluoroarene:arene interactions observed, spectroscopically, in solution. Chapter 2 is a thorough study on the pre-association of pyrene:C6F6 and the impact C6F6 had on the photophysics of dilute and concentrated pyrene solutions. The third chapter summarizes the photophysical results from a variety of rigid polyaromatic molecules, and one flexible polyaromatic (biphenyl). A practical application of this work was observed with nanosecond laser flash photolysis studies outlined in Chapter 4, while the search for other practical applications with quantum dots, oxygen- and carbon-centered radicals in the presence of C6F 6 is detailed in Chapter 5.
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Collings, Jonathan C. "The effect of fluorine substituents on the physical and structural properties of conjugated molecular materials." Thesis, Durham University, 2002. http://etheses.dur.ac.uk/4175/.

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A series of selectively fluorinated tolans of the general formulae C(_6)F(_5)-C=C-C(_6)H(_4)X and C(_6)H(_5)-C=C-C(_6)F(_4)X (where X = I, Br, CI) have been synthesized via homogeneous palladium-catalysed Sonogashira cross-coupling and organolithium chemistry. Several of their crystal structures have been solved from X-ray diffraction data, and their molecular packing is described in terms of arene-perfluoroarene and halogen-halogen interactions. Diffraction-quality crystals of a number of binary arene-perfluoroarene complexes of hexafluorobenzene and octafluoronaphthalene with several mismatched polyaromatic hydrocarbons have been obtained and their crystal structures solved from X-ray diffraction data. All of the structures have been shown to consist of infinite stacks of alternating components. The individual structures are compared and contrasted in detail, and those of the HFB complexes are found to closely resemble those predicted from ab initio DFT calculations, which implies that the interactions are over 90 % electrostatic in nature, in contrast with previous calculations on related complexes. A number of selectively fluorinated 4,4'-bis(phenylethynyl)tolan (BPET) derivatives containing fluorinated and non-fluorinated phenyl rings, have been synthesized from palladium-catalysed Sonogashira cross-coupling of various tolan-based precursors. They are observed to strongly absorb in the UV range 336 - 342nm, which are directly comparable to the absorptions for similarly fluorinated 1,4-bis(phenylethynyl)benzene derivatives which suggests that an effective conjugation length (ECL) of 3-4 repeat units is applicable for these phenylene ethynylene systems. They are observed to fluoresce very strongly in the range 372-410 nm. The diethynylbenzene derivatives 1,4-diethynyltetrafluorobenzene and 1,4- diethynyl-2,5-difluorobenzene have been synthesized from the hydrodesilation of their trimethylsilylated precursors. Their crystal structures have been solved from X-ray diffraction data, and are described in terms of C=C-H F and C=C-H π(C=C) interactions.
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Book chapters on the topic "Arene-perfluoroarene interaction"

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Hori, Akiko. "Arene-Perfluoroarene Interactions in Coordination Architectures." In The Importance of Pi-Interactions in Crystal Engineering, 163–85. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781119945888.ch7.

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