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Journal articles on the topic 'Arene-perfluoroarene interaction'

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

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Yardley, Rebecca E., Joseph A. Paquette, Hi Taing, Heather M. Gaebler, S. Holger Eichhorn, Ian P. Hamilton, and Kenneth E. Maly. "Stabilization of Columnar Liquid Crystal Phases via Arene-Perfluoroarene Interactions." Organic Letters 21, no. 24 (December 5, 2019): 10102–5. http://dx.doi.org/10.1021/acs.orglett.9b04091.

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12

Hori, Akiko, Shohei Takatani, Takeshi K. Miyamoto, and Miki Hasegawa. "Luminescence from π–π stacked bipyridines through arene–perfluoroarene interactions." CrystEngComm 11, no. 4 (2009): 567. http://dx.doi.org/10.1039/b822007g.

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13

Kilbinger, Andreas F. M., and Robert H. Grubbs. "Arene-Perfluoroarene Interactions as Physical Cross-Links for Hydrogel Formation." Angewandte Chemie International Edition 41, no. 9 (May 2, 2002): 1563–66. http://dx.doi.org/10.1002/1521-3773(20020503)41:9<1563::aid-anie1563>3.0.co;2-7.

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14

Kilbinger, Andreas F. M., and Robert H. Grubbs. "Arene-Perfluoroarene Interactions as Physical Cross-Links for Hydrogel Formation." Angewandte Chemie 114, no. 9 (May 2, 2002): 1633–36. http://dx.doi.org/10.1002/1521-3757(20020503)114:9<1633::aid-ange1633>3.0.co;2-s.

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15

Wu, Huixian, Ben-Bo Ni, Chong Wang, Feng Zhai, and Yuguo Ma. "Acid-responsive organogel mediated by arene–perfluoroarene and hydrogen bonding interactions." Soft Matter 8, no. 20 (2012): 5486. http://dx.doi.org/10.1039/c2sm07281e.

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16

Batsanov, Andrei S., Jonathan C. Collings, and Todd B. Marder. "Arene–perfluoroarene interactions in crystal engineering. XV. Ferrocene–decafluorobiphenyl (1/1)." Acta Crystallographica Section C Crystal Structure Communications 62, no. 6 (May 16, 2006): m229—m231. http://dx.doi.org/10.1107/s0108270106014090.

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17

Smith, Caroline E., Philip S. Smith, Rhodri Ll Thomas, Edward G. Robins, Jonathan C. Collings, Chaoyang Dai, Andrew J. Scott, et al. "Arene-perfluoroarene interactions in crystal engineering: structural preferences in polyfluorinated tolans." J. Mater. Chem. 14, no. 3 (2004): 413–20. http://dx.doi.org/10.1039/b314094f.

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18

Wu, Pengfei, Long Zhou, Shuwei Xia, and Liangmin Yu. "Synthesis of luminescent cocrystals based on fluoranthene and the analysis of weak interactions and photophysical properties." Acta Crystallographica Section C Structural Chemistry 77, no. 9 (August 24, 2021): 551–60. http://dx.doi.org/10.1107/s2053229621008652.

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A series of luminescent cocrystals with fluoranthene (C16H10) as the fluorophore and benzene-1,2,4,5-tetracarbonitrile (TCNB, C10H2N4), 2,3,5,6-tetrafluorobenzene-1,4-dicarbonitrile (TFP, C8F4N2) and 1,2,3,4,5,6,7,8-octafluoronaphthalene (OFN, C10F8) as the coformers was designed and synthesized. Structure analysis revealed that these layered structures were due to charge transfer, π–π interactions and hydrogen bonding. Density functional theory (DFT) calculations show that fluoranthene–TCNB and fluoranthene–TFP have charge-transfer properties, while fluoranthene–OFN does not, indicating that fluoranthene–OFN has arene–perfluoroarene (AP) interactions, which was also demonstrated by spectroscopic analysis, which shows that the photophysical properties of luminescent materials can be tuned by forming cocrystals. These results all prove that utilizing supramolecular cocrystals to develop new fluorescent materials is an effective strategy, which has much potential in optoelectronic applications.
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19

Raut, Prasad, Nicole Swanson, Akshata Kulkarni, Coleen Pugh, and Sadhan C. Jana. "Exploiting arene-perfluoroarene interactions for dispersion of carbon black in rubber compounds." Polymer 148 (July 2018): 247–58. http://dx.doi.org/10.1016/j.polymer.2018.06.025.

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20

Hori, Akiko, Ayaka Shinohe, Mikio Yamasaki, Eiji Nishibori, Shinobu Aoyagi, and Makoto Sakata. "1:1 Cross-Assembly of Two β-Diketonate Complexes through Arene–Perfluoroarene Interactions." Angewandte Chemie 119, no. 40 (October 8, 2007): 7761–64. http://dx.doi.org/10.1002/ange.200702662.

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21

Sun, Yanqiu, Yilong Lei, Liangsheng Liao, and Wenping Hu. "Competition between Arene-Perfluoroarene and Charge-Transfer Interactions in Organic Light-Harvesting Systems." Angewandte Chemie International Edition 56, no. 35 (May 19, 2017): 10352–56. http://dx.doi.org/10.1002/anie.201702084.

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22

Hori, Akiko, Ayaka Shinohe, Mikio Yamasaki, Eiji Nishibori, Shinobu Aoyagi, and Makoto Sakata. "1:1 Cross-Assembly of Two β-Diketonate Complexes through Arene–Perfluoroarene Interactions." Angewandte Chemie International Edition 46, no. 40 (October 8, 2007): 7617–20. http://dx.doi.org/10.1002/anie.200702662.

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23

Sun, Yanqiu, Yilong Lei, Liangsheng Liao, and Wenping Hu. "Competition between Arene-Perfluoroarene and Charge-Transfer Interactions in Organic Light-Harvesting Systems." Angewandte Chemie 129, no. 35 (May 19, 2017): 10488–92. http://dx.doi.org/10.1002/ange.201702084.

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24

Hori, Akiko, and Masaya Mizutani. "Synthesis and Crystal Structure Differences between Fully and Partially Fluorinated β-Diketonate Metal (Co2+, Ni2+, and Cu2+) Complexes." International Journal of Inorganic Chemistry 2011 (May 18, 2011): 1–8. http://dx.doi.org/10.1155/2011/291567.

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Coordination complexes, [Co2(1)4(H2O)2] (2), [Ni2(1)4(H2O)2] (3), and [Cu(1)2] (4), by using an asymmetric and partially fluorinated 3-hydroxy-3-pentafluorophenyl-1-phenyl-2-propen-1-one (H1) have been prepared, and the structures were investigated to compare with the corresponding fully fluorinated complexes of [Co2(5)4(H2O)2] (6), [Ni2(5)4(H2O)2] (7), and [Cu(5)2] (8) with bis(pentafluorobenzoyl)methane (H5) and to understand the fluorine-substituted effects. While the coordination mode of the partially fluorinated complexes was quite similar to the fully fluorinated complexes, the intra- and intermolecular π-interactions of the ligand moieties were highly influenced by the fluorination effects; the arene-perfluoroarene interactions were observed in complexes 2 and 3 as a reason of the dinucleation. In this paper, we describe detail structures of the protonated form of the ligand, H1, and complexes 2–4 by X-ray crystallographic studies.
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25

Dai, Chaoyang, Paul Nguyen, Todd B. Marder, Todd B. Marder, Andrew J. Scott, William Clegg, Christopher Viney, and Christopher Viney. "Control of single crystal structure and liquid crystal phase behaviour via arene–perfluoroarene interactions†." Chemical Communications, no. 24 (1999): 2493–94. http://dx.doi.org/10.1039/a906199a.

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26

Habuka, Yusuke, Emily Ami Takeuchi, and Akiko Hori. "Co-crystal structure, Hirshfeld surface analysis and DFT studies of 3,4-ethylenedioxythiophene solvated bis[1,3-bis(pentafluorophenyl)propane-1,3-dionato]copper(II)." Acta Crystallographica Section E Crystallographic Communications 76, no. 6 (May 15, 2020): 820–25. http://dx.doi.org/10.1107/s2056989020006155.

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The title complex, Cu(L)2 or [Cu(C15HF10O2)2], comprised of one copper ion and two fully fluorinated ligands (L −), was crystallized with 3,4-ethylenedioxythiophene (EDOT, C6H6O2S) as a guest molecule to give in a dichloromethane solution a unique co-crystal, Cu(L)2·3C6H6O2S. In the crystal, the oxygen of one guest molecule, EDOT-1, is coordinated to the metal to give an alternate linear arrangement, and the π-planes of the others, EDOT-2 and EDOT-3, interact weakly with the pentafluorophenyl groups of the complex through arene–perfluoroarene interactions. Head-to-tail columnar and head-to-head dimeric arrangements are observed for EDOT-2 and EDOT-3, respectively, in the crystal. The Hirshfeld surface analysis indicated that the most important contributions for the crystal packing are from the F...F (20.4%), F...H/H...F (24.5%) and F...C/C...F (9.6%) interactions. The density functional theory (DFT) optimized structure at the ωB97X-D 6–31G* level was compared with the experimentally determined molecular structure in the solid state.
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27

Ni, Ben-Bo, Chong Wang, Huixian Wu, Jian Pei, and Yuguo Ma. "Copper-free cycloaddition of azide and alkyne in crystalline state facilitated by arene–perfluoroarene interactions." Chem. Commun. 46, no. 5 (2010): 782–84. http://dx.doi.org/10.1039/b912337g.

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28

Weck, Marcus, Alex R. Dunn, Kozo Matsumoto, Geoffrey W. Coates, Emil B. Lobkovsky, and Robert H. Grubbs. "Influence of Perfluoroarene-Arene Interactions on the Phase Behavior of Liquid Crystalline and Polymeric Materials." Angewandte Chemie International Edition 38, no. 18 (September 17, 1999): 2741–45. http://dx.doi.org/10.1002/(sici)1521-3773(19990917)38:18<2741::aid-anie2741>3.0.co;2-1.

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29

Kishikawa, Keiki, Katsuyuki Oda, Sumihiro Aikyo, and Shigeo Kohmoto. "Columnar Superstructures of Non-Disc-Shaped Molecules Generated by Arene–Perfluoroarene Face-to-Face Interactions." Angewandte Chemie International Edition 46, no. 5 (January 22, 2007): 764–68. http://dx.doi.org/10.1002/anie.200603594.

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30

Kishikawa, Keiki, Katsuyuki Oda, Sumihiro Aikyo, and Shigeo Kohmoto. "Columnar Superstructures of Non-Disc-Shaped Molecules Generated by Arene–Perfluoroarene Face-to-Face Interactions." Angewandte Chemie 119, no. 5 (January 22, 2007): 778–82. http://dx.doi.org/10.1002/ange.200603594.

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31

Hori, Akiko, and Tadashi Arii. "Cation–π and arene–perfluoroarene interactions between Cu(ii) fluorine-substituted β-diketonate complex and benzenes." CrystEngComm 9, no. 3 (2007): 215–17. http://dx.doi.org/10.1039/b617808a.

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32

Bacchi, Sergio, Maurizio Benaglia, Franco Cozzi, Francesco Demartin, Giuseppe Filippini, and Angelo Gavezzotti. "X-ray Diffraction and Theoretical Studies for the Quantitative Assessment of Intermolecular Arene–Perfluoroarene Stacking Interactions." Chemistry - A European Journal 12, no. 13 (April 24, 2006): 3538–46. http://dx.doi.org/10.1002/chem.200501248.

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33

Itoh, Takahiro, Mio Kondo, Mari Kanaike, and Shigeyuki Masaoka. "Arene–perfluoroarene interactions for crystal engineering of metal complexes: Controlled self-assembly of paddle-wheel dimers." CrystEngComm 15, no. 31 (2013): 6122. http://dx.doi.org/10.1039/c3ce40777b.

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34

Althagbi, Hanan I., Alison J. Edwards, Brian K. Nicholson, Daniel A. Reason, Graham C. Saunders, Sophie A. Sim, and Danielle A. van der Heijden. "Arene-Perfluoroarene-Anion Stacking and Hydrogen Bonding Interactions in Imidazolium Salts for the Crystal Engineering of Polarity." Crystal Growth & Design 16, no. 1 (December 14, 2015): 174–88. http://dx.doi.org/10.1021/acs.cgd.5b01077.

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35

Ni, Ben-Bo, Chong Wang, Huixian Wu, Jian Pei, and Yuguo Ma. "ChemInform Abstract: Copper-Free Cycloaddition of Azide and Alkyne in Crystalline State Facilitated by Arene-Perfluoroarene Interactions." ChemInform 41, no. 23 (June 8, 2010): no. http://dx.doi.org/10.1002/chin.201023125.

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36

Hori, Akiko, Haruhi Takeda, J. Richard Premkumar, and G. Narahari Sastry. "1:1 and 2:1 cocrystallizations of alkoxy-substituted naphthalene derivatives with octafluoronaphthalene through arene–perfluoroarene interactions." Journal of Fluorine Chemistry 168 (December 2014): 193–97. http://dx.doi.org/10.1016/j.jfluchem.2014.09.025.

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37

Collins, Shawn K., Yassir El-Azizi, and Andreea R. Schmitzer. "Development of Perfluoroarene−Arene Interactions for Macrocyclic En-yne Metathesis and the Total Synthesis of Macrocyclic Natural Products." Journal of Organic Chemistry 72, no. 17 (August 2007): 6397–408. http://dx.doi.org/10.1021/jo070568r.

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38

Sun, Yanqiu, Yilong Lei, Liangsheng Liao, and Wenping Hu. "Titelbild: Competition between Arene-Perfluoroarene and Charge-Transfer Interactions in Organic Light-Harvesting Systems (Angew. Chem. 35/2017)." Angewandte Chemie 129, no. 35 (July 4, 2017): 10383. http://dx.doi.org/10.1002/ange.201706512.

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39

Collings, Jonathan C., Andrei S. Batsanov, Judith AK Howard, and Todd B. Marder. "Arene–perfluoroarene interactions in crystal engineering. Part 14. 1:1 Complexes of octafluoronaphthalene with fluorene and 9,10-dihydrophenanthrene." Canadian Journal of Chemistry 84, no. 2 (February 1, 2006): 238–42. http://dx.doi.org/10.1139/v06-007.

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The 1:1 molecular complexes of octafluoronaphthalene (OFN) with fluorene (1) and with 9,10-dihydrophenanthrene (2) were prepared by cocrystallization of the components and characterized by single-crystal X-ray diffraction. The structure of 1 can be described as a mixed-stack or a laminar checkerboard motif of alternating OFN and fluorene molecules, whilst slanted mixed-stack, herringbone, and face-to-face heteromolecular dimer motifs can all be recognised in 2.Key words: single crystal, X-ray structure, π stacking, fluoroarene.
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40

Collings, Jonathan C., Karl P. Roscoe, Edward G. Robins, Andrei S. Batsanov, Lorna M. Stimson, Judith A. K. Howard, Stewart J. Clark, and Todd B. Marder. "Arene–perfluoroarene interactions in crystal engineering 8: structures of 1∶1 complexes of hexafluorobenzene with fused-ring polyaromatic hydrocarbons." New J. Chem. 26, no. 12 (2002): 1740–46. http://dx.doi.org/10.1039/b207102a.

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41

Collings, J. C., A. S. Batsanov, J. A. K. Howard, and T. B. Marder. "Arene-perfluoroarene interactions in crystal engineering 7: single-crystal structures of 1:1 complexes of octafluoronaphthalene and hexafluorobenzene with acenaphthene." Crystal Engineering 5, no. 1 (March 2002): 37–46. http://dx.doi.org/10.1016/s1463-0184(02)00003-5.

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42

Mandal, Arkalekha, Anwesha Choudhury, Parameswar Krishnan Iyer, and Prasenjit Mal. "Charge Transfer Versus Arene–Perfluoroarene Interactions in Modulation of Optical and Conductivity Properties in Cocrystals of 2,7-Di-tert-butylpyrene." Journal of Physical Chemistry C 123, no. 30 (July 9, 2019): 18198–206. http://dx.doi.org/10.1021/acs.jpcc.9b03827.

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43

Collings, Jonathan C., Philip S. Smith, Dmitri S. Yufit, Andrei S. Batsanov, Judith A. K. Howard, and Todd B. Marder. "Arene–perfluoroarene interactions in crystal engineering. Part 10. Crystal structures of 1∶1 complexes of octafluoronaphthalene with biphenyl and biphenylene." CrystEngComm 6, no. 6 (2004): 25–28. http://dx.doi.org/10.1039/b316169b.

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44

Kishikawa, Keiki, Sumihiro Aikyo, Seiji Akiyama, Takahiro Inoue, Masahiro Takahashi, Shiki Yagai, Hiroaki Aonuma, and Shigeo Kohmoto. "Realization of a lateral directional order in nematic and smectic A phases of rodlike molecules by using perfluoroarene–arene interactions." Soft Matter 7, no. 11 (2011): 5176. http://dx.doi.org/10.1039/c0sm01459a.

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45

Sun, Yanqiu, Yilong Lei, Liangsheng Liao, and Wenping Hu. "Cover Picture: Competition between Arene-Perfluoroarene and Charge-Transfer Interactions in Organic Light-Harvesting Systems (Angew. Chem. Int. Ed. 35/2017)." Angewandte Chemie International Edition 56, no. 35 (July 4, 2017): 10249. http://dx.doi.org/10.1002/anie.201706512.

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46

Zhou, Xing-Hua, Jingdong Luo, Su Huang, Tae-Dong Kim, Zhengwei Shi, Yen-Ju Cheng, Sei-Hum Jang, Daniel B. Knorr, René M. Overney, and Alex K. Y. Jen. "Supramolecular Self-Assembled Dendritic Nonlinear Optical Chromophores: Fine-Tuning of Arene-Perfluoroarene Interactions for Ultralarge Electro-Optic Activity and Enhanced Thermal Stability." Advanced Materials 21, no. 19 (May 18, 2009): 1976–81. http://dx.doi.org/10.1002/adma.200801639.

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47

Constable, Edwin C., Catherine E. Housecroft, Srboljub Vujovic, Jennifer A. Zampese, Aurélien Crochet, and Stuart R. Batten. "Do perfluoroarene⋯arene and C–H⋯F interactions make a difference to the structures of 4,2′:6′,4′′-terpyridine-based coordination polymers?" CrystEngComm 15, no. 46 (2013): 10068. http://dx.doi.org/10.1039/c3ce41384e.

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48

Babu, Sukumaran S, Vakayil K Praveen, Seelam Prasanthkumar, and Ayyappanpillai Ajayaghosh. "Self-Assembly of Oligo(para-phenylenevinylene)s through Arene-Perfluoroarene Interactions: π Gels with Longitudinally Controlled Fiber Growth and Supramolecular Exciplex-Mediated Enhanced Emission." Chemistry - A European Journal 14, no. 31 (October 29, 2008): 9577–84. http://dx.doi.org/10.1002/chem.200801255.

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49

Kishikawa, Keiki, Takahiro Inoue, Yoshiyuki Sasaki, Sumihiro Aikyo, Masahiro Takahashi, and Shigeo Kohmoto. "Generation of biaxiality in smectic A phases by introduction of intermolecular perfluoroarene–arene and C–H/F interactions, and the non-odd–even effect of the molecules in their transition temperatures and layer distances." Soft Matter 7, no. 16 (2011): 7532. http://dx.doi.org/10.1039/c1sm05887h.

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Collings, Jonathan C., Karl P. Roscoe, Rhodri Ll Thomas, Andrei S. Batsanov, Lorna M. Stimson, Judith A. K. Howard, and Todd B. Marder. "Arene-perfluoroarene interactions in crystal engineering. Part 3. Single-crystal structures of 1 : 1 complexes of octafluoronaphthalene with fused-ring polyaromatic hydrocarbonsFor part 1, see ref. 1. For part 2, see ref. 2. Presented at the 16th International Symposium on Fluorine Chemistry, University of Durham, UK, 16–21 July 2000, Abstract no. 308.Electronic supplementary information (ESI) available: experimental data for the re-determination of the crystal structure of triphenylene, tables of the average bond lengths in OFN and the polyaromatic molecules in both the complexes and pure compounds, and a table of distances and angles for intermolecular H···F contacts in the complexes which are below the sum of the van der Waals radii. See http://www.rsc.org/suppdata/nj/b1/b105502j/." New Journal of Chemistry 25, no. 11 (October 19, 2001): 1410–17. http://dx.doi.org/10.1039/b105502j.

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