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Chemical Science
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Journal Name
ARTICLE
Iannaccone, K. Kostarelos, G. Fiori, C. Casiraghi, Nat. 19 J. Cornella, C. Sanchez, D. Banawa, I. Larrosa, Chem. Commun.,
DOI: 10.1039/C9SC05101E
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Chem. Soc., 2017, 139, 11527.
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8
For selected publications on graphene-pyrene-based 20 G. J. P. Perry, J. M. Quibell, A. Panigrahi, I. Larrosa, J. Am.
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Yang, C. Barrow, J. Liu, Compos. Part A: Appl, Sci. Manuf., 22 For examples of the synthesis of polyaromatic hydrocarbons
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For selected publications on graphene-pyrene-based light
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Wibmer, G. Katsukis, G. de la Torre, T. Torres, D. M. Guldi,
Chem. Sci., 2014, 5, 3432; (b) C. B. KC, G. N. Lim, F. D’Souza,
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Harputlu, M. Szalkowski, D. Kowalska, C. G. Unlu, P.
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9
For reviews on the synthesis of pyrene derivatives, see: (a) T.
M. Figueira-Duarte, K. Müllen, Chem. Rev., 2011, 111, 7260; 23 Y. Xu, L. Zhao, H. Bai, W. Hong, C. Li, G. Shi, J. Am. Chem. Soc.,
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Chem., 2014, 12, 212; (c) X. Feng, J.-Y. Hu, C. Redshaw, T. 24 For papers on the analysis of exfoliated graphene flakes, see:
Yamato, Chem. Eur. J., 2016, 22, 11898.
(a) A. Ciesielski, S. Haar, M. El Gemayel, H. Yang, J. Clough, G.
Melinte, M. Gobbi, E. Orgiu, M. V. Nardi, G. Ligorio, V.
Palermo, N. Koch, O. Ersen, C. Casiraghi, P. Samorì, Angew.
Chem. Int. Ed., 2014, 53, 10355; (b) A. Haar, A. Ciesielski, J.
Clough, H. Yang, R. Mazzaro, F. Richard, S. Conti, N. Merstorf,
M. Cecchini, V. Morandi, C. Casiraghi, P. Samorì, Small, 2015,
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Squillaci, O. Ersen, C. Casiraghi, A. Ciesielski, P. Samorì, Sci.
Rep., 2015, 5, 16684; (d) S. Conti, M. G. del Rosso, A. Ciesielski,
J. Weippert, A. Böttcher, Y. Shin, G. Melinte, O. Ersen, C.
Casiraghi, X. Feng, K. Müllen, M. M. Kappes, P. Samorì, M.
Cecchini, ChemPhysChem, 2016, 17, 352; (e) Y. Shin, E.
Prestat, K.-G. Zhou, P. Gorgojo, K. Althumayri, W. Harrison, P.
M. Budd, S. J. Haigh, C. Casiraghi, Carbon, 2016, 102, 357.
10 (a) D. N. Coventry, A. S. Batsanov, A. E. Goeta, J. A. K. Howard,
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Howard, T. B. Marder, Chem. Eur. J., 2012, 18, 5022.
11 For references on the C–H arylation of pyrene derivatives, see:
(a) K. Mochida, K. Kawasumi, Y. Segawa, K. Itami, J. Am. CHem.
Soc., 2011, 133, 10716; (b) L. Ilies, E. Konno, Q. Chen, E.
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Collins, R. Honeker, S. Vásquez-Céspedes, D.-T. D. Tang, F.
Glorious, Chem. Sci., 2015, 6, 1816.
12 For references on the C–H alkynylation of pyrene derivatives,
see: (a) G. Jiang, W. Hu, J. Li, C. Zhu, W. Wu, H. Jiang, Chem.
Commun., 2018, 54, 1746; (b) G. Liao, Q.-J. Yao, Z.-Z. Zhang,
Y.-J. Wu, D.-Y. Huang, B.-F. Shi, Angew. Chem. Int. Ed., 2018,
57, 3661; (c) E. Tan, O. Quinonero, M. E. de Orbe, A. M.
Echevarren, ACS Catal., 2018, 8, 2166.
13 For the directed C–H alkenylation of a pyrene derivatives, see:
J. Zheng, S.-L. You, Angew. Chem. Int. Ed., 2014, 53, 13244.
14 For the directed C–H borylation of a pyrene derivative, see: A.
Ros, B. Estepa, R. López-Rodríguez, E. Álvarez, R. Fernández, J.
M. Lassaletta, Angew. Chem. Int. Ed., 2011, 50, 11724.
15 For reviews on the arylation of aromatic carboxylic acids, see:
(a) J. Cornella, I. Larrosa, Synthesis, 2012, 653; (b) M. P.
Drapeau, L. J. Gooßen, Chem. Eur. J., 2016, 22, 18654; (c) M.
Font, J. Quibell, G. J. P. Perry, I. Larrosa, Chem. Commun.,
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2017, 25, 3517.
16 For references on decarboxylative ortho-arylation of
carboxylic acids, see: (a) J. Cornella, M. Righi, I. Larrosa,
Angew. Chem. Int. Ed., 2011, 50, 9429; (b) J. Luo, S. Preciado,
I. Larrosa, J. Am. Chem. Soc., 2014, 136, 4109; (c) J. Luo, S.
Preciado, I. Larrosa, Chem. Commun., 2015, 51, 3127; (d) Y.
Zhang, H. Zhao, M. Zhang, W. Su, Angew. Chem. Int. Ed., 2015,
54, 3817; (e) M. Font, A. R. A. Spencer, I. Larrosa, Chem. Sci.,
2018, 9, 7133.
17 For references on the palladium-catalysed non-
decarboxylative ortho-arylation of carboxylic acids, see: (a) H.
A. Chiong, Q.-N. Pham, O. Daugulis, J. Am. Chem. Soc., 2007,
129, 9879; (b) C. Arroniz, A. Ironmonger, G. Rassias, I. Larrosa,
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Ironmonger, G. Rassias, I. Larrosa, Chem. Sci., 2014, 5, 3509;
(d) C. Zhu, Y. Zhang, J. Kan, H. Zhao, W. Su, Org. Lett., 2015,
17, 3418.
18 See the Supporting Information for further details.
This journal is © The Royal Society of Chemistry 20xx
J. Name., 2013, 00, 1-3 | 7
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