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| Naji, M. |
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| Motta, Antonella |
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| Aletan, Dirar |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Taccardi, Nicola |
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| Kononenko, Denys |
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| Petrov, R. H. | Madrid |
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| Alshaaer, Mazen | Brussels |
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| Bih, L. |
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| Casati, R. |
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| Muller, Hermance |
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| Kočí, Jan | Prague |
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| Šuljagić, Marija |
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| Kalteremidou, Kalliopi-Artemi | Brussels |
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| Azam, Siraj |
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| Ospanova, Alyiya |
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| Blanpain, Bart |
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| Ali, M. A. |
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| Popa, V. |
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| Rančić, M. |
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| Ollier, Nadège |
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| Azevedo, Nuno Monteiro |
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| Landes, Michael |
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| Rignanese, Gian-Marco |
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Horton, Peter
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (11/11 displayed)
- 2023β,β-directly linked porphyrin ringscitations
- 2023N=8 armchair graphene nanoribbonscitations
- 2020Oxidopolyborate chemistrycitations
- 2020Oxidopolyborate anions templated by transition-metal complex cations: Self-assembled syntheses and structural studies (XRD) of [Co(NH3)6]2[B4O5(OH)4]3·11H2O, [Ni(phen)3][B7O9(OH)5]·9.5H2O and [Zn(dac)2(H2O)2][B7O9(OH)5]·H2Ocitations
- 2019Syntheses, X-ray structures and characterisation of luminescent chromium(III) complexes incorporating 8-quinolinato ligandscitations
- 2018Two 1-D coordination polymers containing zinc(II) hexaborates: [Zn(en{B6O7(OH)6}]2H2O (en =1,2-diaminoethane) and [Zn(pn{B6O7(OH)6}]1.5H2O (pn = 1,2-diaminopropane)citations
- 2017Synthesis, XRD studies and NLO properties of [p-H2NC6H4CH2NH3][B5O6(OH)4]·1/2H2O and NLO properties of some related pentaborate(1−) saltscitations
- 2013The competition between halogen bonds (Br???O) and C–H???O hydrogen bonds: the structure of the acetone–bromine complex revisitedcitations
- 2011Synthesis and structures of mono and binuclear nickel(II) thiolate complexes of a dicompartmental pseudo-macrocycle with N(imine)2S2 and N(oxime)2S2 metal-binding sitescitations
- 2008Synthesis, structure, and supramolecular architecture of benzonitrile and pyridine adducts of bis(pentafluorophenyl)zinc: pentafluorophenyl-aryl interactions versus homoaromatic pairingcitations
- 2004Mixed valence Mn(II)/Mn(III) [3 x 3] grid complexes: structural, electrochemical, spectroscopic, and magnetic propertiescitations
Places of action
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article
N=8 armchair graphene nanoribbons
Abstract
<p>Structurally defined graphene nanoribbons (GNRs) have emerged as promising candidates for nanoelectronic devices. Low band gap (<1 eV) GNRs are particularly important when considering the Schottky barrier in device performance. Here, we demonstrate the first solution synthesis of 8-AGNRs through a carefully designed arylated polynaphthalene precursor. The efficiency of the oxidative cyclodehydrogenation of the tailor-made polymer precursor into 8-AGNRs was validated by FT-IR, Raman, and UV/Vis-near-infrared (NIR) absorption spectroscopy, and further supported by the synthesis of naphtho[1,2,3,4-<i>ghi</i>]perylene derivatives (<b>1</b> and <b>2</b>) as subunits of <b>8-AGNR</b>, with a width of 0.86 nm as suggested by the X-ray single crystal analysis. Low-temperature scanning tunneling microscopy (STM) and solid-state NMR analyses provided further structural support for <b>8-AGNR</b>. The resulting <b>8-AGNR</b> exhibited a remarkable NIR absorption extending up to ∼2400 nm, corresponding to an optical band gap as low as ∼0.52 eV. Moreover, optical-pump TeraHertz-probe spectroscopy revealed charge-carrier mobility in the dc limit of ∼270 cm<sup>2</sup> V<sup>−1</sup> s<sup>−1</sup> for the <b>8-AGNR</b>.</p>