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Correction: Reactivity study of Lewis superacidic carborane-based analogue of 9-bromo-9-borafluorene towards Lewis bases
Libo
Xiang
ab,
Alexander
Matler
ab,
Leibo
Tan
ab and
Qing
Ye
*ab
aInstitute for Inorganic Chemistry, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany. E-mail: qing.ye@uni-wuerzburg.de
bInstitute for Sustainable Chemistry & Catalysis with Boron, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany
First published on 27th August 2024
Abstract
Correction for ‘Reactivity study of Lewis superacidic carborane-based analogue of 9-bromo-9-borafluorene towards Lewis bases’ by Libo Xiang et al., Dalton Trans., 2024, 53, 11655–11658, https://doi.org/10.1039/D4DT01615G.
The authors regret that there was a mismatch between the images and captions for Schemes 1 and 2 and Fig. 2 and 3 in the original article. The correct figures are shown here.
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| Scheme 1 Synthesis of 2–3. | ||
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| Scheme 2 (a) Synthesis of 4; (b) synthesis of 4 via 5. | ||
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| Fig. 1 Single crystal structure of 2a. Hydrogen atoms were omitted for clarity. Thermal ellipsoids are drawn at the 50% probability level. Selected bond lengths [Å]: 2, B1–P 2.032(2), B1–C1 1.671(3), B1–C4 1.667(3), C1–C2 1.667(3), C3–C4 1.670(3), B–Br 2.036(2). | ||
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| Fig. 2 Single crystal structure of 3a. Hydrogen atoms were omitted for clarity. Thermal ellipsoids are drawn at the 50% probability level. Selected bond lengths [Å]: B–C1 1.605(3), B–C2 1.648(3), B–C5 1.643(3), C2–C3 1.656(3), C4–C5 1.653(3), C–N1 1.143(3), B–Br 2.009(2). | ||
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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