Masaki
Yamamura
a,
Shinya
Yazaki
a,
Motofumi
Seki
a,
Yasunori
Matsui
b,
Hiroshi
Ikeda
b and
Tatsuya
Nabeshima
*a
aGraduate School of Pure and Applied Sciences & Tsukuba Research Center for Interdisciplinary Materials Science, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8571, Japan. E-mail: nabesima@chem.tsukuba.ac.jp
bGraduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Sakai, Osaka 599-8531, Japan
First published on 20th July 2018
Correction for ‘A facile and high-yield formation of dipyrrin-boronic acid dyads and triads: a light-harvesting system in the visible region based on the efficient energy transfer’ by Masaki Yamamura et al., Org. Biomol. Chem., 2015, 13, 2574–2581.
In the cited paper, the preparation procedure for compound 1 is not described. The preparative method for 1 is as follows. The authors apologize for the inconvenience this may have caused.
Preparation of 1: To a 300 mL flask were added Ar,O-BODIPY S110 (588.2 mg, 1.076 mmol), methanol (100 mL), and conc. HCl aq. (5 mL). The mixture was stirred at room temperature for 19 h. To the reaction mixure were added sat. NaHCO3 aq. (100 mL) and EtOAc (100 mL). The organic layer was separated, and the aqueous layer was extracted with EtOAc (50 mL × 2). The combined organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by column chromatography (silica gel, EtOAc/hexane = 1/8) to give 1 as a red solid (476.0 mg, 1.034 mmol, 96%). 1H NMR (400 MHz, CDCl3): δ 12.92 (br), 11.96 (br), 7.75 (dd, J = 7.8, 1.4 Hz, 1H), 7.69 (dd, J = 7.8, 1.5 Hz, 1H), 7.32–7.26 (3H), 7.08–6.99 (4H), 6.96 (s, 2H), 6.93 (d, J = 7.1 Hz, 1H), 6.74 (d, J = 4.6 Hz, 2H), 6.30 (br), 3.96 (s, 3H), 2.38 (s, 3H), 2.14 (s, 6H).
10 C. Ikeda, T. Maruyama and T. Nabeshima, Tetrahedron Lett., 2009, 50, 3349–3351.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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