Corrigendum to ‘Recent developments in metal dipyrrin complexes: Design, synthesis, and applications’ [Coord. Chem. Rev. 414 (2020) 213269] (Coordination Chemistry Reviews (2020) 414, (S0010854519304175), (10.1016/j.ccr.2020.213269))

Abstract

The authors regret that some of the copyright permissions were omitted from the published version of this review. The corrected figure captions are listed below. The authors apologize for this omission. Fig. 7. Examples of homoleptic complexes based on trivalent metal ions. Reprinted with permission from ref 56. Copyright @ 2006 American Chemical Society. Fig. 9. Structures of Fe(II) complexes of dipyrromethene. Reprinted with permission from ref 12. Copyright @ 2011 American Chemical Society. Fig. 10. Structure of complexes 2 (a), 3 (b) and 4 (c). Reprinted with permission from ref 11. Copyright @ 2009 American Chemical Society. Fig. 12. Chemical structure of dipyrrin 17 and Ga(III) complex 18. Reprinted with permission from ref 76. Copyright @ 2010 American Chemical Society. Fig. 18. Crystal structure of 80 and 81. Reprinted with permission from ref 77. Copyright 2009 The Royal Society of Chemistry. Fig. 22. Structure of metal complex 101. Reprinted with permission from ref 151. Copyright 2016 The Royal Society of Chemistry. Fig. 33. Zn2+ detection by dipyrromethanes 146–148. Reprinted with permission from ref 173. Copyright 2014 The Royal Society of Chemistry. Fig. 38. Complexation of 160 with Cd2+ and Hg2+ ions (a). Crystal structure of 161 (b). Reprinted with permission from ref 181. Copyright 2017 Centre National de la Recherche Scientifique (CNRS) and The Royal Society of Chemistry. Fig. 39. (a) Chemical structures of 162 and 163. Ar = t-Bu; (b) A photograph showing the color changes of 163 (25 mM) in the presence of various anions (40 equiv.) in DMSO; (c) UV–Vis spectral changes of 163 (10 μM) in the presence of F− (0–180 equiv.) in DMSO. Reprinted with permission from ref 186. Copyright 2010 The Royal Society of Chemistry. Fig. 40. (a) Chemical structures of 164–166; (b) and (c) image showing the color changes of probe 166 in the presence of different anions, (b) in CH2Cl2; (c) in DMSO–H2O. Reprinted with permission from ref 187. Copyright 2012 The Royal Society of Chemistry. Fig. 41. (a) Structures of compounds 167–169 bearing α-formyl groups; (b) photograph showing the color changes of solution of 167 in CHCl3 after addition of different anions (1.2 equiv). Reprinted with permission from ref 188. Copyright 2014 The Royal Society of Chemistry. Fig. 44. (a) ORTEP view of the metallotecton Δ-178b. (b) Showing 1-D zig-zag chains of metallotecton Δ-178b linked by hydrogen bonds involving two of the three carboxyl groups of each tecton. Reprinted with permission from ref 194. Copyright 2007 The Royal Society of Chemistry Fig. 45. Crystal structures of 179 and 180. Reprinted with permission from ref 57. Copyright 2009 The Royal Society of Chemistry. Fig. 46. Dimeric structure of dipyrrin 181 (a) and its nickel (II) complex 182 (b) as determined by X-ray crystallography. Representing a portion of the 1-D networks based on the [Formula presented] (12) connectivity pattern of 181 (c) and the distorted square planar/ tetrahedral coordination bonding motif in 182 (d). Reprinted with permission from ref 195. Copyright 2011 The Royal Society of Chemistry. Fig. 48. Showing space-filling representation of coordination polymers formed 199 (top right) and 200 (top left) and stick representation of 200 (bottom) viewed down the crystallographic c-axis, Reprinted with permission from ref 199. Copyright 2004 American Chemical Society. Fig. 49. Chemical structure of 201 (a), Molecular hexagons (b) and helical coordination polymers (c) comprising the supramolecular structure. Reprinted with permission from ref 200. Copyright © 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Fig. 50. Chemical structure of 202 (a), ORTEP view of 203 (b) and Ag–π interaction 204. Reprinted with permission from ref 201. Copyright 2007 The Royal Society of Chemistry. Fig. 51. Chemical structures of 205–209 and crystal structure of 210. Reprinted with permission from ref 202. Copyright 2004 American Chemical Society. Fig. 52. (a) Layered structure in a crystal of 209 (b) Ribbon like structure and the packing diagram in a crystal of 210. The hydrogen bonds are denoted by dotted lines. Reprinted with permission from ref 202. Copyright 2004 American Chemical Society. Fig. 54. Chemical structure of 216 (a) and 2-D network (b) formed by its complex with Cu(OAc)2. Reprinted with permission from ref 205. Copyright 2009 The Royal Society of Chemistry. Fig. 56. (a) A portion of the 1-D CP observed in the crystalline phase for 221. (b) A portion of the 1-D hydrogen bonded network in the crystal structure of 222. Reprinted with permission from ref 25. Copyright 2012 The Royal Society of Chemistry. Fig. 59. Portions of the crystal structures of CPs 231–234. Reprinted with permission from ref 207. Copyright 2014 The Royal Society of Chemistry. Fig. 60. Chemical structure of 235, portions of crystal structures of 236 and 237. Reprinted with permission from ref 209. Copyright 2007 The Royal Society of Chemistry. Fig. 69. Chemical structures of 256 and 257. Absorption spectrum of 256 in MeCN. The green area covers excitations of the iridium complex due to LC and MLCT transitions, the red shaded region covers π–π* excitations of the NDI and the blue regions covers excitations of the TAA. The absorption spectrum of 257 (violet solid line) and corresponding phosphorescence spectrum (violet line), excitation spectrum (green solid line). Reprinted with permission from ref 217. Copyright 2013 PCCP Owner Societies. Fig. 72. (a) Image of a free-standing film of 268-SWCNT (thickness of 64 μm). (b) TEM image of 268-SWCNT subjected to electron energy-loss spectroscopy (EELS) mapping. EELS mapping for: (c) carbon K edge intensity and (d) Zn M2 and M3 edge intensities. (e) Overlapped image of (b) and (c). (f) Voltage-difference/temperature difference plots for pristine SWCNTs (black) and 33-SWCNT (orange). (Reprinted with permission from ref 221. Copyright 2015 The Royal Society of Chemistry. Fig. 73. Photoelectric conversion profile using 268 as an active material. (a) Image of a thin film of 268 on a SnO2 electrode. (b) Anodic photocurrent signal after irradiation of a working electrode (SnO2 substrate modified with 268 as shown in (a) with intermittent 500 nm light. (c) Action spectrum for the photocurrent generation (orange dots) and absorption spectrum of 268 on a SnO2 substrate (gray solid line). Reprinted with permission from ref 221. Copyright 2015 The Royal Society of Chemistry. Fig. 74. Structures of dipyrromethene ligand and bis(dipyrrinato)Zn(II) complex; nanosheet 269. Reprinted with permission from ref 222. Copyright © 2015, Springer Nature. Fig. 75. (a) Anodic current response after irradiation of the working electrode (SnO2 substrate modified with 36-layer 269) with intermittent 500 nm light (0.1 M tetrabutylammonium perchlorate with 0.05 M TEOA in acetonitrile) (b) action spectrum for the photocurrent generation (magenta dots) and absorption spectrum of 269 (black solid line). (c) Changes in UV–vis spectra upon stepwise depositions of single-layer 269 on a quartz substrate. (d) Showing linear relationship between the absorbance at 500 nm and number of deposition cycles. Reprinted with permission from ref 222. Copyright © 2015, Springer Nature. Fig. 76. Left: chemical structure of porphyrin–dipyrrin hybrid ligand 271. Right: a) Typical photoelectric conversion response upon irradiation of the 270-physisorbed photoanode with intermittent 440 nm monochromatic light. b) Action spectrum for the photocurrent generation (orange dots) and absorption spectrum of 270 (green solid line). Reprinted with permission from ref 223. 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Fig. 82. (a) Chemical structure of 286 (b) UV–vis spectra showing reductive conversion of Cr(VI) to Cr(III) AuNPs (c) AuNPs@prGO500 (d) The plot of conversion vs. time as monitored by UV–vis spectroscopy (e) Schematic presentation for Cr(VI) reduction on AuNPs@prGO500. Reaction conditions: HCOOH = 0.2 mL, [Cr2O72-] = 0.2 mM and catalytic amount = 1 mg/mL (25 µL) levels (0.1 μM to 0.1 M) in 50 mM phosphate buffer solutions at pH = 4.5. Reprinted with permission from ref 233. Copyright 2016 The Royal Society of Chemistry. Fig. 84. Crystal structure of Pd(II)bis-dipyrrinato complex 293 (Reprinted with permission from ref 237. 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) and Mn(III)-bis(phenolate)dipyrrin complex 294. Fig. 85. Crystal structures of U(VI) complex 295 (a) U(IV) complex 296 (b) and Fe(III) complexes 297 (c), 298 (d) and 299 (e), Reprinted with permission from ref 239 (Copyright 2017 American Chemical Society). Scheme 14. Synthesis and crystal structure of compound 100. Reprinted with permission from ref 150. Copyright 2011 The Royal Society of Chemistry. © 2020