82
J. Setsune
Kuroda Y, Kato Y, Higashioji T, Hasegawa J, Kawanami S, Takahashi M, Shiraishi N, Tanabe K,
Ogoshi H (1995) Chiral amino acid recognition by a porphyrin-based artificial receptor. J Am
Chem Soc 117:10950–10958
Kurotobi K, Kim KS, Noh SB, Kim D, Osuka A (2006) A quadruply azulene-fused porphyrin with
intense near-IR absorption and a large two-photon absorption cross section. Angew Chem Int Ed
45:3944–3947
Kurotobi K, Toude Y, Kawamoto K, Fujimori Y, Ito S, Chabera P, Sundström V, Imahori H (2013)
Highly asymmetrical porphyrins with enhanced push-pull character for dye-sensitized solar cells.
Chem Eur J 19:17075–17081
Lewtaka JP, Gryko DT (2012) Synthesis of π-extended porphyrins via intramolecular oxidative
coupling. Chem Commun 48:10069–10086
Lindsey JS (2010) Synthetic routes to meso-patterned porphyrins. Acc Chem Res 43:300–311
Lindsey J (1980) Increased yield of a desired isomer by equilibriums displacement on binding to
silica gel, applied to meso-tetrakis(o-aminophenyl)porphyrin. J Org Chem 45:5215
Lindsey JS, Schreiman IC, Hsu HC, Kearney PC, Marguerettaz AM (1987) Rothemund and AdlerLongo reactions revisited: synthesis of tetraphenylporphyrins under equilibrium conditions. J Org
Chem 52:827–836
Li X, Tanasova M, Vasileiou C, Borhan B (2008) Fluorinated porphyrin tweezer: a powerful reporter
of absolute configuration for erythro and threo diols, amino alcohols, and diamines. J Am Chem
Soc 130:1885–1893
Luo J, Lee S, Son M, Zheng B, Huang K-W, Qi Q, Zeng W, Li G, Kim D, Wu J (2015) Nannulated perylene-substituted and fused porphyrin dimers with intense near-infrared one-photon
and two-photon absorption. Chem Eur J 21:3708–3715
Mandoj F, Nardis S, Pudi R, Lvova L, Fronczek FR, Smith KM, Prodi L, Genovese D, Paolesse R
(2013) β-pyrazino-fused tetrarylporphyrins. Dyes Pigm 99:136–143
Mathew S, Yella A, Gao P, Humphry-Baker R, Curchod BFE, Ashari-Astani N, Tavernelli I, Rothlisberger U, Nazeeruddin MdK, Grätzel M (2014) Dye-sensitized solar cells with 13% efficiency
achieved through the molecular engineering of porphyrin sensitizers. Nat Chem 6:242–247
McCarthy JR, Hyland MA, Brückner C (2004) Synthesis of indaphyrins: meso-tetraarylsecochlorinbased porphyrinoids containing direct o-phenyl-to-β-linkages. Org Biomol Chem 2:1484–1491
Meindl A, Plunkett S, Ryan AA, Flanagan KJ, Callaghan S, Senge MO (2017) Comparative synthetic
strategies for the generation of 5,10- and 5,15-substituted push-pull porphyrins. Eur J Org Chem
3565–3583
Mikhaylov A, Kondratuk DV, Cnossen A, Anderson HL, Drobizhev M, Rebane A (2016) Cooperative enhancement of two-photon absorption in self-assembled zinc-porphyrin nanostructures. J
Phys Chem C 120:11663−11670
Mizuno Y, Aida T, Yamaguchi K (2000) Chirality-memory molecule: crystallographic and spectroscopic studies on dynamic molecular recognition events by fully substituted chiral porphyrins. J
Am Chem Soc 122:5278–5285
Mizuno Y, Alam MdA, Tsuda A, Kinbara K, Yamaguchi K, Aida T (2006) Hermaphroditic chirality
of a D 2-symmetric saddle-shaped porphyrin in multicomponent spontaneous optical resolution:
inclusion cocrystals with double-helical porphyrin arrays. Angew Chem Int Ed 45:3786–3790
Mysłiwiec D, Donnio B, Chmielewski PJ, Heinrich B, Stepien M (2012) Peripherally fused
porphyrins via the Scholl reaction: synthesis, self-assembly, and mesomorphism. J Am Chem
Soc 134:4822−4833
Nakamura Y, Jang SY, Tanaka T, Aratani N, Lim JM, Kim KS, Kim D, Osuka A (2008) Twodimensionally extended porphyrin tapes: synthesis and shape-dependent two-photon absorption
properties. Chem Eur J 14:8279–8289
Nishino N, Kobata K, Mihara H, Fujimoto T (1992) Efficient preparation of αβαβ-atropisomer of
meso-tetra(o-aminophenyl)porphyrin. Chem Lett 1991–1994
Paolesse R, Jaquinod L, Sala FD, Nurco DJ, Prodi L, Montalti M, Natale CD, D’Amico A, Carlo
AD, Lugli P, Smith KM (2000) β-Fused oligoporphyrins: a novel approach to a new type of
extended aromatic system. J Am Chem Soc 122:11295–11302
J. Setsune
Kuroda Y, Kato Y, Higashioji T, Hasegawa J, Kawanami S, Takahashi M, Shiraishi N, Tanabe K,
Ogoshi H (1995) Chiral amino acid recognition by a porphyrin-based artificial receptor. J Am
Chem Soc 117:10950–10958
Kurotobi K, Kim KS, Noh SB, Kim D, Osuka A (2006) A quadruply azulene-fused porphyrin with
intense near-IR absorption and a large two-photon absorption cross section. Angew Chem Int Ed
45:3944–3947
Kurotobi K, Toude Y, Kawamoto K, Fujimori Y, Ito S, Chabera P, Sundström V, Imahori H (2013)
Highly asymmetrical porphyrins with enhanced push-pull character for dye-sensitized solar cells.
Chem Eur J 19:17075–17081
Lewtaka JP, Gryko DT (2012) Synthesis of π-extended porphyrins via intramolecular oxidative
coupling. Chem Commun 48:10069–10086
Lindsey JS (2010) Synthetic routes to meso-patterned porphyrins. Acc Chem Res 43:300–311
Lindsey J (1980) Increased yield of a desired isomer by equilibriums displacement on binding to
silica gel, applied to meso-tetrakis(o-aminophenyl)porphyrin. J Org Chem 45:5215
Lindsey JS, Schreiman IC, Hsu HC, Kearney PC, Marguerettaz AM (1987) Rothemund and AdlerLongo reactions revisited: synthesis of tetraphenylporphyrins under equilibrium conditions. J Org
Chem 52:827–836
Li X, Tanasova M, Vasileiou C, Borhan B (2008) Fluorinated porphyrin tweezer: a powerful reporter
of absolute configuration for erythro and threo diols, amino alcohols, and diamines. J Am Chem
Soc 130:1885–1893
Luo J, Lee S, Son M, Zheng B, Huang K-W, Qi Q, Zeng W, Li G, Kim D, Wu J (2015) Nannulated perylene-substituted and fused porphyrin dimers with intense near-infrared one-photon
and two-photon absorption. Chem Eur J 21:3708–3715
Mandoj F, Nardis S, Pudi R, Lvova L, Fronczek FR, Smith KM, Prodi L, Genovese D, Paolesse R
(2013) β-pyrazino-fused tetrarylporphyrins. Dyes Pigm 99:136–143
Mathew S, Yella A, Gao P, Humphry-Baker R, Curchod BFE, Ashari-Astani N, Tavernelli I, Rothlisberger U, Nazeeruddin MdK, Grätzel M (2014) Dye-sensitized solar cells with 13% efficiency
achieved through the molecular engineering of porphyrin sensitizers. Nat Chem 6:242–247
McCarthy JR, Hyland MA, Brückner C (2004) Synthesis of indaphyrins: meso-tetraarylsecochlorinbased porphyrinoids containing direct o-phenyl-to-β-linkages. Org Biomol Chem 2:1484–1491
Meindl A, Plunkett S, Ryan AA, Flanagan KJ, Callaghan S, Senge MO (2017) Comparative synthetic
strategies for the generation of 5,10- and 5,15-substituted push-pull porphyrins. Eur J Org Chem
3565–3583
Mikhaylov A, Kondratuk DV, Cnossen A, Anderson HL, Drobizhev M, Rebane A (2016) Cooperative enhancement of two-photon absorption in self-assembled zinc-porphyrin nanostructures. J
Phys Chem C 120:11663−11670
Mizuno Y, Aida T, Yamaguchi K (2000) Chirality-memory molecule: crystallographic and spectroscopic studies on dynamic molecular recognition events by fully substituted chiral porphyrins. J
Am Chem Soc 122:5278–5285
Mizuno Y, Alam MdA, Tsuda A, Kinbara K, Yamaguchi K, Aida T (2006) Hermaphroditic chirality
of a D 2-symmetric saddle-shaped porphyrin in multicomponent spontaneous optical resolution:
inclusion cocrystals with double-helical porphyrin arrays. Angew Chem Int Ed 45:3786–3790
Mysłiwiec D, Donnio B, Chmielewski PJ, Heinrich B, Stepien M (2012) Peripherally fused
porphyrins via the Scholl reaction: synthesis, self-assembly, and mesomorphism. J Am Chem
Soc 134:4822−4833
Nakamura Y, Jang SY, Tanaka T, Aratani N, Lim JM, Kim KS, Kim D, Osuka A (2008) Twodimensionally extended porphyrin tapes: synthesis and shape-dependent two-photon absorption
properties. Chem Eur J 14:8279–8289
Nishino N, Kobata K, Mihara H, Fujimoto T (1992) Efficient preparation of αβαβ-atropisomer of
meso-tetra(o-aminophenyl)porphyrin. Chem Lett 1991–1994
Paolesse R, Jaquinod L, Sala FD, Nurco DJ, Prodi L, Montalti M, Natale CD, D’Amico A, Carlo
AD, Lugli P, Smith KM (2000) β-Fused oligoporphyrins: a novel approach to a new type of
extended aromatic system. J Am Chem Soc 122:11295–11302