3 Porphyrins: Syntheses and Properties
81
Drobizhev M, Stepanenko Y, Rebane A, Wilson CJ, Screen TEO, Anderson HL (2006) Strong
cooperative enhancement of two-photon absorption in double-strand conjugated porphyrin ladder
arrays. J Am Chem Soc 128:12432−12433
Finikova O, Cheprakov A, Beletskaya I, Vinogradov S (2001) An expedient synthesis of substituted
tetraaryltetrabenzoporphyrins. Chem Commun 261–262
Finikova O, Cheprakov A, Beletskaya I, Carroll P, Vinogradov S (2004) Novel versatile synthesis
of substituted tetrabenzoporphyrins. J Org Chem 69:522–535
Fujimoto K, Osuka A (2018) A 1,5-naphthyridine-fused porphyrin dimer: intense nir absorption
and facile redox interconversion with its reduced congener. Chem Eur J 24:6530–6533
Fujimoto K, Yorimitsu H, Osuka A (2014) Facile preparation of β-haloporphyrins as useful
precursors of β-substituted porphyrins. Org Lett 16:972−975
Fukui N, Fujimoto K, Yorimitsu H, Osuka A (2017) Embedding heteroatoms: an effective approach
to create porphyrin-based functional materials. Dalton Trans 46:13322–13341
Götz DCG, Gehrold AC, Dorazio SJ, Daddario P, Samankumara L, Bringmann G, Brückner C,
Bruhn T (2015) Indaphyrins and indachlorins: optical and chiroptical properties of a family of
helimeric porphyrinoids. Eur J Org Chem 3913–3922
Grzybowski M, Skonieczny K, Butenschçn H, Gryko DT (2013) Comparison of oxidative aromatic
coupling and the Scholl reaction. Angew Chem Int Ed 52:9900–9930
Hata H, Shinokubo H, Osuka A (2005) Highly regioselective Ir-Catalyzed β-borylation of porphyrins
via C−H bond activation and construction of β−β-linked diporphyrin. J Am Chem Soc 127:8264–
8265
Huang X, Rickman BH, Borhan B, Berova N, Nakanishi K (1998) Zinc porphyrin tweezer in
host−guest complexation: determination of absolute configurations of diamines, amino acids,
and amino alcohols by circular dichroism. J Am Chem Soc 120:6185–6186
Ito S, Murashima T, Uno H, Ono N (1998) A new synthesis of benzoporphyrins using 4,7-dihydro4,7-ethano-2H-isoindole as a synthon of isoindole. Chem Commun 1661–1662
Ito S, Uno H, Murashima T, Ono N (2001) Synthesis of benzoporphyrins functionalized with
octaester groups. Tetrahedron Lett 42:45–47
Ito S, Hiroto S, Lee S, Son M, Hisaki I, Yoshida T, Kim D, Kobayashi N, Shinokubo H (2015)
Synthesis of highly twisted and fully π-conjugated porphyrinic oligomers. J Am Chem Soc
137:142–145
Ito S, Hiroto S, Ousaka N, Yashima E, Shinokubo H (2016) Control of conformation and chirality
of nonplanar π-conjugated diporphyrins using substituents and axial ligands. Chem Asian J
11:936–942
Jaquinod L, Siri O, Khoury RG (1998) Linear fused oligoporphyrins: potential molecular wires with
enhanced electronic communication between bridged metal ions. Chem Commun 1261–1262
Jeandon C, Ruppert R (2011) A porphyrin with two coordination sites: the biquinoline ligand as a
new potential external chelate. Eur J Org Chem 4098−4102
Jiang L, Zaenglein RA, Engle JT, Mittal C, Hartley CS, Ziegler CJ, Wang H (2012) Water-soluble
ionic benzoporphyrins. Chem Commun 48:6927–6929
Kadish KM, Smith KM, Guilard R (eds) (2000) The porphyrin handbook. Academic Press, San
Diego
Kadish KM, Smith KM, Guilard R (eds) (2010) Handbook of porphyrin science. World Scientific,
Singapore
Kondratuk DV, Sprafke JK, O’Sullivan MC, Perdigao LMA, Saywell A, Malfois M, O’Shea JN,
Beton PH, Thompson AL, Anderson HL (2014) Vernier-templated synthesis, crystal structure,
and supramolecular chemistry of a 12-porphyrin nanoring. Chem Eur J 20:12826–12834
Kuimova MK, Botchway SW, Parker AW, Balaz M, Collins HA, Anderson HL, Suhling K, Ogilby
PR (2009) Imaging intracellular viscosity of a single cell during photoinduced cell death. Nat
Chem 1:69–73
Kumar S, Jiang X, Shan W, Jinadasa RGW, Kadish KM, Wang H (2018) β-Functionalized transA2B2 push–pull tetrabenzoporphyrins. Chem Commun 54:5303–5306
81
Drobizhev M, Stepanenko Y, Rebane A, Wilson CJ, Screen TEO, Anderson HL (2006) Strong
cooperative enhancement of two-photon absorption in double-strand conjugated porphyrin ladder
arrays. J Am Chem Soc 128:12432−12433
Finikova O, Cheprakov A, Beletskaya I, Vinogradov S (2001) An expedient synthesis of substituted
tetraaryltetrabenzoporphyrins. Chem Commun 261–262
Finikova O, Cheprakov A, Beletskaya I, Carroll P, Vinogradov S (2004) Novel versatile synthesis
of substituted tetrabenzoporphyrins. J Org Chem 69:522–535
Fujimoto K, Osuka A (2018) A 1,5-naphthyridine-fused porphyrin dimer: intense nir absorption
and facile redox interconversion with its reduced congener. Chem Eur J 24:6530–6533
Fujimoto K, Yorimitsu H, Osuka A (2014) Facile preparation of β-haloporphyrins as useful
precursors of β-substituted porphyrins. Org Lett 16:972−975
Fukui N, Fujimoto K, Yorimitsu H, Osuka A (2017) Embedding heteroatoms: an effective approach
to create porphyrin-based functional materials. Dalton Trans 46:13322–13341
Götz DCG, Gehrold AC, Dorazio SJ, Daddario P, Samankumara L, Bringmann G, Brückner C,
Bruhn T (2015) Indaphyrins and indachlorins: optical and chiroptical properties of a family of
helimeric porphyrinoids. Eur J Org Chem 3913–3922
Grzybowski M, Skonieczny K, Butenschçn H, Gryko DT (2013) Comparison of oxidative aromatic
coupling and the Scholl reaction. Angew Chem Int Ed 52:9900–9930
Hata H, Shinokubo H, Osuka A (2005) Highly regioselective Ir-Catalyzed β-borylation of porphyrins
via C−H bond activation and construction of β−β-linked diporphyrin. J Am Chem Soc 127:8264–
8265
Huang X, Rickman BH, Borhan B, Berova N, Nakanishi K (1998) Zinc porphyrin tweezer in
host−guest complexation: determination of absolute configurations of diamines, amino acids,
and amino alcohols by circular dichroism. J Am Chem Soc 120:6185–6186
Ito S, Murashima T, Uno H, Ono N (1998) A new synthesis of benzoporphyrins using 4,7-dihydro4,7-ethano-2H-isoindole as a synthon of isoindole. Chem Commun 1661–1662
Ito S, Uno H, Murashima T, Ono N (2001) Synthesis of benzoporphyrins functionalized with
octaester groups. Tetrahedron Lett 42:45–47
Ito S, Hiroto S, Lee S, Son M, Hisaki I, Yoshida T, Kim D, Kobayashi N, Shinokubo H (2015)
Synthesis of highly twisted and fully π-conjugated porphyrinic oligomers. J Am Chem Soc
137:142–145
Ito S, Hiroto S, Ousaka N, Yashima E, Shinokubo H (2016) Control of conformation and chirality
of nonplanar π-conjugated diporphyrins using substituents and axial ligands. Chem Asian J
11:936–942
Jaquinod L, Siri O, Khoury RG (1998) Linear fused oligoporphyrins: potential molecular wires with
enhanced electronic communication between bridged metal ions. Chem Commun 1261–1262
Jeandon C, Ruppert R (2011) A porphyrin with two coordination sites: the biquinoline ligand as a
new potential external chelate. Eur J Org Chem 4098−4102
Jiang L, Zaenglein RA, Engle JT, Mittal C, Hartley CS, Ziegler CJ, Wang H (2012) Water-soluble
ionic benzoporphyrins. Chem Commun 48:6927–6929
Kadish KM, Smith KM, Guilard R (eds) (2000) The porphyrin handbook. Academic Press, San
Diego
Kadish KM, Smith KM, Guilard R (eds) (2010) Handbook of porphyrin science. World Scientific,
Singapore
Kondratuk DV, Sprafke JK, O’Sullivan MC, Perdigao LMA, Saywell A, Malfois M, O’Shea JN,
Beton PH, Thompson AL, Anderson HL (2014) Vernier-templated synthesis, crystal structure,
and supramolecular chemistry of a 12-porphyrin nanoring. Chem Eur J 20:12826–12834
Kuimova MK, Botchway SW, Parker AW, Balaz M, Collins HA, Anderson HL, Suhling K, Ogilby
PR (2009) Imaging intracellular viscosity of a single cell during photoinduced cell death. Nat
Chem 1:69–73
Kumar S, Jiang X, Shan W, Jinadasa RGW, Kadish KM, Wang H (2018) β-Functionalized transA2B2 push–pull tetrabenzoporphyrins. Chem Commun 54:5303–5306