Gram-scale synthesis of porphycenes through acid-catalyzed oxidative macrocyclizations of E/Z-mixed 5,6-diaryldipyrroethenes

The gram-scale production of porphycene derivatives is reported. This has been achieved by acid-catalyzed ring closure of an E/Z-mixture of 5,6-diaryldipyrroethenes, resulting in the formation of meso-tetraarylporphycenes in yields of up to 80%. E/Z-isomerization of the 5,6-diaryldipyrroethenes under acidic conditions was key to proceed the effective macrocyclization.

[1]  Y. Hisaeda,et al.  Cobalt–Carbon Bond Formation Reaction via Ligand Reduction of Porphycene–Cobalt(II) Complex and Its Noninnocent Reactivity , 2018, ACS omega.

[2]  H. Sugimoto,et al.  Manganese(V) Porphycene Complex Responsible for Inert C-H Bond Hydroxylation in a Myoglobin Matrix. , 2017, Journal of the American Chemical Society.

[3]  Hiroyuki Meichin,et al.  Catalytic Cyclopropanation by Myoglobin Reconstituted with Iron Porphycene: Acceleration of Catalysis due to Rapid Formation of the Carbene Species. , 2017, Journal of the American Chemical Society.

[4]  Y. Hisaeda,et al.  The first synthesis of meso-dicycloalkylporphycenes: ring strain effects on structural and optical properties of isomeric porphyrins. , 2017, Chemical communications.

[5]  O. Planas,et al.  Acid- and hydrogen-bonding-induced switching between 22-π and 18-π electron conjugations in 2-aminothiazolo[4,5-c]porphycenes. , 2017, Physical chemistry chemical physics : PCCP.

[6]  N. Aratani,et al.  Synthesis, Characterization and Protonation Behavior of Quinoxaline-Fused Porphycenes , 2017, Molecules.

[7]  J. Waluk Spectroscopy and Tautomerization Studies of Porphycenes. , 2017, Chemical reviews.

[8]  David Sánchez-García,et al.  Porphycenes and Related Isomers: Synthetic Aspects. , 2017, Chemical reviews.

[9]  M. Persson,et al.  Force-induced tautomerization in a single molecule. , 2016, Nature chemistry.

[10]  Y. Hisaeda,et al.  An Electropolymerized Crystalline Film Incorporating Axially-Bound Metalloporphycenes: Remarkable Reversibility, Reproducibility, and Coloration Efficiency of Ruthenium(II/III)-Based Electrochromism. , 2015, Inorganic chemistry.

[11]  T. Sarma,et al.  β,β'-Bipyrrole Fusion-Driven cis-Bimetallic Complexation in Isomeric Porphyrin. , 2015, Angewandte Chemie.

[12]  Anup Rana,et al.  β-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties. , 2015, Chemical communications.

[13]  P. Rajakannu,et al.  Stereochemical modulation of emission behaviour in E/Z isomers of diphenyldipyrroethene from aggregation induced emission to crystallization induced emission. , 2015, Physical chemistry chemical physics : PCCP.

[14]  K. Oohora,et al.  meso-Dibenzoporphycene has a Large Bathochromic Shift and a Porphycene Framework with an Unusual cis Tautomeric Form. , 2015, Angewandte Chemie.

[15]  Dongho Kim,et al.  β-Octakis(methylthio)porphycenes: synthesis, characterisation and third order nonlinear optical studies. , 2015, Chemical communications.

[16]  M. Ravikanth,et al.  Facile Synthesis of 9,10,19,20‐Tetraarylporphycenes , 2014 .

[17]  Tsuyoshi Inoue,et al.  C(sp3)-H bond hydroxylation catalyzed by myoglobin reconstituted with manganese porphycene. , 2013, Journal of the American Chemical Society.

[18]  N. Jux,et al.  Electron Accepting Porphycenes on Graphene , 2013, Advanced materials.

[19]  N. Jux,et al.  Poly‐Ortho‐Functionalizable Tetraarylporphycene Platform–Synthesis of Octacationic Derivatives Towards the Layer‐by‐Layer Design of Versatile Graphene Oxide Photoelectrodes , 2013, Advanced materials.

[20]  Tomohiro Ito,et al.  Gram-scale synthesis of nickel(II) norcorrole: the smallest antiaromatic porphyrinoid. , 2012, Angewandte Chemie.

[21]  Miquel Duran-Frigola,et al.  Dual fluorescence in 9-amino-2,7,12,17-tetraphenylporphycene. , 2011, Physical chemistry chemical physics : PCCP.

[22]  S. V. Rao,et al.  Dinaphthoporphycenes: synthesis and nonlinear optical studies. , 2011, Organic letters.

[23]  H. Yamada,et al.  Synthesis, structures, and optical and electrochemical properties of benzoporphycenes. , 2009, Chemistry.

[24]  K. Ohkubo,et al.  Metalloporphycenes: synthesis and characterization of (pentamethylcyclopentadienyl)ruthenium sitting-atop and pi-complexes. , 2009, Journal of the American Chemical Society.

[25]  E. Suresh,et al.  9,10,19,20-Tetraarylporphycenes. , 2008, Organic letters.

[26]  Á. Villanueva,et al.  Porphycenes: facts and prospects in photodynamic therapy of cancer. , 2007, Current medicinal chemistry.

[27]  D. Gryko,et al.  Efficient synthesis of meso-substituted corroles in a H2O-MeOH mixture. , 2006, The Journal of organic chemistry.

[28]  Hideaki Sato,et al.  Blue myoglobin reconstituted with an iron porphycene shows extremely high oxygen affinity. , 2002, Journal of the American Chemical Society.

[29]  E. Vogel,et al.  New Porphycene Ligands: Octaethyl‐ and Etioporphycene (OEPc and EtioPc)—Tetra‐ and Pentacoordinated Zinc Complexes of OEPc , 1993 .

[30]  E. Vogel,et al.  2,7,12,17‐Tetrapropylporphycene—Counterpart of Octaethylporphyrin in the Porphycene Series , 1987 .

[31]  P. Batail,et al.  Acid-mediated trans-cis isomerization of substituted tetrathiafulvalenes. Selective precipitation of the trans isomer , 1987 .

[32]  Johann Lex,et al.  Porphycene—a Novel Porphin Isomer , 1986 .

[33]  Y. Hisaeda,et al.  Facile Synthesis of 9,10,19,20-Tetraalkylporphycenes , 2017 .

[34]  M. Persson,et al.  Controlling intramolecular hydrogen transfer in a porphycene molecule with single atoms or molecules located nearby. , 2014, Nature chemistry.

[35]  C. Che,et al.  Catalytic and asymmetric cyclopropanation of styrenes catalysed by ruthenium porphyrin and porphycene complexes , 1997 .

[36]  E. Vogel,et al.  Steric Modulation of the Porphycene System by Alkyl Substituents: 9,10,19,20‐Tetraalkylporphycenes , 1989 .

[37]  J. Lindsey,et al.  Synthesis of tetraphenylporphyrins under very mild conditions , 1986 .

[38]  A. Adler,et al.  A simplified synthesis for meso-tetraphenylporphine , 1967 .