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Volumn 41, Issue 2, 2008, Pages 265-279

Structural diversity in expanded porphyrins

Author keywords

[No Author keywords available]

Indexed keywords

PORPHYRIN;

EID: 40549097448     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar700091k     Document Type: Article
Times cited : (226)

References (53)
  • 3
    • 0001299658 scopus 로고    scopus 로고
    • Jasat, A.; Dolphin, D. Exapnded Porphyrins and Their Heterologs. Chem. Rev. 1997, 97, 2267-2234.
    • Jasat, A.; Dolphin, D. Exapnded Porphyrins and Their Heterologs. Chem. Rev. 1997, 97, 2267-2234.
  • 4
    • 84990113780 scopus 로고    scopus 로고
    • Vogel, E.; Sicken, M.; Rohrig, P.; Schmickler, H.; Lex, J.; Ermer, O. Tetraoxaporphycene Dication. Angew. Chem., Int. Ed. Engl. 1988, 27, 411-414.
    • (a) Vogel, E.; Sicken, M.; Rohrig, P.; Schmickler, H.; Lex, J.; Ermer, O. Tetraoxaporphycene Dication. Angew. Chem., Int. Ed. Engl. 1988, 27, 411-414.
  • 5
    • 0031574005 scopus 로고    scopus 로고
    • Vogel, E.; Frode, C.; Brehian, A.; Schmickler, H.; Lex, J. Octaethyltetraselenaporphyrin Dication. Angew. Chem., Int. Ed. Engl. 1997, 36, 2609-2612.
    • (b) Vogel, E.; Frode, C.; Brehian, A.; Schmickler, H.; Lex, J. Octaethyltetraselenaporphyrin Dication. Angew. Chem., Int. Ed. Engl. 1997, 36, 2609-2612.
  • 6
    • 0242551254 scopus 로고    scopus 로고
    • Synthetic Expanded Porphyrin Chemistry
    • Sessler, J. L.; Seidel, D. Synthetic Expanded Porphyrin Chemistry. Angew. Chem., Int. Ed. 2003, 42, 5134-5175.
    • (2003) Angew. Chem., Int. Ed , vol.42 , pp. 5134-5175
    • Sessler, J.L.1    Seidel, D.2
  • 8
    • 0035543097 scopus 로고    scopus 로고
    • Sessler, J. L.; Davis, J. M. Sapphyrins: Versatile Anion Binding Agents. Acc. Chem. Res. 2001, 34, 989-997.
    • (b) Sessler, J. L.; Davis, J. M. Sapphyrins: Versatile Anion Binding Agents. Acc. Chem. Res. 2001, 34, 989-997.
  • 9
    • 28144435824 scopus 로고    scopus 로고
    • Modified Push-Pull Expanded Corroies: Syntheses, Structure and Nonlinear Optical Properties
    • (a) Misra, R.; Kumar, R.; Prabhuraja, V.; Chandrashekar, T. K. Modified Push-Pull Expanded Corroies: Syntheses, Structure and Nonlinear Optical Properties. J. Photochem. Photobiol. A: Chem. 2005, 75, 108-117.
    • (2005) J. Photochem. Photobiol. A: Chem , vol.75 , pp. 108-117
    • Misra, R.1    Kumar, R.2    Prabhuraja, V.3    Chandrashekar, T.K.4
  • 10
    • 33644774387 scopus 로고    scopus 로고
    • Modified (22π) Smaragdyrins with Large Two-Photon Absorption Cross Section: A Structure Function Correlation
    • (b) Misra, R.; Kumar, R.; Chandrashekar, T. K.; Nag, A.; Goswami, D. Modified (22π) Smaragdyrins with Large Two-Photon Absorption Cross Section: A Structure Function Correlation. Org. Lett. 2006, 8, 629-631.
    • (2006) Org. Lett , vol.8 , pp. 629-631
    • Misra, R.1    Kumar, R.2    Chandrashekar, T.K.3    Nag, A.4    Goswami, D.5
  • 11
    • 33845590327 scopus 로고    scopus 로고
    • 22π Smaragdyrin Molecular Conjugates with Aromatic Phenylacetylenes and Ferrocenes; Syntheses, Electrochemical and Photonic Properties
    • (c) Misra, R.; Kumar, R.; Chandrashekar, T. K.; Suresh, C. H.; Nag, A.; Goswami, D. 22π Smaragdyrin Molecular Conjugates with Aromatic Phenylacetylenes and Ferrocenes; Syntheses, Electrochemical and Photonic Properties. J. Am. Chem. Soc. 2006, 128, 16083-16091.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 16083-16091
    • Misra, R.1    Kumar, R.2    Chandrashekar, T.K.3    Suresh, C.H.4    Nag, A.5    Goswami, D.6
  • 12
    • 0036967746 scopus 로고    scopus 로고
    • Confusion, Inversion, And Creation- A New Spring from Porphyrin Chemistry
    • (a) Furuta, H.; Maeda, H.; Osuka, A. Confusion, Inversion, And Creation- A New Spring from Porphyrin Chemistry. Chem. Commun. 2002, 1795-1804.
    • (2002) Chem. Commun , pp. 1795-1804
    • Furuta, H.1    Maeda, H.2    Osuka, A.3
  • 13
    • 12344319203 scopus 로고    scopus 로고
    • Confusion Approach to Porphyrinoid Chemistry
    • (b) Srinivasan, A.; Furuta, H. Confusion Approach to Porphyrinoid Chemistry. Acc. Chem. Res. 2005, 38, 10-20.
    • (2005) Acc. Chem. Res , vol.38 , pp. 10-20
    • Srinivasan, A.1    Furuta, H.2
  • 14
    • 0141654013 scopus 로고    scopus 로고
    • Core-Modified Expanded Porphyrins: New Generation Organic Materials
    • Chandrashekar, T. K.; Venkatraman, S. Core-Modified Expanded Porphyrins: New Generation Organic Materials. Acc. Chem. Res. 2003, 36, 676-691.
    • (2003) Acc. Chem. Res , vol.36 , pp. 676-691
    • Chandrashekar, T.K.1    Venkatraman, S.2
  • 15
    • 33845551269 scopus 로고    scopus 로고
    • Bauer, V. J.; Clive, D. L. J.; Dolphin, D.; Paine, J. B.; Harris, F. L.; King, M. M.; Loder, J.; Wand, S. -W. C.; Woodward, R. B. Sapphyrins: Novel Aromatic Pentapyrrolic Macrocylces. J. Am. Chem. Soc. 1983, 105, 6429-6436.
    • Bauer, V. J.; Clive, D. L. J.; Dolphin, D.; Paine, J. B.; Harris, F. L.; King, M. M.; Loder, J.; Wand, S. -W. C.; Woodward, R. B. Sapphyrins: Novel Aromatic Pentapyrrolic Macrocylces. J. Am. Chem. Soc. 1983, 105, 6429-6436.
  • 16
    • 84989509330 scopus 로고    scopus 로고
    • Chmielewski, P. J.; Latos-Grazynski, L.; Rachlewicz, K. 5,10,15,20-Tetraphenylsapphyrin. Identification of a Pentapyrrolic Expanded Porphyrin in the Rothemund Synthesis. Chem.-Eur. J. 1995, 1, 68-73.
    • Chmielewski, P. J.; Latos-Grazynski, L.; Rachlewicz, K. 5,10,15,20-Tetraphenylsapphyrin. Identification of a Pentapyrrolic Expanded Porphyrin in the Rothemund Synthesis. Chem.-Eur. J. 1995, 1, 68-73.
  • 18
    • 0032850669 scopus 로고    scopus 로고
    • Narayanan, S. J.; Sridevi, B.; Chandrashekar, T. K.; Vij, A.; Roy, R. Novel Core-Modified Expanded Porphyrins with meso-Aryl Substituents: Synthesis, Spectral and Structural Characterization. J. Am. Chem. Soc. 1999, 121, 9053-9068.
    • Narayanan, S. J.; Sridevi, B.; Chandrashekar, T. K.; Vij, A.; Roy, R. Novel Core-Modified Expanded Porphyrins with meso-Aryl Substituents: Synthesis, Spectral and Structural Characterization. J. Am. Chem. Soc. 1999, 121, 9053-9068.
  • 20
    • 0033236843 scopus 로고    scopus 로고
    • Synthesis and X-Ray Crystal Structure of 27-Oxa-25,29-Dithiasapphyrin: Bithiophene-Containing Sapphyrin Have an Inverted Structure
    • Shin, K.; Lim, C.; Choi, C.; Kim, Y.; Lee, C.-H. Synthesis and X-Ray Crystal Structure of 27-Oxa-25,29-Dithiasapphyrin: Bithiophene-Containing Sapphyrin Have an Inverted Structure. Chem. Lett. 1999, 28, 1331-1332.
    • (1999) Chem. Lett , vol.28 , pp. 1331-1332
    • Shin, K.1    Lim, C.2    Choi, C.3    Kim, Y.4    Lee, C.-H.5
  • 21
    • 18044401781 scopus 로고    scopus 로고
    • 25,27-Dithiasapphyrin and Pyrrole-Inverted Isomer of 21,23-Dithiaporphyrin from Condensation of Pyrrole and 2,5-Bis(p-tolylhydroxymethyl)thiophene
    • Sprutta, N.; Latos-Grazynski, L. 25,27-Dithiasapphyrin and Pyrrole-Inverted Isomer of 21,23-Dithiaporphyrin from Condensation of Pyrrole and 2,5-Bis(p-tolylhydroxymethyl)thiophene. Org. Lett. 2001, 3, 1933-1936.
    • (2001) Org. Lett , vol.3 , pp. 1933-1936
    • Sprutta, N.1    Latos-Grazynski, L.2
  • 26
    • 17644395337 scopus 로고    scopus 로고
    • Shimizu, S.; Taniguchi, R.; Osuka, A. meso-Aryl-Substituted [26]Hexaphyrin (1.1.0.1.1.0) and [38]Nonaphyrin(1.1.0.1.1.0.1.1.0) from Oxidative Coupling of a Tripyrrane. Angew. Chem., Int. Ed. 2005, 44, 2225-2229.
    • Shimizu, S.; Taniguchi, R.; Osuka, A. meso-Aryl-Substituted [26]Hexaphyrin (1.1.0.1.1.0) and [38]Nonaphyrin(1.1.0.1.1.0.1.1.0) from Oxidative Coupling of a Tripyrrane. Angew. Chem., Int. Ed. 2005, 44, 2225-2229.
  • 27
    • 0034699055 scopus 로고    scopus 로고
    • 26]Hexaphyrin(1.1.1.1. 0.0): An All-Aza Isomer of Rubyrin with an Inverted Pyrrole Subunit
    • Sessler, J. L.; Seidel, D.; Bucher, C.; Lynch, V. [26]Hexaphyrin(1.1.1.1. 0.0): An All-Aza Isomer of Rubyrin with an Inverted Pyrrole Subunit. Chem. Commun. 2000, 1473-1474.
    • (2000) Chem. Commun , pp. 1473-1474
    • Sessler, J.L.1    Seidel, D.2    Bucher, C.3    Lynch, V.4
  • 28
    • 0035821254 scopus 로고    scopus 로고
    • Pushpan, S. K.; Anand, V. G.; Venkatraman, S.; Srinivasan, A.; Gupta, A. K.; Chandrashekar, T. K. Characterization of a New meso-Aryl Rubyrin Isomer: [26] Hexaphyrin (1.1.1.0.1.0) with an Inverted Heterocyclic Ring. Tetrahedron Lett. 2001, 42, 3391-3394.
    • Pushpan, S. K.; Anand, V. G.; Venkatraman, S.; Srinivasan, A.; Gupta, A. K.; Chandrashekar, T. K. Characterization of a New meso-Aryl Rubyrin Isomer: [26] Hexaphyrin (1.1.1.0.1.0) with an Inverted Heterocyclic Ring. Tetrahedron Lett. 2001, 42, 3391-3394.
  • 29
    • 33750352788 scopus 로고    scopus 로고
    • Effect of Meso-Aryl Substituents on the Synthesis of Core-Modified Expanded Porphyrins
    • Kumar, R.; Misra, R.; Chandrashekar, T. K. Effect of Meso-Aryl Substituents on the Synthesis of Core-Modified Expanded Porphyrins. Org. Lett. 2006, 8, 4847-4850.
    • (2006) Org. Lett , vol.8 , pp. 4847-4850
    • Kumar, R.1    Misra, R.2    Chandrashekar, T.K.3
  • 32
    • 0034822674 scopus 로고    scopus 로고
    • Shin, J.-Y.; Furuta, H.; Yoza, K.; Igarashi, S.; Osuka, A. meso-Aryl Substituted Expanded Porphyrins. J. Am. Chem. Soc. 2001, 123, 7190-7191.
    • (c) Shin, J.-Y.; Furuta, H.; Yoza, K.; Igarashi, S.; Osuka, A. meso-Aryl Substituted Expanded Porphyrins. J. Am. Chem. Soc. 2001, 123, 7190-7191.
  • 33
    • 0345413223 scopus 로고    scopus 로고
    • Synthesis and Crystal Structure of meso-Trialkynyl-[28]hexaphyrin
    • (d) Krivokapic, A.; Anderson, H. L. Synthesis and Crystal Structure of meso-Trialkynyl-[28]hexaphyrin. Org. Biomol. Chem. 2003, 1, 3639-3641.
    • (2003) Org. Biomol. Chem , vol.1 , pp. 3639-3641
    • Krivokapic, A.1    Anderson, H.L.2
  • 34
    • 33846941251 scopus 로고    scopus 로고
    • 26π Aromatic Core-Modified Hexaphyrins: Syntheses, Characterization and Structural Diversity
    • (a) Misra, R.; Kumar, R.; Chandrashekar, T. K.; Joshi, B. S. 26π Aromatic Core-Modified Hexaphyrins: Syntheses, Characterization and Structural Diversity. J. Org. Chem. 2007, 72, 1153-1160.
    • (2007) J. Org. Chem , vol.72 , pp. 1153-1160
    • Misra, R.1    Kumar, R.2    Chandrashekar, T.K.3    Joshi, B.S.4
  • 36
    • 0037020292 scopus 로고    scopus 로고
    • Cu-Mediated Syntheses of N-Fused and Ring-Modified Trithiahexaphyrins
    • Hung, C.-H.; Jong, J.-P.; Ho, M.-Y.; Lee, G. H.; Peng, S.-M. Cu-Mediated Syntheses of N-Fused and Ring-Modified Trithiahexaphyrins. Chem.-Eur. J. 2002, 8, 4542-4548.
    • (2002) Chem.-Eur. J , vol.8 , pp. 4542-4548
    • Hung, C.-H.1    Jong, J.-P.2    Ho, M.-Y.3    Lee, G.H.4    Peng, S.-M.5
  • 37
    • 0037471634 scopus 로고    scopus 로고
    • Doubly N-Confused Hexaphyrins: A Novel Aromatic Expanded Porphyrin that Complexes Bis-metals in the Core
    • Srinivasan, A.; Ishizuka, T.; Osuka, A.; Furuta, H. Doubly N-Confused Hexaphyrins: A Novel Aromatic Expanded Porphyrin that Complexes Bis-metals in the Core. J. Am. Chem. Soc. 2003, 125, 878-879.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 878-879
    • Srinivasan, A.1    Ishizuka, T.2    Osuka, A.3    Furuta, H.4
  • 38
    • 0033537021 scopus 로고    scopus 로고
    • Sessler, J. L.; Seidel, J.; Lynch, V. Synthesis of [28]Heptaphyrin(1.0.0. 1.0.0.0) and [32]Octaphyrin(1.0.0.0.1.0.0.0) via a Directed Oxidative Ring Closure: The First Expanded Porphyrins Containing a Quaterpyrrole Subunit. J. Am. Chem. Soc. 1999, 121, 11257-11258.
    • Sessler, J. L.; Seidel, J.; Lynch, V. Synthesis of [28]Heptaphyrin(1.0.0. 1.0.0.0) and [32]Octaphyrin(1.0.0.0.1.0.0.0) via a Directed Oxidative Ring Closure: The First Expanded Porphyrins Containing a Quaterpyrrole Subunit. J. Am. Chem. Soc. 1999, 121, 11257-11258.
  • 39
    • 0037148749 scopus 로고    scopus 로고
    • 30] Heptaphyrin (1.1.1.1.0.0): An Aromatic Expanded Porphyrin with a "Figure Eight" Like Structure
    • Bucher, C.; Seidel, D.; Lynch, V.; Sessler, J. L. [30] Heptaphyrin (1.1.1.1.0.0): An Aromatic Expanded Porphyrin with a "Figure Eight" Like Structure. Chem. Commun 2002, 328-329.
    • (2002) Chem. Commun , pp. 328-329
    • Bucher, C.1    Seidel, D.2    Lynch, V.3    Sessler, J.L.4
  • 41
    • 28844465769 scopus 로고    scopus 로고
    • Rath, H.; Sankar, J.; Prabhuraja, V.; Chandrashekar, T. K.; Joshi, B. S. Aromatic Core-Modified Twisted Heptaphyrins[1.1.1.1.1.1.0]: Syntheses and Structural Characterization. Org. Lett. 2005, 7, 5445-5448.
    • Rath, H.; Sankar, J.; Prabhuraja, V.; Chandrashekar, T. K.; Joshi, B. S. Aromatic Core-Modified Twisted Heptaphyrins[1.1.1.1.1.1.0]: Syntheses and Structural Characterization. Org. Lett. 2005, 7, 5445-5448.
  • 42
    • 33646731146 scopus 로고    scopus 로고
    • Porphyrin Synthesis in Water Provides New Expanded Porphyrins with Direct Bipyrrole Linkages: Isolation and Characterization of Two Heptaphyrins
    • Hiroto, S.; Shinokubo, H.; Osuka, A. Porphyrin Synthesis in Water Provides New Expanded Porphyrins with Direct Bipyrrole Linkages: Isolation and Characterization of Two Heptaphyrins. J. Am. Chem. Soc. 2006, 128, 6568-6569.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 6568-6569
    • Hiroto, S.1    Shinokubo, H.2    Osuka, A.3
  • 43
    • 33845465820 scopus 로고    scopus 로고
    • Saito, S.; Osuka, A. N-Fusion Reaction Sequence of Heptaphyrin(1.1.1.1.1. 1.1): Singly, Doubly and Quadruply N-Fused Hepataphyrins. Chem.-Eur. J. 2006, 12, 9095-9102.
    • Saito, S.; Osuka, A. N-Fusion Reaction Sequence of Heptaphyrin(1.1.1.1.1. 1.1): Singly, Doubly and Quadruply N-Fused Hepataphyrins. Chem.-Eur. J. 2006, 12, 9095-9102.
  • 45
    • 0037090998 scopus 로고    scopus 로고
    • Cyclo[8] Pyrrole: A Simple To Make Expanded Porphyrin with No Meso Bridges
    • Seidel, D.; Lynch, V.; Sessler, J. L. Cyclo[8] Pyrrole: A Simple To Make Expanded Porphyrin with No Meso Bridges. Angew. Chem., Int. Ed. 2002, 41, 1422-1425.
    • (2002) Angew. Chem., Int. Ed , vol.41 , pp. 1422-1425
    • Seidel, D.1    Lynch, V.2    Sessler, J.L.3
  • 46
    • 0035812425 scopus 로고    scopus 로고
    • Anand, V. G.; Pushpan, S. K.; Venkatraman, S.; Dey, A.; Chandrashekar, T. K.; Joshi, B. S.; Roy, R.; Teng, W.; Senge, K. R. 34π Octaphyrin: First Structural Characterization of a Planar, Aromatic [1.0.1.0.1.0.1.0] Octaphyrin with Inverted Heterocyclic Rings. J. Am. Chem. Soc. 2001, 123, 8620-8621.
    • Anand, V. G.; Pushpan, S. K.; Venkatraman, S.; Dey, A.; Chandrashekar, T. K.; Joshi, B. S.; Roy, R.; Teng, W.; Senge, K. R. 34π Octaphyrin: First Structural Characterization of a Planar, Aromatic [1.0.1.0.1.0.1.0] Octaphyrin with Inverted Heterocyclic Rings. J. Am. Chem. Soc. 2001, 123, 8620-8621.
  • 47
    • 0037495971 scopus 로고    scopus 로고
    • meso-Substituted Aromatic 34π Core-Modified Octaphyrins: Syntheses, Characterization and Anion Binding Properties
    • Anand, V. G.; Venkatraman, S.; Chandrashekar, T. K.; Teng, W.; Senge, K. R. meso-Substituted Aromatic 34π Core-Modified Octaphyrins: Syntheses, Characterization and Anion Binding Properties. Chem.-Eur. J. 2003, 9, 2282-2290.
    • (2003) Chem.-Eur. J , vol.9 , pp. 2282-2290
    • Anand, V.G.1    Venkatraman, S.2    Chandrashekar, T.K.3    Teng, W.4    Senge, K.R.5
  • 48
    • 33845473641 scopus 로고    scopus 로고
    • Kumar, R.; Misra, R.; Chandrashekar, T. K.; Suresh, E. Near IR absorbing planar aromatic [34]octaphyrins(1.1.0.1.1.0.0.0) containing a quaterthiophene subunit. Chem. Commun. 2007, 43-45.
    • Kumar, R.; Misra, R.; Chandrashekar, T. K.; Suresh, E. Near IR absorbing planar aromatic [34]octaphyrins(1.1.0.1.1.0.0.0) containing a quaterthiophene subunit. Chem. Commun. 2007, 43-45.
  • 49
    • 22544431652 scopus 로고    scopus 로고
    • Figure-Eight Aromatic Core-Modified Octaphyrins with six meso links: Synthesis and Structural Characterization
    • Rath, H.; Sankar, J.; Prabhuraja, V.; Chandrashekar, T. K.; Joshi, B. S.; Roy, R. Figure-Eight Aromatic Core-Modified Octaphyrins with six meso links: Synthesis and Structural Characterization. Chem. Commun. 2005, 3343-3345.
    • (2005) Chem. Commun , pp. 3343-3345
    • Rath, H.1    Sankar, J.2    Prabhuraja, V.3    Chandrashekar, T.K.4    Joshi, B.S.5    Roy, R.6
  • 50
    • 0034822674 scopus 로고    scopus 로고
    • Shin, J-Y.; Furuta, H.; Yoza.; Igarashi, S.; Osuka, A. meso-Aryl-Substituted Expanded Porphyrins. J. Am. Chem. Soc. 2001, 123, 7190-7191.
    • Shin, J-Y.; Furuta, H.; Yoza.; Igarashi, S.; Osuka, A. meso-Aryl-Substituted Expanded Porphyrins. J. Am. Chem. Soc. 2001, 123, 7190-7191.
  • 51
    • 34250343301 scopus 로고    scopus 로고
    • Kamimura, Y.; Shimizu, S.; Osuka, A. [40]Nonaphyrin(1.1.1.1.1.1.1.1.1) and Its Heterometallic Complexes with Palladium- Carbon Bonds. Chem.-Eur. J. 2007, 13, 1620-1628.
    • Kamimura, Y.; Shimizu, S.; Osuka, A. [40]Nonaphyrin(1.1.1.1.1.1.1.1.1) and Its Heterometallic Complexes with Palladium- Carbon Bonds. Chem.-Eur. J. 2007, 13, 1620-1628.
  • 53
    • 33745697783 scopus 로고    scopus 로고
    • Aromatic Core Modified Decaphyrins with the Largest Two-Photon Absorption Cross-Sections: Syntheses and Characterization
    • Rath, H.; Sankar, J.; Prabhuraja, V.; Chandrashekar, T. K.; Joshi, B. S.; Nag, A.; Goswami, D. Aromatic Core Modified Decaphyrins with the Largest Two-Photon Absorption Cross-Sections: Syntheses and Characterization. Org. Lett. 2006, 8, 2325-2328.
    • (2006) Org. Lett , vol.8 , pp. 2325-2328
    • Rath, H.1    Sankar, J.2    Prabhuraja, V.3    Chandrashekar, T.K.4    Joshi, B.S.5    Nag, A.6    Goswami, D.7


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