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Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Efficient Synthesis of Novel Porphyrin Dimers with Versatile Linkers via Bis(dipyrromethanes) in an Excellent Mixed-Solvent

Hongbin Zhao A B C , Junxu Liao A , Deliang Yang A , Yujia Xie A B , Yongjun Xu A , Hongke Wang A and Bangying Wang A B
+ Author Affiliations
- Author Affiliations

A College of Chemistry and Environmental Engineering, Dongguan University of Technology, Guangdong 523808, China.

B College of Chemistry, Xiangtan University, Hunan 411105, China.

C Corresponding author. Email: zhaohbhanlf@163.com

Australian Journal of Chemistry 66(8) 972-982 https://doi.org/10.1071/CH12521
Submitted: 22 November 2012  Accepted: 2 May 2013   Published: 29 May 2013

Abstract

A general and efficient protocol has been developed to synthesise a series of novel porphyrin dimers with versatile aryl linkers via a simultaneous condensation-cyclisation-oxidation reaction of diverse bis(dipyrromethanes) with dipyrromethane-dicarbinol catalysed by indium(iii) chloride at room temperature in an efficient CH2Cl2 and CH3CN mixed-solvent. The reaction yields increased to 21–26 % based on liquid chromatography-mass spectrometry (LCMS) and isolated yields were 13–19 % due to the use of the proper mixed-solvent. This mild method is applicable to the preparation of linker-tunable porphyrin dimers with targeted functionalities and could potentially be extended to the single-step construction of longer functionalised multiporphyrin arrays.


References

[1]  (a) M. J. Crossley, P. L. J. Burn, J. Chem. Soc., Chem. Commun. 1991, 1569.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK38XotlChtA%3D%3D&md5=aafaa0c85ed38c25395595163a38d668CAS |
      (b) V. Y. Lin, S. G. DiMagno, M. J. Therien, Science 1994, 264, 1105.
         | Crossref | GoogleScholarGoogle Scholar |
      (c) M. O. Senge, M. Fazekas, E. G. A. Notaras, W. J. Blau, M. Zawadzka, O. B. Locos, E. M. N. Mhuircheartaigh, Adv. Mater. 2007, 19, 2737.
         | Crossref | GoogleScholarGoogle Scholar |
      (d) N. Aratani, A. Osuka, H. S. Cho, D. Kim, J. Photochem. Photobiol. C 2002, 3, 25.
         | Crossref | GoogleScholarGoogle Scholar |

[2]  D. Holten, D. F. Bocian, J. S. Lindsey, Acc. Chem. Res. 2002, 35, 57.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXos1Cjs7Y%3D&md5=f5f7fb1cd770ebf9a323b9d0400d3258CAS | 11790089PubMed |

[3]  (a) Y. Terazono, G. Kodis, K. Bhushan, J. Zaks, C. Madden, A. L. Moore, T. A. Moore, G. R. Fleming, D. J. Gust, J. Am. Chem. Soc. 2011, 133, 2916.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhvVWis7c%3D&md5=53159976ccdbe7747386e522a1bde8eeCAS | 21314185PubMed |
      (b) T. Ishizuka, L. E. Sinks, K. Song, S. T. Hung, A. Nayak, K. Clays, M. J. J. Therien, J. Am. Chem. Soc. 2011, 133, 2884.
         | Crossref | GoogleScholarGoogle Scholar |
      (c) J. K. Sprafke, S. D. Stranks, J. H. Warner, R. J. Nicholas, H. L. Anderson, Angew. Chem. Int. Ed. 2011, 50, 2313.
         | Crossref | GoogleScholarGoogle Scholar |

[4]  K. Osawa, N. Aratani, A. Osuka, Tetrahedron Lett. 2009, 50, 3333.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXmtVemsro%3D&md5=0f8e425c5387399c07cdb6d45c09a832CAS |

[5]  (a) S. I. Yang, R. K. Lammi, J. Seth, J. A. Riggs, T. Arai, D. Kim, D. F. Bocian, D. Holten, J. S. J. Lindsey, J. Phys. Chem. B 1998, 102, 9426.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXmvFChtr0%3D&md5=3bb61674fa3b991509660933b3d9f217CAS |
      (b) S. Cho, M. C. Yoon, C. H. Kim, N. Aratani, G. Mori, T. Joo, A. Osuka, D. Kim, J. Phys. Chem. C 2007, 111, 14881.
         | Crossref | GoogleScholarGoogle Scholar |
      (c) A. J. Mozer, M. J. Griffith, G. Tsekouras, P. Wagner, G. G. Wallace, S. Mori, K. Sunahara, M. Miyashita, J. C. Earles, K. C. Gordon, L. Du, R. Katoh, A. Furube, D. L. J. Officer, J. Am. Chem. Soc. 2009, 131, 15621.
         | Crossref | GoogleScholarGoogle Scholar |

[6]  N. Aratani, A. Takagi, Y. Yanagawa, T. Matsumoto, T. Kawai, Z. S. Yoon, D. Kim, A. Osuka, Chem. – Eur. J. 2005, 11, 3389.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXkvV2jurk%3D&md5=f9ca7303dda261144174f375a25edbe8CAS | 15798970PubMed |

[7]  G. P. Arsenault, E. Bullock, S. F. J. MacDonald, J. Am. Chem. Soc. 1960, 82, 4384.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaF3MXhtlCksw%3D%3D&md5=9d6604677513873a504fe9536ea44d5dCAS |

[8]  P. Thamyongkit, J. S. J. Lindsey, J. Org. Chem. 2004, 69, 5796.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXmtVeisrg%3D&md5=a5b5a6ce7836fe01012e2fd1ce4454aeCAS | 15307763PubMed |

[9]  J. K. Laha, S. Dhanalekshmi, M. Taniguchi, A. Ambroise, J. S. Lindsey, Org. Process Res. Dev. 2003, 7, 799.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXnt1Onsb0%3D&md5=3b01bc44dc25c708d823f23569307314CAS |

[10]  G. R. Geier, B. J. Littler, J. S. J. Lindsey, J. Chem. Soc., Perkin Trans. 2 2001, 701.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXjtFOqsrk%3D&md5=fa3ba23655cdff2f4aa03e24f4c8ef56CAS |

[11]  H. Zhao, J. Liao, J. Ning, Y. Xie, Y. Cao, L. Chen, D. Yang, B. Wang, Adv. Synth. Catal. 2010, 352, 3083.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhsVCjsLvK&md5=61ee555dde51f45b34bb8f4607f7d9eeCAS |

[12]  (a) D. L. Yang, H. B. Zhao, J. X. Liao, L. Chen, D. L. Yang, B. Y. Wang, Acta. Cryst. 2011, E67, m1673.
      (b) L. Chen, H. B. Zhao, Y. J. Xie, D. L. Yang, B. Y. Wang, Acta Crystallogr. 2010, E66, m1455.
      (c) P. K. Kumar, P. Bhyrappa, B. Varghese, Tetrahedron Lett. 2003, 44, 4849.
         | Crossref | GoogleScholarGoogle Scholar |

[13]  M. Taniguchi, J. S. Lindsey, Tetrahedron 2010, 66, 5549.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXpt1eqsbg%3D&md5=32d93c075d58b95ad31edbd4919f27e6CAS |

[14]  (a) P. S. Reeta, J. Kandhadi, G. Lingamallu, Tetrahedron Lett. 2010, 51, 2865.
         | Crossref | GoogleScholarGoogle Scholar |
      (b) K. K. Pasunooti, J. L. Song, H. Chai, P. Amaladass, W. Q. Deng, X. W. Liu, J. Photochem. Photobiol. A 2011, 218, 219.
         | Crossref | GoogleScholarGoogle Scholar |

[15]  B. Wang, M. R. Wasielewski, J. Am. Chem. Soc. 1997, 119, 12.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28XnsVChur8%3D&md5=b62063316e15b55eca23d852799337a2CAS |

[16]  S. Shi, Z. Li, J. Wang, J. Polym. Res. 2007, 14, 305.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXntlCjsL4%3D&md5=2c886c5d40a2bea67345e9822fb8ccc0CAS |

[17]  X. C. Li, Y. Liu, M. S. Liu, A. K.-Y. Jen, Chem. Mater. 1999, 11, 1568.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXivVarsrY%3D&md5=5cf36095db898edd97f1ea13a1fb5bf4CAS |

[18]  F. Liu, K. Wang, G. Bai, Y. Zhang, L. Gao, Inorg. Chem. 2004, 43, 1799.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXhtVylsbw%3D&md5=61acef28be6467c133b3031ccbb8065fCAS | 14989674PubMed |

[19]  S. Kim, C.-K. Lim, J. Na, Y.-D. Lee, K. Kim, K. Choi, J. F. Leary, I. C. Kwon, Chem. Commun. 2010, 46, 1617.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXit1Orsrk%3D&md5=f9a4d7314f6ccdb8878b659b3cc7c533CAS |