Literature DB >> 19514027

pi-Conjugation enlargement toward the creation of multi-porphyrinic systems with large two-photon absorption properties.

Naoki Aratani1, Dongho Kim, Atsuhiro Osuka.   

Abstract

Recent progress in the synthesis of covalently linked porphyrin arrays with large two-Photon absorption (TPA) cross-section values has been reviewed with a particular focus on the relation of TPA properties with molecular structures. Covalently linked porphyrin arrays continue to be important and useful for the creation of functional materials owing to their chemical robustness, fine-tuning, and easy manipulation. More importantly, the porphyrin electronic systems are quite susceptible to periphery conjugative perturbations, hence allowing facile fabrications to extensively delocalized systems. This property has been used for exploration of porphyrin-based molecular systems with large TPA values, demonstrating a general trend that enhancement in electronic interactions leads to large TPA cross-section values. As a representative example, the porphyrin tapes exhibit larger TPA values owing to the fully delocalized nature of the pi-electrons. This Focus Review will help understand the structural requirements of porphyrin arrays with large TPA values, which will be useful for future applications in optical communication in the IR region.

Entities:  

Year:  2009        PMID: 19514027     DOI: 10.1002/asia.200900045

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  4 in total

1.  Two-Photon Absorbing Phosphorescent Metalloporphyrins: Effects of π-Extension and Peripheral Substitution.

Authors:  Tatiana V Esipova; Héctor J Rivera-Jacquez; Bruno Weber; Artëm E Masunov; Sergei A Vinogradov
Journal:  J Am Chem Soc       Date:  2016-11-23       Impact factor: 15.419

2.  Regioselective phenylene-fusion reactions of Ni(ii)-porphyrins controlled by an electron-withdrawing meso-substituent.

Authors:  Norihito Fukui; Seung-Kyu Lee; Kenichi Kato; Daiki Shimizu; Takayuki Tanaka; Sangsu Lee; Hideki Yorimitsu; Dongho Kim; Atsuhiro Osuka
Journal:  Chem Sci       Date:  2016-03-01       Impact factor: 9.825

3.  Covalent Porphyrin Hybrids Linked with Dipyrrin, Bidipyrrin or Thiacorrole.

Authors:  Renbao He; Huan Yue; Jiahui Kong
Journal:  Molecules       Date:  2017-08-23       Impact factor: 4.411

4.  Macroscopically Anisotropic Structures Produced by Light-induced Solvothermal Assembly of Porphyrin Dimers.

Authors:  Yasuyuki Yamamoto; Yushi Nishimura; Shiho Tokonami; Norihito Fukui; Takayuki Tanaka; Atsuhiro Osuka; Hideki Yorimitsu; Takuya Iida
Journal:  Sci Rep       Date:  2018-07-23       Impact factor: 4.379

  4 in total

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