Ultrafast photoinduced electron transfer in face-to-face charge-transfer π-complexes of planar porphyrins and hexaazatriphenylene derivatives† †Electronic supplementary information (ESI) available: 1H, 13C NMR and MALDI-TOF mass spectra, cyclic voltammograms, fluorescence spectra, fluorescence titration spectra, 1H NMR titration, femtosecond laser-induced transient absorption spectral measurement data, and DFT data. See DOI: 10.1039/c4sc02787f Click here for additional data file.

نویسندگان

  • Toru Aoki
  • Hayato Sakai
  • Kei Ohkubo
  • Tomo Sakanoue
  • Taishi Takenobu
  • Shunichi Fukuzumi
  • Taku Hasobe
چکیده

Department of Chemistry, Faculty of Sc Yokohama, 223-8522, Japan. E-mail: hasob Department of Material and Life Science, University, ALCA, Japan Science and Tech 0871, Japan. E-mail: [email protected] Department of Applied Physics, Waseda U 169-8555, Japan. E-mail: takenobu@waseda † Electronic supplementary information MALDI-TOF mass spectra, cyclic vo uorescence titration spectra, H NMR transient absorption spectral measurem 10.1039/c4sc02787f Cite this: Chem. Sci., 2015, 6, 1498

منابع مشابه

Ultrafast photoinduced electron transfer in face-to-face charge-transfer π-complexes of planar porphyrins and hexaazatriphenylene derivatives.

Charge-transfer (CT) π-complexes are formed between planar porphyrins and 1,4,5,8,9,12-hexaazatriphenylene (HAT) derivatives with large formation constants (e.g., 104 M-1), exhibiting broad CT absorption bands. The unusually large formation constants result from close face-to-face contact between two planar π-planes of porphyrins and HAT derivatives. The redox potentials of porphyrins and HAT d...

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5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents† †Electronic supplementary information (ESI) available: General experimental methods, HR-ESI-TOF mass spectra, UV/Vis absorption spectra, NMR spectra, cyclic voltammograms, X-ray crystal structures and results of DFT calculations. CCDC 1025770, 1025771 and 1025772. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c4sc03394a Click here for additional data file. Click here for additional data file.

Department of Chemistry, Graduate Schoo Kyoto 606-8502, Japan. E-mail: osuka@kuc Spectroscopy Laboratory for Functional p Chemistry Yonsei University, Seoul 120-749 † Electronic supplementary information methods, HR-ESI-TOF mass spectra, UV cyclic voltammograms, X-ray crystal struc CCDC 1025770, 1025771 and 1025772. Fo or other electronic format see DOI: 10.103 Cite this: Chem. Sci., 2015, 6, 1696

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عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2015