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Volumn , Issue 13, 2010, Pages 2576-2586

Meso-indolo[3,2-6]carbazolyl-substitutedporphyrmoids: synthesis, characterization and effect of the number of indolocarbazole moieties on the photophysical properties

Author keywords

Excitation energy deactivation; Luminescence; Molecular electronics; Nitrogen heterocycles; Photophysical properties; Porphyrinoids

Indexed keywords


EID: 77951172792     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201000180     Document Type: Article
Times cited : (19)

References (81)
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    • 2-porphyrin 11a could be pursued under optimized Lindsey "minimal scrambling" conditions: B. J. Littler, Y. Ciringh, J. S. Lindsey, J. Org. Chem. 1999, 64, 2864-2872. At this stage, however, the observed scrambling was considered more an advantage to obtain all differently substituted ?neio-indolocarbazolylporphyins from a single reaction, enabling their photophysical comparison.
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    • 13C NMR spectra for ICZ precursor 9 and the novel porphyrinoids can be found in the Supporting Information. Additional data on the VT NMR studies and (two-dimensional) representations of the different atropoisomers for 11a,12a are presented as well.
    • 13C NMR spectra for ICZ precursor 9 and the novel porphyrinoids can be found in the Supporting Information. Additional data on the VT NMR studies and (two-dimensional) representations of the different atropoisomers for 11a,12a are presented as well.
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    • UV/Vis absorption spectra of a few ICZ precursors and mesoindolocarbazolylcorroles 6 and 14 can be consulted in the Supporting Information
    • UV/Vis absorption spectra of a few ICZ precursors and mesoindolocarbazolylcorroles 6 and 14 can be consulted in the Supporting Information.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.