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Volumn 132, Issue 37, 2010, Pages 12991-12999

Scrutinizing the chemical nature and photophysics of an expanded hemiporphyrazine: The special case of [30]trithia-2,3,5,10,12,13,15,20,22,23,25, 30-dodecaazahexaphyrin

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL NATURE; DIFFRACTION ANALYSIS; ELECTROCHEMICAL TECHNIQUES; ELECTRON TRANSFER; ELECTRONIC DELOCALIZATION; EXCITED-STATE ENERGY; HEXAMERS; IN-PROCESS; INTRAMOLECULAR HYDROGEN BONDING; MACROCYCLES; NMR STUDIES; ONE-ELECTRON OXIDATION; ONE-ELECTRON REDUCTIONS; OXIDIZED STATE; PHOTOPHYSICS; PHTHALONITRILES; PHYSICOCHEMICAL FEATURES; PLANAR CONFORMATIONS; THIADIAZOLES;

EID: 77956680651     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja104577d     Document Type: Article
Times cited : (51)

References (73)
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    • note
    • Two canonical forms can be outlined for compound 7; both of them imply the coexistence of three aromatic (either pyrrole or thiadiazole) and three nonaromatic heterocyclic components within the macrocycle. We have represented compound 7 in Figure 3 according to the structure found for the benzo fused congeners 1a-c.
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    • Resolvable fluorescence decays were only noted for 1b
    • Resolvable fluorescence decays were only noted for 1b.
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    • Singlet oxygen quantum yields were determined via the characteristic near-infrared emission and afforded values of 0.05 (1), 0.78 (1b), and 0.11 (1c)
    • Singlet oxygen quantum yields were determined via the characteristic near-infrared emission and afforded values of 0.05 (1), 0.78 (1b), and 0.11 (1c).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.