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Volumn 1, Issue 6, 2006, Pages 832-844

Halide-anion binding by singly and doubly N-confused porphyrins

Author keywords

Anions; Binding studies; N confused porphyrins; pi interactions; Porphyrinoids

Indexed keywords

ANION; BROMIDE; CHLORIDE; IODIDE; PORPHYRIN; QUATERNARY AMMONIUM DERIVATIVE; TETRABUTYLAMMONIUM;

EID: 33846006925     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.200600182     Document Type: Article
Times cited : (69)

References (69)
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    • a values including errors are shown in the Supporting Figures.
    • a values including errors are shown in the Supporting Figures.
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    • 1H NMR signals of 2 and 3 resonate at δ = 0.53 and ≈ 1.1 ppm for the inner CH and δ = 14.37 and 13.88 ppm for the outer NH, respectively.
    • 1H NMR signals of 2 and 3 resonate at δ = 0.53 and ≈ 1.1 ppm for the inner CH and δ = 14.37 and 13.88 ppm for the outer NH, respectively.
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    • Fluorescence change of NCTPP by F- binding was reported briefly in reference [7 a].
    • Fluorescence change of NCTPP by F- binding was reported briefly in reference [7 a].
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    • NPA charges of the complexes were shown in the Supporting Information
    • NPA charges of the complexes were shown in the Supporting Information.
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    • A direct comparison between 1-Cu and NCTPP-Cu was extremely difficult because the latter phenyl derivative was too unstable for anion-binding studies.
    • A direct comparison between 1-Cu and NCTPP-Cu was extremely difficult because the latter phenyl derivative was too unstable for anion-binding studies.
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    • For the calculations, the basis-set superposition error and zero-point energy correction were not considered.[14c
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    • Tris(pentafluorophenyl)-substituted NCPs 4-6 were prepared by [2 + 2] condensation of N-confused dipyrromethane derivatives and normal dipyrromethanes. See also reference [11].
    • Tris(pentafluorophenyl)-substituted NCPs 4-6 were prepared by [2 + 2] condensation of N-confused dipyrromethane derivatives and normal dipyrromethanes. See also reference [11].
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    • The data were analyzed by assuming a normal porphyrin structure, because the pyrrole groups in the crystal were disordered and only the 1/8 of the structure was available due to the symmetrical space group
    • The data were analyzed by assuming a normal porphyrin structure, because the pyrrole groups in the crystal were disordered and only the 1/8 of the structure was available due to the symmetrical space group.
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    • The similar deprotonation of pyrrole NH by halide anions and the formation of ion-pair complexes was previously reported with 3,4-dichloro-2,5-diamidopyrroles: a S. Camiolo, P. A. Gale, M. B. Hursthouse, M. E. Light, A. J. Shi, Chem. Commun. 2002, 758-759;
    • The similar deprotonation of pyrrole NH by halide anions and the formation of ion-pair complexes was previously reported with 3,4-dichloro-2,5-diamidopyrroles: a) S. Camiolo, P. A. Gale, M. B. Hursthouse, M. E. Light, A. J. Shi, Chem. Commun. 2002, 758-759;


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.