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Synthesis, spectroscopic and electrochemical properties of axially symmetric fullerene-porphyrin dyad with a rigid pyrrolo[3,4-c]pyrrole spacer. / Konev, A.S.; Khlebnikov, A.F.; Nikiforova, T.G.; Virtsev, A.A.; Frauendorf, H.

In: Journal of Organic Chemistry, Vol. 78, No. 6, 2013, p. 2542-2552.

Research output: Contribution to journal › Article

Harvard

Konev, AS, Khlebnikov, AF, Nikiforova, TG, Virtsev, AA & Frauendorf, H 2013, 'Synthesis, spectroscopic and electrochemical properties of axially symmetric fullerene-porphyrin dyad with a rigid pyrrolo[3,4-c]pyrrole spacer', Journal of Organic Chemistry, vol. 78, no. 6, pp. 2542-2552. https://doi.org/10.1021/jo302763a

APA

Konev, A. S., Khlebnikov, A. F., Nikiforova, T. G., Virtsev, A. A., & Frauendorf, H. (2013). Synthesis, spectroscopic and electrochemical properties of axially symmetric fullerene-porphyrin dyad with a rigid pyrrolo[3,4-c]pyrrole spacer. Journal of Organic Chemistry, 78(6), 2542-2552. https://doi.org/10.1021/jo302763a

Vancouver

Konev AS, Khlebnikov AF, Nikiforova TG, Virtsev AA, Frauendorf H. Synthesis, spectroscopic and electrochemical properties of axially symmetric fullerene-porphyrin dyad with a rigid pyrrolo[3,4-c]pyrrole spacer. Journal of Organic Chemistry. 2013;78(6):2542-2552. https://doi.org/10.1021/jo302763a

Author

Konev, A.S. ; Khlebnikov, A.F. ; Nikiforova, T.G. ; Virtsev, A.A. ; Frauendorf, H. / Synthesis, spectroscopic and electrochemical properties of axially symmetric fullerene-porphyrin dyad with a rigid pyrrolo[3,4-c]pyrrole spacer. In: Journal of Organic Chemistry. 2013 ; Vol. 78, No. 6. pp. 2542-2552.

BibTeX

@article{68e31e90821749a1a516c072ae9b729e,
title = "Synthesis, spectroscopic and electrochemical properties of axially symmetric fullerene-porphyrin dyad with a rigid pyrrolo[3,4-c]pyrrole spacer",
abstract = "A new approach to porphyrinofullerene donor-acceptor dyads, based on consecutive 1,3-dipolar cycloaddition of azomethine ylides, generated from bis-aziridinedicarboxylate, to C60 and to porphyrin with a maleimidophenyl substituent, was developed. A synthesis of the axially symmetric porphyrin-fullerene-C60 ensemble 5 with a novel rigid pyrrolo[3,4-c]pyrrolic linker was realized. Theoretical, electrochemical, and spectroscopic studies of compound 5 showed that it is capable of forming a charge-separated state. {\textcopyright} 2013 American Chemical Society.",
author = "A.S. Konev and A.F. Khlebnikov and T.G. Nikiforova and A.A. Virtsev and H. Frauendorf",
year = "2013",
doi = "10.1021/jo302763a",
language = "English",
volume = "78",
pages = "2542--2552",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "6",

}

RIS

TY - JOUR

T1 - Synthesis, spectroscopic and electrochemical properties of axially symmetric fullerene-porphyrin dyad with a rigid pyrrolo[3,4-c]pyrrole spacer

AU - Konev, A.S.

AU - Khlebnikov, A.F.

AU - Nikiforova, T.G.

AU - Virtsev, A.A.

AU - Frauendorf, H.

PY - 2013

Y1 - 2013

N2 - A new approach to porphyrinofullerene donor-acceptor dyads, based on consecutive 1,3-dipolar cycloaddition of azomethine ylides, generated from bis-aziridinedicarboxylate, to C60 and to porphyrin with a maleimidophenyl substituent, was developed. A synthesis of the axially symmetric porphyrin-fullerene-C60 ensemble 5 with a novel rigid pyrrolo[3,4-c]pyrrolic linker was realized. Theoretical, electrochemical, and spectroscopic studies of compound 5 showed that it is capable of forming a charge-separated state. © 2013 American Chemical Society.

AB - A new approach to porphyrinofullerene donor-acceptor dyads, based on consecutive 1,3-dipolar cycloaddition of azomethine ylides, generated from bis-aziridinedicarboxylate, to C60 and to porphyrin with a maleimidophenyl substituent, was developed. A synthesis of the axially symmetric porphyrin-fullerene-C60 ensemble 5 with a novel rigid pyrrolo[3,4-c]pyrrolic linker was realized. Theoretical, electrochemical, and spectroscopic studies of compound 5 showed that it is capable of forming a charge-separated state. © 2013 American Chemical Society.

U2 - 10.1021/jo302763a

DO - 10.1021/jo302763a

M3 - Article

VL - 78

SP - 2542

EP - 2552

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 6

ER -

ID: 5628999