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Design of diethynyl porphyrin derivatives with high near infrared fluorescence quantum yields

Publication ,  Journal Article
Susumu, K; Therien, MJ
Published in: Journal of Porphyrins and Phthalocyanines
January 1, 2015

A design strategy for (porphinato)zinc-based fluorophores that possess large near infrared fluorescence quantum yields is described. These fluorophores are based on a (5,15-diethynylporphinato)zinc(II) framework and feature symmetric donor or acceptor units appended at the meso-ethynyl positions via benzo[c][1,2,5]thiadiazole moieties. These (5,15-bis(benzo[c][1′,2′,5′]thiadiazol-4′-ylethynyl)-10,20-bis[2′,6′-bis(3'',3''-dimethyl-1''-butyloxy)phenyl]porphinato)zinc(II) (4), (5,15-bis[4′-(N,N-dihexylamino) benzo[c][1′,2′,5′]thiadiazol-7′-ylethynyl]-10,20-bis[2′,6′-bis(3'',3''-dimethyl-1''-butyloxy)phenyl]porphinato)zinc(II) (5), (5,15-bis([7′-(4''-n-dodecyloxyphenylethynyl)benzo[c][1′,2′,5′]thiadiazol-4′-yl]ethynyl)-10,20-bis[2′,6′-bis(3'',3''-dimethyl-1''-butyloxy)phenyl]porphinato)zinc(II) (6), (5,15-bis([7′-([7''-(4'' ′-n-dodecyloxyphenyl)benzo[c][1'',2'',5'']thiadiazol-4''-yl]ethynyl)benzo[c][1′,2′,5′]thiadiazol-4′-yl]ethynyl)-10,20-bis[2′,6′-bis(3'',3''-dimethyl-1''-butyloxy)phenyl]porphinato)zinc(II) (7), 5,15-bis ([7′-(4''-N,N-dihexylaminophenylethynyl)benzo[c][1′,2′,5′]thiadiazol-4′-yl]ethynyl)-10,20-bis[2′,6′-bis(3'',3''-dimethyl-1''-butyloxy)phenyl]porphinato)zinc(II) (8), and (5,15-bis([7′-(4''-N,N-dihexylaminophenylethenyl)benzo[c][1′,2′,5′]thiadiazol-4′-yl]ethynyl)-10,20-bis[2′,6′-bis(3'',3''-dimethyl-1''-butyloxy)phenyl]porphinato)zinc(II) (9) chromophores possess red-shifted absorption and emission bands that range between 650 and 750 nm that bear distinct similarities to those of the chlorophylls and structurally related molecules. Interestingly, the measured radiative decay rate constants for these emitters track with the integrated oscillator strengths of their respective x-polarized Q-band absorptions, and thus define an unusual family of high quantum yield near infrared fluorophores in which emission intensity is governed by a simple Strickler-Berg dependence.

Duke Scholars

Published In

Journal of Porphyrins and Phthalocyanines

DOI

EISSN

1099-1409

ISSN

1088-4246

Publication Date

January 1, 2015

Volume

19

Issue

1-3

Start / End Page

205 / 218

Related Subject Headings

  • Organic Chemistry
  • 3405 Organic chemistry
  • 0305 Organic Chemistry
 

Citation

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ICMJE
MLA
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Susumu, K., & Therien, M. J. (2015). Design of diethynyl porphyrin derivatives with high near infrared fluorescence quantum yields. Journal of Porphyrins and Phthalocyanines, 19(1–3), 205–218. https://doi.org/10.1142/S1088424614501107
Susumu, K., and M. J. Therien. “Design of diethynyl porphyrin derivatives with high near infrared fluorescence quantum yields.” Journal of Porphyrins and Phthalocyanines 19, no. 1–3 (January 1, 2015): 205–18. https://doi.org/10.1142/S1088424614501107.
Susumu K, Therien MJ. Design of diethynyl porphyrin derivatives with high near infrared fluorescence quantum yields. Journal of Porphyrins and Phthalocyanines. 2015 Jan 1;19(1–3):205–18.
Susumu, K., and M. J. Therien. “Design of diethynyl porphyrin derivatives with high near infrared fluorescence quantum yields.” Journal of Porphyrins and Phthalocyanines, vol. 19, no. 1–3, Jan. 2015, pp. 205–18. Scopus, doi:10.1142/S1088424614501107.
Susumu K, Therien MJ. Design of diethynyl porphyrin derivatives with high near infrared fluorescence quantum yields. Journal of Porphyrins and Phthalocyanines. 2015 Jan 1;19(1–3):205–218.
Journal cover image

Published In

Journal of Porphyrins and Phthalocyanines

DOI

EISSN

1099-1409

ISSN

1088-4246

Publication Date

January 1, 2015

Volume

19

Issue

1-3

Start / End Page

205 / 218

Related Subject Headings

  • Organic Chemistry
  • 3405 Organic chemistry
  • 0305 Organic Chemistry