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Distorted Phthalocyanines by Click Chemistry: Photoacoustic, Photothermal, and Surface-Enhanced Resonance Raman Studies.


ABSTRACT: Distortion of nominally planar phthalocyanine macrocycles affects the excited state dynamics in that most of the excited-state energy decays through internal conversion. A click-type annulation reaction on a perfluorophthalocyanine platform appending a seven-membered ring to the ?-positions on one or more of the isoindoles distorts the macrocycle and modulates solubility. The distorted derivative enables photoacoustic imaging, photothermal effects, and strong surface-enhanced resonance Raman signals.

SUBMITTER: Rizvi W 

PROVIDER: S-EPMC6861660 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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Distorted Phthalocyanines by Click Chemistry: Photoacoustic, Photothermal, and Surface-Enhanced Resonance Raman Studies.

Rizvi Waqar W   Berisha Naxhije N   Farley Christopher C   Bhupathiraju N V S Dinesh K NVSDK   Andreou Chrysafis C   Khwaja Emaad E   Fuentes German V GV   Kircher Moritz F MF   Gao Ruomei R   Drain Charles Michael CM  

Chemistry (Weinheim an der Bergstrasse, Germany) 20191021 64


Distortion of nominally planar phthalocyanine macrocycles affects the excited state dynamics in that most of the excited-state energy decays through internal conversion. A click-type annulation reaction on a perfluorophthalocyanine platform appending a seven-membered ring to the β-positions on one or more of the isoindoles distorts the macrocycle and modulates solubility. The distorted derivative enables photoacoustic imaging, photothermal effects, and strong surface-enhanced resonance Raman sig  ...[more]

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