Synthesis of Photoresponsive Dual NIR Two-Photon Absorptive [60]Fullerene Triads and Tetrads
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Author(s) • • • • •
Jeon, Seaho
Wang, Min
Tan, Loon-Seng
Cooper, Thomas
Hamblin, Michael R.
Chiang, Long Y.
Date Issued
August 2013
Journal
Molecules
Publisher
MDPI AG
Citation
Jeon, Seaho, Min Wang, Loon-Seng Tan, Thomas Cooper, Michael Hamblin, and Long Chiang. “Synthesis of Photoresponsive Dual NIR Two-Photon Absorptive [60]Fullerene Triads and Tetrads.” Molecules 18, no. 8 (August 12, 2013): 9603–9622.
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Final published version
Abstract
Broadband nonlinear optical (NLO) organic nanostructures exhibiting both ultrafast photoresponse and a large cross-section of two-photon absorption throughout a wide NIR spectrum may make them suitable for use as nonlinear biophotonic materials. We report here the synthesis and characterization of two C60-(antenna)x analogous compounds as branched triad C60(>DPAF-C18)(>CPAF-C2M) and tetrad C60(>DPAF-C18)(>CPAF-C2M)2 nanostructures. These compounds showed approximately equal extinction coefficients of optical absorption over 400–550 nm that corresponds to near-IR two-photon based excitation wavelengths at 780–1,100 nm. Accordingly, they may be utilized as potential precursor candidates to the active-core structures of photosensitizing nanodrugs for 2γ-PDT in the biological optical window of 800–1,050 nm.
MIT Department
Harvard University--MIT Division of Health Sciences and Technology
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DOI of Published Version
https://doi.org/10.3390/molecules18089603