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Synthesis of Photoresponsive Dual NIR Two-Photon Absorptive 60Fullerene Triads and Tetrads

机译:光响应双近红外双光子吸收性60富勒烯三联体和四联体的合成

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摘要

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.
机译:宽带非线性光学(NLO)有机纳米结构在超宽的NIR光谱范围内具有超快的光响应和大的双光子吸收截面,可使其适合用作非线性生物光子材料。我们在这里报告了两个C60-(antenna)x类似化合物的合成和表征,分别是分支三联体C60(> DPAF-C18)(> CPAF-C2M)和四键C60(> DPAF-C18)(> CPAF-C2M)2纳米结构。这些化合物在400–550 nm范围内显示出大致相等的消光系数,这对应于在780–1,100 nm处基于近红外双光子的激发波长。因此,它们可以在800–1,050 nm的生物光学窗口中用作2γ-PDT的光敏纳米药物活性核心结构的潜在前体候选物。

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