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硼二吡咯甲烷(BODIPY)衍生物的双光子吸收增强。

Enhancement of Two-Photon Absorption in Boron-Dipyrromethene (BODIPY) Derivatives.

机构信息

Department of Physics, Harbin Institute of Technology, Harbin 150001, China.

School of Electronic and Information Engineering, Changshu Institute of Technology, Changshu 215500, China.

出版信息

Molecules. 2022 Apr 29;27(9):2849. doi: 10.3390/molecules27092849.

DOI:10.3390/molecules27092849
PMID:35566197
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9099460/
Abstract

The linear and nonlinear optical properties of two BODIPY derivatives, 1,7-Diphenyl-3,5-bis(9,9-dimethyl-9H-fluoren-2-yl)-boron-diuoride-azadipyrromethene (ZL-61) and 1,7-Diphenyl-3,5-bis(4-(1,2,2-triphenylvinyl)phenyl)-boron-diuoride-azadipyrromethene (ZL-22), were comprehensively investigated based on experimental and theoretical studies. It was found that both compounds show a strong two-photon absorption response in the near-infrared regime, and the two-photon-absorption cross-section values of ZL-61 and ZL-22 were determined to be 8321 GM and 1864 GM at 800 nm, respectively. The improvement of the two-photon absorption cross section in ZL-61 was attributed to the enhancement of the donor group, which was confirmed by transient absorption measurements and DFT calculation. Our results indicate that these BODIPY derivatives are a promising candidate for optical limiting and two-photon imaging applications.

摘要

两种 BODIPY 衍生物,1,7-二苯基-3,5-双(9,9-二甲基-9H-芴-2-基)-硼二氟-偶氮吡咯甲川(ZL-61)和 1,7-二苯基-3,5-双(4-(1,2,2-三苯基乙烯基)苯基)-硼二氟-偶氮吡咯甲川(ZL-22)的线性和非线性光学性质通过实验和理论研究进行了综合研究。结果发现,这两种化合物在近红外区域均表现出较强的双光子吸收响应,ZL-61 和 ZL-22 在 800nm 处的双光子吸收截面值分别为 8321GM 和 1864GM。ZL-61 中双光子吸收截面的提高归因于供体基团的增强,这通过瞬态吸收测量和 DFT 计算得到了证实。我们的研究结果表明,这些 BODIPY 衍生物是用于光限幅和双光子成像应用的有前途的候选材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/b6522c13e9f7/molecules-27-02849-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/b6bbab3e7f4f/molecules-27-02849-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/77a757756bff/molecules-27-02849-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/b5364dcb1749/molecules-27-02849-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/f2824a1de1ef/molecules-27-02849-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/edf58d8d558b/molecules-27-02849-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/6c6989b080c2/molecules-27-02849-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/da36107335c5/molecules-27-02849-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/36c193b4f1a8/molecules-27-02849-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/61a6a2ff14af/molecules-27-02849-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/03db77aa2912/molecules-27-02849-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/b6522c13e9f7/molecules-27-02849-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/b6bbab3e7f4f/molecules-27-02849-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/77a757756bff/molecules-27-02849-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/b5364dcb1749/molecules-27-02849-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/f2824a1de1ef/molecules-27-02849-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/edf58d8d558b/molecules-27-02849-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/6c6989b080c2/molecules-27-02849-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/da36107335c5/molecules-27-02849-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/36c193b4f1a8/molecules-27-02849-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/61a6a2ff14af/molecules-27-02849-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/03db77aa2912/molecules-27-02849-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9598/9099460/b6522c13e9f7/molecules-27-02849-g010.jpg

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