Computational Design of Two-Photon Fluorescent Probes for a Zinc Ion Based on a Salen Ligand

被引:25
|
作者
Huang, Shuang [1 ,2 ]
Zou, Lu-Yi [1 ]
Ren, Ai-Min [1 ]
Guo, Jing-Fu [3 ]
Liu, Xiao-Ting [1 ]
Feng, Ji-Kang [1 ]
Yang, Bao-Zhu [2 ]
机构
[1] Jilin Univ, Inst Theoret Chem, State Key Lab Theoret & Computat Chem, Changchun 130023, Peoples R China
[2] Changzhou Univ, Sch Math & Phys, Changzhou 213164, Peoples R China
[3] NE Normal Univ, Sch Phys, Changchun 130021, Peoples R China
关键词
DENSITY-FUNCTIONAL THERMOCHEMISTRY; ABSORPTION CROSS-SECTIONS; MOLECULAR-ORBITAL METHODS; NONCOVALENT INTERACTIONS; IMAGING ZINC; SENSOR; ZN2+; LIGHT; POLARIZATION; CHEMOSENSOR;
D O I
10.1021/ic3022062
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A two-photon fluorescent probe has become a critical tool in biology and medicine owing to its capability of imaging intact tissue for a long period of time, such as in two-photon fluorescence microscopy (TPM). In this context, a series of Salen-based zinc-ion bioimaging reagents that were designed based on an intramolecular charge-transfer mechanism were studied through the quantum-chemical method. The increase of one-photon absorption and fluorescence emission wavelength and the reduction of the oscillator strength upon coordination with a zinc ion reveal that they are fluorescent bioimaging reagents used for ratiometric detection. When the Salen ligand is incorporated with Zn2+, the value of the two-photon absorption (TPA) cross-section (delta(max)) will decrease, and most of the ligands and complexes exhibit a TPA peak in the near-infrared spectral region. That is, a substituent at the end of the ligand can influence the luminescence property, besides increasing solubility. In addition, the effect of an end-substituted position on the TPA property was considered, such as ortho and meta substitution. The detailed investigations will provide a theoretical basis to synthesize zinc-ion-responsive two-photon fluorescent bioimaging reagents as powerful tools for TPM and biological detection in vivo.
引用
收藏
页码:5702 / 5713
页数:12
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