Boronic acid derived salicylidenehydrazinopyridine (BOSPY) complexes with aggregation-induced emission for fluorescence imaging of cellular organelles. (February 2023)
- Record Type:
- Journal Article
- Title:
- Boronic acid derived salicylidenehydrazinopyridine (BOSPY) complexes with aggregation-induced emission for fluorescence imaging of cellular organelles. (February 2023)
- Main Title:
- Boronic acid derived salicylidenehydrazinopyridine (BOSPY) complexes with aggregation-induced emission for fluorescence imaging of cellular organelles
- Authors:
- Wang, Hua
Guo, Xing
Bu, Weibin
Kang, Zhengxin
Yu, Changjiang
Wu, Qinghua
Jiao, Lijuan
Hao, Erhong - Abstract:
- Abstract: A series of boronic acid derived salicylidenehydrazinopyridine complexes have been synthesized from the condensation of 2-hydrazinopyridine or 2-hydrazinoquinoline and salicylaldehyde then followed by complexation with various boronic acids. Their X-ray structures demonstrate that the boron atoms adopt a tetrahedral geometry and the aryl substituents from arylboric acids along the vertical axis gave the molecule stereotactic structure and induced molecular chirality. These dyes have good solubility on organic solvents due to the nonplanar curved structure and the presence of axial-substituted groups that provide steric protection. They have strong visible-light absorption, weak emission and large Stoke shifts in organic solvents. Interestingly, molecular aggregates of these new boron complexes experienced the transformation from H -type aggregation to J- type aggregation and exhibited strong aggregation-induced emission (AIE) activities. These novel AIE dyes showed great potential as bioimaging dyes, and two complexes were mainly distributed in lipid droplets of cells in colocalization experiments. Graphical abstract: Image 1 Highlights: New boron complexed fluorophore (BOSPY ) has been developed from various arylboric acids. Molecular chirality of these dyes after boron complexation was confirmed by X-ray structures. These dyes exhibit strong aggregation-induced emission (AIE). These AIE dyes are suitable for fluorescence imaging and two dyes can specificallyAbstract: A series of boronic acid derived salicylidenehydrazinopyridine complexes have been synthesized from the condensation of 2-hydrazinopyridine or 2-hydrazinoquinoline and salicylaldehyde then followed by complexation with various boronic acids. Their X-ray structures demonstrate that the boron atoms adopt a tetrahedral geometry and the aryl substituents from arylboric acids along the vertical axis gave the molecule stereotactic structure and induced molecular chirality. These dyes have good solubility on organic solvents due to the nonplanar curved structure and the presence of axial-substituted groups that provide steric protection. They have strong visible-light absorption, weak emission and large Stoke shifts in organic solvents. Interestingly, molecular aggregates of these new boron complexes experienced the transformation from H -type aggregation to J- type aggregation and exhibited strong aggregation-induced emission (AIE) activities. These novel AIE dyes showed great potential as bioimaging dyes, and two complexes were mainly distributed in lipid droplets of cells in colocalization experiments. Graphical abstract: Image 1 Highlights: New boron complexed fluorophore (BOSPY ) has been developed from various arylboric acids. Molecular chirality of these dyes after boron complexation was confirmed by X-ray structures. These dyes exhibit strong aggregation-induced emission (AIE). These AIE dyes are suitable for fluorescence imaging and two dyes can specifically localize in lipid droplets of cells. … (more)
- Is Part Of:
- Dyes and pigments. Volume 210(2023)
- Journal:
- Dyes and pigments
- Issue:
- Volume 210(2023)
- Issue Display:
- Volume 210, Issue 2023 (2023)
- Year:
- 2023
- Volume:
- 210
- Issue:
- 2023
- Issue Sort Value:
- 2023-0210-2023-0000
- Page Start:
- Page End:
- Publication Date:
- 2023-02
- Subjects:
- BODIPY dyes -- Boron complexes -- Aggregation-induced emission -- Fluorescent probes -- Bioimaging
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2022.111013 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24863.xml