scholarly journals Novel NIR-II organic fluorophores for bioimaging beyond 1550 nm

2020 ◽  
Vol 11 (10) ◽  
pp. 2621-2626 ◽  
Author(s):  
Yang Li ◽  
Yufang Liu ◽  
Qianqian Li ◽  
Xiaodong Zeng ◽  
Tian Tian ◽  
...  
Keyword(s):  
Organic Fluorophores ◽  
Donor Acceptor ◽  
Bio Imaging

Novel NIR-II organic fluorophores were designed and synthesized using an AIE and highly twisted donor–acceptor distortion strategy for bio-imaging beyond 1550 nm.

scholarly journals “CinNapht” Dyes as New Cinnoline/Naphthalimide Fused Hybrids Fluorophores: Synthesis, Photo-Physical Study and Use for Bio-Imaging

2021 ◽  
Author(s):  
Minh-Duc Hoang ◽  
Jean-Baptiste Bodin ◽  
Farah Savina ◽  
Vincent Steinmetz ◽  
Jérôme Bignon ◽  
...  
Keyword(s):  
Quantum Yield ◽  
Red Emission ◽  
Solvatochromic Effect ◽  
Physical Study ◽  
Donor Acceptor ◽  
Bio Imaging ◽  
Naphthalimide Dye

Six-membered diaza ring of Cinnoline have been fused on Naphthalimide dye to give donor–acceptor system called CinNapht. These red shifted fluorophore, that can be synthetised in gram scale, exhibits a large Stoke Shift and quantum yield up to 0.33. It is also caracterized by strong solvatochromic effect for green to red emission as well and can be used for bio-imaging

Ratiometric O2 sensing based on selective self-sensitized photooxidation of donor–acceptor fluorophores

2019 ◽  
Vol 55 (49) ◽  
pp. 7017-7020 ◽  
Author(s):  
Jian-Xin Wang ◽  
Li-Ya Niu ◽  
Peng-Zhong Chen ◽  
Yu-Zhe Chen ◽  
Qing-Zheng Yang ◽  
...  
Keyword(s):  
Light Irradiation ◽  
Organic Fluorophores ◽  
Donor Acceptor ◽  
O2 Sensing

We report a series of organic fluorophores that undergo selective self-sensitized photooxidation upon light irradiation in air.

Live bio-imaging with fully bio-compatible organic fluorophores

2017 ◽  
Vol 166 ◽  
pp. 52-57 ◽  
Author(s):  
Ilseung Yang ◽  
Jong Woo Lee ◽  
Sunjin Hwang ◽  
Jung Eun Lee ◽  
Eunhak Lim ◽  
...  
Keyword(s):  
Organic Fluorophores ◽  
Bio Imaging

scholarly journals “CinNapht” Dyes as New Cinnoline/Naphthalimide Fused Hybrids Fluorophores: Synthesis, Photo-Physical Study and Use for Bio-Imaging

2021 ◽  
Author(s):  
Minh-Duc Hoang ◽  
Jean-Baptiste Bodin ◽  
Farah Savina ◽  
Vincent Steinmetz ◽  
Jérôme Bignon ◽  
...  
Keyword(s):  
Quantum Yield ◽  
Red Emission ◽  
Solvatochromic Effect ◽  
Physical Study ◽  
Donor Acceptor ◽  
Bio Imaging ◽  
Naphthalimide Dye

Six-membered diaza ring of Cinnoline have been fused on Naphthalimide dye to give donor–acceptor system called CinNapht. These red shifted fluorophore, that can be synthetised in gram scale, exhibits a large Stoke Shift and quantum yield up to 0.33. It is also caracterized by strong solvatochromic effect for green to red emission as well and can be used for bio-imaging

scholarly journals “CinNapht” dyes: a new cinnoline/naphthalimide fused hybrid fluorophore. Synthesis, photo-physical study and use for bio-imaging

RSC Advances ◽  
2021 ◽  
Vol 11 (48) ◽  
pp. 30088-30092
Author(s):  
Minh-Duc Hoang ◽  
Jean-Baptiste Bodin ◽  
Farah Savina ◽  
Vincent Steinmetz ◽  
Jérôme Bignon ◽  
...  
Keyword(s):  
Physical Study ◽  
Donor Acceptor ◽  
Bio Imaging ◽  
Naphthalimide Dye

Six-membered-diaza ring of cinnoline has been fused on naphthalimide dye to give a donor–acceptor system called CinNapht.

scholarly journals Shielding Unit Engineering of NIR-II Molecular Fluorophores for Improved Fluorescence Performance and Renal Excretion Ability

2021 ◽  
Vol 9 ◽  
Author(s):  
Chunchen Liu ◽  
Huilong Ma ◽  
Zhubin Hu ◽  
Rui Tian ◽  
Rui Ma ◽  
...  
Keyword(s):  
Quantum Yield ◽  
Near Infrared ◽  
Renal Excretion ◽  
Side Chain ◽  
Side Chains ◽  
High Brightness ◽  
Calculation Results ◽  
Donor Acceptor ◽  
Bio Imaging

Molecular fluorophores emitting in the second near-infrared (NIR-II) window with good renal excretion ability are favorable for in vivo bio-imaging and clinical applications. So far, renally excretable fluorophores are still less studied. Understanding the influences of molecular structure on optical properties and renal excretion abilities are vital for fluorophore optimization. Herein, a series of shielding unit-donor-acceptor-donor-shielding unit (S-D-A-D-S) NIR-II molecular fluorophores are designed and synthesized with dialkoxy chains substituted benzene as the S unit. The anchoring positions of dialkoxy chains on benzene are tuned as meso-2,6, para-2,5, or ortho-3,4 to afford three fluorophores: BGM6P, BGP6P and BGO6P, respectively. Experimental and calculation results reveal that alkoxy side chains anchored closer to the conjugated backbone can provide better protection from water molecules and PEG chains, affording higher fluorescence quantum yield (QY) in aqueous solutions. Further, these side chains can enable good encapsulation of backbone, resulting in decreased binding with albumin and improved renal excretion. Thus, fluorophore BGM6P with meso-2,6-dialkoxy chains exhibits the highest quantum yield and fastest renal excretion. This work emphasizes the important roles of side chain patterns on optimizing NIR-II fluorophores with high brightness and renal excretion ability.

Evidence of a donor-acceptor type transition in CuGaSe2

1980 ◽  
Vol 41 (7) ◽  
pp. 707-712 ◽  
Author(s):  
A. Poure ◽  
G. Aguero ◽  
G. Masse ◽  
J.P. Aicardi
Keyword(s):  
Type Transition ◽  
Donor Acceptor
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