scholarly journals Preparation of Carbon Dots with High-Fluorescence Quantum Yield and Their Application in Dopamine Fluorescence Probe and Cellular Imaging

2019 ◽  
Vol 2019 ◽  
pp. 1-9 ◽  
Author(s):  
Haitao Lin ◽  
Jun Huang ◽  
Liyun Ding

Carbon dots represent a kind of fluorescent nanomaterial and have broad application prospects in the field of biosensing and optoelectronics. Here, we explored carbon dots with a high-fluorescence quantum yield rate synthesized from L-cysteine and citric acid by the microwave-assisted method. The characteristics of the carbon dots were studied using a transmission electron microscope, an X-ray diffractometer, X-ray photoelectron spectra, a UV-Vis absorption spectrometer, a FTIR spectrometer, and a fluorescence spectrophotometer. The obtained carbon dots exhibited a high-fluorescence quantum yield (up to 85%), which is due to the combination of amidogens and sulfydryl with carbon dots, and hence bring the improved fluorescence property. We used carbon dots for in vitro imaging of CRL-5822 cells and human umbilical vein endothelial cells, which showed the low inhibitory rate (0.8%) of cells for 48 h with good biocompatibility demonstrated by the cell viability assay. The image of cells can be observed clearly under UV light. The Stern-Volmer equation was introduced to describe the quenching effect between the fluorescence intensity of carbon dots and the concentration of aqueous dopamine (DA).

2015 ◽  
Vol 3 (2) ◽  
pp. 542-546 ◽  
Author(s):  
Quan Xu ◽  
Peng Pu ◽  
Jungang Zhao ◽  
Chenbo Dong ◽  
Chun Gao ◽  
...  

Sulfur-doped carbon dots were synthesized by a one-step hydrothermal method and exhibited high fluorescence quantum yield (67%) and exceptional emission behavior.


Nanoscale ◽  
2016 ◽  
Vol 8 (30) ◽  
pp. 14374-14378 ◽  
Author(s):  
Lei Shi ◽  
Jian Hai Yang ◽  
Hai Bo Zeng ◽  
Yong Mei Chen ◽  
Sheng Chun Yang ◽  
...  

2021 ◽  
Author(s):  
Hai-Jiao Wang ◽  
Wan-Yi Hou ◽  
Jing Kang ◽  
Xin-Yu Zhai ◽  
Hongli Chen ◽  
...  

Due to the direct π - π interaction and excessive energy resonance transfer, it is very challenging to prepare CDs with high fluorescence quantum yield (QY) in solid state. In...


2020 ◽  
Vol 56 (47) ◽  
pp. 6384-6387
Author(s):  
Vlad A. Neacşu ◽  
Cecilia Cerretani ◽  
Mikkel B. Liisberg ◽  
Steven M. Swasey ◽  
Elisabeth G. Gwinn ◽  
...  

Silver nanoclusters stabilized by 5′-CCCGGAGAAG-3′ DNA strands display an unusually high fluorescence quantum yield in the near-infrared region.


2020 ◽  
Vol 4 (3) ◽  
pp. 941-949 ◽  
Author(s):  
Xinzhe Yang ◽  
Qian Wang ◽  
Peiyu Hu ◽  
Chao Xu ◽  
Wenjing Guo ◽  
...  

An ionic AIEgen with high fluorescence quantum yield shows remarkable and reversible mechanochromism as well as excellent mitochondrial imaging of cancer cells and long-term tracking of tumors.


2020 ◽  
Vol 8 (30) ◽  
pp. 10416-10421
Author(s):  
Feng-Yan Hao ◽  
Yi-Zhong Shi ◽  
Kai Wang ◽  
Xiao-Chun Fan ◽  
Lin Wu ◽  
...  

By crooking conventional donor segments via suitable steric hindrance, nearly planar geometries, a small singlet–triplet energy splitting and a high fluorescence quantum yield can be realized simultaneously.


2020 ◽  
Vol 8 (17) ◽  
pp. 5873-5881 ◽  
Author(s):  
Yeasin Khan ◽  
Yohan Ahn ◽  
Hyuna Lee ◽  
Jaeki Jeong ◽  
Yun Seop Shin ◽  
...  

We’ve observed intense, water-stable fluorescence from lead formate crystals when they are precipitated from a CH3NH3PbBr3 (MAPbBr3) perovskite precursor solution.


1987 ◽  
Vol 42 (9) ◽  
pp. 987-993
Author(s):  
P. Nikolova ◽  
N. Tyutyulkova ◽  
V. Dryanska

The spectral properties of a group of 3-(2-benzthiazolyl)-coumarins and coumarinimines, some of them having high fluorescence quantum yield (Qf > 0.7), are described.The quantum -chemical investigations show that the main chromophore of this group of dyes is the 3 -(2-thiazolyl)-2 H -pyran -2-one fragmenti.e . the coumarin (coumarinimine) and the benzthiazolyl fragments are not separate chromophores.


Synthesis ◽  
2019 ◽  
Vol 51 (22) ◽  
pp. 4147-4152 ◽  
Author(s):  
Michael Fingerle ◽  
Simon Stocker ◽  
Holger F. Bettinger

A dibenzoperylene motif featuring a doubly boron–nitrogen-doped bay region is accessible from an aniline derivative in six steps in good overall yield. Two n-butyl groups provide the BN-doped polycyclic aromatic hydrocarbon with sufficient solubility in common organic solvents. The synthesis sequence allows installation of a second boron atom next to a weakly nucleophilic nitrogen by using a protected boron species. The title compound shows blue fluorescence, an extremely high fluorescence quantum yield, and an interesting doped bay region.


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