scholarly journals Short-time preparation and electrochemical properties of a single layer of tetraoctylammonium bromide capped Au nanoparticles on dithiol self-assembled monolayer-modified Au electrode

2009 ◽  
Vol 633 (1) ◽  
pp. 175-181 ◽  
Author(s):  
S. Abraham John ◽  
Takamasa Sagara
2016 ◽  
Vol 45 (47) ◽  
pp. 19053-19061 ◽  
Author(s):  
Charlotte Buron ◽  
Sihem Groni ◽  
Nathalie Ségaud ◽  
Sandra Mazerat ◽  
Diana Dragoe ◽  
...  

The first coordination sphere of (N5)FeII–X complexes grafted on a gold electrode can be tuned in a similar way to that in solution.


2011 ◽  
Vol 239-242 ◽  
pp. 1442-1447 ◽  
Author(s):  
Shu Zhen Tan ◽  
Pu Ni Zeng ◽  
Zhong Cao ◽  
Jiao Yun Xia ◽  
Wei Li

A novel technique to covalently immobilize indicator dyes with terminal amino groups for preparing optical sensors is investigated. Au nanoparticles are used as bridges and carriers for anchoring indicator dyes on the surface of a quartz glass slide. 1-Aminopyrene (AP) was employed as an example of indicator dyes and covalently immobilized onto the outmost surface of the glass slide. First, the glass slide was functionalized by (3-mercaptopropyl) trimethoxysilane (MPS) to form a thiol-terminated self-assembled monolayer, where Au nanoparticles were strongly anchored via covalent link. Then, 16-mercaptohexadecanoic acid (MHDA) was self-assembled to bring carboxylic groups onto the surfaces of Au nanoparticles. A further activation by using 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS) converted the carboxylic group into succinimide ester. Finally, the active succinimide ester was reacted with 1-aminopyrene (AP). Thus, AP was covalently immobilized to the glass slide and an AP-immobilized sensor was obtained. The resulting sensor was used to determine rutin based on fluorescence quenching. It showed a linear response toward rutin (R) from 5.0 × 10-7 to 6.0 × 10-4 mol L-1 with a detection limit of 2.0× 10-7 mol L-1. This AP-immobilized sensor has very satisfactory reproducibility, reversibility, rapid response and no dye-leaching.


2007 ◽  
Vol 32 (2) ◽  
pp. 575-578
Author(s):  
Yuya Hayashi ◽  
Tomohiko Inomata ◽  
Kazuma Shinozaki ◽  
Yasuhiro Funahashi ◽  
Tomohiro Ozawa ◽  
...  

2014 ◽  
Vol 134 (10) ◽  
pp. 315-319
Author(s):  
Miyuki Tabata ◽  
Kozue Nogami ◽  
Tatsuro Goda ◽  
Akira Matsumoto ◽  
Yuji Miyahara

RSC Advances ◽  
2014 ◽  
Vol 4 (109) ◽  
pp. 64310-64318 ◽  
Author(s):  
Piotr Piotrowski ◽  
Joanna Pawłowska ◽  
Jan Pawłowski ◽  
Lidia Jagoda Opuchlik ◽  
Renata Bilewicz ◽  
...  

Two types of nanocomposites were synthesized: Au electrode covered with self-assembled in situ deprotected aromatic S-acetyl-derivatized C60 fullerenes and Au nanoparticles decorated with high number of C60 fullerenes.


2011 ◽  
Vol 298 ◽  
pp. 78-83
Author(s):  
Yan Liu ◽  
Zhao Dai ◽  
Shi Chao Xu ◽  
Ji Mei Zhang ◽  
Guo Zheng ◽  
...  

A novel electrochemical DNA biosensor system based on Au nanoparticles (AuNPs) modified Au electrode and anthraquinone-2,6-disulfonic acid (AQDS) as hybridization indicator was presented in this paper. AuNPs with different particle sizes were prepared from gold chloride by reduction, and self-assembled on Au electrode (AuNPs/Au electrode) by cysteamine as linker. Then, 5’ end –SH modified DNA (HS-DNA) as nucleotide probes were self-assembled onto the surface of AuNPs modified Au electrode (HS-DNA/AuNPs/Au electrode), and the HS-DNA/AuNPs/Au electrode could detect target DNA (completely complementary with HS-DNA). Because AuNPs were on Au electrode, the surface of Au electrode was increased. Therefore, this would result in the increase of electrochemical signal and increase the sensitivity of biosensor. If a completely complementary single stranded DNA (ssDNA) as target existed in the detection system, the cathodic peak current (△Ip) of AuNPs modified Au electrode was increased about 3 times than the HS-DNA/AuNPs/Au electrode because of the hybridization between HS-DNA and complementary DNA target and the formation of double stranded DNA (dsDNA), and if the target was a mismatching base-pair with HS-DNA, the electrochemical signal of electrode would have no obviously change. These results showed that this DNA biosensor system based on AuNPs self-assembled Au electrode had an excellent sensitivity with a complete complementary DNA sequence.


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