Surface activity and redox behavior of nonionic surfactants containing an anthraquinone group as the redox-active site

1999 ◽  
Vol 277 (12) ◽  
pp. 1125-1133 ◽  
Author(s):  
M. A. B. H. Susan ◽  
K. Tani ◽  
M. Watanabe
Molecules ◽  
2020 ◽  
Vol 25 (24) ◽  
pp. 5917
Author(s):  
Yang Pan ◽  
Shogo Morisako ◽  
Shinobu Aoyagi ◽  
Takahiro Sasamori

Divalent silicon species, the so-called silylenes, represent attractive organosilicon building blocks. Isolable stable silylenes remain scarce, and in most hitherto reported examples, the silicon center is stabilized by electron-donating substituents (e.g., heteroatoms such as nitrogen), which results in electronic perturbation. In order to avoid such electronic perturbation, we have been interested in the chemistry of reactive silylenes with carbon-based substituents such as ferrocenyl groups. Due to the presence of a divalent silicon center and the redox-active transition metal iron, ferrocenylsilylenes can be expected to exhibit interesting redox behavior. Herein, we report the design and synthesis of a bis(ferrocenyl)silirane as a precursor for a bis(ferrocenyl)silylene, which could potentially be used as a building block for redox-active organosilicon compounds. It was found that the isolated bis(ferrocenyl)siliranes could be a bottleable precursor for the bis(ferrocenyl)silylene under mild conditions.


2015 ◽  
Vol 223 ◽  
pp. 122-130 ◽  
Author(s):  
Anton S. Lytvynenko ◽  
Mikhail A. Kiskin ◽  
Victoria N. Dorofeeva ◽  
Andrey M. Mishura ◽  
Vladimir E. Titov ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 24 (44) ◽  
pp. no-no
Author(s):  
E. MEISSNER ◽  
J. MYSZKOWSKI ◽  
J. SZYMANOWSKI ◽  
R. BARHOUM

1993 ◽  
Vol 115 (22) ◽  
pp. 10029-10035 ◽  
Author(s):  
Mei M. Whittaker ◽  
Yao Yuan Chuang ◽  
James W. Whittaker

2012 ◽  
Vol 02 (02) ◽  
pp. 93-97 ◽  
Author(s):  
Haiyan Li ◽  
Jun Wang ◽  
Changhuan Liu ◽  
Jun Han ◽  
Cuiqin Li ◽  
...  

2012 ◽  
Vol 390 ◽  
pp. 47-52 ◽  
Author(s):  
Isao Ando ◽  
Takemasa Fukuishi ◽  
Kikujiro Ujimoto ◽  
Hirondo Kurihara

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