Characterization of the Microenvironments in AOT Reverse Micelles Using Multidimensional Spectral Analysis

1996 ◽  
Vol 100 (26) ◽  
pp. 11133-11138 ◽  
Author(s):  
Kerry K. Karukstis ◽  
April A. Frazier ◽  
D. Stefan Martula ◽  
Jennifer A. Whiles
2017 ◽  
Vol 77 (11) ◽  
pp. 989-996
Author(s):  
Shannon Anderson ◽  
Mikael Nilsson ◽  
Clayton Clark ◽  
Egwu Eric Kalu

2018 ◽  
Vol 149 (14) ◽  
pp. 144901 ◽  
Author(s):  
Ryo Urano ◽  
George A. Pantelopulos ◽  
Shanshan Song ◽  
John E. Straub

2013 ◽  
Vol 31 (2) ◽  
pp. 435-437 ◽  
Author(s):  
Xiangyan Chen ◽  
Yi Ru ◽  
Fengliang Chen ◽  
Xianchang Wang ◽  
Xiaoyan Zhao ◽  
...  

2017 ◽  
Vol 16 (10) ◽  
pp. 1750200 ◽  
Author(s):  
László Székelyhidi ◽  
Bettina Wilkens

In 2004, a counterexample was given for a 1965 result of R. J. Elliott claiming that discrete spectral synthesis holds on every Abelian group. Since then the investigation of discrete spectral analysis and synthesis has gained traction. Characterizations of the Abelian groups that possess spectral analysis and spectral synthesis, respectively, were published in 2005. A characterization of the varieties on discrete Abelian groups enjoying spectral synthesis is still missing. We present a ring theoretical approach to the issue. In particular, we provide a generalization of the Principal Ideal Theorem on discrete Abelian groups.


2016 ◽  
Vol 12 ◽  
pp. 2663-2667 ◽  
Author(s):  
Makoto Masaoka ◽  
Tomohiro Michitaka ◽  
Akihito Hashidzume

The formose reaction in reverse micelles of aerosol-OT (AOT), triton X-100 (TX), and hexadecyltrimethylammonium bromide (CTAB) was investigated. Time–conversion data have indicated that the interfacial water layer of AOT reverse micelles is a medium that accelerates formation of glycolaldehyde in the formose reaction. The 13C NMR spectra for the products of the formose reaction using formaldehyde-13C as starting material are indicative of the formation of ethylene glycol as a major product.


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