Hydrophobic Collapse of Foldamer Capsules Drives Picomolar-Level Chloride Binding in Aqueous Acetonitrile Solutions

2013 ◽  
Vol 135 (38) ◽  
pp. 14401-14412 ◽  
Author(s):  
Yuran Hua ◽  
Yun Liu ◽  
Chun-Hsing Chen ◽  
Amar H. Flood
1988 ◽  
Vol 66 (7) ◽  
pp. 1757-1762 ◽  
Author(s):  
J. A. Caram ◽  
M. E. Martins ◽  
E. G. Gros ◽  
C. M. Marschoff

The anodic behaviour of limonene on Pt electrodes was studied in LiCl solutions in acetonitrile with low water content. It was found that cis-6-acetamido-p-menth-1,8-diene is formed with acceptable yields. This compound is of interest as a potential intermediate for obtaining oxidation derivatives of limonene. Other products, among them the new compound 8-acetamido-2,4,8-trimethyl-4-chloromethyl-3-aza-bicyclo[3.3.1]non-2-ene, were identified. Reaction routes are proposed.


1993 ◽  
Vol 328 ◽  
Author(s):  
T. F. Otero ◽  
E. Brillas ◽  
J. Carrasco ◽  
A. Figueras

ABSTRACTThe electrogeneration and electrodissolution of poly (SNS) have been improved by using aqueous acetonitrile solutions having a 1% (ν/ν) of water constant. Compact, adherent and thick films (until 0.4 Mg cm-2) were galvanostatically electrogenerated. The electrodeposited (oxidized) polymer is insoluble in 0.1 M L?CIO4 aqueous acetonitrile solution and solubilizes by cathodic reduction. Both, electrogeneration and electrodissolution, are faradaic processes. Those facts mimic electrodeposition and electroerosion of metals and their concomitant industrial applications. New technological possibilities using polymers in electrophotography, electroreprography, electropolishing, electro-erosion and electromachining are open through polymeric electrodissolution altogether to a new processible way, through the obtained solution, for the conducting polymers.


1985 ◽  
Vol 63 (2) ◽  
pp. 469-475 ◽  
Author(s):  
Ghulam Ghaus Choudhry ◽  
Frans W. M. van der Wielen ◽  
G. R. Barrie Webster ◽  
Otto Hutzinger

Laboratory photochemical studies of aqueous acetonitrile solutions of some polychlorinated phenols (PCPs) such as 2,3,4,5-tetrachlorophenol (2,3,4,5-Cl4-Pn) (1), 2,3,4,6-Cl4-Pn (2), 2,3,5,6-Cl4-Pn (3), and pentachlorophenol (Cl5-Pn) (4) at λ > 285 nm have been carried out for 6 and 24 h exposure times. All the investigated PCPs underwent reductive dechlorination. This process was dependent not only upon the position of OH group but also upon the relative positions of the Cl substituents on the benzene ring. The Cl4-Pn 2 (and 3) and Cl5-Pn (4) also yielded photoproducts of molecular formulae C8H4Cl3NO (M+• = 235) and C8H3Cl4NO (M+• = 269), respectively. Furthermore, phenol 3 is unique amongst the investigated PCPs; in addition to the above mentioned photoproducts, it yielded hexa-, hepta-, and octachlorodihydroxybiphenyl(s) as well as heptachlorohydroxydiphenyl ether.


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