ESR Studies of Poly(aniline-co-m-aminophenol) in the Solid State and Nonaqueous Solution

2007 ◽  
Vol 111 (25) ◽  
pp. 6998-7002 ◽  
Author(s):  
Shaolin Mu ◽  
Chong Chen
Solar Energy ◽  
2020 ◽  
Vol 195 ◽  
pp. 565-572 ◽  
Author(s):  
Mücella Özbay Karakuş ◽  
Merve Eren Yakışıklıer ◽  
Ali Delibaş ◽  
Enise Ayyıldız ◽  
Hidayet Çetin

1997 ◽  
Vol 75 (3) ◽  
pp. 333-341 ◽  
Author(s):  
Martyn A. Brown ◽  
Jesus A. Castro ◽  
Dennis G. Tuck

The solid state structures of the compounds GaI3•PPh3 and Ga2I6•dppe ( dppe = 1,2-bis(diphenylphosphino)ethane ) have been determined. For the former, in which the GaI3P core has C3v symmetry, the structure is trigonal, with a = 14.961(2) Å, c = 16.509(3) Å, V = 3199.5(4) Å3, Z = 6, space group [Formula: see text]. In Ga2I6•dppe, the ligand bridges two GaI3P centres; the structure is monoclinic, a = 10.196(7) Å, b = 15.363(1) Å, c = 23.027(9) Å, β = 98.735(4)°, V = 3565.1(3.2) Å3Z = 4, space group P21/n The use of 31P NMR spectroscopy shows that GaI3•PPh3 is slightly dissociated in nonaqueous solution, and the effect of adding Ph3P or I− has been investigated. Similar studies with Ga2I6•dppe are also reported. In each system, four-coordination at gallium is dominant; an equally important factor is the dimerization of uncomplexed GaI3 to Ga2I6 in these solutions. Keywords: gallium(III) iodide, complexes, phosphorus, NMR, crystallography.


1993 ◽  
Vol 55 (1) ◽  
pp. 702-707 ◽  
Author(s):  
P.C. Stein ◽  
William L. Earl ◽  
A. Ray

1997 ◽  
Vol 85 (1-3) ◽  
pp. 1367-1368 ◽  
Author(s):  
Euakyoung Kim ◽  
Kwang-Yong Lee ◽  
Myong-Hoon Lee ◽  
Jae-Sup Shin ◽  
Suh Bong Rhee

Polymers ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 1191 ◽  
Author(s):  
Ke Qu ◽  
Mingxi Fang ◽  
Shuwei Zhang ◽  
Haiying Liu ◽  
Xiangqun Zeng

This work reports the design, synthesis, and characterization of a novel redox-active conjugated polyaniline containing quinone moiety as a solid state reference electrode. The union of electro-active quinone with π-conjugated polyaniline was created by the first chemical synthesis of para-dimethoxybenzene-functionalized aniline as a monomer using a palladium-mediated coupling. The successful polymerization of the as-prepared monomer was accomplished without acid additives. Its post-polymerization modification with strong Lewis acid boron tribromide furnished unique poly (aniline quinone/hydroquinone) with desired properties for all-solid-state reference electrode (RE) applications. The electrochemical responses from the conjugated polyaniline backbone in this unique polymer have been “suppressed” by the quinone pendant. The resulting poly (aniline quinone) showed a quasi-reversible redox process from the redox behavior of the pendant quinone. The stable electrode potential of this poly (aniline quinone/hydroquinone) suggested that it was a single phase in which the amounts of totally reduced and totally oxidized species could be maintained at a constant in various solvents and electrolytes. Its electrochemical stability was excellent with 95% peak current retention after continuous cyclic voltammetric testing. The aniline and quinone moieties in poly (aniline quinone/hydroquinone) render it to have both hydrophilic and hydrophobic compatibility. It showed excellent behavior as a reference electrode in aqueous and non-aqueous media and can be used in both non-zero current and zero-current conditions, providing a stable potential with a maximum potential drift of ~4.7 mV over ten consecutive days.


2019 ◽  
Vol 7 (29) ◽  
pp. 17292-17298 ◽  
Author(s):  
Ping Li ◽  
Zhengsong Fang ◽  
You Zhang ◽  
Chunshao Mo ◽  
Xuanhe Hu ◽  
...  

A specially designed poly(aniline-co-azure C) (PANAC) copolymer cathode harnesses intelligent proton-self-buffering capability and fast electron/ion transport in a highly bendable, quasi-solid-state Zn–PANAC battery.


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