New Boronic-Acid- and Boronate-Substituted Aromatic Compounds as Precursors of Fluoride-Responsive Conjugated Polymer Films

Nicolas, Maël; Fabre, Bruno; Marchand, Gilles; Simonet, Jacques

doi:10.1002/(sici)1099-0690(200005)2000:9<1703::aid-ejoc1703>3.0.co;2-s

Cited by 99 publications

(79 citation statements)

References 19 publications

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“…Nitrate-selective electrodes [1], humidity sensors [2], fluoride electrodes [3], and devices for detection of metal ions [4,5] based on ICP have been described. Polypyrrole (PPy) has attracted most attention because it is one of the most stable ICP known [6] and one of the easiest to synthesize, and so has tremendous technological potential.…”

Section: Introductionmentioning

confidence: 99%

Simple PVC–PPy electrode for pH measurement and titrations

et al. 2002

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Cobaltabis(dicarbollide) [3,3'-Co(1,2-C2B9H11)](-)-doped polypyrrole (PPy) films have been prepared galvanostatically on glassy carbon electrodes in acetonitrile solution. The potential response behavior of the film of this new material has been investigated in some common pH buffers and in acid-base titrations. The potentiometric characteristics of the resulting films are indicative of a quasi-Nernstian response (approximately 50 mV/pH unit), a linearity range from pH 12 to 3 and correlation coefficients (r2) of approximately 0.98. The electrode is suitable for pH measurements and for monoprotic titrations of strong alkalis with strong acids, and weak bases with strong acids, but the long response time hinders the use of this electrode for multiprotic titrations. The time response has been dramatically improved by reducing the film thickness by using the template effect of a non-conducting polymer (PVC) cast over the graphite surface before PPy deposition. PPy polymerization occurs in the free channels of PVC leading to the formation of PPy wires. The morphological change of PPy does not affect the slope or linearity range. The response of the PVC-PPy electrochemical sensor is rapid and the sensor is easy to prepare, at low cost, and its performance is comparable with that of commercial glass electrodes.

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Section: Introductionmentioning

confidence: 99%

Simple PVC–PPy electrode for pH measurement and titrations

et al. 2002

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“…5-Phenylbarbituric acid, 1-n-butyl-5-phenylbarbituric acid, 14 and 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-benzophenone 19 were prepared according to published procedures. Dichloromethane was distilled from calcium hydride, dioxane from sodium/benzophenone.…”

Section: Methodsmentioning

confidence: 99%

“…NMR spectra were obtained on a Bruker Avance 250, a Bruker Avance III 500, or a Varian Inova-400 spectrometer. 1 H and 13 C NMR spectra were internally referenced to the solvent signal, 19 F NMR spectra were externally referenced to CFCl 3 . Elemental analyses were carried out using an "Elementanalysator Vario EL" (Elementar Analysengeräte GmbH) or a "Flash EA 112 Series" (Thermo).…”

Section: Methodsmentioning

confidence: 99%

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A one-step synthesis of tricyclic pyrimidines

Bauer¹,

Spange

2011

Arkivoc

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The reaction of triflic anhydride activated carbonyl compounds with 5-phenylbarbituric acids in a mild, non-catalyzed one-step procedure yields unusual tricyclic pyrano[2,3-d]pyrimidines or oxazolo[3,2-c]pyrimidines containing an ADA hydrogen bond pattern. By subsequent functionalisation, other derivatives are accessible, including for instance a pyrimidine containing phenolphthalein analogue, thereby combining established chromophoric systems with a supramolecular recognition unit.

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“…Fabre and coworkers homopolymerized anilineboronic acid, in the presence of fluoride [82], to produce a self-doped polyaniline. The copolymer and the homopolymer react easily with sacharides (e.g.…”

Section: Polyaniline Substituted With Boronic Acids Groupsmentioning

confidence: 99%

Organic Chemistry of Polyanilines: Tailoring Properties to Technological Applications~!2008-08-19~!2008-09-11~!2008-11-28~!

Miras¹,

Acevedo²,

Monge³

et al. 2008

TOMACROJ

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Abstract:The use of organic chemistry reactions to introduce additional functional groups on polyanilines is described. Among the reactions discussed are: electrophilic aromatic substitution, nucleophilic addition to the aromatic rings, nucleophilic substitution on the amine groups and reactions on pendant groups. The use of combinatorial chemistry techniques, by coupling of combinatorially synthesised diazonium salts with polyaniline, to produce a functionalized polyanilines library is also reviewed. The modification of polyaniline introduces or alters different properties of the materials: solubility, self-doping and redox coupled ion exchange. The tailoring of those properties to technical applications is therefore examined.

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New Boronic-Acid- and Boronate-Substituted Aromatic Compounds as Precursors of Fluoride-Responsive Conjugated Polymer Films

Cited by 99 publications

References 19 publications

Simple PVC–PPy electrode for pH measurement and titrations

Simple PVC–PPy electrode for pH measurement and titrations

A one-step synthesis of tricyclic pyrimidines

Organic Chemistry of Polyanilines: Tailoring Properties to Technological Applications~!2008-08-19~!2008-09-11~!2008-11-28~!

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