From chain collapse to new structures: Spectroscopic properties of poly(3-thiophene acetic acid) upon binding by alkyl trimethylammonium bromide surfactants

Langmuir

Volumn 28, Issue 10, 2012, Pages 4815-4828

  Franco, I Echavarri ^a   Lorchat, P ^a   Lamps, J P ^a   Schmutz, M ^a   Schroder A ^a   Catala, J M ^a   Combet, J ^a,b   Schosseler, F ^a  

^a UNIVERSITÉ DE STRASBOURG   (France)

^b INSTITUT LAUE LANGEVIN   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ABSORPTION AND EMISSION SPECTROSCOPY; ALKYL CHAIN LENGTHS; AQUEOUS BUFFER; AQUEOUS SOLUBILITY; BLUE SHIFT; BROMIDE SURFACTANTS; COLORIMETRIC BIOSENSORS; COMPOSITION RANGES; COMPOSITION RATIO; CONJUGATION LENGTH; CONTOUR LENGTHS; CRITICAL MICELLAR CONCENTRATIONS; CRYOGENIC TRANSMISSION ELECTRON MICROSCOPY; EMISSION MAXIMA; INTENSE EMISSION; ISOTHERMAL TITRATION CALORIMETRY; MIXED AGGREGATES; MIXED SOLUTION; MOLAR CONCENTRATION; MONOMER UNITS; PERSISTENCE LENGTH; POLYANIONS; POLYMER CONCENTRATIONS; RED-SHIFTED; REGIORANDOM; SPECTROSCOPIC PROPERTY; SURFACTANT BINDING; SURFACTANT CONCENTRATIONS; SURFACTANT MOLECULES; SURFACTANT TAILS;

ACETIC ACID; BIOSENSORS; BROMINE COMPOUNDS; CATIONIC SURFACTANTS; DYES; ELECTROMAGNETIC WAVE ABSORPTION; EMISSION SPECTROSCOPY; PH; PHOTON CORRELATION SPECTROSCOPY; THIOPHENE; TRANSMISSION ELECTRON MICROSCOPY;

STRUCTURE (COMPOSITION);

ACETIC ACID DERIVATIVE; DODECYLTRIMETHYLAMMONIUM; POLY(THIOPHENE 3 ACETIC ACID); POLY(THIOPHENE-3-ACETIC ACID); QUATERNARY AMMONIUM DERIVATIVE; SURFACTANT; THIOPHENE DERIVATIVE; TRIMETHYLAMMONIUM SALT DERIVATIVE;

ARTICLE; BIOPHYSICS; CALORIMETRY; CHEMICAL STRUCTURE; CHEMISTRY; CRYOELECTRON MICROSCOPY; GENETIC PROCEDURES; HYDRODYNAMICS; MACROMOLECULE; SPECTROSCOPY; THERMODYNAMICS;

ACETATES; BIOPHYSICAL PHENOMENA; BIOSENSING TECHNIQUES; CALORIMETRY; CRYOELECTRON MICROSCOPY; HYDRODYNAMICS; MACROMOLECULAR SUBSTANCES; MOLECULAR STRUCTURE; QUATERNARY AMMONIUM COMPOUNDS; SPECTRUM ANALYSIS; SURFACE-ACTIVE AGENTS; THERMODYNAMICS; THIOPHENES; TRIMETHYL AMMONIUM COMPOUNDS;

EID: 84858228862     PISSN: 07437463     EISSN: 15205827     Source Type: Journal    
DOI: 10.1021/la204862u     Document Type: Article

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