Polarity assessment of thermoresponsive poly(NIPAM-co-NtBA) copolymer films using fluorescence methods

Journal of Fluorescence

Volumn 20, Issue 3, 2010, Pages 719-731

  Szczupak, Boguslaw ^a   Ryder, Alan G ^a   Togashi, Denisio M ^a   Klymchenko, Andrey S ^b   Rochev, Yuri A ^a   Gorelov, Alexander ^c   Glynn, Thomas J ^a  

^a NATIONAL UNIVERSITY OF IRELAND   (Ireland)

^b UNIVERSITÉ DE STRASBOURG   (France)

^c UNIVERSITY COLLEGE DUBLIN   (Ireland)

Author keywords

3 Hydroxyflavone; ESIPT; Fluorescence; Polarity; Polymer; Proton Transfer; Pyrene; Thermoresponsive

Indexed keywords

3-HYDROXYFLAVONE; COMPLEX FACTORS; COPOLYMER COMPOSITIONS; COPOLYMER FILMS; DUAL BAND; EMISSION PROPERTIES; EMISSION SPECTRUMS; ESIPT; EXCITED-STATE INTRAMOLECULAR PROTON TRANSFER; FLUORESCENCE EMISSION; FLUORESCENCE METHOD; HYDROGEN BONDINGS; HYDROPHILIC POLYMER FILMS; IN-SITU; LINEAR RELATIONSHIPS; MEASUREMENT METHODS; N-TERT-BUTYLACRYLAMIDE; NON-CONTACT; NON-COVALENT INTERACTION; NON-DESTRUCTIVE MEASUREMENT; PHYSICOCHEMICAL PROPERTY; POLARITY; POLYMER COMPOSITION; POLYMER SCIENCE; SOLVATOCHROMISMS; THERMO-RESPONSIVE; TIME-SCALES; VIBRONIC BANDS;

COPOLYMERIZATION; EMISSION SPECTROSCOPY; EXCITED STATES; FLUOROPHORES; HYDROGEN BONDS; HYDROPHILICITY; PLASTIC FILMS; PROTONS;

POLYMER FILMS;

3 HYDROXYFLAVONE; 3-HYDROXYFLAVONE; 4' DIETHYLAMINO 3 HYDROXYFLAVONE; 4'-DIETHYLAMINO-3-HYDROXYFLAVONE; 7 METHOXYFLAVONE; 7-METHOXYFLAVONE; ACRYLAMIDE DERIVATIVE; ACRYLIC ACID RESIN; FLAVONE DERIVATIVE; FLAVONOID; FLUORESCENT DYE; N ISOPROPYLACRYLAMIDE; N-ISOPROPYLACRYLAMIDE; POLY N ISOPROPYLACRYLAMIDE; POLY-N-ISOPROPYLACRYLAMIDE; POLYMER; PROTON; PYRENE; PYRENE DERIVATIVE; SOLVENT; TERT BUTYLACRYLAMIDE; TERT-BUTYLACRYLAMIDE;

ARTICLE; CHEMISTRY; DRUG DOSAGE FORM; FLUORESCENCE; HYDROGEN BOND; TEMPERATURE;

ACRYLAMIDES; ACRYLIC RESINS; DOSAGE FORMS; FLAVONES; FLAVONOIDS; FLUORESCENCE; FLUORESCENT DYES; HYDROGEN BONDING; POLYMERS; PROTONS; PYRENES; SOLVENTS; TEMPERATURE;

EID: 77955923542     PISSN: 10530509     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10895-010-0613-5     Document Type: Article

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