Tunable solvatochromic response of newly synthesized antioxidative naphthalimide derivatives: Intramolecular charge transfer associated with hydrogen bonding effect

Journal of Physical Chemistry A

Volumn 115, Issue 11, 2011, Pages 2216-2224

  Dhar, Sayaree ^a   Singha Roy, Somnath ^b   Rana, Dipak Kumar ^a   Bhattacharya, Sudin ^b   Bhattacharya, Sumanta ^c   Bhattacharya, Subhash Chandra ^a  

^a JADAVPUR UNIVERSITY   (India)

^b CHITTARANJAN NATIONAL CANCER INSTITUTE   (India)

^c UNIVERSITY OF BURDWAN   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO GROUP; ANTI OXIDATIVE ACTIVITY; APROTIC SOLVENTS; DIFFERENT SOLVENTS; DRUG DEVELOPMENT; ELECTRONIC EXCITATION; ENERGY TRANSITIONS; EXPERIMENTAL DATA; GROUND STATE GEOMETRY; HYDROGEN BONDING INTERACTIONS; HYDROGEN-BONDING EFFECTS; INTRA-MOLECULAR CHARGE TRANSFER; INTRAMOLECULAR CHARGE TRANSFERS; NAPHTHALIMIDE; NAPHTHALIMIDE DERIVATIVE; NONRADIATIVE RELAXATION PROCESS; PHOTOPHYSICAL; SOLVATOCHROMIC; SOLVATOCHROMIC BEHAVIOR; SOLVENT POLARITY; SPECTRAL CHARACTERIZATION; TIME DEPENDENT DENSITY FUNCTIONAL THEORY; TIME-RESOLVED FLUORESCENCE; UV-VIS ABSORPTIONS;

CHARGE TRANSFER; FLUORESCENCE; HYDROGEN; HYDROGEN BONDS; ION EXCHANGE; MASS TRANSFER; SOLVENTS; SPECTRUM ANALYZERS;

DENSITY FUNCTIONAL THEORY;

ANTINEOPLASTIC AGENT; ANTIOXIDANT; NAPHTHALIMIDE DERIVATIVE; SOLVENT;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; ELECTRON; ENERGY TRANSFER; HYDROGEN BOND; SYNTHESIS;

ANTINEOPLASTIC AGENTS; ANTIOXIDANTS; ELECTRONS; ENERGY TRANSFER; HYDROGEN BONDING; MODELS, MOLECULAR; NAPHTHALIMIDES; SOLVENTS;

EID: 79952758402     PISSN: 10895639     EISSN: 15205215     Source Type: Journal    
DOI: 10.1021/jp1117773     Document Type: Article

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