Synthesis, optical properties, and LFER analysis of solvent-dependent binding constants of Hamilton-receptor-connected merocyanine chromophores

Journal of Organic Chemistry

Volumn 73, Issue 16, 2008, Pages 6355-6362

  Schmidt, Johann ^a   Schmidt, Ralf ^a   Würthner, Frank ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING ENERGY; CHEMICAL REACTIONS; CHLORINE COMPOUNDS; CHROMOPHORES; COMPLEXATION; DICHLOROMETHANE; DYES; ETHERS; HYDROGEN; HYDROGEN BONDS; NONMETALS; NUCLEAR MAGNETIC RESONANCE; OPTICAL PROPERTIES; SEMICONDUCTING CADMIUM TELLURIDE; SOLVENTS; TITRATION; TOLUENE; VOLUMETRIC ANALYSIS;

ACCEPTOR GROUPS; ASSEMBLY STRUCTURES; BARBITURIC ACID; BINDING CONSTANTS; BINDING STRENGTHS; CHEMICAL EQUATIONS; HAMILTON; MEROCYANINE; MEROCYANINE DYES; NON-COVALENT BINDING;

ORGANIC SOLVENTS;

1 (3,5 DICARBETHOXY)PHENYL 2,6 DIMETHYL 4 PYRIDONE; 1 (3,5 DICARBOXY)PHENYL 2,6 DIMETHYL 4 PYRIDONE HYDROCHLORIDE; 1 [3,5 BIS(6 AMINOPYRIDINE 2 YL)CARBAMOYL]PHENYL 2,6 DIMETHYL 4 PYRIDONE; 1 [3,5 BIS[(6 BUTYRYLAMINO)PYRIDINE 2 YL]CARBAMOYL]PHENYL 2,6 DIMETHYL 4 PYRIDONE; 1,3 BIS[[(6 (3,3 DIMETHYL)BUTYRYLAMINO)PYRIDINE 2 YL]CARBAMOYL]BENZENE; 5 [1 [3,5 BIS[(6 BUTYRYLAMINO)PYRIDINE 2 YL]CARBAMOYL]PHENYL 2,6 DIMETHYLPYRIDINE 4 YLIDENE] 1,3 DIBUTYLPYRDIMIDINE 1,4,6 TRIONE; 5 [2 (1,3 DIHYDRO 3,3 DIMETHYL 1 ISOPROPYL 2H INDOL 2 YLIDENE)ETHYLIDENE]PYRIMIDINE 2,4,6 TRIONE; 5 [2 (2,6 DIUNDECYL 1 DODECYLPYRIDINE 4 YLIDENE)EHTYLIDENE]PYRIMIDINE 2,4,6 TRIONE; 5 [2,6 DIMETHYL 1 (2 ETHYL)HEXYLPYRIDINE 4 YLIDENE]PYRIMIDINE 2,4,6 TRIONE; BARBITURIC ACID; CHLOROFORM; DICHLOROMETHANE; DIOXANE; MEROCYANINE; PERYLENE; PYRIDONE DERIVATIVE; PYRIMIDINE DERIVATIVE; SOLVENT; TETRAHYDROFURAN; TOLUENE;

ARTICLE; BINDING AFFINITY; CHEMICAL BINDING; CHEMICAL STRUCTURE; COMPLEX FORMATION; ELECTRIC FIELD; HYDROGEN BOND; LIGHT REFRACTION; NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; TITRIMETRY; ULTRAVIOLET SPECTROSCOPY;

EID: 50149113908     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo801083b     Document Type: Article

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