Structural identification of a novel axially chiral binaphthyl fluorene based salen ligand in solution using electronic circular dichroism: A theoretical-experimental analysis

Keyphrases

• Stereoisomers 100%
• Structural Identification 100%
• Fluorene 100%
• Tetrahydrofuran 100%
• Binaphthyl 100%
• Electronic Circular Dichroism 100%
• Salen Ligand 100%
• Ylidenes 100%
• Axially chiral 100%
• Ethynyl 100%
• Biophotonics 50%
• Gas Phase 50%
• Force Field 50%
• Unique Structure 50%
• Steric Energy 50%
• B3LYP 50%
• Steric Hindrance 50%
• UV-VIS Spectroscopy 50%
• (R)-1 50%
• 4-hydroxybenzaldehyde 50%
• Optimal Structure 50%
• B3LYP Level 50%
• 1,1′-binaphthyl 50%
• Structural Conformation 50%
• Optical Isomer 50%
• Electronic Circular Dichroism Spectrum 50%
• Electronic Excited States 50%
• Gaussian 09 50%
• Homogeneous Sensing 50%
• Bürgi-Dunitz Trajectory 50%
• Diamino 50%
• Homogeneous Catalysis 50%
• Methan 50%
• Axial chirality 50%

Chemistry

• Stereoisomer 100%
• Structure 100%
• Fluorene 100%
• Conformational Isomer 100%
• Electronic Circular Dichroism 100%
• Tetrahydrofuran 100%
• Salen 100%
• Ethynyl 100%
• Chirality 50%
• Phenol 50%
• Gaussian Distribution 50%
• DFT-B3LYP Calculation 50%
• UV/VIS Spectroscopy 50%
• Homogeneous Catalysis 50%
• Hydroxybenzaldehyde 50%
• Excited Electronic State 50%
• Steric Hindrance 50%
• Circular Dichroism 50%