Amanote Research
Register
Sign In
Luminescence Tuning of Organoboron Quinolates Through Substituent Variation at the 5-Position of the Quinolato Moiety
doi 10.1021/ol0619664.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Tuning Order-Disorder Phase Transition Through Regulating the Substituent Group of Anion
Chinese Journal of Chemistry
Chemistry
Tuning Luminescence and Conductivity Through Controlled Growth of Polymorphous Molecular Crystals
Advanced Electronic Materials
Optical
Electronic
Magnetic Materials
Fine Tuning the Performance of Multiorbital Radical Conductors by Substituent Effects
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Effect of an Electron-Donating Substituent at the 3,4-Position of 3-Hydroxyflavone: Photophysics in Bulk Solvents
Tuning the Photonic Behavior of Symmetrical Bis-Bodipy Architectures: The Key Role of the Spacer Moiety
Frontiers in Chemistry
Chemistry
Synthesis and Antihypertensive Activities of New 1,4-Dihydropyridine Derivatives Containing a Nitrooxy Moiety at the 3-Ester Position.
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
Structure-Activity Relationships of Cephalosporins Having a (Dimethylisoxazolidinio)vinyl Moiety at Their 3-Position.
Journal of Antibiotics
Drug Discovery
Pharmacology
Luminescence Tuning of MEH-PPV for Organic Electronic Applications
Acta Physica Polonica A
Astronomy
Physics
Primary Aminothiourea-Catalyzed Enantioselective Synthesis of RauhutCurrier Adducts of 3Arylcyclohexenone With a Tethered Enone on the Aryl Moiety at the Ortho-Position
