866416-39-9

Upstream product

• 865087-56-5 4-(4-iodo-2,6-dimethyl-phenyl)-3,5-dimethyl-pyridine 
• 109-77-3 malononitrile 
• 361543-99-9 4-methoxy-2,6-dimethylphenylboronic acid 
• 6267-34-1 2-bromo-5-methoxy-1,3-dimethyl-benzene 
• 7463-51-6 4-bromo-3,5-dimethylphenol 
• 70564-92-0 4-bromo-3,5-dimethyl-pyridine 1-oxide 
• 865087-48-5 4-(3,5-dimethylpyridin-4-yl)-N-(diphenylmethylene)-3,5-dimethyl-benzenamine 
• 865087-54-3 trifluoromethane sulfonic acid 4-(3,5-dimethyl-pyridin-4-yl)-3,5-dimethyl-phenyl ester 
• 865087-44-1 4-(4-methoxy-2,6-dimethylphenyl)-3,5-dimethyl-pyridin-1-ol 
• 865087-49-6 4-(3,5-dimethylpyridin-4-yl)-3,5-dimethyl-phenylamine 
• 865087-45-2 4-(4-methoxy-2,6-dimethylphenyl)-3,5-dimethyl-pyridine 

Relevant academic research and scientific papers

TWISTED PI-ELECTRON SYSTEM CHROMOPHORE COMPOUNDS WITH VERY LARGE MOLECULAR HYPERPOLARIZABILITIES AND RELATED COMPOSITIONS AND DEVICES

Unconventional twisted π-electron system electro-optic (EO) chromophores/compounds, compositions and related device structures. Crystallographic analysis of several non-limiting chromophores reveals, for instance, large ring-ring dihedral twist angles and

Ultralarge hyperpolarizability twisted π-electron system electro-optic chromophores: Synthesis, solid-state and solution-phase structural characteristics, electronic structures, linear and nonlinear optical properties, and computational studies

This contribution details the synthesis and chemical/physical characterization of a series of unconventional twisted π-electron system electro-optic (EO) chromophores. Crystallographic analysis of these chromophores reveals large ring-ring dihedral twist

Exceptional molecular hyperpolarizabilities in twisted π-electron system chromophores

(Chemical Equation Presented) Nonlinear optics: Twisted π-electron system electrooptic (EO) chromophores with exceptional molecular hyperpolarizabilities (-488 000×10-48 esu at 1907 nm) were designed and synthesized. Crystallographic analysis r