439610-93-2

Upstream product

• 120-47-8 Ethyl 4-hydroxybenzoate 
• 439610-89-6 4-(5-benzyloxypent-1-oxy)biphenyl-4'-carboxylic acid 
• 481725-56-8 4-(1,3,2-dioxaborinan-2-yl)benzoyl chloride 
• 540-38-5 p-Iodophenol 
• 6169-06-8 (S)-2-Octanol 
• 4541-15-5 5-(benzyloxy)-1-pentanol 
• 111-29-5 1 ,5-pentanediol 
• 439610-87-4 5-benzyloxypentyl benzenesulfonate 
• 111153-20-9 (S)-(+)-1-methylheptyl 4-benzyloxybenzoate 
• 111153-21-0 4-hydroxybenzoic acid (S)-1-methylheptyl ester 
• 50670-76-3 ethyl 4-hydroxy-4-biphenyl carboxylate 
• 1486-51-7 p-(benzyloxy)benzoic acid 
• 1486-50-6 4-(benzyloxy)benzoic acid chloride 

Relevant academic research and scientific papers

Self-assembling behaviour of chiral calamitic monoacrylates targeted for polymer stabilisation of polar smectic phases in chiral liquid crystals

The stabilisation and control of synclinic and anticlinic chiral liquid crystalline phases remain an actual and highlighted task. This work presents the design and mesomorphic properties of new chiral calamitic reactive mesogens, monoacrylates, based on biphenyl benzoate and phenyl biphenyl-4-carboxylate cores with reactive terminal groups placed far from the chiral chain. The compound's structures, compatible with the components of modern ferroelectric and antiferroelectric liquid crystalline mixtures, are confirmed by mass spectrometry (electron ionization) analysis and proton/carbon nuclear magnetic resonance. All the reactive mesogens possess the self-assembling, i.e. liquid crystalline behaviour with high tendency to create smectic phases in a broad temperature range, which was confirmed by a polarizing optical microscopy, differential scanning calorimetry and broad-band dielectric spectroscopy. Doping of advanced multicomponent mixtures possessing the chiral smectic phases by the designed monoacrylates with further cross-linking procedure, can be an effective and functional tool for stabilising ferroelectric and antiferroelectric phases in various states and hence, can allow the symmetrisation of the switching times in the modes employed surface stabilised geometry; this is a very highlighted task for optoelectronics. Moreover, an evident considerable tendency for thermal polymerisation of specific reactive mesogens can reduce the drawbacks of polymer stabilisation.

Synthesis and mesomorphic properties of achiral and chiral esters with high tilted synclinic and anticlinic phases

Two series of three ring esters with chiral chain (derivative of (S)-octanol-2) and achiral chain (the swallow type) with high tilted synclinic and anticlinic phases were chosen to studies. The aim of presented studies was to find how the changes of diffe

Orthoconic antiferroelectrics. Synthesis and mesomorphic properties of optically active (S)-(+)-4-(1-methylheptyloxycarbonyl)phenyl 4′-(fluoroalkanoyloxyalkoxy)biphenyl-4-carboxylates and 4′-(alkanoyloxyalkoxy)biphenyl-4-carboxylates

Convenient methods for preparing optically active (S)-(+)-4-(1-methylheptyloxycarbonyl)-phenyl 4′-(ω-perfluoroalkanoyloxyalkoxy)- and 4′-(ω-alkanoyloxyalkoxy)biphenyl-4-carboxylates and their intermediates have been described and discussed. The phase transitions of the prepared esters have been investigated by differential scanning calorimetry.