120654-22-0

Upstream product

• 93-61-8 N-methyl-N-phenylformamide 
• 120654-37-7 6-[methyl(phenyl)amino]hexyl acetate 
• 68-12-2 N,N-dimethyl-formamide 
• 100-61-8 N-methylaniline 
• 120654-36-6 N-(6-hydrooxyhexyl)-N-methylaminobenzene 
• 4286-55-9 1-bromo-6-hexanol 

Downstream Products

• 177087-88-6 4-[N-(6-acetoxyhexyl)-N-methylamino]benzyl alcohol 
• 146823-49-6 2-Methyl-acrylic acid 6-{methyl-[4-((E)-2-thiophen-2-yl-vinyl)-phenyl]-amino}-hexyl ester 
• 146823-48-5 6-{Methyl-[4-((E)-2-thiophen-2-yl-vinyl)-phenyl]-amino}-hexan-1-ol 

Relevant academic research and scientific papers

Synthesis, self-assembly and characterization of a novel push-pull thiophene-based chromophore on a gold surface

Push-pull chromophores are widely used and investigated due to their intrinsic electro-optical and non-linear optical properties that are suitable for a variety of applications. However, the grafting and the control of self-organization of such derivatives onto surfaces have been less considered although this may enhance the pre-cited properties and/or enlarge the scope of their use. In this work we present the stepwise synthesis of a novel non-charged push-pull chromophore modified with a fleeting thioacetate group, and the study of its self-assembling abilities onto a gold surface. Self-assembled dense monolayer formation is clearly demonstrated by electrochemical, XPS and STM measurements. Besides, associated with good film quality a conducting behavior consistent with the structure of the SAM-organized push-pull is also highlighted.

Synthesis and characterization of end-functionalized oligo- (vinylthiophenes) with liquid crystal properties

A general scheme for the synthesis of end-functionalized conjugated (E)-vinylthiophene oligomers with liquid crystal and potential second-order non-linear optical properties is described. These push-pull thiophene-containing aromatic molecules show mesogenic properties over different temperature ranges depending on the chain length and the functional end-groups.

Functionalized heteroaromatic compounds for nonlinear optical applications

Heteroaromatic nonlinear optical compounds, alone, and in combination with a chemically inert medium to provide a combination exhibiting second order nonlinear optical properties, including combinations that dispose a layer of the nonlinear optical compounds on chemically inert substrates, blend guest molecules of the nonlinear optical compounds with a chemically inert host matrix of a thermoplastic polymer, or covalently bond pendant side chains of the nonlinear optical compounds to chemically inert polymers.