640736-48-7

Upstream product

• 64-18-6 formic acid 
• 640736-36-3 (S)-4-(4-(1-methylhexyloxy)-2,6-dimethylphenylethynyl)-2,6-dimethylaniline 
• 255850-24-9 4-acetylenyl-2,6-dimethylaniline 

Downstream Products

• 640736-60-3 (S)-4-(4-(1-methylhexyloxy)-2,6-dimethylphenylethynyl)-2,6-dimethylphenylisocyanide 

Relevant academic research and scientific papers

Synthesis, structure, and liquid crystal properties of a series of platinum(II) complexes containing chiral 4-(4-alkoxyphenylethynyl) phenylisocyanide ligands

Several platinum(II) isocyanide complexes of the type PtI2 (CNC6H2-2,6-R2-4-CC-(C6 H2-3,5-R′2-4-(R or S )-OCHMeCn-1 (H2(n-1)CH3))2 have been prepared and their mesomorphic properties have been investigated. The complexes with R=Me, R′=H, and n=4-7 exhibit a broader N* phase than the corresponding complexes with R=R′=H, indicating that the methyl substituents on the phenylisocyanide group improve the liquid crystal properties by creating a smooth transition between the bulky PtI2 center and the more slender organic units. The complexes with R=Me and R′=Me exhibit a SmA phase. The presence of methyl groups in the R′-positions in addition to the methyl groups in the R-positions increases the melting point, but does not significantly change the clearing temperature. For the complexes with R=Me and R′=H the temperature-dependent pitches of the N* phase range from 350 to 400 nm.