Synthesis and Characterization of Organic Materials with Conveniently Accessible Supercooled Liquid and Glassy Phases:  Isomeric 1,3,5-Tris(naphthyl)benzenes

1996 ◽  
Vol 100 (3) ◽  
pp. 1081-1090 ◽  
Author(s):  
Craig M. Whitaker ◽  
Robert J. McMahon
1999 ◽  
Vol 561 ◽  
Author(s):  
R.C. Advincula ◽  
S. Inaoka ◽  
M. Park ◽  
D. Phillips ◽  
D.M. Shin

ABSTRACTIn this report, we describe our initial synthesis and characterization of mono-functional and bi-functional dibromoalkyl oligothiophenes to achieve amphiphilicity and telechelic functionality. Oligothiophenes are an important class of organic materials for opto-electronic devices and display applications. We have mono-functionalized oligothiophenes by the synthesis of a quinquethiophene bromoalkyl derivative. A bi-functional sexithiophene was derived primarily by the symmetrical coupling of terthiophene derivatives. Both were synthesized using Grignard coupling and lithiation reaction methodologies. UV-Vis, IR, NMR, MALDI-TOF-MS, and DSC confirmed the structure and physical properties of the oligomers. In addition, we have also synthesized an amphiphilic diamine derivative from the reaction of hexamethylenediamine with a bromoalkyl terthiophene derivative. Using photoluminescence, the photophysical properties of the oligomers were found to be that of typical oligothiophenes. Processing as ultrathin films for devices is currently being investigated.


2016 ◽  
Vol 1819 ◽  
Author(s):  
Olivia Monroy ◽  
Lioudmila Fomina ◽  
Roberto Salcedo

ABSTRACTNew organic materials with semiconductor behavior were prepared from diphenyldiacetylene and aromatic amines with withdrawing groups by Reisch-Schulte reaction and characterized by IR, RMN spectroscopy. The obtained materials share the property of having electron withdrawing groups joint to the attached aromatic ring, it seems this feature accounts in large fashion to improve the semiconducting behavior of this kind of substances, this topic was studied by means theoretical calculations and the results are also discussed. The calculations were carried out by means the Gaussian09 software and all the involved species were geometrically optimized.


2014 ◽  
Vol 5 (9) ◽  
pp. 3627-3633 ◽  
Author(s):  
Gabriel E. Rudebusch ◽  
Aaron G. Fix ◽  
Hillary A. Henthorn ◽  
Chris L. Vonnegut ◽  
Lev N. Zakharov ◽  
...  

The synthesis and characterization of a series of quinoidal diindeno(thieno)thiophenes (DI[n]Ts) are reported. NIR absorption, deep LUMO energy levels and progressively tighter solid-state packing allude to organic materials applications.


2020 ◽  
Vol 75 (4) ◽  
pp. 359-363 ◽  
Author(s):  
Sacha Legrand ◽  
Milja Hannu-Kuure ◽  
Ari Kärkkäinen

AbstractA new polymerizable naphthalene derivative has been designed, prepared, and characterized by 1H, 13C NMR, and MS. The new monomer synthesis has successfully been accomplished from a cheap commercially available raw material, in only four steps with good yields. The four steps can be easily scaled up for manufacturing purposes. It is anticipated that the new precursor can be very useful in the preparation of valuable materials with high refractive index for numerous opto-electronic applications.


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