1087349-15-2Relevant academic research and scientific papers
Synthesis of nitro- and amino-functionalized π-conjugated oligomers incorporating 3,4-ethylenedioxythiophene (EDOT) units
Trippé-Allard, Ga?lle,Lacroix, Jean-Christophe
, p. 861 - 866 (2013/07/27)
Dissymmetric π-conjugated oligomers incorporating 3,4- ethylenedioxythiophene (EDOT) units and bearing nitro and amino end-groups were synthesized in good yields through Pd-catalyzed Suzuki coupling reactions and direct C-H bond arylation. Their spectrosc
ORGANIC COMPOUNDS, PROCESS FOR PREPARING SAME AND USES IN ELECTRONICS
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Paragraph 0135; 0136; 0137; 0138; 0139; 0140; 0141, (2013/04/10)
The present disclosure relates to novel organic compounds, to the processes for preparing same and to the uses thereof, firstly in the electronics field, in particular in the fields referred to as plastic electronics and molecular electronics, and, secondly, in the coatings field, in particular in the fields of adhesion primers and intelligent coatings. The disclosure also relates to a material comprising a novel compound according to the invention.
Preparation of aryl and heteroaryl indium(III) reagents by the direct insertion of indium in the presence of LiCl
Chen, Yi-Hung,Knochel, Paul
supporting information; experimental part, p. 7648 - 7651 (2009/04/06)
Sensitive functional groups, including ketone, aldehyde, and ester groups, may be present in aryl indium reagents prepared in good to excellent yields by the treatment of aryl and heteroaryl iodides with indium powder in the presence of LiCl (see example)
