Showing posts with label fullerene. Show all posts
Showing posts with label fullerene. Show all posts

Wednesday 11 June 2014

Ionic Liquid Solubilizes Fullerene in Water



Ionic Liquid Solubilizes Fullerene in Water

Modeling shows imidazolium ionic liquid facilitates the dispersion of C60 in water by forming solute pair
Read more

Wednesday 14 May 2014

First Solid-State Study of a Functionalized Fullerene Radical Anion Salt



First Solid-State Study of a Functionalized Fullerene Radical Anion Salt

A radical anion of a highly functionalized fullerene derivative with twelve bulky addends shows promising magnetic properties
Read more

Monday 29 July 2013

Co-Catalyzed Radical Cycloaddition of [60]Fullerene with Active Dibromides: Selective Synthesis of Carbocycle-Fused Fullerene Monoadducts

Figure


Co-Catalyzed Radical Cycloaddition of [60]Fullerene with Active Dibromides: Selective Synthesis of Carbocycle-Fused Fullerene Monoadducts

Org. Lett., Article ASAP
Publication Date (Web): July 23, 2013 (Letter)
DOI: 10.1021/ol401876n

An efficient and highly selective Co-catalyzed radical cycloaddition of [60]fullerene with active dibromides for the synthesis of three-, five-, six-, and seven-membered carbocycle-fused fullerene monoadducts has been reported. The controlled experiments unambiguously disclosed that the reaction proceeds through the formation of a fullerene monoradical as a key intermediate.

Co-Catalyzed Radical Cycloaddition of [60]Fullerene with Active Dibromides: Selective Synthesis of Carbocycle-Fused Fullerene Monoadducts

Figure


Co-Catalyzed Radical Cycloaddition of [60]Fullerene with Active Dibromides: Selective Synthesis of Carbocycle-Fused Fullerene Monoadducts

Org. Lett., Article ASAP
Publication Date (Web): July 23, 2013 (Letter)
DOI: 10.1021/ol401876n

An efficient and highly selective Co-catalyzed radical cycloaddition of [60]fullerene with active dibromides for the synthesis of three-, five-, six-, and seven-membered carbocycle-fused fullerene monoadducts has been reported. The controlled experiments unambiguously disclosed that the reaction proceeds through the formation of a fullerene monoradical as a key intermediate.