Literature DB >> 22692299

Highly selective reactions of C60Cl6 with thiols for the synthesis of functionalized [60]fullerene derivatives.

Ekaterina A Khakina1, Anastasiya A Yurkova, Alexander S Peregudov, Sergey I Troyanov, Vyacheslav V Trush, Andrey I Vovk, Alexander V Mumyatov, Vyacheslav M Martynenko, Jan Balzarini, Pavel A Troshin.   

Abstract

Chlorofullerene C(60)Cl(6) undergoes highly selective reactions with thiols forming compounds C(60)[SR](5)H with high yields. These reactions open up straightforward synthetic routes to many functionalized fullerene derivatives, e.g. water-soluble compounds showing interesting biological activities.

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Year:  2012        PMID： 22692299     DOI： 10.1039/c2cc32517a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  3 in total

1.  Fullerenes in Biology and Medicine.

Authors:  Edison Castro; Andrea Hernandez Garcia; Gerardo Zavala; Luis Echegoyen
Journal:  J Mater Chem B       Date:  2017-07-08       Impact factor: 6.331

2.  A zeta potential value determines the aggregate's size of penta-substituted [60]fullerene derivatives in aqueous suspension whereas positive charge is required for toxicity against bacterial cells.

Authors:  Dmitry G Deryabin; Ludmila V Efremova; Alexey S Vasilchenko; Evgeniya V Saidakova; Elena A Sizova; Pavel A Troshin; Alexander V Zhilenkov; Ekaterina A Khakina; Ekaterina E Khakina
Journal:  J Nanobiotechnology       Date:  2015-08-08       Impact factor: 10.435

Review 3.  Progress in Antiviral Fullerene Research.

Authors:  Piao-Yang Xu; Xiao-Qing Li; Wei-Guang Chen; Lin-Long Deng; Yuan-Zhi Tan; Qianyan Zhang; Su-Yuan Xie; Lan-Sun Zheng
Journal:  Nanomaterials (Basel)       Date:  2022-07-24       Impact factor: 5.719
  3 in total

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