Literature DB >> 21109874

The reactivity of endohedral fullerenes. What can be learnt from computational studies?

Sílvia Osuna1, Marcel Swart, Miquel Solà.   

Abstract

The last two decades have witnessed major advances in the synthesis and characterization of endohedral fullerenes. These species have interesting physicochemical properties with many potential interesting applications in the fields of magnetism, superconductivity, nonlinear optical properties, radioimmunotherapy, and magnetic resonance imaging contrast agents, among others. In addition to the synthesis and characterization, the chemical functionalization of these species has been a main focus of research for at least four reasons: first, to help characterize endohedral fullerenes that could not be well described structurally otherwise; second, to generate materials with fine-tuned properties leading to enhanced functionality in one of their multiple potential applications; third, to produce water-soluble endohedral fullerenes needed for their use in medicinal sciences; and fourth, to generate electron donor-acceptor conjugates that can be used in solar energy conversion/storage. The functionalization of these species has been achieved through different types of reactions, the most common being the Diels-Alder reactions, 1,3-dipolar cycloadditions, Bingel-Hirsch reactions, and free-radical reactions. It has been found that the performance of these reactions in endohedral fullerenes may be quite different from that of the empty fullerenes. Indeed, encapsulated species have a large influence on the thermodynamics, kinetics, and regiochemistry of these reactions. A detailed understanding of the changes in chemical reactivity due to incarceration of atoms or clusters of atoms is essential to assist the synthesis of new functionalized endohedral fullerenes with specific properties. This Perspective seeks to highlight the key role played by computational chemistry in the analysis of the chemical reactivity of these systems. It is shown that the information obtained through calculations is highly valuable in the process of designing new materials based on endohedral fullerenes.

Entities:  

Year:  2010        PMID: 21109874     DOI: 10.1039/c0cp01594f

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  6 in total

1.  Changes in Structure and Reactivity of Ng2 Encapsulated in Fullerenes: A Density Functional Theory Study.

Authors:  Meng Li; Xin He; Bin Wang; Dongbo Zhao; Chunying Rong; Pratim K Chattaraj; Shubin Liu
Journal:  Front Chem       Date:  2020-07-03       Impact factor: 5.221

Review 2.  Coordination modes and different hapticities for fullerene organometallic complexes.

Authors:  Delia Soto; Roberto Salcedo
Journal:  Molecules       Date:  2012-06-12       Impact factor: 4.411

3.  Successive Diels-Alder Cycloadditions of Cyclopentadiene to [10]CPP⊃C60: A Computational Study.

Authors:  Gerard Pareras; Sílvia Simon; Albert Poater; Miquel Solà
Journal:  J Org Chem       Date:  2022-03-23       Impact factor: 4.198

4.  Synergic effects between boron and nitrogen atoms in BN-codoped C59-n BN n fullerenes (n = 1-3) for metal-free reduction of greenhouse N2O gas.

Authors:  Mehdi D Esrafili; Adnan Ali Khan; Parisasadat Mousavian
Journal:  RSC Adv       Date:  2021-06-28       Impact factor: 4.036

5.  On the regioselectivity of the Diels-Alder cycloaddition to C60 in high spin states.

Authors:  Ouissam El Bakouri; Marc Garcia-Borràs; Rosa M Girón; Salvatore Filippone; Nazario Martín; Miquel Solà
Journal:  Phys Chem Chem Phys       Date:  2018-05-03       Impact factor: 3.676

6.  Stability computations for isomers of La@C(n) (n = 72, 74, 76).

Authors:  Zdeněk Slanina; Filip Uhlík; Shyi-Long Lee; Ludwik Adamowicz; Takeshi Akasaka; Shigeru Nagase
Journal:  Molecules       Date:  2012-11-05       Impact factor: 4.411

  6 in total

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