Although progress has recently been made toward understanding the health and environmental consequences of these materials, challenges ramain for future research.

http://pubs.acs.org/doi/pdf/10.1021/es062726m

Assessing the risks of manufactured nanomaterials.

In this review article we discuss the progress of lithium storage in different carbon forms starting from intercalation in graphite to the lithium storage in fullerenes, nanotubes, diamond and most recently, graphene. The recent advances in lithium storage in various novel morphological variants of carbons prepared by a variety of techniques are also discussed with the most important models in literature that have been set out to explain the excess lithium storage. The major emphasis lies on the real structure.

Lithium Storage in Carbon Nanostructures

The properties of an organic molecular ferromagnet [C(60)TDAE(086); TDAE is tetrakis(dimethylamino)ethylene] with a Curie temperature ;T(c) = 161 kelvin are described The ferromagnetic state shows no remanence, and the temperature dependence of the magnetization below ;T(c) does not follow the behavior expected of a conventional ferromagnet These results are interpreted as a reflection of a three-dimensional system leading to a soft ferromagnet

https://science.sciencemag.org/content/sci/253/5017/301.full.pdf

Organic molecular soft ferromagnetism in a fullerene c60.

THE recent syntheses1,2 of macroscopic quantities of C60 have suggested possible applications in host–guest and organic chemistry, tribology, electrochemistry and semiconductor tech-nology. Here we report the preparation of alkali-metal-doped films of C60 and C70 which have electrical conductivities at room temperature that are comparable to those attained by n-type doped polyacetylene. The highest conductivities observed in the doped films are: 4Scm−1 (Cs/C60), 100 (Rb/C60), 500 (K/C60), 20 (Na/C60), 10 (Li/C60), 2 (K/C70). The doping process is reversed on exposure of the films to the atmosphere. At high doping levels, the films become more resistive. We attribute the conductivity induced in these films to the formation of energy bands from the π orbitals of C60 or C70, which become partially filled with carriers on doping. The smaller alkali metal ions should be able to fit into the interstices in the lattice without disrupting the network of contacts between the carbon spheroids. In the case of C60, this would allow the development of an isotropic band structure, and we therefore propose that these materials may constitute the first three-dimensional 'organic' conductors.

Conducting films of C60 and C70 by alkali-metal doping

Within the wr-orbital axis vector theory, the total rehybridization required for closure of the fullerenes is approximately conserved. This result allows the development of a structure-based index of strain in the fullerenes, and it is estimated that about 80 percent of the heat of formation of the carbon atoms in C60 may be attributed to a combination of v strain and steric inhibition of resonance. Application of this analysis to the geometries of structurally characterized organometallic derivatives of C60 and C70 shows that the reactivity exhibited by the fullerenes may be attributed to the relief of a combination of local and global strain energy. C60 is of ambiguous aromatic character with anomalous magnetic properties but with the reactivity of a continuous aromatic molecule, moderated only by the tremendous strain inherent in the spheroidal structure.

https://science.sciencemag.org/content/sci/261/5128/1545.full.pdf

Chemistry of the fullerenes: the manifestation of strain in a class of continuous aromatic molecules.

Buckminsterfullerene, C{sub 60}, was prepared in gram quantities by contact-arc vaporization of a graphite rod in a 100-Torr atmosphere of helium, followed by extraction of the resultant graphite soot with toluene. The dominance of C{sub 60} in this extract was verified by mass, FTIR, and NMR spectroscopy. The molecule was successfully hydrogenated to C{sub 60}H{sub 36} via a Birch reduction and dehydrogenated back to bare C{sub 60} by treatment with DDQ reagent. Cyclic voltammetry of C{sub 60} in methylene chloride revealed highly reversible formation of at least two stable anionic forms of C{sub 60} in solution. A broad new class of these fulleride and fulleronium ions is anticipated, both with the internal cavity empty and with any one of a large number of elements inside, thus providing a means of fine-tuning the chemical, optical, and redox properties.

Efficient production of C60 (buckminsterfullerene), C60H36, and the solvated buckide ion

The total synthesis of cystodytins

Chemoenzymatic preparation of trans-2,6-dialkylpiperidines and of other azacycle building blocks. Total synthesis of (+)-desoxoprosopinine

Dihydropyrans obtained by cyclocondensation of aromatic enones with vinyl ethers are transformed into pyridines by treatment with hydroxylamine hydrochloride.

N. E. Byrne

Papers

Efficient production of C60 (buckminsterfullerene), C60H36, and the solvated buckide ion

The total synthesis of cystodytins

Chemoenzymatic preparation of trans-2,6-dialkylpiperidines and of other azacycle building blocks. Total synthesis of (+)-desoxoprosopinine

Modified Knoevenagel–Stobbe preparation of substituted pyridines: a new approach to streptonigrinoids

Synthetic studies towards cystodytin A: The preparation of novel cystodytin congeners