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Beilstein J. Nanotechnol. 2014, 5, 1580–1589, doi:10.3762/bjnano.5.170
Scheme 1: General chemical modification routes for exfoliated graphene sheets. (a) [3 + 2] 1,3-dipolar cycloa...
Figure 1: Illustrative energy diagram for the photo-induced formation of the charge-separated state of graphe...
Figure 2: Tetraphenylporphyrin (TTP) condensed onto graphene oxide (GO) yielding GO–TPP hybrid material [44].
Figure 3: Ferrocene units anchored to graphene oxide (GO) forming a GO–Fc hybrid material [50].
Scheme 2: Iron(II) coordinated on terpyridine (tpy) moieties covalently anchored to graphene oxide (GO) formi...
Scheme 3: “Click” reaction for the grafting of a porphyrin onto reduced graphene oxide sheets that was pre-mo...
Figure 4: Free and Pd-metallated tetraphenylporphyrin moieties as substituents of pyrrolidine rings covalentl...
Figure 5: Covalent grafting of (2-aminoethoxy)(tri-tert-butyl)phthalocyanine zinc to exfoliated graphene shee...
Figure 6: Phthalocyanine–graphene hybrid material, prepared upon condensation of mono-OH-derivatized phthaloc...
Figure 7: Sulfonyl-substituted zinc phthalocyanine covalently bound to pre-modified graphene via “click” chem...
Figure 8: Extended tetrathiafulvalene units covalently attached to exfoliated graphene via Bingel cycloadditi...
Figure 9: Graphene sheets covalently functionalized with a Ru-bipyridine complex [62].