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      Unlocking the Stability of Reduced Graphene Oxide Nanosheets in Biological Media via Use of Sodium Ascorbate

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          Abstract

          Graphene oxide and reduced graphene oxide (RGO) are carbon bidimensional nanomaterials largely exploited in biomedicine. Their unique interactions with eukaryotic and prokaryotic cells are used to obtain precise intracellular delivery, to create device coatings, and to design theranostic materials for both therapeutic and imaging applications, mainly in the cancer research field. It is known, however, that the hydrophobic behavior of RGO limits its stability in biological media. Here, the employment of sodium ascorbate (NaA) as a reducing agent for the preparation of RGO to provide a nanomaterial with remarkable suitability for applications in cell culture media is proposed. It is demonstrated via a combined experimental and theoretical approach that NaA is able to yield a peculiar RGO derivative, exerting a twofold effect, that is, C sp 2 network restoration upon epoxide reduction and RGO edge functionalization via H‐bonding, lending RGO a so far unexampled dispersibility in aqueous‐based media. The kinetic stability of the bidimensional layers of RGO obtained from NaA is demonstrated together with its superior biocompatibility for drug delivery, unlocking outstanding potentialities for biological applications.

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          Density-functional thermochemistry. III. The role of exact exchange

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            Improved synthesis of graphene oxide.

            An improved method for the preparation of graphene oxide (GO) is described. Currently, Hummers' method (KMnO(4), NaNO(3), H(2)SO(4)) is the most common method used for preparing graphene oxide. We have found that excluding the NaNO(3), increasing the amount of KMnO(4), and performing the reaction in a 9:1 mixture of H(2)SO(4)/H(3)PO(4) improves the efficiency of the oxidation process. This improved method provides a greater amount of hydrophilic oxidized graphene material as compared to Hummers' method or Hummers' method with additional KMnO(4). Moreover, even though the GO produced by our method is more oxidized than that prepared by Hummers' method, when both are reduced in the same chamber with hydrazine, chemically converted graphene (CCG) produced from this new method is equivalent in its electrical conductivity. In contrast to Hummers' method, the new method does not generate toxic gas and the temperature is easily controlled. This improved synthesis of GO may be important for large-scale production of GO as well as the construction of devices composed of the subsequent CCG.
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              The chemistry of graphene oxide.

              The chemistry of graphene oxide is discussed in this critical review. Particular emphasis is directed toward the synthesis of graphene oxide, as well as its structure. Graphene oxide as a substrate for a variety of chemical transformations, including its reduction to graphene-like materials, is also discussed. This review will be of value to synthetic chemists interested in this emerging field of materials science, as well as those investigating applications of graphene who would find a more thorough treatment of the chemistry of graphene oxide useful in understanding the scope and limitations of current approaches which utilize this material (91 references).
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                Journal
                Advanced Materials Interfaces
                Adv Materials Inter
                2196-7350
                2196-7350
                August 2023
                July 03 2023
                August 2023
                : 10
                : 22
                Affiliations
                [1 ] Dipartimento di Chimica Università di Roma La Sapienza p.le A. Moro 5 I‐00185 Rome Italy
                [2 ] Dipartimento di Neuroscienze Università Cattolica del Sacro Cuore Largo Francesco Vito 1 I‐00168 Rome Italy
                [3 ] Fondazione Policlinico Universitario “A. Gemelli” IRCSS Largo A. Gemelli 8 I‐00168 Rome Italy
                [4 ] Consorzio INSTM UdR Roma “La Sapienza” p.le A. Moro 5 I‐00185 Rome Italy
                [5 ] Istituto dei Sistemi Complessi CNR Via dei Taurini 19 I‐00185 Rome Italy
                Article
                10.1002/admi.202300105
                aacbb30b-43d2-45d9-872b-14f08656af6f
                © 2023

                http://creativecommons.org/licenses/by/4.0/

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