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Literature DB >> 22722186

Materials chemistry: carbon origami.

Jay S Siegel¹.

Abstract

Entities: Chemical

Year: 2012 PMID： 22722186 DOI： 10.1038/486327a

Source DB: PubMed Journal: Nature ISSN： 0028-0836 Impact factor: 49.962

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13 in total

1. Aryl-aryl bond formation one century after the discovery of the Ullmann reaction.

Authors: Jwanro Hassan; Marc Sévignon; Christel Gozzi; Emmanuelle Schulz; Marc Lemaire
Journal: Chem Rev Date: 2002-05 Impact factor: 60.622

2. A short, rigid, structurally pure carbon nanotube by stepwise chemical synthesis.

Authors: Lawrence T Scott; Edward A Jackson; Qianyan Zhang; Brian D Steinberg; Mihail Bancu; Bo Li
Journal: J Am Chem Soc Date: 2011-12-13 Impact factor: 15.419

3. Facile bucky-bowl synthesis by regiospecific cove-region closure by HF elimination.

Authors: K Yu Amsharov; M A Kabdulov; Martin Jansen
Journal: Angew Chem Int Ed Engl Date: 2012-04-04 Impact factor: 15.336

4. One step closer to isomerically pure fullerenes and heterofullerenes: harnessing the potential of catalytic surfaces.

Authors: Lawrence T Scott
Journal: Angew Chem Int Ed Engl Date: 2009 Impact factor: 15.336

5. Atomically precise bottom-up fabrication of graphene nanoribbons.

Authors: Jinming Cai; Pascal Ruffieux; Rached Jaafar; Marco Bieri; Thomas Braun; Stephan Blankenburg; Matthias Muoth; Ari P Seitsonen; Moussa Saleh; Xinliang Feng; Klaus Müllen; Roman Fasel
Journal: Nature Date: 2010-07-22 Impact factor: 49.962

6. Roll-to-roll production of 30-inch graphene films for transparent electrodes.

Authors: Sukang Bae; Hyeongkeun Kim; Youngbin Lee; Xiangfan Xu; Jae-Sung Park; Yi Zheng; Jayakumar Balakrishnan; Tian Lei; Hye Ri Kim; Young Il Song; Young-Jin Kim; Kwang S Kim; Barbaros Ozyilmaz; Jong-Hyun Ahn; Byung Hee Hong; Sumio Iijima
Journal: Nat Nanotechnol Date: 2010-06-20 Impact factor: 39.213

Materials chemistry: carbon origami.

1. Aryl-aryl bond formation one century after the discovery of the Ullmann reaction.

2. A short, rigid, structurally pure carbon nanotube by stepwise chemical synthesis.

3. Facile bucky-bowl synthesis by regiospecific cove-region closure by HF elimination.

4. One step closer to isomerically pure fullerenes and heterofullerenes: harnessing the potential of catalytic surfaces.

5. Atomically precise bottom-up fabrication of graphene nanoribbons.

6. Roll-to-roll production of 30-inch graphene films for transparent electrodes.

7. A rational chemical synthesis of C60.

8. Proton-catalyzed, silane-fueled Friedel-Crafts coupling of fluoroarenes.

9. Hydrodefluorination of perfluoroalkyl groups using silylium-carborane catalysts.

10. Synthesis, characterization, and theory of [9]-, [12]-, and [18]cycloparaphenylene: carbon nanohoop structures.