Literature DB >> 19374354

Solvent engineering for shape-shifter pure fullerene (C60).

Marappan Sathish1, Kun'ichi Miyazawa, Jonathan P Hill, Katsuhiko Ariga.   

Abstract

As a highly anticipated technique for bottom-up nanotechnology, i.e., shape control of pure functional molecules, we here report controlled formation of two-dimensional (2D) objects such as hexagons and rhombi and their selective shape shifting into one-dimensional (1D) rods through solvent-dependent changes of crystal lattice, all from pure C(60). Uniformly shaped rhombi and hexagons were obtained at tert-butyl alcohol/toluene and i-propyl alcohol/CCl(4) interfaces, respectively. In addition, exposure of these 2D nanosheets to water induced selective transformation into 1D nanorods. Nanorhombi were converted to short nanorods upon exposure to water. This shape shift is accompanied by changes in crystalline structures from a mixed fcc/hexagonal to pure fcc lattice, the latter of which is almost identical with morphologically similar C(60) nanowhiskers. Metastable nanorhombi which possess a strained mixed crystalline structure metamorphosize into the more stable short nanowhisker (nanorods). In contrast, the stable nanohexagon of a single lattice (and so less strain) does not undergo shape shifting. These results clearly demonstrate controlled formation of 2D nanosheets with various shapes (hexagons, rhombi, etc.) and selective shape shifting to nanorods (short nanowhiskers) all from pure C(60) molecules by very simple solvent treatments.

Entities:  

Year:  2009        PMID: 19374354     DOI: 10.1021/ja902061r

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  7 in total

Review 1.  Paradigm shift from self-assembly to commanded assembly of functional materials: recent examples in porphyrin/fullerene supramolecular systems.

Authors:  Mao Li; Shinsuke Ishihara; Qingmin Ji; Misaho Akada; Jonathan P Hill; Katsuhiko Ariga
Journal:  Sci Technol Adv Mater       Date:  2012-09-11       Impact factor: 8.090

2.  Directed assembly of optoelectronically active alkyl-π-conjugated molecules by adding n-alkanes or π-conjugated species.

Authors:  Martin J Hollamby; Maciej Karny; Paul H H Bomans; Nico A J M Sommerdijk; Nico A J M Sommerdjik; Akinori Saeki; Shu Seki; Hiroyuki Minamikawa; Isabelle Grillo; Brian R Pauw; Paul Brown; Julian Eastoe; Helmuth Möhwald; Takashi Nakanishi
Journal:  Nat Chem       Date:  2014-06-22       Impact factor: 24.427

Review 3.  Intelligent chiral sensing based on supramolecular and interfacial concepts.

Authors:  Katsuhiko Ariga; Gary J Richards; Shinsuke Ishihara; Hironori Izawa; Jonathan P Hill
Journal:  Sensors (Basel)       Date:  2010-07-13       Impact factor: 3.576

4.  Synthesis and characterization of fullerene nanowhiskers by liquid-liquid interfacial precipitation: influence of C60 solubility.

Authors:  Marappan Sathish; Kun'ichi Miyazawa
Journal:  Molecules       Date:  2012-03-29       Impact factor: 4.411

5.  Synthesis, crystal structure, self-assembly of C60 derivatives bearing rigid pyridine substituents.

Authors:  Min Ai; Jie Li; Zijuan Ji; Chuanhui Wang; Rui Li; Wei Dai; Muqing Chen
Journal:  RSC Adv       Date:  2019-01-23       Impact factor: 4.036

6.  A π-gel scaffold for assembling fullerene to photoconducting supramolecular rods.

Authors:  Vishnu Sukumaran Nair; Rahul Dev Mukhopadhyay; Akinori Saeki; Shu Seki; Ayyappanpillai Ajayaghosh
Journal:  Sci Adv       Date:  2016-09-23       Impact factor: 14.136

7.  Rubrene-Directed Structural Transformation of Fullerene (C60) Microsheets to Nanorod Arrays with Enhanced Photoelectrochemical Properties.

Authors:  Ning Chen; Pengwei Yu; Kun Guo; Xing Lu
Journal:  Nanomaterials (Basel)       Date:  2022-03-14       Impact factor: 5.076

  7 in total

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