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Tailoring Bicomponent Supramolecular Nanoporous Networks : Phase Segregation, Polymorphism, and Glasses at the Solid−Liquid Interface

Palma, Carlos-Andres (författare)
University of Strasbourg, France
Björk, Jonas (författare)
University of Liverpool, UK
Bonini, Massimo (författare)
BASF SE.
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Dyer, Matthew S. (författare)
University of Liverpool, UK
Llanas-Pallas, Anna (författare)
University of Trieste, Italy
Bonifazi, Davide (författare)
University of Trieste, Italy
Persson, Mats (författare)
University of Liverpool, UK
Samorì, Paolo (författare)
University of Strasbourg, France
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 (creator_code:org_t)
2009-08-24
2009
Engelska.
Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 131:36, s. 13062-13071
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • We study the formation of four supramolecular bicomponent networks based on four linear modules (linkers) bridging melamine via triple hydrogen-bonds. We explore at the nanoscale level the phenomena of polymorphism and phase segregation which rule the generation of highly crystalline nanoporous patterns self-assembled at the solid-liquid interface. The investigated linkers include two systems exposing diuracil groups in the R and ω position, naphthalene tetracarboxylic diimide and pyromellitic diimide. In situ scanning tunneling microscopy (STM) investigations revealed that, when blended with melamine, out of the four systems, three are able to form two-dimensional (2D) porous architectures, two of which exhibit highly ordered hexagonal structures, while pyromellitic diimide assembles only into one- dimensional (1D) supramolecular arrays. These bicomponent self-assembled monolayers are used as a test bed to gain detailed insight into phase segregation and polymorphism in 2D supramolecular systems by exploring the contribution of hydrogen-bond energy and periodicity, molecular flexibility, concentration and ratio of the components in solution as well as the effect of annealing via time-dependent and temperature-modulated experiments. These comparative studies, obtained through a joint experimental and computational analysis, offer new insights into strategies toward the bottom-up fabrication of highly ordered tunable nanopatterning at interfaces mediated by hydrogen bonds.

Ämnesord

NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)
NATURVETENSKAP  -- Fysik -- Den kondenserade materiens fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Condensed Matter Physics (hsv//eng)

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