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Synthesis and Photophysics of Coaxial Threaded Molecular Wires: Polyrotaxanes with Triarylamine Jackets

Sforazzini, G. (author)
University Of Oxford
Kahnt, Axel, 1980 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Wykes, Michael (author)
Universite de Mons
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Sprafke, Johannes K. (author)
University Of Oxford
Brovelli, S. (author)
Universita' degli Studi di Milano-Bicocca,University of Milano-Bicocca,University College London (UCL)
Montarnal, D. (author)
University of California
Meinardi, F. (author)
Universita' degli Studi di Milano-Bicocca,University of Milano-Bicocca
Cacialli, F. (author)
University College London (UCL)
Beljonne, David (author)
Universite de Mons
Albinsson, Bo, 1963 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Anderson, Harry L. (author)
University Of Oxford
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 (creator_code:org_t)
2014-02-14
2014
English.
In: Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 118:8, s. 4553-4566
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Conjugated polyrotaxanes jacketed with hole-transport groups have been synthesized from water-soluble polyrotaxanes consisting of a polyfluorene-alt-biphenylene (PFBP) conjugated polymer threaded through beta-cyclodextrin macrocycles. The hydroxyl groups of the oligosaccharides were efficiently functionalized with triphenylamine (TPA) so that every polyrotaxane molecule carries a coat of about 200 TPA units, forming a supramolecular coaxial structure. This architecture was characterized using a range of techniques, including small-angle X-ray scattering. Absorption of light by the TPA units results in excitation energy transfer (EET) and photoinduced electron transfer (ET) to the inner conjugated polymer core. These energy- and charge-transfer processes were explored by steady-state and time-resolved fluorescence spectroscopy, femtosecond transient absorption spectroscopy, and molecular modeling. The time-resolved measurements yielded insights into the heterogeneity of the TPA coat: those TPA units which are close to the central polymer core tend to undergo ET, whereas those on the outer surface of the polyrotaxane, far from the core, undergo EET. Sections of the backbone that are excited indirectly via EET tend to be more remote from the TPA units and thus are less susceptible to electron-transfer quenching. The rate of EET from the TPA units to the PFBP core was effectively modeled by taking account of the heterogeneity in the TPA-PFBP distance, using a distributed monopole approach. This work represents a new strategy for building and studying well-defined arrays of >100 covalently linked chromophores.

Subject headings

NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Keyword

ENERGY-TRANSFER
DERMOTT G
CHARGE-TRANSPORT
1995
WHITE
PHOTOSYNTHETIC BACTERIA
RSTER T
P269
P55
1948
ARCHIVES OF MICROBIOLOGY
ELECTROLUMINESCENCE
ANNALEN DER PHYSIK
P517
ATOM FORCE-FIELD
NATURE
ELECTRON-TRANSFER
V2
AEHELIN LA
V119
V374
1978
CYCLODEXTRIN
SUPRAMOLECULAR CONTROL
BINARY BLENDS
CONJUGATED POLYROTAXANES

Publication and Content Type

art (subject category)
ref (subject category)

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