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Sökning: onr:"swepub:oai:research.chalmers.se:1ca4bb91-9f70-453b-a4c3-ed1016d3f5ec" > Norbornadiene-dihyd...

Norbornadiene-dihydroazulene conjugates

Kilde, Martin Drohse (författare)
Köpenhamns universitet,University of Copenhagen
Manso, Mads, 1991 (författare)
Köpenhamns universitet,University of Copenhagen,Chalmers tekniska högskola,Chalmers University of Technology
Ree, Nicolai (författare)
Köpenhamns universitet,University of Copenhagen
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Petersen, Anne Ugleholdt (författare)
Köpenhamns universitet,University of Copenhagen
Moth-Poulsen, Kasper, 1978 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Mikkelsen, Kurt V. (författare)
Köpenhamns universitet,University of Copenhagen
Nielsen, Mogens Brondsted (författare)
Köpenhamns universitet,University of Copenhagen
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 (creator_code:org_t)
2019
2019
Engelska.
Ingår i: Organic and Biomolecular Chemistry. - : Royal Society of Chemistry (RSC). - 1477-0539 .- 1477-0520. ; 17:33, s. 7735-7746
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The introduction of various photochromic units into the same molecule is an attractive approach for the development of novel molecular solar thermal (MOST) energy storage systems. Here, we present the synthesis and characterisation of a series of covalently linked norbornadiene/dihydroazulene (NBD/DHA) conjugates, using the Sonogashira coupling as the key synthetic step. Generation of the fully photoisomerized quadricyclane/vinylheptafulvene (QC/VHF) isomer was found to depend strongly on how the two units are connected - by linear conjugation (a para-phenylene bridge) or cross-conjugation (a meta-phenylene bridge) or by linking to the five- or seven-membered ring of DHA - as well as on the electronic character of another substituent group on the NBD unit. When the QC-VHF system could be reached, the QC-to-NBD back-reaction occurred faster than the VHF-to-DHA back-reaction, while the latter could be promoted simply by the addition of Cu(i) ions. The absence or presence of Cu(i) can thus be used to control whether heat releases should occur on different or identical time scales. The experimental findings were rationalized in a computational study by comparing natural transition orbitals (NTOs). Moreover, the calculations revealed an energy storage capacity of 106-110 kJ mol(-1) of the QC-VHF isomers, which is higher than the sum of the capacities of the individual, separate units. The major contribution to the energy storage relates to the energetic QC form, while the major contribution to the absorption of visible light originates from the DHA photochrome; some of the NBD-DHA conjugates had absorption onsets at 450 nm or beyond.

Ämnesord

NATURVETENSKAP  -- Fysik -- Atom- och molekylfysik och optik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Atom and Molecular Physics and Optics (hsv//eng)
NATURVETENSKAP  -- Kemi -- Teoretisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Theoretical Chemistry (hsv//eng)
NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)

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