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Diels-Alder reactivity of triisopropylsilyl ethynyl substituted acenes [data]

We investigated the Diels-Alder reaction of 6,13-bis(triisopropylsilyl)pentacene (1) with small dienophiles such as (bridged) dihydronaphthalenes/cyclohexenes that yielded adducts at the central ring, the other dienophiles predominantly or exclusively attacked the unsubstituted off-center ring. The...

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Main Authors: Jester, Fabian (Author) , Kaczun, Tobias (Author) , Maier, Steffen (Author) , Meiners, Paul (Author) , Weigold, Svenja (Author) , Rominger, Frank (Author) , Dreuw, Andreas (Author) , Freudenberg, Jan (Author) , Bunz, Uwe H. F. (Author)
Format: Database Research Data
Language:English
Published: Heidelberg Universität 2024-10-17
DOI:10.11588/DATA/HCEAB4
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Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.11588/DATA/HCEAB4
Verlag, kostenfrei, Volltext: https://heidata.uni-heidelberg.de/dataset.xhtml?persistentId=doi:10.11588/DATA/HCEAB4
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Author Notes:Fabian Jester, Tobias Kaczun, Steffen Maier, Paul Meiners, Svenja Weigold, Frank Rominger, Andreas Dreuw, Jan Freudenberg, Uwe H. F. Bunz
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Summary:We investigated the Diels-Alder reaction of 6,13-bis(triisopropylsilyl)pentacene (1) with small dienophiles such as (bridged) dihydronaphthalenes/cyclohexenes that yielded adducts at the central ring, the other dienophiles predominantly or exclusively attacked the unsubstituted off-center ring. The difference in regioselectivity was investigated by DFT calculations. Apart from dispersion interactions, it is due to the steric demand of the dienophiles, which need to fit in between the silylethynyl substituents to react at the central ring. Epoxynaphthalene adducts of 1 as well as its anthracene and tetracene congeners were deoxygenated, easily furnishing triarenobarrelenes with TIPS-ethynyl substituents at the bridge heads, attractive building blocks for porous solids and higher acene-based trimers.
Item Description:Gefördert durch: Deutsche Forschungsgemeinschaft (SFB): 1249, Deutsche Forschungsgemeinschaft: INST 40/575-1 FUGG, Deutsche Forschungsgemeinschaft: INST 35/1596-1 FUGG
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Physical Description:Online Resource
DOI:10.11588/DATA/HCEAB4

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