Fabian, Kai H. H. ; Lindner, Hans-Jörg ; Nimmerfroh, Norbert ; Hafner, Klaus (2022)
Synthesis and Properties of the First [4.4]Ferrocenophane-1,3,15,17-tetrayne.
In: Angewandte Chemie International Edition, 2001, 40 (18)
doi: 10.26083/tuprints-00022368
Article, Secondary publication, Publisher's Version
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Angew Chem Int Ed - 2001 - Fabian - Synthesis and Properties of the First 4 4 Ferrocenophane‐1 3 15 17‐tetrayne.pdf Copyright Information: In Copyright. Download (674kB) |
| Item Type: | Article |
|---|---|
| Type of entry: | Secondary publication |
| Title: | Synthesis and Properties of the First [4.4]Ferrocenophane-1,3,15,17-tetrayne |
| Language: | English |
| Date: | 2022 |
| Place of Publication: | Darmstadt |
| Year of primary publication: | 2001 |
| Publisher: | Wiley |
| Journal or Publication Title: | Angewandte Chemie International Edition |
| Volume of the journal: | 40 |
| Issue Number: | 18 |
| DOI: | 10.26083/tuprints-00022368 |
| Corresponding Links: | |
| Origin: | Secondary publication service |
| Abstract: | Building butadiyne bridges: The kinetically stabilized 1,1′-diethynylferrocene, readily prepared from the pentafulvenoid allene 1, can be transformed into the [4.4]ferrocenophane 2 by oxidative coupling. This compound exhibits a remarkably symmetrical structure in which the electrons are delocalized through the butadiyne bridges; in the crystalline state 2 exists in a helical-chiral conformation. |
| Status: | Publisher's Version |
| URN: | urn:nbn:de:tuda-tuprints-223685 |
| Classification DDC: | 500 Science and mathematics > 540 Chemistry |
| Divisions: | 07 Department of Chemistry > Clemens-Schöpf-Institut > Organ Chemistry |
| Date Deposited: | 28 Nov 2022 09:05 |
| Last Modified: | 21 Apr 2023 11:38 |
| URI: | https://tuprints.ulb.tu-darmstadt.de/id/eprint/22368 |
| PPN: | 507137620 |
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