Sunlight photolysis of cyclopentadienyl–tethered titanium(iv) permethyltitanocene chlorides

0532837 - ÚFCH JH 2021 RIV CH eng J - Článek v odborném periodiku
Pinkas, Jiří - Kubišta, Jiří - Mach, Karel - Gyepes, Robert - Horáček, Michal
Sunlight photolysis of cyclopentadienyl–tethered titanium(iv) permethyltitanocene chlorides.
Journal of Organometallic Chemistry. Roč. 927, NOV 2020 (2020), č. článku 121536. ISSN 0022-328X. E-ISSN 1872-8561
Institucionální podpora: RVO:61388955
Klíčová slova: Density functional calculation * Isomerization * Photolysis * Solid-state structures * Titanium
Obor OECD: Physical chemistry
Impakt faktor: 2.369, rok: 2020
Způsob publikování: Omezený přístup

Solutions of permethylcyclopentadienyl-tethered titanium(IV) chlorides incorporating one double bond in their tethers were exposed in glass vessels to sunlight, which triggered their photolytical reactions providing mixtures of products. Although the formation of several different products was apparent from 1H NMR spectra, only a single product could be identified in the crude reaction mixtures. This product was dicyclopentadiene [C10Me10], which arose from the recombination of the generally photodissociated C5Me5 radical. Amongst products that contained titanium, three complexes (3a, 3b and 4a) could be isolated after employing fractional crystallization and these complexes were characterized. The mechanism of 3a formation involves photodissociation of one η5-C5Me5 ligand from the parent complex, complemented by chlorine abstraction from another reactant molecule. Complexes 3b and 4a become formed via tether rearrangement, which starts with dissociating the tether Ti–C bond and is followed by rotating the tether, reattaching it subsequently through its available radical terminus.
Trvalý link: http://hdl.handle.net/11104/0311221