Alkyne Cyclotrimerisation, Acyclic Oligomerisation, and Transfer Hydrogenation Catalysed by a Titanium(IV) Phosphinoaryloxide Complex and its Redox Chemistry.

Bibliographic Details
Title: Alkyne Cyclotrimerisation, Acyclic Oligomerisation, and Transfer Hydrogenation Catalysed by a Titanium(IV) Phosphinoaryloxide Complex and its Redox Chemistry.
Authors: Steiner, Matthias R.1 (AUTHOR), Jouikov, Viatcheslav V.2 (AUTHOR), Fischer, Roland C.3 (AUTHOR), Uher, Johanna M.1 (AUTHOR), y Medina, Isabel‐Maria Ramirez4 (AUTHOR), Hlina, Johann A.5 (AUTHOR) johann.hlina@uni-graz.at
Source: European Journal of Inorganic Chemistry. Jul2024, Vol. 27 Issue 19, p1-10. 10p.
Subject Terms: *TITANIUM, *TRANSFER hydrogenation, *ELECTRON paramagnetic resonance spectroscopy, *OPTICAL spectroscopy, *OXIDATION-reduction reaction, *ELEMENTAL analysis
Abstract: The reaction of sodium 2,4‐di‐tert‐butyl‐6‐(diphenylphos‐phino)phenolate (1, NaOArP) with TiIVCl4(THF)2 in a 2 : 1 molar ratio yielded TiIV(OArP)2Cl2 (2). The reduction of 2 with magnesium gave the dimeric titanium(III) compound [TiIII(OArP)2Cl]2 (3). In the presence of magnesium, compound 2 was found to catalyse the cyclotrimerization, acyclic oligomerisation, and hydrogenation of terminal alkynes. The complexes were characterised by single‐crystal X‐ray diffraction, optical spectroscopy, elemental analysis, and NMR or EPR spectroscopy, respectively. [ABSTRACT FROM AUTHOR]
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Database: Academic Search Complete
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ISSN:14341948
DOI:10.1002/ejic.202300791
Published in:European Journal of Inorganic Chemistry
Language:English