Alkyne Cyclotrimerisation, Acyclic Oligomerisation, and Transfer Hydrogenation Catalysed by a Titanium(IV) Phosphinoaryloxide Complex and its Redox Chemistry.
Title: | Alkyne Cyclotrimerisation, Acyclic Oligomerisation, and Transfer Hydrogenation Catalysed by a Titanium(IV) Phosphinoaryloxide Complex and its Redox Chemistry. |
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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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Items | – Name: Title Label: Title Group: Ti Data: Alkyne Cyclotrimerisation, Acyclic Oligomerisation, and Transfer Hydrogenation Catalysed by a Titanium(IV) Phosphinoaryloxide Complex and its Redox Chemistry. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Steiner%2C+Matthias+R%2E%22">Steiner, Matthias R.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jouikov%2C+Viatcheslav+V%2E%22">Jouikov, Viatcheslav V.</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fischer%2C+Roland+C%2E%22">Fischer, Roland C.</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Uher%2C+Johanna+M%2E%22">Uher, Johanna M.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22y+Medina%2C+Isabel‐Maria+Ramirez%22">y Medina, Isabel‐Maria Ramirez</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hlina%2C+Johann+A%2E%22">Hlina, Johann A.</searchLink><relatesTo>5</relatesTo> (AUTHOR)<i> johann.hlina@uni-graz.at</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Inorganic+Chemistry%22">European Journal of Inorganic Chemistry</searchLink>. Jul2024, Vol. 27 Issue 19, p1-10. 10p. – Name: Subject Label: Subject Terms Group: Su Data: *<searchLink fieldCode="DE" term="%22TITANIUM%22">TITANIUM</searchLink><br />*<searchLink fieldCode="DE" term="%22TRANSFER+hydrogenation%22">TRANSFER hydrogenation</searchLink><br />*<searchLink fieldCode="DE" term="%22ELECTRON+paramagnetic+resonance+spectroscopy%22">ELECTRON paramagnetic resonance spectroscopy</searchLink><br />*<searchLink fieldCode="DE" term="%22OPTICAL+spectroscopy%22">OPTICAL spectroscopy</searchLink><br />*<searchLink fieldCode="DE" term="%22OXIDATION-reduction+reaction%22">OXIDATION-reduction reaction</searchLink><br />*<searchLink fieldCode="DE" term="%22ELEMENTAL+analysis%22">ELEMENTAL analysis</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: 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] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of European Journal of Inorganic Chemistry is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ejic.202300791 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 10 StartPage: 1 Subjects: – SubjectFull: TITANIUM Type: general – SubjectFull: TRANSFER hydrogenation Type: general – SubjectFull: ELECTRON paramagnetic resonance spectroscopy Type: general – SubjectFull: OPTICAL spectroscopy Type: general – SubjectFull: OXIDATION-reduction reaction Type: general – SubjectFull: ELEMENTAL analysis Type: general Titles: – TitleFull: Alkyne Cyclotrimerisation, Acyclic Oligomerisation, and Transfer Hydrogenation Catalysed by a Titanium(IV) Phosphinoaryloxide Complex and its Redox Chemistry. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Steiner, Matthias R. – PersonEntity: Name: NameFull: Jouikov, Viatcheslav V. – PersonEntity: Name: NameFull: Fischer, Roland C. – PersonEntity: Name: NameFull: Uher, Johanna M. – PersonEntity: Name: NameFull: y Medina, Isabel‐Maria Ramirez – PersonEntity: Name: NameFull: Hlina, Johann A. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: Jul2024 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 14341948 Numbering: – Type: volume Value: 27 – Type: issue Value: 19 Titles: – TitleFull: European Journal of Inorganic Chemistry Type: main |
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