A Heteroleptic Ferrous Complex with Mesoionic Bis(1, 2, 3‐triazol‐5‐ylidene) Ligands: Taming the MLCT Excited State of Iron(II). Issue 9 (11th December 2014)
- Record Type:
- Journal Article
- Title:
- A Heteroleptic Ferrous Complex with Mesoionic Bis(1, 2, 3‐triazol‐5‐ylidene) Ligands: Taming the MLCT Excited State of Iron(II). Issue 9 (11th December 2014)
- Main Title:
- A Heteroleptic Ferrous Complex with Mesoionic Bis(1, 2, 3‐triazol‐5‐ylidene) Ligands: Taming the MLCT Excited State of Iron(II)
- Authors:
- Liu, Yizhu
Kjær, Kasper S.
Fredin, Lisa A.
Chábera, Pavel
Harlang, Tobias
Canton, Sophie E.
Lidin, Sven
Zhang, Jianxin
Lomoth, Reiner
Bergquist, Karl‐Erik
Persson, Petter
Wärnmark, Kenneth
Sundström, Villy - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Strongly σ‐donating N‐heterocyclic carbenes (NHCs) have revived research interest in the catalytic chemistry of iron, and are now also starting to bring the photochemistry and photophysics of this abundant element into a new era. In this work, a heteroleptic Fe<sup>II</sup> complex (<bold>1</bold>) was synthesized based on sequentially furnishing the Fe<sup>II</sup> center with the benchmark 2, 2′‐bipyridine (bpy) ligand and the more strongly σ‐donating mesoionic ligand, 4, 4′‐bis(1, 2, 3‐triazol‐5‐ylidene) (btz). Complex <bold>1</bold> was comprehensively characterized by electrochemistry, static and ultrafast spectroscopy, and quantum chemical calculations and compared to [Fe(bpy)<sub>3</sub>](PF<sub>6</sub>)<sub>2</sub> and (TBA)<sub>2</sub>[Fe(bpy)(CN)<sub>4</sub>]. Heteroleptic complex <bold>1</bold> extends the absorption spectrum towards longer wavelengths compared to a previously synthesized homoleptic Fe<sup>II</sup> NHC complex. The combination of the mesoionic nature of btz and the heteroleptic structure effectively destabilizes the metal‐centered (MC) states relative to the triplet metal‐to‐ligand charge transfer (<sup>3</sup>MLCT) state in <bold>1</bold>, rendering it a lifetime of 13 ps, the longest to date of a photochemically stable Fe<sup>II</sup> complex. Deactivation of the <sup>3</sup>MLCT state is proposed to proceed via the <sup>3</sup>MC state that strongly couples with the<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Strongly σ‐donating N‐heterocyclic carbenes (NHCs) have revived research interest in the catalytic chemistry of iron, and are now also starting to bring the photochemistry and photophysics of this abundant element into a new era. In this work, a heteroleptic Fe<sup>II</sup> complex (<bold>1</bold>) was synthesized based on sequentially furnishing the Fe<sup>II</sup> center with the benchmark 2, 2′‐bipyridine (bpy) ligand and the more strongly σ‐donating mesoionic ligand, 4, 4′‐bis(1, 2, 3‐triazol‐5‐ylidene) (btz). Complex <bold>1</bold> was comprehensively characterized by electrochemistry, static and ultrafast spectroscopy, and quantum chemical calculations and compared to [Fe(bpy)<sub>3</sub>](PF<sub>6</sub>)<sub>2</sub> and (TBA)<sub>2</sub>[Fe(bpy)(CN)<sub>4</sub>]. Heteroleptic complex <bold>1</bold> extends the absorption spectrum towards longer wavelengths compared to a previously synthesized homoleptic Fe<sup>II</sup> NHC complex. The combination of the mesoionic nature of btz and the heteroleptic structure effectively destabilizes the metal‐centered (MC) states relative to the triplet metal‐to‐ligand charge transfer (<sup>3</sup>MLCT) state in <bold>1</bold>, rendering it a lifetime of 13 ps, the longest to date of a photochemically stable Fe<sup>II</sup> complex. Deactivation of the <sup>3</sup>MLCT state is proposed to proceed via the <sup>3</sup>MC state that strongly couples with the singlet ground state.</p> </abstract> … (more)
- Is Part Of:
- Chemistry. Volume 21:Issue 9(2015)
- Journal:
- Chemistry
- Issue:
- Volume 21:Issue 9(2015)
- Issue Display:
- Volume 21, Issue 9 (2015)
- Year:
- 2015
- Volume:
- 21
- Issue:
- 9
- Issue Sort Value:
- 2015-0021-0009-0000
- Page Start:
- 3628
- Page End:
- 3639
- Publication Date:
- 2014-12-11
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201405184 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4017.xml