Nitrogen activation and cleavage by a multimetallic uranium complex. Issue 27 (30th June 2022)
- Record Type:
- Journal Article
- Title:
- Nitrogen activation and cleavage by a multimetallic uranium complex. Issue 27 (30th June 2022)
- Main Title:
- Nitrogen activation and cleavage by a multimetallic uranium complex
- Authors:
- Keener, Megan
Fadaei-Tirani, Farzaneh
Scopelliti, Rosario
Zivkovic, Ivica
Mazzanti, Marinella - Abstract:
- Abstract : Combinations of ligands were used to tune UNU complexes yielding a U(iii )/U(iii ) nitride, which activates N2 . Parallel N2 reduction pathways were identified, leading to the first example of N2 cleavage by U without external alkali reducing agents. Abstract : Multimetallic-multielectron cooperativity plays a key role in the metal-mediated cleavage of N2 to nitrides (N 3− ). In particular, low-valent uranium complexes coupled with strong alkali metal reducing agents can lead to N2 cleavage, but often, it is ambiguous how many electrons are transferred from the uranium centers to cleave N2 . Herein, we designed new dinuclear uranium nitride complexes presenting a combination of electronically diverse ancillary ligands to promote the multielectron transformation of N2 . Two heteroleptic diuranium nitride complexes, [K{U IV (OSi(O t Bu)3 )(N(SiMe3 )2 )2 }2 (μ-N)] (1 ) and [Cs{U IV (OSi(O t Bu)3 )2 (N(SiMe3 )2 )}2 (μ-N)] (3-Cs ), containing different combinations of OSi(O t Bu)3 and N(SiMe3 )2 ancillary ligands, were synthesized. We found that both complexes could be reduced to their U(iii )/U(iv ) analogues, and the complex, [K2 {U IV/III (OSi(O t Bu)3 )2 (N(SiMe3 )2 )}2 (μ-N)] (6-K ), could be further reduced to a putative U(iii )/U(iii ) species that is capable of promoting the 4e − reduction of N2, yielding the N2 4− complex [K3 {U V (OSi(O t Bu)3 )2 (N(SiMe3 )2 )}2 (μ-N)(μ-η 2 :η 2 -N2 )], 7 . Parallel N2 reduction pathways were also identified, leading to theAbstract : Combinations of ligands were used to tune UNU complexes yielding a U(iii )/U(iii ) nitride, which activates N2 . Parallel N2 reduction pathways were identified, leading to the first example of N2 cleavage by U without external alkali reducing agents. Abstract : Multimetallic-multielectron cooperativity plays a key role in the metal-mediated cleavage of N2 to nitrides (N 3− ). In particular, low-valent uranium complexes coupled with strong alkali metal reducing agents can lead to N2 cleavage, but often, it is ambiguous how many electrons are transferred from the uranium centers to cleave N2 . Herein, we designed new dinuclear uranium nitride complexes presenting a combination of electronically diverse ancillary ligands to promote the multielectron transformation of N2 . Two heteroleptic diuranium nitride complexes, [K{U IV (OSi(O t Bu)3 )(N(SiMe3 )2 )2 }2 (μ-N)] (1 ) and [Cs{U IV (OSi(O t Bu)3 )2 (N(SiMe3 )2 )}2 (μ-N)] (3-Cs ), containing different combinations of OSi(O t Bu)3 and N(SiMe3 )2 ancillary ligands, were synthesized. We found that both complexes could be reduced to their U(iii )/U(iv ) analogues, and the complex, [K2 {U IV/III (OSi(O t Bu)3 )2 (N(SiMe3 )2 )}2 (μ-N)] (6-K ), could be further reduced to a putative U(iii )/U(iii ) species that is capable of promoting the 4e − reduction of N2, yielding the N2 4− complex [K3 {U V (OSi(O t Bu)3 )2 (N(SiMe3 )2 )}2 (μ-N)(μ-η 2 :η 2 -N2 )], 7 . Parallel N2 reduction pathways were also identified, leading to the isolation of N2 cleavage products, [K3 {U VI (OSi(O t Bu)3 )2 (N(SiMe3 )2 )(N)}(μ-N)2 {U V (OSi(O t Bu)3 )2 (N(SiMe3 )2 )}]2, 8, and [K4 {(OSi(O t Bu)3 )2 U V )(N)}(μ-NH)(μ-κ 2 :C, N-CH2 SiMe2 NSiMe3 )-{U V (OSi(O t Bu)3 )2 ][K(N(SiMe3 )2 ]2, 9 . These complexes provide the first example of N2 cleavage to nitride by a uranium complex in the absence of reducing alkali metals. … (more)
- Is Part Of:
- Chemical science. Volume 13:Issue 27(2022)
- Journal:
- Chemical science
- Issue:
- Volume 13:Issue 27(2022)
- Issue Display:
- Volume 13, Issue 27 (2022)
- Year:
- 2022
- Volume:
- 13
- Issue:
- 27
- Issue Sort Value:
- 2022-0013-0027-0000
- Page Start:
- 8025
- Page End:
- 8035
- Publication Date:
- 2022-06-30
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/SC ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2sc02997a ↗
- Languages:
- English
- ISSNs:
- 2041-6520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.490000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22567.xml