Unusual coordination mode for 1,3-diphosphete ligands towards a Cr-Cr quintuple bond complex

Elsayed Moussa, M. and Rummel, E. -m. and Balazs, G. and Riesinger, C. and Noor, A. and Kempe, R. and Scheer, M. (2023) Unusual coordination mode for 1,3-diphosphete ligands towards a Cr-Cr quintuple bond complex. CHEMICAL COMMUNICATIONS, 59 (55). pp. 8588-8591. ISSN 1359-7345, 1364-548X

Full text not available from this repository. (Request a copy)

Abstract

The reaction of (LCrCrL)-Cr-5 (L = N2C25H29, 1) with the phosphaalkynes R-C P (R = tBu, Me, Ad) yields the neutral dimerisation compounds [L2Cr2(mu,eta(1): eta(1): eta(2): eta(2)-P2C2R2)] (R = tBu (2), Me (3)) and the tetrahedrane complex [L2Cr2(mu,eta(2): eta(2)-P = CAd)] (4). The 1,3-diphosphete ligands in complexes 2 and 3 are the first to possess this structural feature spanned over a metal-metal multiple bond, while the slightly bigger adamantyl phosphaalkyne remains a monomer in 4 with a side-on coordination mode.

Item Type: Article
Uncontrolled Keywords: PHOSPHORUS-COMPOUNDS; PHOSPHAALKYNE; ACTIVATION; REACTIVITY; CHEMISTRY; PCME;
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie > Chair Prof. Dr. Manfred Scheer
Depositing User: Dr. Gernot Deinzer
Date Deposited: 10 Mar 2024 15:09
Last Modified: 10 Mar 2024 15:09
URI: https://pred.uni-regensburg.de/id/eprint/59630

Actions (login required)

View Item View Item