For the first time, the tetrahedral diphosphorus complex [CpW(CO)(µ,η:η-P)] (Cp = CH) () is used as a connecter in supramolecular chemistry. The treatment of with Cu halides leads to the formation of the new one-dimensional (1D) linear polymers [Cu(µ-X){CpW(CO)(µ,η:η:η:η-P)}] {X = Cl (), Br (), I ()}. The coordination polymers (CPs) - are almost insoluble in organic solvents, thus, their P MAS-NMR spectra were recorded and found to be remarkably influenced by their solid-state structures. Additionally, we demonstrate that by reacting the Cp-substituted diphosphorus complex [Cp'W(CO)(µ,η:η-P)] {Cp' = CH{C(CH)}} () with CuBr, the unprecedented soluble 1D CP [Cu(µ-Br){Cp'W(CO)(µ,η:η:η:η-P)}] () is obtained. Furthermore, the reactions of with the Ag salts Ag[CFSO] and Ag[PF] result in the formation of the oligomeric dicationic species [Ag{CpW(CO)(µ,η:η:η-P)} {CpW(CO)(µ,η:η:η:η-P)}][X'] {X' = [CFSO] (), [PF] ()}.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853230 | PMC |
http://dx.doi.org/10.1002/ejic.201900580 | DOI Listing |
J Am Chem Soc
January 2025
Department of Chemistry, Texas A&M University, College Station, Texas 77843, United States.
Terminal metal-phosphorus (M-P) complexes are of significant contemporary interest as potential platforms for P-atom transfer (PAT) chemistry. Decarbonylation of metal-phosphaethynolate (M-PCO) complexes has emerged as a general synthetic approach to terminal M-P complexes. M-P complexes that are stabilized by strong M-P multiple bonds are kinetically persistent and isolable.
View Article and Find Full Text PDFOrganometallics
June 2024
Department of Chemistry, Texas A&M University, PO Box 30012, College Station, Texas 77842-3012, United States.
Photolyses of -Fe(CO)(As((CH) )As) ( = , 10; , 12; , 14) in the presence of PMe, or reactions of -[Fe(CO)(NO)(As((CH) )As)] BF and -BuN Cl, afford the air stable title complexes As((CH) )As (-) in 79-34% yields. With , the , and , isomers are separable and each is crystallographically characterized. With ,, the isomers rapidly interconvert by homeomorphic isomerization, but each crystallizes (contrathermodynamically) as an , isomer.
View Article and Find Full Text PDFChem Asian J
January 2024
Department of Chemistry, Indian Institute of Science Education and Research (IISER) Tirupati, Tirupati, 517507, India.
The stability and reactivity studies of heavier di-atomic group-15 congeners of alkynes, e. g., the di-phosphorus (P≡P) compounds have been the topic of huge interest because of their contrasting transient properties and lower stability compared to those of the stable molecular di-nitrogen (N≡N).
View Article and Find Full Text PDFInorg Chem
August 2023
Department of Chemistry and Biochemistry, Materials Science Institute, Knight Campus for Accelerating Scientific Impart, and Institute of Molecular Biology, University of Oregon, Eugene, Oregon, 97403-1253, United States.
We investigated the differential oxidative and nucleophilic chemistry of reactive sulfur and oxygen anions (SSNO, SNO, NO, S, and HS) using the simple reducing electrophile PPhCl. In the case of SSNO reacting with PPhCl, a complex mixture of mono and diphosphorus products is formed exclusively in the P(V) oxidation state. We found that the phosphine stoichiometry dictates selectivity for oxidation to P=S/P=O products or transformation to P species.
View Article and Find Full Text PDFChemistry
October 2023
University of Regensburg, Institute of Inorganic Chemistry, 93040, Regensburg, Germany.
The reaction between diphosphorus derivatives [( Im )P (Dipp)]OTf (1[OTf]) and [( Im )P (Dipp)Cl] (1[Cl]) with the cyclotetraphosphido cobalt complex [K(18c-6)][(PHDI)Co(η -cyclo-P )] (2) leads to the formation of complex [(PHDI)Co{η -cyclo-P (Dipp)( Im )}] (3), which features an unusual hexaphosphido ligand [ Im =4,5-dichloro-1,3-bis(2,6-diisopropylphenyl)imidazol-2-yl, Dipp=2,6-diisopropylphenyl, 18c-6=18-crown-6, PHDI=bis(2,6-diisopropylphenyl)phenanthrene-9,10-diimine]. Complex 3 was obtained as a crystalline material with a moderate yield at low temperature. Upon exposure to ambient temperature, compound 3 slowly transforms into two other compounds, [K(18c-6)][(PHDI)Co(η -P Dipp)] (4) and [(PHDI)Co{cyclo-P ( Im )}] (5).
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!