The reactions of diselenophosphates, [dsep, (RO)2PSe2-; R = Et, (n)Pr and (i)Pr] with cadmium(II) and mercury(II) perchlorates in a 2 : 1 molar ratio formed compounds of stoichiometry M[Se2P(OR)2]2{M = Cd, R = Et (1), (n)Pr (2), (i)Pr (3); Hg, Et(4), (n)Pr (5), (i)Pr (6)}, and with zinc(II) perchlorates, chalcogen centered tetranuclear clusters, [Zn4(micro4-E){Se2P(OR)2}6]{E = Se, R = Et (7), (n)Pr (8), (i)Pr (9); E = O, R = Et (10), (n)Pr (11), (i)Pr (12)} were formed. All these complexes have been characterized with the help of analytical data, X-ray crystallography (1, 3, 6, 10, 11 and 12), and FAB-mass spectrometry (7-12). Compound 1 is a linear double-chain polymer, in which each pair of Cd atoms is bridged by two dsep ligands; the mercury 6 polymer has a helical chain structure, in which two Hg atoms are bridged by one dsep ligand, and the other ligand chelates the Hg atom. The chelating dsep ligands lie on either side of the helical chain. Compound 3 exists as a dimer in which two cadmium atoms are connected by two bridging dsep ligands, and each cadmium atom is further chelated by a dsep ligand. The metal atoms in 1, 3 and 6 are each coordinated by four selenium atoms in a distorted tetrahedral geometry. Clusters 10-12 have tetrahedral array of zinc atoms with an oxygen atom in the center with edge-bridging dsep ligands. Positive FAB-mass spectra support the formation of selenium-centered clusters,7-9, of which the cluster 8 was structurally confirmed earlier. The solution state behavior of compounds 1-12 has been studied by using multinuclear NMR spectroscopy. Dimer 3 in CD2Cl2 showed monomer-dimer exchange equilibrium in the temperature range 20 to -90 degrees C and the free energy of activation is calculated from the coalescence temperature as DeltaG++(223 K)= 38.5 kJ mol(-1). Polymer undergoes depolymerization in CDCl3 and exhibits monomer-dimer exchange equilibrium in the temperature range 20 to -60 degrees C.
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http://dx.doi.org/10.1039/b510728h | DOI Listing |
Chemistry
December 2024
Department of Chemistry, Central University of Punjab, Bathinda, 151401, India.
The heterometallic [Ag(I)/Fe(II)] molecular electrocatalysts for hydrogen production were introduced here to recognize the mutual role of metallic nuclearity and ligand engineering. A series of ferrocenyl dithiophosphonate stabilized mononuclear [Ag(PPh){SPFc(OR)}] {where R=Me (1), Et (2), Pr (3), Pr (4), Amyl (5); Fc=Fe (ɳ-CH) (ɳ-CH)} and dinuclear [Ag(PPh){SPFc(OR}] {where R=Et (2 a), and Pr (3 a)} complexes were synthesized and characterized by SCXRD, NMR (P and H), ESI-MS, UV-Vis, and FT-IR spectroscopy. The comparative electrocatalytic HER behavior of 1-5 and 2 a-3 a showed effective current density of 1 mA/cm with overpotentials ranging from 772 to 991 mV, demonstrating the influence of extended and branched carbon chains in dithiophosphonates and metallic (mono-/di-) nuclearity, which correlates with documented tetra-nuclear [Ag(SPFc(OPr)], 6.
View Article and Find Full Text PDFCell Mol Life Sci
February 2024
Center for Genomic Regulation (CRG), Barcelona Institute for Science and Technology (BIST), Barcelona, Spain.
In hormone-responsive breast cancer cells, progesterone (P4) has been shown to act via its nuclear receptor (nPR), a ligand-activated transcription factor. A small fraction of progesterone receptor is palmitoylated and anchored to the cell membrane (mbPR) forming a complex with estrogen receptor alpha (ERα). Upon hormone exposure, either directly or via interaction with ERα, mbPR activates the SRC/RAS/ERK kinase pathway leading to phosphorylation of nPR by ERK.
View Article and Find Full Text PDFACS Catal
November 2023
Institute of Applied Synthetic Chemistry, TU Wien, Getreidemarkt 9/163-AC, A-1060 Wien, Austria.
Two bench-stable Fe(II) alkyl complexes [Fe(κPCP-PCP-Pr)(CO)(R)] (R = CHCHCH, CH) were obtained by the treatment of [Fe(κPCP-PCP-Pr)(CO)(H)] with NaNH and subsequent addition of CHCHCHBr and CHI, respectively. The reaction proceeds via the anionic Fe(0) intermediate Na[Fe(κPCP-PCP-Pr)(CO)]. The catalytic performance of both alkyl complexes was investigated for the transfer hydrogenation of terminal and internal alkynes utilizing PhSiH and PrOH as a hydrogen source.
View Article and Find Full Text PDFInt J Mol Sci
October 2022
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, 31 Leninsky Prosp., 119071 Moscow, Russia.
A new series of compounds based on perbrominated disubstituted sulfonium derivatives of the -decaborate anion (-BuN)[2-BBrSR] (R = -Pr, -Pr, -Bu, -CH, -CH, -CH) was obtained, characterised by modern physicochemical methods of analysis. According to the results of an X-ray diffraction study, some of the anions and solvate molecules were disordered. The cations (-BuN) and anions [2-BBrSR] were associated via C-H…Br and H…H contacts.
View Article and Find Full Text PDFJ Am Chem Soc
October 2022
Department of Chemistry, Brandeis University, 415 South Street, Waltham, Massachusetts 02453, United States.
Azobispyrazole, 4pzMe-5pzH, derivatives with small terminal substituents (Me, Et, -Pr, and -Pr) are reported to undergo facile reversible photoswitching in condensed phases at room temperature, exhibiting unprecedentedly large effective light penetration depths (1400 μm of UV at 365 nm and 1400 μm of visible light at 530 nm). These small photoswitches exhibit crystal-to-liquid phase transitions upon UV irradiation, which increases the overall energy storage density of this material beyond 300 J/g that is similar to the specific energy of commercial Na-ion batteries. The impact of heteroarene design, the presence of methyl substituents, and the terminal functional groups is explored for both condensed-phase switching and energy storage.
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