The synthesis and crystal structure of the multidentate PPN ligand 2-[bis(diisopropylphosphanyl)methyl]-6-methylpyridine (L), CHNP, are described. In the isostructural tetrahedral Fe and Co complexes of type LMCl (M = Fe, Co), namely {2-[bis(diisopropylphosphanyl)methyl]-6-methylpyridine-κP,N}dichloridoiron(II), [FeCl(CHNP)], and {2-[bis(diisopropylphosphanyl)methyl]-6-methylpyridine-κP,N}dichloridocobalt(II), [CoCl(CHNP)], the ligand adopts a bidentate P,N-coordination, whereas in the case of the octahedral Mn complex {2-[bis(diisopropylphosphanyl)methyl]-6-methylpyridine-κP,P'}bromidotricarbonylmanganese(I), [MnBr(CHNP)(CO)], the ligand coordinates via both P atoms to the metal centre.
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http://dx.doi.org/10.1107/S205322961701261X | DOI Listing |
Org Biomol Chem
December 2024
Shenzhen Key Laboratory of Small Molecule Drug Discovery and Synthesis, Department of Chemistry, and Medi-Pingshan, Southern University of Science and Technology, 1088 Xueyuan Road, Shenzhen 518055, China.
A new type of ferrocenyl P,P,N,N,O-ligand has been developed through a one-step transformation. This represents a rare example of a ligand containing both chiral bisphosphine and diamine groups suitable for ruthenium-catalyzed asymmetric hydrogenation. Its ruthenium complex can be directly prepared by stirring the ligand and [Ru(benzene)Cl] at 90 °C in DMF for 4 hours.
View Article and Find Full Text PDFInt J Mol Sci
October 2024
Faculty of Chemistry, Lomonosov Moscow State University, Lenin Hills, 1, Bld. 3, 119991 Moscow, Russia.
A comparative study of the copolymerization of racemic propylene oxide (PO) with CO catalyzed by racemic (salcy)CoX (salcy = ,'-bis(3,5-di--butylsalicylidene)-1,2-diaminocyclohexane; X = perfluorobenzoate (OBzF) or 2,4-dinitrophenoxy (DNP)) in the presence of a [PPN]Cl ([PPN] = bis(triphenylphosphine)iminium) cocatalyst is performed in bulk at 21 °C and a 2.5 MPa pressure of CO. The increase in the nucleophilicity of an attacking anion results in the increase in the copolymerization rate.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Shanghai Key Laboratory of Functional Materials Chemistry, Feringa Nobel Prize Scientist Joint Research Center, Institute of Fine Chemicals, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Photodynamic therapy (PDT) is a clinically approved therapeutic modality that has shown great potential for cancer treatment. However, there exist two major problems hindering PDT applications: the nonspecific phototoxicity requiring patients to stay in dark post-PDT, and the limited photodynamic efficiency. Herein, we report a photo-triggered porphyrin polyelectrolyte nanoassembling (photo-triggered PPN) strategy, in which porphyrin photosensitizer and photoswitchable energy accepter are assembled into polyelectrolyte micelles by a combined force of charge interaction and metal-ligand coordination.
View Article and Find Full Text PDFNat Prod Res
October 2024
Department of Pharmacy, Bangabandhu Sheikh Mujibur Rahman Science and Technology University, Gopalganj, Bangladesh.
Nanoscale
October 2024
Centro de Química Estrutural, Institute of Molecular Sciences, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001, Lisboa, Portugal.
The synthesis of a high nuclear (CuNa) complex 1 the self-assembly of copper(II) phenylsilsesquioxane induced by complexation with bis(triphenylphosphine)iminium chloride (PPNCl) was successfully achieved. This complex, which includes two bis(triphenylphosphine)iminium PPN cations, represents the first example of a metallasilsesquioxane/phosphazene compound. The CuNa-silsesquioxane cage demonstrates a nontrivial combination of two pairs of Si-cyclic/Si-acyclic silsesquioxane ligands and a fusion of two SiCuNa fragments, combined the central ninth copper ion.
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