A pair of enantiomeric ligands, (2R,3R)-dibenzyl-2,3-bis(isonicotinoyloxy)succinate ((R,R)-L) and (2S,3S)-dibenzyl-2,3-bis(isonicotinoyloxy)succinate ((S,S)-L), are designed and synthesized. Seven copper (II) coordination polymers {[Cu((R,R)-L)Br (THF)] ⋅ CH CN} (1 a) and {[Cu((S,S)-L)Br (THF)] ⋅ CH CN} (1 b), {[Cu((R,R)-L)Cl (THF)] ⋅ CH CN} (2 a) and {[Cu((S,S)-L)Cl (THF)] ⋅ CH CN} (2 b), {[Cu((R,R)-L)(NO ) (CH CN)]} (3 a) and {[Cu((S,S)-L)(NO ) (CH CN)]} (3 b), {[Cu((R,R)-L) (CH CN) ](ClO ) ⋅ 3CH CN} (4) were obtained through the assemblies with CuBr , CuCl ⋅ 2H O, Cu(NO ) ⋅ 3H O, Cu(ClO ) ⋅ 6H O, respectively. Single-crystal X-ray diffraction and circular dichroism analysis demonstrate that 1 a-3 a, 1 b-3 b have a mono chiral one-dimensional (1D) chain-like spiral structure, while 4 have 1D chain-like structure whose metal centers have chiral propeller coordination environment. Ligand structure, anions and solvent systems have a regulatory effect on the formation of chiral helical structure. Further investigation has proved that 1 a can be used as circular dichroism spectrum probe for monitoring L-/D-cysteine and L-/D-penicillamine configuration and concentration in aqueous media based on ligand interchange mechanism.
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http://dx.doi.org/10.1002/asia.202200263 | DOI Listing |
Dalton Trans
December 2024
Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Jiangwan Campus, Fudan University, Shanghai 200438, China.
The phosphaguanidinate rare-earth-metal bis(aminobenzyl) complexes [(PhP)C(NCHPr-2,6)]Ln(CHCH NMe-) (Ln = Y(1-Y) and Lu(1-Lu)) were synthesized by the protonolysis of (PhP)[C(NHR)(NR)] (R = 2,6-(Pr)CH) with Ln(CHCHNMe-) (Ln = Y and Lu). Interestingly, the ring-opening rearrangement product [-MeNCHCHC(NCHPr-2,6)]Lu(CHCHNMe-)[O(CH)PPh] (2) was obtained when the acid-base reaction was carried out in THF solution at 60 °C for 36 h. Additionally, the trinuclear homometallic yttrium multimethyl/methylidene complex {[(PhP)C(NCHPr-2,6)]Y(μ-Me)}(μ-Me)(μ-CH) (3) was synthesized by the treatment of 1-Y with AlMe (2 equiv.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
Key Laboratory of Industrial Fermentation Microbiology, Ministry of Education, Tianjin 300457, PR China; Tianjin Key Laboratory of Industrial Microbiology, Tianjin 300457, PR China; College of Biotechnology, Tianjin University of Science and Technology, Tianjin 300457, PR China. Electronic address:
Soluble cytotoxic oligomers produced during the fibrillation of both α-synuclein (αS) and amyloid-β protein (Aβ) are key pathogenic factors in Parkinson's disease (PD) and Alzheimer's disease (AD). Reducing toxic oligomers by regulating the aggregation process of αS and Aβ is an important strategy for the treatment of PD and AD. Herein, tetrahydrofolic acid (THF) is found to accelerate amyloid fibrillization, decreases cytotoxic oligomers and suppresses their toxicity.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Department of Chemistry and Materials Science, College of Science, Nanjing Forestry University, Nanjing 210037, P. R. China.
Covalent-organic-framework (COF) materials with a designable periodic framework have been expected as a kind of promising anode material for potassium ion batteries (PIBs). However, these materials suffer seriously from low capacity, poor rate performance, and slow reaction kinetics during the K-storage process, significantly limiting their widespread applications. Herein, a three-dimensional (3D) COF material denoted as CN-COF with a high N content and defined configuration as well as a graphite-like layer stacking structure was developed as a promising anode to realize efficient 3D K-storage performance with enhanced interfacial stability and reaction kinetics via an electrolyte chemistry compatibility strategy.
View Article and Find Full Text PDFChemistry
December 2024
Departamento de Química Orgánica y Química Inorgánica, Instituto de Investigación Química "Andrés M. del Río" (IQAR), Universidad de Alcalá, Campus Universitario, Alcalá de Henares, Madrid, E-28805, Spain.
Literature on Group One organoelement chemistry is dominated by lithium, though sodium and potassium also feature prominently, whereas rubidium and caesium are rarely mentioned. With recent breakthroughs hinting that organoelement compounds of these two heavier metals can perform better than their lighter congeners in particular applications, important advantages could be missed unless complete sets of alkali metals are included in studies. Here, we report the synthesis and characterisation of a complete set of multi-alkali-metallated molecular compounds of the 1,3,5-tris[(4,6-dimethylpyridin-2-yl)aminomethyl]-2,4,6-triethylbenzene framework.
View Article and Find Full Text PDFChem Commun (Camb)
December 2024
Anhui Provincial Engineering Center for High Performance Biobased Nylon, School of Materials and Chemistry, Anhui Agricultural University, Hefei, Anhui, 230036, P. R. China.
Phenolic polymers with catechol groups easily undergo oxidative crosslinking. Through the incorporation of pendant amide groups, the thermal stability of linear phenolic polymers with catechol moieties was significantly improved with maintained antioxidation performance and solubility in THF after storing at 80 °C for 96 hours.
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